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The 25th
Conference of the Egyptian Society for Medical Microbiology
1
The 25th
Conference of the Egyptian Society
for Medical Microbiology (ESMM)
Infection, Prevention and
Control; the Role of Microbiology
18th
April 2019
Helnan Dreamland Hotel. 6th
October. Giza
Program &
Abstract Book
Announcement
We have the pleasure to announce that the EJMM had been
published on the Google scholar link.
For Online Submission Use This Website:
www.ejmm-eg.com/e
The 25th
Conference of the Egyptian Society for Medical Microbiology
2
Welcome Message
On behalf of the Egyptian Society for Medical Microbiology
(ESMM), we have the pleasure to welcome you to share the activities of
the 25th Annual ESMM Conference.
The conference theme "Infection, Prevention and Control; the Role of
Microbiology" was selected to express the real need for updating our
knowledge, understanding and following up the enormous development
and the latest recent advances in treatment of some vital problems we are
facing in our microbiology practice.
Also we have the pleasure to meet several eminent guest speakers who
will focus on recent advances in infection control, and the problem of
drug resistance.
Many of the eminent scientists, both the leading generation and the
young promising researchers, are meeting to communicate and exchange
ideas and thoughts that will surely find the proper approaches for solving
medical problems and to celebrate our traditional annual meeting of
almost all microbiologists and immunologists in our beloved Egypt.
The scientific program covers about 30 topics including plenary
lectures and research oral presentations delivered by distinguished
professors, in addition to poster presentations.
We are looking forward to meeting you in the conference
participating in its activities to make it a successful and fruitful one.
President of ESSM President of the Conference
Prof. Samira Shoeb Prof. A. Ashraf Wegdan
Prof. Ahmed Omar Shafeik
The 25th
Conference of the Egyptian Society for Medical Microbiology
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ESMM BOARD
President Prof. Samira Shoeb
Treasurer Prof. Ahmed Ashraf Wegdan
Secretary General Prof. Ahmed Amer Mossaad
Members Prof. Ahmed Omar Shafeik
Prof. Ahmed Sadek
Prof. Ahmed Saeed Osman
Prof. Ayman Allam
Prof. Mohamed Sherif
Prof. Rasha Bassyouni
Scientific Committee
Prof. Dr. Ahmed Amer Mossaad
Prof. Dr. Ahmed Ashraf Wegdan
Prof. Dr. Ahmed Omar Shafeik
Prof. Dr. Azza Al-Sharkawy
Prof. Dr. Ensaf Alazzazy
Prof. Dr. Ismail Sedeik
Prof. Dr. Rasha Bassiouny
Organizing Committee Mrs.: Soad Abou Elenein
Mr. Maher Mobarak
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Program Overview
Thursday, 18th
April 2019
8:00-9:30 Registration
9:30-10:00 Opening Ceremony
Plenary Session 10:00-11:40
Chairmen: Prof. Awatef Awaad
Prof. Azza Al Sharkawy
Prof. Ensaf E Azzazy
Prof. Saeed Al Abbady
10:00-10:20
Abeer Ezzat El-Sayed Mohamed Central Line Associated Infections and Bundle Care
10:20-10:40 Ahmed Morad Asaad
Proficiency of Information Technology for Surveillance of
antimicrobial resistance in Healthcare settings
10:40-11:00 Marwa Nasser
Phage Therapy: A Potential Solution in the Era of Multi-drug
Resistance
11:00-11:20 Nermine Elmaraghy
The Dilemma of Antibiotic Resistance
11:20-11:40 Rania Ahmed Hassan
Antibiotic resistance: A public health challenge
11:40:12:00 Coffee Break
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Session I 12:00-02:00
Chairmen:
Prof. Ashraf Wegdan
Prof. Ismail Sedeik
Prof. Mona Abdel Wahab
12:00-12:15 Phenotypic and Genotypic Characterization of
Stenotrophomonas maltophilia in Alexandria Main University
Hospital
Mona Gamal El Din Morsi, May Moheb El Din Raouf,
Marwa Ahmed Meheissen, Mabrouka Abdelsalam Hamad
12:15-12:30 Microbiological Studies on the Effect of Medicinal Plant
Extracts on Diabetic Foot Ulcer Bacteria
Mohamed E. Sarhan, Dalia Moemen, Manal Tarshoby,
Mahmoud A. Swelim, Mohamed Abd El-Raouf
12:30-12:45 Accuracy of Human Immunodeficiency Virus Diagnostic Tests
Simulating the CDC Algorithm
Youssra M. Mostafa and Doaa T. Masallat
12:45-01:00 MRSA Screening and Spa Gene Detection in Isolates from
Ophthalmology Hospital in Egypt Compared to MRSA Spa
Detection in USA
Maha G Haggag, Tamara Revazishvili, Amal E Abo Elnour,
Mai Al-Kaffas
01:00-01:15 Detection of Carbapenemase Genes among Carbapenem-
Resistant Enterobacteriaceae Isolates in Suez Canal University
Hospitals in Ismailia
Hasnaa A. Mohamed,Said H. Abbadi, Waheed F. Hessam,
Atef S. Raheel, Abeer Ezzat El Sayed
01:15-01:30 Correlation of Virulence Determinants of Staphylococcus
aureus to the Severity of Diabetic Foot Ulcers in a Tertiary
Care Centre, Egypt
Yasmin Nabiel
01:30-01:45 Human Papillomavirus Types, 16 and 18 Among HIV Sero
Positive Women Attending Aminu Kano Teaching Hospital,
Kano, Nigeria
Emmanuela CN, Taysir RH, Usman AD
01:45-02:00 Trouble Shooting in H pylori Diagnostics…. A Glance from
Real Life Stories
Marwa Saad Fathi and Nermin Mahmoud
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Session II 02:00-04:00
Chairmen:
Prof. Rasha Mohamed Fathi
Prof. Ahmed Omar Shafeik
Prof. Rasha Bassyouni
02:00-02:15 Could Training Programs Eliminate Hospital Environmental
Surfaces Contaminations with Multidrug Resistant Bacteria
Rasha H. Bassyouni, Sylvana Nady Gaber, Asmaa Younis Elsary,
Mohamed Safaa Arafa
02:15-02:30 Fluoroquinolone Resistance of Clinical E. coli Isolates in
Mansoura University Hospitals and its Control
Eldegla H.E., Abdel-Fattah G.M., and Salem A.M.
02:30-02:45 The Art of Article Critique" How to Review a Medical Article;
Advice From a Reviewer
Noha Tharwat Abou El-Khier
02:45-03:00 Single Closed Tube Tm-shift Method Versus PCR-Restriction
Fragment Length Polymorphism in Detection of Macrophage
Migration Inhibitory Factor-173 G>C (s755622) Single
Nucleotid Polymorphism in Patients with Rheumatoid
Arthritis
Hala A.Tabl and Nashwa I. Hashaad
03:00-03:15 Biochemical and Immunological Characterization of
Hemolysin Produced by Pseudomonas aeruginosa PAO1
Isolated from Burn Patients
Ayman A. Allam, Ashraf M. El-shawadfy, Wesam A. Hassanein,
Esraa H. Hamza
03:15-03:30 Human Herpes Virus Type 8 (HHV-8) Among People Living
with HIV Attending General Hospital, Jigawa State, Nigeria
Nazir A.Y., Taysir, R. H., Usman, A. D.
