Nuclear Orthologs Derived from Whole Genome Sequencing Indicate Cryptic Diversity in the Bemisia tabaci (Insecta: Aleyrodidae) Complex of Whiteflies
Authorde Moya, Robert S.
Brown, Judith K.
Sweet, Andrew D.
Walden, Kimberly K. O.
Paredes-Montero, Jorge R.
Waterhouse, Robert M.
Johnson, Kevin P.
AffiliationUniv Arizona, Sch Plant Sci
MetadataShow full item record
Citationde Moya, R. S., Brown, J. K., Sweet, A. D., Walden, K. K., Paredes-Montero, J. R., Waterhouse, R. M., & Johnson, K. P. (2019). Nuclear Orthologs Derived from Whole Genome Sequencing Indicate Cryptic Diversity in the Bemisia tabaci (Insecta: Aleyrodidae) Complex of Whiteflies. Diversity, 11(9), 151.
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AbstractThe Bemisia tabaci complex of whiteflies contains globally important pests thought to contain cryptic species corresponding to geographically structured phylogenetic clades. Although mostly morphologically indistinguishable, differences have been shown to exist among populations in behavior, plant virus vector capacity, ability to hybridize, and DNA sequence divergence. These differences allow for certain populations to become invasive and cause great economic damage in a monoculture setting. Although high mitochondrial DNA divergences have been reported between putative conspecifics of the B. tabaci species complex, there is limited data that exists across the whole genome for this group. Using data from 2184 orthologs obtained from whole genome sequencing (Illumina), a phylogenetic analysis using maximum likelihood and coalescent methodologies was completed on ten individuals of the B. tabaci complex. In addition, automatic barcode gap discovery methods were employed, and results suggest the existence of five species. Although the divergences of the mitochondrial cytochrome oxidase I gene are high among members of this complex, nuclear divergences are much lower in comparison. Single-copy orthologs from whole genome sequencing demonstrate divergent population structures among members of the B. tabaci complex and the sequences provide an important resource to aid in future genomic studies of the group.
NoteOpen access journal
VersionFinal published version
SponsorsSupport for this work was provided to K.P.J. by the National Science Foundation (grant number DEB-1342604). Support for R.M.W. was provided by the Swiss National Science Foundation (grant number PP00P3_170664).