The Bemisia tabaci complex
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Transcript of The Bemisia tabaci complex
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The The Bemisia tabaciBemisia tabaci complex complex
J.K. Brown Department of Plant Sciences,
The University of Arizona Tucson, AZ 85721
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V. The Whitefly V. The Whitefly VectorVector Pupal stagePupal stage
AdultAdult /4th Instar /4th Instar
Bemisia tabaciBemisia tabaci (Genn.) (Genn.)• Worldwide, most important whitefly vector of plant Worldwide, most important whitefly vector of plant
viruses: irrigated cropping systems viruses: irrigated cropping systems subtropics/tropicssubtropics/tropics
• Only whitefly vector for BegomovirusesOnly whitefly vector for Begomoviruses• Species rich in biological variants-lacks Species rich in biological variants-lacks
distinguishing morphological (4th instar) distinguishing morphological (4th instar) characteristicscharacteristics
• Synonymized from numerous species and variants Synonymized from numerous species and variants by Russell, 1957 (historical evidence: cryptic by Russell, 1957 (historical evidence: cryptic species)species)
• Recent evidence for phenotypic & genotypic Recent evidence for phenotypic & genotypic variantsvariants
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Bemisia tabaci has been here for a long time…Bemisia tabaci has been here for a long time…• Tropical originTropical origin• Phloem specialists -Phloem specialists -
intercellular stylet penetrationintercellular stylet penetration
• ParthenogenesisParthenogenesis
Primitive whitefly, Bernaea neocomica Schlee in Lebanese amber - 120 to130 MY BP -Stuttgart Natural History Museum collection
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Extant B. tabaci - widely distributed ~b/t 300 parallels N& S
-Evidence for morphological variation = -Evidence for morphological variation = taxonomic confusion (Basu & taxonomic confusion (Basu &
Mohanty; MoundMohanty; Mound) )
-Most - highly polyphagous, but some are ‘host-adapted’-Most - highly polyphagous, but some are ‘host-adapted’
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First evidence for biologically distinct populationsFirst evidence for biologically distinct populations
Jatropha
Sida
Dr. JulioBird
Bird (1957) recognized Jatropha Bird (1957) recognized Jatropha race was ‘host-restricted’; Low race was ‘host-restricted’; Low fecundityfecundity
Sida race was polyphagous; Sida race was polyphagous; moderate to high fecundity moderate to high fecundity
Proposed ‘concept’ of racesProposed ‘concept’ of races
Then Costa and Russell (1975) recognized Then Costa and Russell (1975) recognized that that BB. . tabacitabaci from Brazil did not colonize from Brazil did not colonize cassava (its center of origin) adding to J. cassava (its center of origin) adding to J. Bird’s’ race’ hypothesis; cassava associated Bird’s’ race’ hypothesis; cassava associated populations discovered on cassava in Africa populations discovered on cassava in Africa (Burban et al., 1991) (begomovirus vectors)(Burban et al., 1991) (begomovirus vectors)
AZ-A and B biotypes recognized after the introduction of the B type in 1988-89
(Costa & Brown)
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1987/88 B biotype introduced to US & Caribbean, C& So America &
worldwide - SSL diagnostic phenotype (Costa& Brown 1990)
-Polyphagous; preferred cotton, cucurbits, poinsettia, tomato
Using general esterases first demonstrated widespread genetic polymorphisms genus-wide throughout the subtropics
Brown et al., UAZ - 1989-1993)
‘Discovery’ ofthe Bbiotype
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A number of A number of biotypes are now known, but cannot be distinguished biotypes are now known, but cannot be distinguished using morphological charactersusing morphological characters
Biological Characters That Can Differ
-Geographic range: limited vs. widespread/
-Fecundity: ~50 to 300+ offspring
-Begomovirus transmission competency - co-evolution
-Host range: monophagous to polyphagous
-Dispersal behavior: short or long distance
-Mating behavior /some are isolated by geography/host?
-Hybrids for certain haplotype crosses, others incompatible (produce only males = no fertilization)
-Insecticide resistance - highly variable and plastic
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Molecular marker-DNA sequence used for identification
• Mitochondria
-Cytochrome oxidase I gene
-Primer locations
UEA3-UEA10
850 bp
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PCR Primers
Forward C1-J-2195
5’ ttg att ttt tgg tca tcc aga agt 3’
Reverse L2-N-3014
5’ tcc aat gca cta atc tgc cat att a 3’
(UBC Insect Mitochondrial DNA Primer Oligonucleotide Set, compiled by B. J. Crespi and C. Simon, with most sequences
taken from Simon et al., 1994)
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MT COI MT COI sequence sequence revealsrevealsphylogeo-phylogeo-graphic graphic clustersclusters
Hypothesis: Hypothesis: species complexspecies complex
Q biotype
A biotype
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The Big
Picture
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Table 3. Percent shared nucleotide identity and nucleotide divergence for within-clade comparisons of Bemisia tabaci, calculated by PAUP.
Clade% nt identity % nt divergence
New Worldn = 8
91.4 - 99.0 1.0 - 8.6
Indian Subcontinent/ FarEastn = 7
82.8 - 98.6 1.4 - 17.2
N. Africa- Middle East-Mediterranean Region
n = 1381.9 - 97.2 2.8 - 18.1
Sub-Saharan Africa(w/o ABA, IC cassava)
n = 4288.9 - 99.7 0.3 - 11.1
Sub-Saharan AfricaN = 44
80.3 - 99.7 0.3 - 19.7
Outgroups
T. vaporariorum xAll B. tabaci
B. afer x All B. tabaci
71.3 - 76.5
71.6
23.5 - 28.7
28.4
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Global origins of B. tabaciGlobal origins of B. tabaci + Begomoviruses + Begomoviruses
Q
BA
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Begomoviruses Begomoviruses can be carried bycan be carried by B. tabaci B. tabaci or plantsor plants
-‘Paired icosahedra’ (geminate) particles
20 x 30 nm
The insect vector is theBemisia tabaci speciescomplex
Examples of begomovirus symptoms in AZ/CA/Sonora Mexico crops
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Transmission Transmission Pathway - Pathway -
Geminiviruses are transmitted by Geminiviruses are transmitted by different biotypes with similar different biotypes with similar
competency if plant host is competency if plant host is compatiblecompatible
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Where to go from here?Know who and where the enemy isKnow what to do when it’s found
1. Accept that the Q biotype could likely become established in the U.S. and the Americas; we will not likely be able to eradicate it.
2. The Q biotype has a very broad host range; thought to be similar to the B biotype.
3. Conduct surveys (self monitoring) to find out where it is and where it is not presently: Hot spot states: AZ, CA, TX, FL cotton, vegetables, ornamentals. Share information, not blame.
4. Diligent monitor over time to track movement and distribution to identifyHot spots for directed control to reduce potential for outbreaks.
5. Obtain additional information about host range, potential to hybridize, vector aspects, new viruses anticipated?, biology in niches in U.S., identify/optimize effective insecticides.
6. Continue to self monitor and judicious use of insecticides - effective control.
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Thank you