03:30-03:45 Interleukin-18 and Vascular Endothelial Growth Factor as
Predictors for End-stage Renal Disease Aml F.A. Makled, Eman H.M. Salem, Amira H.A. El-Khayat,
Mahmoud M.A. Emara, Sara I.M. El Shohady
03:45-04:00 Phenotypic and Molecular Characterization of Clinical
Acinetobacter isolates from Menoufia University Hospitals
Ahmed M. Baker, Amal F. Makled, Eman H. Salem,
Ahmed A. Salama,Soma E. Ajlan
04:00 Lunch
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Conference of the Egyptian Society for Medical Microbiology
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Poster
1. Assessment of the level of Knowledge, Attitude and Practice Regarding
Influenza Vaccination in Community and Healthcare Settings in
Riyadh, Saudi Arabia
Dalia Saad ElFeky, Yomna Khaled Ramadan, Alhanouf Alsarhan, Rawabi
AlQurashi, Malak Alkhodaidi, Malak Albalawi
2. Antimicrobial Activities of Commercially Available Obturating
Materials in Primary Teeth Israa A. Ibrahim, Doaa T. Masallat, Ahmed H. Ibrahim, Ibrahim H. El Kalla
3. Helicobacter Pylori, Chlamydia Pneumoniae and c. Trachomatis as
Probable Etiological Agents of Preeclampsia
Yasmin Nabiel
4. Screening of the Antimicrobial Activity of Some Plant Aqueous Extracts
and Plant Oils and Enhancement of the Antimicrobial Activity of
Selected Plant Oil Using Liposomes as Nanoscale Carrier
Maha G Haggag, Medhat W Shafaa, Hossam S Kareem, Hoda H El-
Hendawy and Amir M El-Gamil
5. Colistin Resistance in Klebsiella pneumoniae and Esherichia coli Clinical
Isolates: A Microbiological and Molecular Study Amina Nour Eldin, Reem Abdelhamid Harfouh, Marwa Ahmed Meheissen,
Ahmed Mostafa Elmenshawy, Sara Mustafa Hendawy
6. Characterization of Fluoroquinolones-resistant Salmonella enterica
serovar typhi in Egypt
Amira Hisham El- Ashry, Mohammad Ahmed Abou El-Ela, Mohammad Abd
El- Razik El-Farrash, Hamdia Yehia Askar, Monir Hussein Hussein Bahgat
7. Association between Single-nucleotide Polymorphism of miR-146a and
Psoriasis
Hala A. Tabl and Hanan H. Sabry
8. Molecular Detection of bla OXA-48 Carbapenemase in Uropathogenic
Klebsiella pneumoniae strains from Suez Canal University Hospital
Rania Kishk, Marwa Azab, Ranya Hassan, Omar Dessouki
9. Molecular detection of Helicobacter pylori in children with Otitis media
with effusion at Assiut University and Sohag teaching Hospitals
Mohamed S Abd Elaal, Mohamed A Alfeky, Mohamed M Osman, Essam Abo
ELmagd, Trek A Hassan, Amal A Elkhawaga
10. In Vitro Assessment of Colistin-Carbapenem Combination Against
Multi Drug Resistant Enterobacteriaceae Isolates in Suez Canal
University Hospitals
Maha Mahdi, Omayma Aboul- Ola, Anwar Heiba, Rania Kishk
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Plenary Session
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Central Line Associated Infections and Bundle Care
Prof. Dr. Abeer Ezzat El-Sayed Mohamed Professor of Microbiology & Medical Immunology,
Head of Infection prevention & Control Unit Suez Canal Specialized Hospital,
Faculty of Medicine, SCU, Ismailia, Egypt
Intravascular catheter represents an essential part of the management of
critically ill patients, who present as acute emergency. However, their use is
often complicated by serious infections, mostly catheter related-blood stream
infections (CRBSIs) which are associated with increased morbidity & mortality,
increase in duration of hospitalization and additional medical costs. The
incidence of CRBSIs varies considerably by the type of catheter, frequency of
catheter manipulation, adherence to bundle care especially hand hygiene, patient
related factors and severity of illness. Accessing the catheter to administer
medications, flush the line & change tubing or caps introduces microorganisms
into the lumen. Hub manipulation is the most common source of infection in
long-term catheters, however it can trigger CR-BSIs in short term catheters as
well. The primary focus is on CVC insertion and nursing intervensions include
insertion and maintainance bundle care as:-
Perform proper hand hygiene.
Use maximal barriers during catheter insertion.
Provide antisepsis with chlorhexidine gluconate.
Choose an appropriate insertion site.
Avoid routine CVC replacement.
Evaluate the catheter insertion site daily for signs of infection and to
assess dressing integrity.
Daily review of catheter necessity with prompt removal when no longer
essential.
Conclusion: Most catheter-related BSIs with short term percutaneously
inserted, noncuffed CVCs were extraluminally acquired and derived from
cutaneous microflora. Strategies achieving successful suppression of cutaneous
colonization can substantially reduce the risk of catheter related blood stream
infection with short term CVCs.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Proficiency of Information Technology for Surveillance of
antimicrobial resistance in Healthcare settings
Ahmed Morad Asaad Professor of Medical Microbiology and Immunology, Faculty of Medicine,
Zagazig University, ZUMJ Editor-In-Chief
Antimicrobial resistance (AMR) is a major global health problem. It is
estimated that 300 million people will die prematurely because of infections as a
result of antimicrobial-resistant organisms over the next 35 years. Besides, the
world can expect to lose 60-100 trillion Dollars in economic output if AMR is
not effectively tackled. The WHO has for many years promoted the global
monitoring of AMR and taken steps to raise awareness of the impending public
health crisis it will cause. Surveillance is essential to all aspects of the
management of healthcare-associated infections and antimicrobial resistance
because it provides the necessary information to develop and monitor therapy
guidelines, antibiotic formularies, antibiotic stewardship programmes, public
health interventions, infection control policies, and novel antimicrobials and
vaccines. With advances in information technology, the use of soft programs in
AMR surveillance becomes highly warranted. Many software programs are now
available including WHONET, SaTScan, FleXScan, FluNet, Google Flu Trend,
Google Maps, and HealthMap. However, WHONET is considered the best
choice in clinical and epidemiological fields. The WHONET is free and has
been used in >3000 hospitals over >200 countries. This microbiological and
epidemiological program can be used efficiently to study the emergence of
resistant genes, detect an outbreak within a hospital, identify antibiotic
resistance profiles, and to provide automated reporting with the ability for
space-time visualisation.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Phage Therapy: A Potential Solution in the
Era of Multi-drug Resistance
Marwa Nasser
Microbiology Department, Faculty of Medicine, Ain Shams University
The emergence of multiple drug-resistant bacteria has prompted interest in
alternatives to conventional antimicrobials. One of the possible replacement
options for antibiotics is the use of bacteriophages. These naturally occurring
viruses attack and replicate only within specific bacteria. This is useful in
humans because not only do the bacteriophages not attack human cells, but they
also do not affect our normal flora. Phage therapy has less adverse effects than
antibiotics, can overcome resistance more efficiently, and can more easily
penetrate into biofilm. In this talk, we aim to discuss the history, recent
developments as well as the advantages and other challenges of bacteriophage
therapy as an alternative to antimicrobial chemotherapy.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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The Dilemma of Antibiotic Resistance
Nermine Elmaraghy
Faculty of Medicine, Suez Canal University; Ismailia, Egypt
Using antibiotics can lead to resistance. Each time you take antibiotics, sensitive
bacteria are killed. But resistant germs may be left to grow and multiply. They
can spread to other people. They can also cause infections that certain
antibiotics cannot cure. The world urgently needs to change the way it
prescribes and uses antibiotics. Even if new medicines are developed, without
behavior change, antibiotic resistance will remain a major threat.
Antibiotic resistance is rising to dangerously high levels in all parts of the
world. New resistance mechanisms are emerging and spreading globally,
threatening our ability to treat common infectious diseases. Where antibiotics
can be bought for human or animal use without a prescription, the emergence
and spread of resistance is made worse. Similarly, in countries without standard
treatment guidelines, antibiotics are often over-prescribed by health workers and
veterinarians and over-used by the public. Without urgent action, we are
heading for a post-antibiotic era, in which common infections and minor
injuries can once again kill.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Antibiotic resistance: A public health challenge
Rania Ahmed Hassan
Assistant Professor of Medical Microbiology and Immunology
Faculty of Medicine, Ain Shams University
According to the CDC, An increasing number of infections became resistant
to available antibiotics; the ability to effectively prevent and treat a growing
list of diseases is being compromised. These diseases become harder,
and sometimes impossible, to treat. The diminishing number of effective
antibiotics also increases the risk of many medical procedures including
surgery, chemotherapy, and organ transplants.
In this presentation, I am going to highlight three serious resistance traits:
1. New Delhi metallo-β- lactamase (blaNDM-1): constitutes a critical medical
issue. there is a quite systematic association with other antibiotic resistance
determinants is observed in almost all blaNDM-1 producers
(Enterobacteriaceae, Acinetobacter, and Pseudomonas)
2. Emergence of E. coli sequence type 131 (ST131) which markedly
contributed to the increased prevalence of antimicrobial resistance among E.
coli isolates
3. Inducible resistance to macrolides, lincosamides and streptogramins B group
of antibiotics “termed as MLSB resistance”, that are used of treatment of
methicillin resistant Staphylococci (MRS) with decreased susceptibility or
resistance to glycopeptides.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Session I
The 25th
Conference of the Egyptian Society for Medical Microbiology
15
Phenotypic and Genotypic Characterization of Stenotrophomonas
maltophilia in Alexandria Main University Hospital
Mona Gamal El Din Morsi, May Moheb El Din Raouf,
Marwa Ahmed Meheissen, Mabrouka Abdelsalam Hamad
Department of Medical Microbiology and Immunology,
Faculty of Medicine, Alexandria University, Egypt
Background and Objectives: Stenotrophomonas maltophilia emerged as an
important opportunistic nosoocomial pathogen, that causes a variety of infections
difficult to treat due to the intrinsic resistance to the important antimicrobial agents and
mobile genetic elements. Our aim was to determine the prevalence of S. maltophilia
among the clinical isolates of Alexandria Main University, to examine their
antimicrobial susceptibility, biofilm production, extracellular enzymes profile, and to
investigate the presence of class 1 and 2 integrons by PCR. Methodology: Fourteen
clinical isolates of S. maltophilia were collected from different specimens submitted to
Diagnostic Medical Microbiology Laboratory of AMUH over one year period, starting
from the first of April 2017 till the end of March 2018. All isolates were subjected to
antimicrobial susceptibility testing using the VITEK-AST-GN222 Cards (BioMerieux).
Biofilm production was tested by quantitative gold standard mirotitre plate test. The
extracellular enzymes were tested by inoculation of purified single colony on 5% blood
agar, Muller-Hinton agar plate contain 3% skimmed milk, and tryptic soya agar plates
contain 1% Tween 80, to test for hemolytic , protease and lipase activity respectively.
S. maltophilia integron class1 and 2 were identified by PCR. Results: The prevalence
of S. maltophilia (14) isolates among the non- lactose fermenters clinical isolate of
AMUH (1725) was 0.81%. The isolation of S. maltophilia was highest in blood
cultures (12; 85.7%), followed by sputum (1; 7.14%) and urine cultures (1; 7.14%). All
isolates (100%) were positive for hemolytic activity, while seven (50%) produced
protease activity. Eight (57.14%) produced lipase activity. Regarding biofilm
production, nine (64.28%) were moderate biofilm producers, while five (35.71%) were
weak biofilm producers. All isolates (100%) were susceptible to ticarcillin/clavulanic
acid, trimethoprime/sulphamethoxazole, minocycline. On other hand three (21.42%)
were resistance and one (7.14%) was intermediate susceptible to ceftazidime. Class 1
integrase was identified in four isolates (28.5%). Class 2 integrase was not detected in
any of the isolates. Conclusion: Our findings suggest that S. maltophilia can cause
serious healthcare associated infections particularly blood stream infections, though its
very low prevalence in our hospital. Trimethoprim/sulphamethoxazole (SXT) is still
the antibiotic of choice for treatment of S. maltophilia infections in our settings.
The 25th
Conference of the Egyptian Society for Medical Microbiology
16
Microbiological Studies on the Effect of Medicinal Plant
Extracts on Diabetic Foot Ulcer Bacteria
1Mohamed E. Sarhan,
2Dalia Moemen*,
3Manal Tarshoby,
1Mahmoud A. Swelim, and
4Mohamed Abd El-Raouf
1Botany Department, Faculty of Science, Banha University;
2Microbiology
Department, Faculty of Medicine, Mansoura University; 3Endocrinology and Diabetes
Department, Faculty of Medicine, Mansoura University; 4Botany Department, Faculty
of Science, Mansoura University, Egypt.
Background: The emergence of microbial resistance towards antibiotics
increased in a terrible rate. Screening of antimicrobial effect of plant extracts
represents hope for discovery of new antimicrobial agents.
Objectives: This research aimed to study the influence of the extracts of several
medicinal plants on diabetic foot ulcer bacteria.
Methodology: Swabs from deep tissues were collected from 56 patients
attending the outpatient clinic of diabetic foot Unit, and diagnosed clinically as
diabetic foot infections. The specimens were examined to identify the causative
bacteria and their antibiotic susceptibility pattern. Antimicrobial activity of
ethanol extracts of ten medicinal plant parts (cinnamon, henna, fennel, black
cumin, eucalyptus, clove, chamomile, ginger, sloenstemma and basil) were
investigated using well diffusion method. Phytochemical screening of effective
plants extracts were performed using tests for alkaloids, glycosides, cardiac
glycosides, saponins, phenols, sterols, tannins, flavonoids and diterpen. Results:
The commonest isolated organisms were S. aureus (33.9%), followed by S.
epidermidis (16.9%), P. aeruginosa (15.3%), P. mirabilis (13.6%), K.
pneumoniae (10.2%), E. coli (6.8%) and P. vulgaris (3.4%). Most bacteria were
resistant to tested antibiotics and 33.9% were multi-drug resistant bacteria.
Ethanol extract of solenstemma, clove, black cumin, and basil had effective
growth inhibition effect against isolated bacteria. Phytochemical screening
clarified that these plant parts contain powerful secondary metabolites and
active materials which explained their antimicrobial activity.
Conclusions: Some medical plants showed antimicrobial activity against
resistant bacteria, thus could be leading and useful therapeutic agents against
many bacterial infections.
The 25th
Conference of the Egyptian Society for Medical Microbiology
17
Accuracy of Human Immunodeficiency Virus Diagnostic Tests
Simulating the CDC Algorithm
1Youssra M. Mostafa and
2Doaa T. Masallat*
1Resident Microbiologist, Mansoura Fever Hospital, Ministry of health
2Medical Microbiology Department, Faculty of Medicine, Mansoura University
Background: The detection of HIV in Egypt is started by screening for HIV
antibodies or antigen by EIA and confirming the reactive samples by Western
blot test (WB). In many countries, a new algorithm has been proposed by
Centers for Disease Control and Prevention that uses an HIV-1/HIV-2 antibody
differentiation immunoassay instead of WB or immunofluoresence (IFA) for
confirmation. The initially reactive specimens are followed by same day
confirmation rapid assay that approved by FDA and if this test is negative they
make a nucleic acid test (NAT) to confirm. Objectives: comparing different
diagnostic tests results with WB result in HIV diagnosis and detecting the
accuracy of each assay. Methodology: This study was conducted from January
2016 to September 2017 on 100 people who were seeking for HIV diagnosis.
Blood samples were tested by Fourth generation Enzyme linked immunosorbent
assay (ELISA), Multispot rapid diagnostic test, and nested PCR. Results: The
sensitivity was the best with ELISA. PCR was the most specific test, followed
by Multispot, and finally ELISA. Conclusion: This algorithm provides accurate
results in short time.
The 25th
Conference of the Egyptian Society for Medical Microbiology
18
MRSA Screening and Spa Gene Detection in Isolates from
Ophthalmology Hospital in Egypt Compared to MRSA Spa
Detection in USA
Maha G Haggag1,2*
,Tamara Revazishvili3, Amal E Abo Elnour
4,
Mai Al-Kaffas1
1Microbiology & Immunology Unite, Microbiology & Parasitology Department,
2Allergy lab, Research Institute of Ophthalmology, Giza, Egypt.
3Department of Pathology, Immunology & Laboratory Medicine, College of Medicine,
University of Florida, Emerging Pathogen Institute, Gainesville, FL 32611, USA. 4Infection Control Team, Microbiology & Immunology Unite, Microbiology &
Parasitology Department, Research Institute of Ophthalmology, Giza, Egypt.
Background: Staphylococcus aureus is a major cause of ocular infections as
conjunctivitis, keratitis and endophthalmitis. Methicillin resistant Staphylococcus
aureus (MRSA) was almost restricted to hospitals but its prevalence has been
increased in peoples outside hospitals. Protein A is a cell wall component of
Staphylococcus aureus that binds to the Fc portion of IgG. The spa gene of
Staphylococcus aureus encodes protein A contains a highly polymorphic sequence
which is composed of repeats of 24 bp. Sequence typing of the spa gene repeat
region is used to study the epidemiology of MRSA. Methodology: In this study
screening of MRSA among healthcare workers in the Hospital of the Research
Institute of Ophthalmology in Egypt was done and detection of spa gene by PCR
was compared with that was done in USA as part of spa typing of MRSA referred
to the Department of Pathology, Immunology and Laboratory Medicine, Emerging
Pathogens Institute, University of Florida, Gainesville, FL, USA. Results: In the
present study 81 samples from healthcare providers in the Hospital of the Research
Institute of Ophthalmology (RIO), Egypt, were screened for MRSA. Out of these
81 samples, 41 isolates (50.6%) were identified as coagulase positive
Staphylococcus aureus. Twelve staphylococcal isolates were resistant to both
oxacillin and cefoxitin and those were identified as MRSA with percentage 14.8%
(12/81). Conventional PCR could detect spa gene in 10 out of 12 DNA MRSA with
percentage of 83.3% (10/12). On the other hand spa gene was identified by PCR in
all 28 DNA MRSA isolated from patients in the USA (100%). Conclusion: In the
present study the prevalence of MRSA in HCWs was 14.8%. Since amplification of
spa gene by PCR is a necessarily preliminary step for spa typing of MRSA and
since using different sequences for primers of spa gene in this study as well as in
others might affect PCR results then proper selection of the primers and thermal
cycling reaction conditions are recommended for PCR performance and spa typing.
The 25th
Conference of the Egyptian Society for Medical Microbiology
19
Detection of Carbapenemase Genes among Carbapenem-
Resistant Enterobacteriaceae Isolates in Suez Canal University
Hospitals in Ismailia
Hasnaa A. Mohamed1,Said H. Abbadi
1, Waheed F. Hessam
1, Atef S. Raheel
1,
Abeer Ezzat El Sayed1
1 Depatment of Medical Microbiology & Immunology, Faculty of Medicine,
Suez Canal University
Background: Carbapenem antibiotics are important therapeutic agents in the health
care setting, they are frequently used as an empiric therapy for life-threatening
infections as well as infections with multi-drug-resistant gram-negative bacilli.
Carbapenemase-producing Carbapenem-Resistant Enterobacteriaceae (CRE) are a
significant public health challenge worldwide. The detection of carbapenemases
productions in CRE strains is performed by phenotypic and genotypic methods.
The phenotypic methods target carbapenemases production but provide no
guidance regarding the specific carbapenemases types, while the genotypic
diagnosis has the benefit of determining the exact mechanism conferring
carbapenems resistance. Objective: Improvement of the antibiotic policy and
infection control strategies in Suez Canal University Hospitals in Ismailia; through
adequate detection of carbapenem resistance in the hospitals. Methodology: All the
CRE isolates were tested by the phenotypic methods (mCIM) test to detect
carbapenemases production, and screened by the conventional PCR for the
presence of five carbapenemase genes, namely blaKPC, blaIMI, blaVIM, blaNDM,
blaOXA-48. Results: The study showed that 34.1% of the Enterobacteriaceae
isolates were carbapenems resistant. Carbapenemases activity was detected in
67.9% of the examined CRE isolates using mCIM test,55.6% showed Metallo-
carbapenemases , 44.4% showed Serine-carbapenemases using the e CIM test.
Using PCR all the isolates (100%) harbor one or more carbapenemases genes. 51
(96.2%) were proved to harbor blaOXA-48 gene, 47 (88.7%) were proved to harbor
blaNDM gene, 28 (52.8%), were proved to harbor blaVIM,gene, the rate of blaIMI,
blaKPC isolation was 17 (32.1%), 4 (7.5%) respectively. Conclusion: The study
results suggest high frequencies of carbapenemase genes among CRE isolates with
carbapenemases activity detected in 67.9% of the examined CRE isolates.It is
extremely concerning and important element need proper antibiotic policy with
wise use of carbapenems and proper implementation of IPC isolation precautions to
monitor the spread of such isolates in the hospital.
The 25th
Conference of the Egyptian Society for Medical Microbiology
20
Correlation of Virulence Determinants of Staphylococcus aureus
to the Severity of Diabetic Foot Ulcers in a Tertiary Care
Centre, Egypt
Yasmin Nabiel
Microbiology and Immunology Department,
Faculty of Medicine, Mansoura University
Objectives: This study aimed to estimate the correlation of the Staphylococcus
aureus virulence determinants to the severity of the diabetic foot ulcers in
patients admitted to diabetic foot Unit at Mansoura University Hospitals.
Methodology: A prospective study was performed at the diabetic foot Unit of
Mansoura University hospital, Egypt. The study included 95 patients clinically
diagnosed as diabetic foot ulcers from whom swabs were obtained from the foot
lesions to be processed followed by detecting virulence determinants in isolated
S. aureus by PCR. Results: Staphylococcus aureus was isolated from 34 cases
(35.8%). icaA, icaD, pvl and tst genes were detected in 61.8%, 67.6%, 53%, and
32.4% of S. aureus isolates respectively with higher prevalence in isolated
strains from more severe infections and results were stastically significant. coa
and clfA genes were positive 97.1% and 94.1% isolates respectively.
Conclusion: The results showed that the S. aureus strains causing infections in
diabetic foot patients having genes: icaA, icaD, pvl and tst may be correlated to
the severity of lesions whereas coa and clfA were not.
The 25th
Conference of the Egyptian Society for Medical Microbiology
21
Human Papillomavirus Types, 16 and 18 Among HIV Sero
Positive Women Attending Aminu Kano Teaching Hospital,
Kano, Nigeria
1Emmanuela, C. N.,
2Taysir, R. H. and Usman, A. D.
1Department of Medical Microbiology and Parasitology Faculty of Clinical
Sciences, Bayero University Kano, Nigeria;
2Faculty of Medicine, Al-Azhar University, Cairo
Background: Human Papillomavirus (HPV) is one of the most common
sexually transmitted infections. It is the main etiologic agent in cervical cancer
development. HPV types 16 and 18 are more virulent, causing more than 16%
of all cervical carcinomas. It has been suggested that the oncogenic potential of
high-risk genital HPV types may be influenced by a concomitant infection with
the Human Immunodeficiency Virus (HIV). Objective: To determine the
prevalence of Human Papillo mavirus types 16 and 18 infection among HIV
sero positive women attending Aminu Kano Teaching Hospital (AKTH), Kano,
Nigeria. Methodology: The CD4 counts and HIV-viral load of the subject
women were obtained from their medical record. Data generated were analyzed
using SPSS software version 20. Results: This research involved 86 sexually
active HIV positive women in which 25(29.1) % were single, 61(70) % were
married. Their age group was between 20-50 years. 50 (58.1%) out of the 86
women enrolled in this study were positive for HPV, while 36 (41.9%) were
negative for HPV. From the pap smear carried out, low squamous intra-
epithelial lesion (LSIL) that were found was 17 (19.8%), atypical Squamous
Cell-High Squamous intra-epithelial lesion (ASC-HSIL cannot be excluded)
seen were 11 (12.8%) and negative with inflammation were 38 (44.2%). From
the 28 samples that have cell abnormalities, 6 (21.4%) were positive for HPV
type 16, while 16 (57.1%) were positive for HPV type 18. This study showed
that women living with HIV are prone to develop cervical cancer, as 28 (32.6%)
out of 86 women enrolled in this study had cell abnormalities, which indicate
that, there is a possibility for cervical cancer occurrence. This study also showed
that there is a high prevalence of Human Papillomavirus Infection, as type 16
and 18 were detected from these women. Conclusion: There should be an
effective pap smear annual screening among women living with HIV, and early
treatment of precancerous cervical lesions, to prevent cervical cancer
occurrence.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Trouble shooting in H pylori diagnostics…. A glance from real
life stories
Marwa Saad Fathi and Nermin Mahmoud
Medical Microbiology & Immunology Department, Faculty of Medicine
Ain shams University
H. pylori stands as one of the most important pathogens causing gastritis &
gastric erosions that may extend to gastric ulcer. Different studies illustrated the
methods attempted for successful yielding of the pathogen & thus performing an
adequate antibiogram to target the ultimate goal of clearance of the pathogen
after treatment; yet very few researchers highlighted definite solutions to
overcome difficulties clouding the process of culture & sensitivity as well as the
molecular tools for diagnosis. The pathway for accurate diagnosis is full of
obstacles that may obviously hinder back the adequacy of culture & sensitivity
steps. We faced several troubles within our series of studies which we tried to
plan it out to reach a solution that may help in further studies. Problems starts
from sampling including the technique, site of biopsy, rapid urease test,
transport medium, this is followed by culture troubles including high cost media
supplement availability, contamination after long incubation, anaerobic
supplementation, reaching up to susceptibility lack of antimicrobial
susceptibility CLSI guidelines as well as difficulty in yielding & reding
susceptibility patterns. The standard treatment for eradication of H. pylori is a
combination regimen of clarithromycin, amoxicillin and proton pump inhibitor.
In one study high resistance to metronidazole and clarithromycin have been
reported to be 86.7% and 50%, respectively. While resistance to amoxicillin
was 20% however tetracycline and levofloxacin resistance was rare 13.3% and
6.7%, respectively. Predictors for antibiotic resistance were either the body
weight, endoscopic findings or abuse of antibiotics and metronidazole.
Consequently, it is mandatory that antimicrobial susceptibility testing should be
done before initiating treatment; thus, better benefits is achieved for patient care
and also cost effective.
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The 25th
Conference of the Egyptian Society for Medical Microbiology
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The 25th
Conference of the Egyptian Society for Medical Microbiology
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Session II
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Could Training Programs Eliminate Hospital Environmental
Surfaces Contaminations with Multidrug Resistant Bacteria
1Rasha H. Bassyouni,
1Sylvana Nady Gaber,
2Asmaa Younis Elsary,
3Mohamed Safaa Arafa
1Department of Medical Microbiology and Immunology, Faculty of Medicine,
Fayoum University, Egypt. 2
Department of Public Health and Community
Medicine, Faculty of Medicine, Fayoum University, Egypt. 3
Department of
Orthopaedic surgery, Faculty of Medicine, Fayoum University, Egypt.
Background: Hospital environment could be a risk for transmission of
nosocomial infections. Objective: This study aimed to evaluate the effect of
training program on the elimination of microbial contamination of hospital
environmental surfaces, devices and health care workers (HCWs) hands.
Methodology: Two phases interventional study was conducted for basal
evaluation and training of HCWs and housekeepers on standard precautions
with evaluation of environmental surfaces, devices and hands contamination at
basal level before as well as after routine cleaning and hand hygiene, also after
implantation of a training program. Results: Significant reduction of
environmental surfaces and devices contamination was detected after
educational intervention at all departments (p-value >0.001). The most
common isolate was S. aureus in operating rooms, orthopedic, and general
surgery departments (44.4%, 26.9%, and 22.2% respectively), E.coli was the
most common isolate in urology department (21.8%). Bed ledges/ bed arms
samples showed the highest contamination level (39%) while curtain edges
showed the least contamination site (4.2%). Nurses had the lowest frequency of
hand contamination (30%) followed by physicians, the highest hand
contamination recorded for housekeepers (50%). E.coli isolated from 47.4% of
hands. The most isolated Multidrug Resistant Bacteria was MRSA (54.3%)
followed by ESBLs producing E.coli (38.7%). After education there were
significant improvements in practice observed for all subjects (p-value< 0.05)
and environmental contamination decreased to zero level. Conclusion:
Intervention with a training program has a positive impact on elimination of
hospital environment contamination.
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Conference of the Egyptian Society for Medical Microbiology
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Fluoroquinolone resistance of clinical E. coli isolates in Mansoura
University Hospitals and its Control
1Eldegla H.E.,
2Abdel-Fattah
G.M.,
2Salem A.M.
1Department Medical Microbiology and Immunology, Faculty of Medicine,
Mansoura University, Mansoura, Egypt; 2Department of Botany, Faculty of
Science, Mansoura University, Mansoura, Egypt
Background: Fluoroquinolones resistance usually occurs due to mutation in the
quinolone resistance-determining regions (QRDRs) in the gyrA and parC genes
that can be detected by multiplex allele-specific PCR (MAS-PCR). Herbal
medicines are used as alternative treatment for disease caused by resistant
bacteria. Objectives: This work aimed to detect resistance to fluoroquinolones in
E. coli isolates from patient admitted in Mansoura University Hospitals;
additionally, to identify certain natural plant extracts that could be used against
fluoroquinolone resistant E. coli. Methodology: Fifty clinical E. coli isolates were
collected from patients admitted in Mansoura University Hospitals.
Fluoroquinolones susceptibility pattern was tested by disk diffusion method. Out
of 50 isolates, 25 fluoroquinolone resistant E. coli were selected to detect
mutations in gyrA and parC genes by MAS-PCR. Ethanolic plant extracts were
tested against FQ resistant E. coli isolates by using agar well diffusion method.
Results: E. coli isolates showed highest resistance to ciprofloxacin (76%)
followed by norfloxacin (72%), levofloxacin (70%), and ofloxacin (68%). Double
mutations at gyrA gene were detected at position 83 and 87 of QRDRs in 12
(48%) FQ resistant E. coli and at parC gene at position 80 and 84 of QRDRs in 3
(12%) FQ resistant E. coli. While single mutation at position 83 and 87 was found
in QRDR of gyrA in 8 (32%) and 5 (20%) of FQ-resistant E. coli, respectively
and single mutation at position 80 and 84 was found in QRDR of parC in 21
(84%) and 1 (4%) of FQ-resistant E. coli, respectively. Ethanolic extract of Clove
had more antibacterial activity compared to other extracts. Conclusion: high rate
of fluoroquinolone resistance among clinical E. coli isolates was detected and this
necessitates monitoring the microbial trends and resistance patterns. Plants may
be used as natural antibiotics in the treatments of antibiotic resistant E. coli
infections.
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Conference of the Egyptian Society for Medical Microbiology
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"The art of article critique"
How to Review a Medical Article; Advice from a reviewer
Noha Tharwat Abou El-Khier
Medical Microbiology & Immunology, Faculty of Medicine, Mansoura
University, Egypt
Peer review is the process used to assess an academic paper before deciding
whether it should be published or not. The paper is looked at by experts in the
field, known as reviewers or referees. The peer-review system is essential in
order to ensure that only credible, high- quality research is published. It not only
improves the quality of published papers, it also ensures that readers can trust a
journal to provide reliable information. As members of the scientific
community, researchers are expected to review papers. The role of a peer
reviewer is substantial. First and foremost, the reviewer’s role is to tell the
author the strengths and weaknesses of the manuscript and to provide
constructive criticism about how it could be improved. The second
responsibility of the reviewer is to suggest to the Editors whether the manuscript
should be accepted, rejected, or revised and resubmitted. The responsibility of
the peer reviewer is to thoroughly evaluate the science of a submitted
manuscript. The time spent reading, evaluating, and writing a peer review is
substantial.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Single closed tube Tm-shift method versus PCR-Restriction
Fragment Length Polymorphism in detection of Macrophage
Migration Inhibitory Factor-173 G>C (s755622) single nucleotid
polymorphism in patients with rheumatoid arthritis
1Hala A.Tabl, and
2Nashwa I. Hashaad
Departments of 1Medical Microbiology &Immunology and
2Rheumatology, Rehabilitation & Physical Medicine, Faculty of Medicine,
Benha University
Background: Macrophage migration inhibitory factor (MIF) might has a role in
the development and disease activity of Rheumatoid arthritis (RA). There are
several disadvantages in the conventional methods for MIF genotyping and
there is a strong need for convenient, flexible, accurate and inexpensive method.
Objectives: This study was designed to study the application of single closed
tube melting temperature (Tm)-shift method in genotyping of MIF-173 G>C
(s755622) gene in RA patients and to compare its result with the conventional
PCR-Restriction Fragment Length Polymorphism (PCR-RFLP) and to
investigate the potential association of these variants of MIF gene with
susceptibility and activity of RA. Methodology: GC-rich tail was attached to 5'-
end of one of the two allele specific forward primers, such that MIF alleles can
be discriminated by the Tm of the PCR products. One hundred RA patients and
40 healthy controls were genotyped for MIF-173 G>C by both Tm-shift method
and conventional PCR-RFLP. Results: The comparison of the PCR-RFLP and
the Tm-shift method showed one discordant result in 140 samples tested.
Retesting this sample with prolonged time of incubation with the restriction
enzyme, corrected the result to become 100% agreement between the two
methods. No significant association could be found between MIF-173 G>C
SNP and risk of RA. C/C genotype is more prone to higher disease activity than
other genotypes. Conclusion: The single closed-tube Tm-shift method is
reliable, rapid and cost-effective and it is superior to conventional PCR-RFLP in
genotyping of MIF.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Biochemical and Immunological Characterization of Hemolysin
Produced by Pseudomonas aeruginosa PAO1 Isolated from Burn
Patients
1Ayman A. Allam,
2Ashraf M. El-shawadfy,
2Wesam A. Hassanein, and
2Esraa H. Hamza
*Medical Microbiology and Immunology Department, Faculty of medicine,
**Botany and Microbiology Department, Faculty of science, Zagazig
University, Egypt.
Objectives: The aim of the study was to purify and characterize the haemolysin
produced by multidrug resistant Pseudomonas aeruginosa PAO1 isolated from
burn patients. Methodology: Isolation and identification of Pseudomonas
aeruginosa from burn patients was done by standard bacteriology methods.
Characterizarion of Pseudomonas aeruginosa PAO1 was done by PCR
amplification and sequencing of the gene 16 S rRNA. The hemolysin produced
by Pseudomonas aeruginosa PAO1 (NR 074828 1) under optimal cultural
conditions (pH 7, incubation at 37 °C, yeast extract as nitrogen source and
glucose as carbon source) was purified by successive fractional precipitation
using ammonium sulphate 70% concentration followed by gel filtration on
Sephadex G -100. Results: The specific activity of purified enzyme increased to
30-fold with a 15.6 % yield after gel filtration on Sephadex G -100. Pure
enzyme revealed an apparent molecular weight of 37 KDa after SDS-poly
acrylamide Gel Electrophoresis. High performance liquid chromatography
showed that the hemolysin is rich in glycine (26.7) %. The physical
characteristics of the haemolysin were determined, and the obtained results
showed that it was inactivated above 70C. Purified enzyme was stable within
pH range of 4-9 and the maximum activity was at pH 7. It was also activated by
metal ions such as Ca2+, Fe3+ and Cu2+ while iodine and EDTA inhibited the
enzyme activity. The hemolysin lost its half activity after storage period of 48
day at 4°C. It completely lost its toxicity after heating for 15 min in boiling
water bath. Mice toxicity of the fresh and heated hemolysin revealed that
injecting mice with 0.5 ml of fresh hemolysin hemolytic titer (128 HU/ml)
caused 100 % mortality within 5 days while 0.5 ml of hemolytic titer 64 HU/ml
of the heated hemolysin (toxoid) caused 50% mortality. In vitro toxin antitoxin
neutralization test revealed that anti-hemolysin antitoxin was present in the
serum of the mice that previously injected by heated toxin (toxoid).
Conclusion: The study concluded that this hemolysin can be a component of a
vaccine for preventing hemolysis caused by multidrug resistant Pseudomonas
aeruginosa in burn patients.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Human Herpes Virus Type 8 (HHV-8) among People Living with HIV
Attending General Hospital, Jigawa State, Nigeria
1Nazir A.Y.,
2Taysir R. H. and Usman A. D.
1Department of Medical Microbiology and Parasitology
Faculty of Clinical Sciences, Bayero University Kano, Nigeria and 2Faculty of Medicine, Al-Azhar University, Cairo
Background: Human Herpes virus type 8 is among the frequent opportunistic
infections among individuals infected with human immunodeficiency virus
(HIV) and may result in severe morbidity and mortality among this group of
patients. It is known to be the causative agent of Kaposi’s Sarcoma (KS), as
well as other malignancies such as primary effusion lymphoma. Objective: This
study investigates the prevalence of HHV8 antigen among people live with HIV
as well as its correlation with the patients CD4 counts and Viral loads.
Methodology: This cross-sectional study involved 182 blood sample collected
from HIV sero positive individuals attending antiretroviral therapy clinic
(ART), Babura General Hospital, Jigawa State, Nigeria. Samples were analyzed
for HHV-8 antigen using Enzyme linked immunosorbent assay and CD4+ cell
Count. Socio-demographic informations such as age, gender, and marital status
were obtained from patient folder. Results: Of the 182 subject studied 6(3.3%)
were positive for HHV-8 antigen. All subjects (100%) who were HHV8
Positive have low CD4 Count and high HIV Viral loads. There was a
statistically significant difference between HHV8 and respondents CD4 count (p
= 0.001). However no association was observed between HHV8 and
respondents gender and their age.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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Interleukin-18 and Vascular Endothelial Growth Factor as
Predictors for End-stage Renal Disease
1Aml F.A. Makled,
1Eman H.M. Salem,
1Amira H.A. El-Khayat,
2Mahmoud M.A. Emara,
3Sara I.M. El Shohady
Departments of 1Microbiology and Immunology and
2Internal Medicine, Faulty
of Medicine, Menoufia Universality, Shebin Elkom 3Menoufia University
Hospital, Menoufia University, Menoufia Governorate, Egypt
Background: IL-18 and VEGF are inflammatory cytokines playing important
roles in the pathogenesis of ESRD and related comorbidities like diabetic
nephropathy and viral hepatitis. Objective: The objective of this study was to
evaluate the role of interleukin-18 (IL-18) and vascular endothelial growth
factor (VEGF) in end-stage renal disease (ESRD), and the influence of
comorbidities like diabetes and viral hepatitis on their levels. Methodology:
This study was conducted on 96 patients undergoing hemodialysis (25 diabetic
patients with hepatic viral infections, 25 diabetic patients without hepatic viral
infections, 25 nondiabetic patients with hepatic viral infections, and 21
age-matched and sex-matched healthy individuals as a control group). All
patients were subjected to full history taking, clinical examination, and
laboratory investigations. Serum IL-18 and VEGF levels were measured for all
the study individuals by using enzyme-linked immunosorbent assay technique.
Results: The prevalence of IL-18 and VEGF was higher in diabetic patients and
patients with hepatitis comparing with the controls (P = 0.001). A detectable
level of IL-18 was found in 100% of diabetic patients with and without viral
hepatitis, and in 44% of the ones with only hepatitis (P = 0.001). A detectable
level of VEFG was found in 100% of the patients with only diabetes and only
hepatitis, and in 80% of the ones with combined diabetes and hepatitis (P =
0.001). Conclusion: There is high elevation of both IL-18 and VEGF serum
levels in ESRD associated with diabetic nephropathy and viral hepatitis. Serum
IL-18 is higher in diabetic than hepatic nephropathy, whereas the opposite is
seen with VEGF.
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Phenotypic and molecular characterization of clinical
Acinetobacter isolates from Menoufia University Hospitals
Ahmed M. Baker, Amal F. Makled, Eman H. Salem, Ahmed A. Salama,
Soma E. Ajlan
Department of Microbiology and Immunology, Faulty of Medicine,
Menoufia Universality, Shebin Elkom
Background: Acinetobacter spp. is important opportunistic pathogens
responsible for nosocomial infections. Objectives: The aims of this study were
to investigate the prevalence of Acinetobacter spp. in Menoufia University
Hospitals, to investigate their antimicrobial susceptibility patterns, and to assess
carbapenemases production in these isolates. Methodology: This study was
conducted on 603 clinical samples from patients admitted to Menoufia
University Hospitals. Acinetobacter spp. were identified by standard
microbiological methods and API20NE test kits. Antimicrobial susceptibility
was tested using disk diffusion and agar dilution methods. Imipenem‑resistant
Acinetobacter isolates were further tested for metallo‑β‑lactamase (MβL)
production. Results: This study was conducted at Medical Microbiology and
Immunology Laboratory, Faculty of Medicine, Menoufia University.
Acinetobacter spp. represented 10.6% of all collected nosocomial isolates. With
regards to API20NE results, A. baumanii was the predominant Acinetobacter
spp. (80.8%) followed by A. baumannii–A. calcoaceticus complex (7.7%), A.
lwoffii (5.8%), A. haemolyticus (3.8%), and A. pitti (2.6%). Acinetobacter
isolates were highly resistant to cefepime (92.3%), ampicillin–sulbactam,
piperacillin, piperacillin–tazobactam, ceftazidime, tobramycin (91% for each),
amikacin (84.6%), and imipenem (67.9%). Overall, 56.4% of Acinetobacter
isolates were susceptible to tigecycline. On agar dilution method, 96.2% of
Acinetobacter isolates were found to be susceptible to colistin and 66.7% were
imipenem resistant. Imipenem/ethylenediaminetetraacetic acid combined disk
test showed that 81.1% of imipenem‑resistant Acinetobacter were MβL
producers, and multiplex PCR showed that 15.1% of imipenem‑resistant
Acinetobacter were positive for blaVIM2, but none of them were positive for
blaIMP1 gene. Conclusion: Acinetobacter spp. are serious nosocomial
pathogens with high prevalence of carbapenems resistance. Production of
carbapenemases, especially MβLs, is considered the main
carbapenem‑resistance mechanism. Tigecycline and colistin can be valuable
therapeutic options for the treatment of Acinetobacter infections.
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Posters
The 25th
Conference of the Egyptian Society for Medical Microbiology
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[1] Assessment of the level of Knowledge, attitude and practice regarding
influenza vaccination in Community and healthcare settings in Riyadh,
Saudi Arabia
Dalia Saad ElFeky1&2
, Yomna Khaled Ramadan1&3
, Alhanouf Alsarhan1,
Rawabi AlQurashi1, Malak Alkhodaidi
1, Malak Albalawi
1
1College of Medicine, Princess Nourah Bint Abdulrahman University, Riyadh,
2Department of Medical Micrrobiology and Imunology, Faculty of Medicine; Cairo
University; 3Department of Internal Medicine, Faculty of Medicine, Cairo University
Introduction: Seasonal influenza is a major health issue. Each year, about 3–5
million cases of severe illness and 250,000–500,000 deaths globally result from
epidemic seasonal influenza. Vaccination against influenza viruses is the most
efficient way to prevent influenza related complications. Compliance to receive
the influenza vaccination is very low and potential barriers of influenza
vaccination are in need to be identified to raise awareness and acceptance of the
vaccine. Objectives: The Aim of this study was to assess knowledge, beliefs
and attitudes regarding influenza vaccination in community and healthcare
settings in Riyadh city and to identify reasons for electing or declining the
immunization. Methodology: It is a cross-sectional questionnaire based study
conducted between January and March 2018 using a closed ended, interviewer
based questionnaire. The study enrolled 500 adults of Riyadh city population
including participants from general population, students and HCWs. The
questionnaire was distributed in shopping malls and parks in different areas in
Riyadh, in Princess Nourah Bint Abdulrahman University and in King Abdullah
Bin Abdulaziz University Hospital. Results: A total of 500 participants were
included in the study including 124 HCWs (24.8%), 195 students (39%) and
181 (36.2%) participants from general population. The knowledge score of
participants in this study ranged between 5-35 with mean of 18 ±5.85. Mean
knowledge score was highest among HCWs followed by students and lastly
general population with a statistically significant difference (p<0.00). However,
the majority of participants in all groups have poor knowledge when using a cut
off 60% and 70% of knowledge score for the general population and HCWs,
respectively. Conclusion: There is poor knowledge about influenza disease and
influenza vaccination among the studied population including HCWs.
Compliance to influenza vaccination was poor among different groups of the
studied population.
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[2]
Antimicrobial Activities of Commercially Available Obturating
Materials in Primary Teeth
1Israa A. Ibrahim,
2Doaa T. Masallat,
3Ahmed H. Ibrahim,
3Ibrahim H. El Kalla
1Faculty of Dentistry, Science and Technology University, Republic of the
Sudan; 2Department of Microbiology and Immunology, Faculty of Medicine,
Mansoura University, Egypt; 3Department of Pedodontics and Preventive
Dentistry, Faculty of Dentistry, Mansoura University, Egypt
Background: Preservation of primary dentition is a must for orofacial
development as it helps to maintain the eruption of permanent teeth, aids in
mastication, and phonation. Objectives: The present study compares the
antimicrobial activities of commonly used obturating materials for filling the
root canals of primary teeth against the microorganisms commonly infect the
roots. Methodology: the antimicrobial activities of four commonly used
obturating materials, ZOE; Iodoform; Vitapex; and Endoflas, were evaluated by
three methods; the first method was electron microscope images which detected
the presence of the bacteria in dentinal tubules. The second method was CFU
count method in which thirty extracted deciduous mandibular molars were
incubated in a mixed-species suspension, obturated, cultured and the numbers of
the bacterial colonies were reported for each obturated group. The third method
was the agar diffusion method in which the antimicrobial activities of the
obturating materials were tested against four microbial isolates (E. faecalis; E.
coli; S. aureus and Ps. aeruginosa). Results: The four obturating materials
reported different antimicrobial effect in CFU test which was not statistically
significant; however, Endoflas and ZOE were superior to Vitapex and
Iodoform. Bacterial resistances were detected against Vitapex and Iodoform.
Conclusion: Obturating materials containing eugenol were more effective than
other materials without eugenol.
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[3]
Helicobacter pylori, Chlamydia pneumoniae and c. trachomatis as
Probable Etiological Agents of Preeclampsia
Yasmin Nabiel
Microbiology and Immunology Department,
Faculty of Medicine, Mansoura University
Objectives: The aim of this study was to evaluate the evidence for Helicobacter
pylori, Chlamydiae pneumoniae and trachomatis to act as a probable etiology
for preeclampsia (PE), together with estimating the prevalence of such
infections in pregnant women with PE. Methodology: We performed a
prospective study in Mansoura University Hospitals, Egypt, for detecting H.
pylori infection by estimating H. pylori IgG and IgM, in addition to detection of
Chlamydiae infections by PCR in 90 pregnant women with PE and 90
normotensive pregnant women of the same age and body mass index who were
studied as control. Results: The prevalence of H. pylori infection in
preeclamptic pregnant women was 54.4% with a statistically significant
association to PE. The prevalence of C. pneumoniae was 27.8% whereas that of
C. trachomatis was 4.44%. The infected preeclamptic cases showed high levels
of leucocytes besides elevated C-reactive protein concentrations. Conclusion:
Helicobacter pylori were found to act as a cofactor in the development of PE.
Occurrence of C. trachomatis was low in pregnant women in our community;
however, it showed that it may act as a cofactor in PE, whereas C. pneumoniae
was attributed to have no role in PE pathogenesis until supported by further
studies.
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[4]
Screening of the Antimicrobial Activity of Some Plant Aqueous
Extracts and Plant Oils and Enhancement of the Antimicrobial
Activity of Selected Plant Oil Using Liposomes as Nanoscale
Carrier
Maha G Haggag1*, Medhat W Shafaa
2, Hossam S Kareem
3,
Hoda H El-Hendawy4and Amir M El-Gamil
4
1Department of Microbiology & Immunology, Research Institute of
Ophthalmology, Giza, Egypt. 2Department of Physics, Faculty of Science,
Helwan University, Cairo, Egypt; 3Department of physiological Optics,
Research Institute of Ophthalmology, Giza, Egypt. 4Department of Botany and
Microbiology, Faculty of Science, Helwan University, Egypt.
Background: A considerable interest in the possible use of natural alternatives as food
preservative either to delay food spoilage or to prevent food-borne pathogens growth. Many
spices and herbs extracts possess antimicrobial activity, almost invariably due to the
essential oil fraction. Liposomes can encapsulate both hydrophilic and lipophilic materials.
Liposome entrapment may stabilize encapsulated bioactive materials against a range of
environmental and chemical stresses, including the presence of enzymes or reactive
chemicals and exposure to extreme pH, temperature, and high ion concentration thus
providing protection of the antimicrobial peptides, enhancing their efficacy and stability for
food applications. Objectives: This study aimed to test the antimicrobial activity of
Aqueous plant extracts & oils against selected strains of pathogenic Gram-positive and
Gram-negative bacteria and yeast. Furthermore clove oil was selected to be encapsulated
into liposomes as nanoscale carriers to examine the possible enhancement of its
antimicrobial activity. Methodology: Aqueous extracts of clove flower buds, black seed,
Lupine, curcuma, cinnamon, ginger, and chamomile were prepared and their antimicrobial
activities were tested against 5 types of pathogenic isolates; Staphylococcus aureus, salmonella, Escherichia coli, Pseudomonas aeruginosa, Klebsiella and Candida spp using
agar well diffusion method. Also six ready-made oils of clove, black seed, thyme, garlic,
rosemary and green tea were purchased and tested for their antimicrobial activity. Clove oil
was selected to be encapsulated into liposomes and antimicrobial activity enhancement was
tested by MIC and MBC. Results: Antimicrobial activity of Clove extract was stronger
than other plant aqueous extracts. All oils showed antimicrobial activity against at least two
of the tested microorganisms. The antimicrobial activity of liposome encapsulated clove oil
was enhanced by 5 times more than that of un-encapsulated clove oil. Tetracycline was also
encapsulated into liposomes and its antimicrobial activity was found to be improved by 12
times when compared with un-encapsulated one. Conclusion: Liposome is an efficient
carrier that significantly enhancing the antimicrobial activity of some plant oils as clove and
also significantly strengthen the antibiotic activity in vitro.
The 25th
Conference of the Egyptian Society for Medical Microbiology
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[5]
Colistin Resistance in Klebsiella pneumoniae and Esherichia coli
clinical Isolates: A Microbiological and Molecular Study
Amina Nour Eldin1, Reem Abdelhamid Harfouh
1, Marwa Ahmed Meheissen
1, Ahmed Mostafa Elmenshawy
2, Sara Mustafa Hendawy
1
1Medical Microbiology & Immunology Department, faculty of Medicine,
University of Alexandria; 2 Critical care Department, faculty of Medicine,
University of Alexandria
Background: The global increase in multidrug resistant Enterobacteriaceae has
resulted in increased use of colistin with the inevitable risk of emerging
resistance. Klebsiella pneumoniae and Esherichia coli have been recently
showing an appreciable resistance to colistin. Objectives: The aim of the
present work was to: 1. Evaluate the performance of the rapid polymyxin
Nordmann Poirel test for phenotypic detection of colistin resistance in K.
pneumoniae and E. coli clinical isolates. 2. Determine the antimicrobial
susceptibility pattern of those isolates. 3. Estimate the prevalence of plasmid
mediated colistin resistance among resistant clinical isolates. Mothodology: A
total of 50 K. pneumoniae and E. coli (25 colistin susceptible and 25 colistin-
resistant) isolated from different clinical specimens collected from Alexandria
University hospitals intensive care units were included in the study. All isolates
were subjected to the following: 1. Identification to the species level by
MALDI-TOF. 2. Detection of colistin resistance by phenotypic methods. a.
Broth microdilution method according to EUCAST 2018 guidelines.b. Rapid
Polymyxin NP Test. 3. PCR for detection of mcr-1 and mcr-2 genes for plasmid
mediated colistin resistance. Results: Using broth microdilution test, the MIC of
colistin susceptible isolates ranged from 0.12- < 2 μg/mL, while that of colistin
resistant isolates ranged from 4 – 128 ug/ml. With regard to performance of the
rapid polymyxin NP test with colistin-susceptible isolates (13 K. pneumoniae,
12 E. coli), the 25 isolates tested (MICs of colistin) gave negative results,
similarly all colistin resistant isolates (20 K. pneumoniae, 5 E. coli) gave a
positive result. Thus the test provided 100% sensitivity and specificity. None of
the colistin resistant isolates harbored mcr-1 or mcr-2 genes. Conclusions: The
rapid polymyxin NP test is useful for first-step screening of colistin resistance in
K. pneumoniae and E. coli. The mechanism of colistin resistance could be
explained by mechanisms other than plasmid-mediated resistance. Further study
with larger sample size is needed to investigate the presence of plasmid
mediated colistin resistance genes.
The 25th
Conference of the Egyptian Society for Medical Microbiology
40
[6]
Characterization of Fluoroquinolones-resistant Salmonella
enterica serovar Typhi in Egypt
1Amira Hisham El- Ashry,
1Mohammad Ahmed Abou El-Ela,
1Mohammad Abd El- Razik El-Farrash,
1Hamdia Yehia Askar,
1Monir Hussein Hussein Bahgat,
2Mansoura, Egypt
Department of Medical Microbiology and Immunology a and the Department of
Internal Medicine, b Faculty of Medicine, Mansoura University, Egypt
Background: Typhoid fever is endemic in developing countries including
Egypt, producing major public health problems with high mortality and
morbidity. The emergence of resistant serovar Typhi (S. typhi) to commonly
recommended antimicrobials is alarming in developing countries.
Fluoroquinolones have been the empirical drug of choice for multidrug-resistant
MDR typhoid. However, there have been several alarming reports of
fluoroquinolones therapeutic failure in typhoid patients. Resistance of S. typhi to
fluoroquinolones commonly results from target site mutation. Objectives:
Determination of antimicrobial resistance pattern of S. typhi isolated from
Egyptian patients with typhoid fever admitted to or attended Mansoura
University
Hospitals (MUHs) and Mansoura Fever Hospital, detection of
quinolones resistant strains and using PCR-RFLP and sequencing techniques for
testing mutation at QRDR of gyrA gene in the isolated strains. Methodology:
Blood and Stool samples from clinically suspected typhoid patients were
screened by culture on suitable media and were identified biochemically. The
identified S. typhi isolates were tested for susceptibility to antimicrobials using
the Kirby Bauer disk diffusion method. Minimum inhibitory concentrations of
ciprofloxacin was determined by E test. Interpretation of all results was done
according to the CLSI guidelines 2015. Mutations in gyrA gene were detected
by PCR-RFLP and sequencing methods. Results: Out of 500 blood and stool
samples, 57 isolates were S. typhi (96.6%) and only two were S. paratyphi A
(3.4%). Of the 57 S. typhi, 80.7% were resistant to nalidixic acid, 50.9% had
ciprofloxacin MIC 0.125-0.5 μg/ml and 19.3% had ciprofloxacin MIC >1
μg/ml. Ser 83 mutation in gyrA was detected in 63.1% of the isolates.
Conclusion: Increased emergence of fluoroquinolones -resistant typhoidal
Salmonella in Egypt which is caused mainly by point mutation at codon 83
(Ser83-Phe substitution TCC→TTC) in QRDR of gyrA gene.
The 25th
Conference of the Egyptian Society for Medical Microbiology
41
[7]
Association between single-nucleotide polymorphism of miR-
146a and psoriasis
Hala A. Tabl and Hanan H. Sabry
Departments of Medical Microbiology & Immunology and Dermatology,
Venereology and Andorology Faculty of Medicine, Benha University, Egypt
Background: Micro-RNAs (miRNAs) play important roles in the development
of different inflammatory conditions of the skin. However, few studies
investigated the association between miR-146a and psoriasis. Objectives: This
work aimed to study the association between miR-146a single-nucleotide
polymorphism (SNP) rs2910164 and the risk of psoriasis and to study the
association between levels of skin expression of miR-146a and the response to
treatment. Methodology: The study was carried out on 120 patients with
psoriasis and 60 control subjects. The miR-146a rs2910164 SNP was detected
by using polymerase chain reaction-restriction fragment length polymorphism
(PCR-RFLP) analysis. Levels of skin expression of miR-146a were detected by
Real Time PCR before and 3 months after treatment with PUVA therapy.
Results: Non significant association could be found between combined (CG +
GG) genotypes and risk of psoriasis [OR (95% CI) = 0.81 (0.41-1.60)],
(P=0.52). The level of miR-146a expression was significantly increased in
patients compared to controls, with the highest level recorded in patients with
CC genotype. There was a significant decrease in the miR-146a levels after
treatment in both CC (P<0.001) & CG (P=0.01) genotypes but not in GG
genotype (P=0.29). MiR-146a levels were higher in patients responding to
treatment than non-responders (P<0.001). Also, there was significantly higher
response to PUVA treatment in CC genotype (100%) than in CG genotype
(50%) and GG genotype (20%) (P<0.001). In conclusion, no significant
association could be found between combined rs2910164 genotypes (CG + GG)
and risk of psoriasis. Moreover, measuring miR-146a level and knowing
patients' genotype could be useful predictors of therapeutic response.
The 25th
Conference of the Egyptian Society for Medical Microbiology
42
[8]
Molecular detection of bla OXA-48 carbapenemase in
uropathogenic Klebsiella pneumoniae strains from Suez Canal
University Hospital
1Rania Kishk,
2Marwa Azab,
3Ranya Hassan,
3Omar Dessouki
1Microbiology and Immunology department, Faculty of Medicine, Suez Canal
University; 2Microbiology and Immunology department, Faculty of pharmacy,
Suez Canal University; 3
Clinical Pathology department, Faculty of Medicine,
Suez Canal University
Background: The emergence of multidrug resistant Klebsiella pneumoniae (K.
pneumonia) has a new concern in antibiotic resistant threats. The emergence of
carbapenems resistance, antibiotics of last resort, is considered a critical clinical
and public problem. Aim: this study aimed to make recommendations for the
identification and detection of Klebsiella Producing Carbapenemases (KPC) to
improve patient management and antimicrobial stewardship. Methodology: this
study included 120 consecutive and non-duplicate clinical strains of K.
pneumoniae isolated from cases of urinary tract infections. Phenotypic detection
of ESBL and Carbapenemases production were performed. Identification of
class D carbapenemases by 16S rRNA gene sequence was performed.
Carbapenem resistance bla OXA-48 gene was detected using conventional
PCR. Results: Phenotypic tests show 57 strains (47.5%) were carbapenem
resistance (p value = 0.002) and 47 strains (39.1%) were ESBL producers (p
value = 0.001). By 16S rRNA sequencing analysis, most of class D
carbapenemases were K. pneumoniae (17 strains out of 20 strains). Two strains
were K. oxytoca and the other strain was Bacillus cereus. Among class D
carbapenemase resistant K. pneumoniae identified by 16S rRNA sequencing,
PCR for bla OXA-48 gene produced amplified product of 744 bp and was
positive in 10 isolates (58.8%). All these isolates were ESBL producers by
phenotypic tests and resistant to ciprofloxacin, levofloxacin, gentamycin and
amikacin. Conclusion: There are high frequencies of both carbapenem
resistance (47.5%) and ESBL production (39.1%) among K. pneumoniae
isolates. Effective infection control and strict antimicrobial stewardship are
crucial elements to limit the spread of resentence genes.
The 25th
Conference of the Egyptian Society for Medical Microbiology
43
[9] Molecular detection of Helicobacter pylori in children with Otitis
media with effusion at Assiut University and Sohag Teaching
Hospitals
Mohamed S Abd Elaal a, Mohamed A Alfeky
b, Mohamed M Osman
a, Essam
Abo ELmagd, c Trek A Hassan
a and Amal A Elkhawaga
b
aOtolaryngology department, Faculty of Medicine, Assiut University
bMedical Microbiology and Immunology department, Faculty of Medicine,
Assiut University cOtolaryngology Department, Faculty of Medicine, Aswan University
Background: Otitis media with effusion (OME) is a commonest cause of
hearing loss in childhood especially in developing countries. The study included
50 patients with OME. In all cases, myringotomy operation was done.
Objectives: Our work aimed to investigate the prevalence of aerobic and
anaerobic bacteria in children with OME; to determine the presence of H. pylori
in middle ear effusions (MEE) using polymerase chain reaction (PCR); and to
examine the antibiotic susceptibility profile of isolated bacterial strains. Results:
Staphylococcus aureus (28%) was the most prevalent, followed by
Peptostreptococcus species (19.2%), Coagulase negative staphylococci
(17.5%), Klebsiella species (8.7%), E. coli (5.2%), and Pseudomonas
aeruginosa (3.2%). H. pylori could be detected in (5.2%) cases using PCR.
Regarding antibiotic sensitivity, most isolated strains were sensitive for
ciprofloxacin and chloramphenicol while they were resistant to cephalothin
except Peptostreptococcus species. Conclusion: The obtained results indicate
that H. pylori may play a role in the pathogenesis of OME.
The 25th
Conference of the Egyptian Society for Medical Microbiology
44
[10] In Vitro Assessment of Colistin-Carbapenem Combination
Against Multi Drug Resistant Enterobacteriaceae Isolates in
Suez Canal University Hospitals Maha Mahdi, Omayma Aboul- Ola, Anwar Heiba, Rania Kishk
Microbiology and Immunology Department, Faculty of Medicine, Suez Canal
University, Ismailia, Egypt
Background: Health crisis of Multi-Drug Resistant (MDR) Gram Negative
Bacteria, including Enterobacteriaceae, seems overwhelming as its persistence
and worldwide spread causes clinical failures in the treatment of infections by
these organisms and results in significant morbidity and mortality. Combination
therapy, using two or more drugs, may be the last resort for treatment of these
MDR organisms. Objective: this study aimed to assess the effect of colistin
carbapenem combination on MDR-Enterobacteriaceae in vitro. Methodology:
Out of 219 of Enterobacteriaceae strains isolated from different types of
infections in SCUHs, 21.91% were detected to be MDR. In vitro assessment of
Imipenem-colistin combination on the 46 MDR-Enterobacteriaceae strains was
performed using the checkerboard technique. Results: The combination had a
synergistic effect on 63.04% of the isolates and additive effect on 23.9%.
Indifferent effect was shown in 10.8%, while antagonism was shown in 2.1% of
the strains. At least, four-fold decrease in imipenem MIC was proved in 86.9%
of the strains, 30.43% had a reversal of imipenem resistance with change of
MICs from ≥ 4 to ≤ 1μg/ml, 15.21% changed to intermediate resistance with
MIC decrease from ≥ 4 to 2 μg/ml. Three of the 5 strains that showed
indifference and the only strain which showed antagonism were the colistin
resistant strains. Conclusion: Carbapenem and colistin combination against
MDR-Enterobacteriaceae is supported in vitro by high synergy and the reversal
of imipenem resistance with low antagonism, which may encourage clinical
trials of combination therapy in treatment of HAIs by MDR pathogens.