Evidence map›Paper›PMID 27974049›Full record

ArticleBMC biology2016

The draft genome of whitefly Bemisia tabaci MEAM1, a global crop pest, provides novel insights into virus transmission, host adaptation, and insecticide resistance.

Wenbo Chen, Daniel K Hasegawa, Navneet Kaur, Adi Kliot, Patricia Valle Pinheiro, Junbo Luan, Marcus C Stensmyr, Yi Zheng, Wenli Liu, Honghe Sun and 18 more

Abstract read
In one paragraph

Article in BMC biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 151 papers.

0numbers the graph read from it
0cells of the map it votes in
151citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

151 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

91 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

Wenbo ChenBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Daniel K HasegawaBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Navneet KaurUS Department of Agriculture-Agricultural Research Service, Crop Improvement and Protection Research, Salinas, CA, 93905, USA.
Adi KliotDepartment of Entomology, The Volcani Center, Bet Dagan, 50250, Israel.
Patricia Valle PinheiroBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Junbo LuanDepartment of Entomology, Cornell University, Ithaca, NY, 14853, USA.
Marcus C StensmyrDepartment of Biology, Lund University, Lund, SE-223 62, Sweden.
Yi ZhengBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Wenli LiuBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Honghe SunBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Yimin XuBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Yuan LuoDepartment of Entomology, Cornell University, Ithaca, NY, 14853, USA.
Angela KruseBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Xiaowei YangDepartment of Entomology, Cornell University, Ithaca, NY, 14853, USA.
Svetlana KontsedalovDepartment of Entomology, The Volcani Center, Bet Dagan, 50250, Israel.
Galina LebedevDepartment of Entomology, The Volcani Center, Bet Dagan, 50250, Israel.
Tonja W FisherDepartment of Plant Sciences, The University of Arizona, Tucson, AZ, 85721, USA.
David R NelsonDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN, 38163, USA.
Wayne B HunterUS Department of Agriculture-Agricultural Research Service, US Horticultural Laboratory, Fort Pierce, FL, 34945, USA.
Judith K BrownDepartment of Plant Pathology and Plant-Microbe Biology, Cornell University, Ithaca, NY, 14853, USA.
Georg JanderBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Michelle CiliaBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA.
Angela E DouglasDepartment of Entomology, Cornell University, Ithaca, NY, 14853, USA.
Murad GhanimDepartment of Entomology, The Volcani Center, Bet Dagan, 50250, Israel.
Alvin M SimmonsUS Department of Agriculture-Agricultural Research Service, US Vegetable Laboratory, Charleston, SC, 29414, USA.
William M WintermantelUS Department of Agriculture-Agricultural Research Service, Crop Improvement and Protection Research, Salinas, CA, 93905, USA. bill.wintermantel@ars.usda.gov.
Kai-Shu LingUS Department of Agriculture-Agricultural Research Service, US Vegetable Laboratory, Charleston, SC, 29414, USA. kai.ling@ars.usda.gov.
Zhangjun FeiBoyce Thompson Institute, Cornell University, Ithaca, NY, 14853, USA. zf25@cornell.edu.ORCID 0000-0001-9684-1450

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe whitefly Bemisia tabaci (Hemiptera: Aleyrodidae) is among the 100 worst invasive species in the world. As one of the most important crop pests and virus vectors, B. tabaci causes substantial crop losses and poses a serious threat to global food security.

resultsWe report the 615-Mb high-quality genome sequence of B. tabaci Middle East-Asia Minor 1 (MEAM1), the first genome sequence in the Aleyrodidae family, which contains 15,664 protein-coding genes. The B. tabaci genome is highly divergent from other sequenced hemipteran genomes, sharing no detectable synteny. A number of known detoxification gene families, including cytochrome P450s and UDP-glucuronosyltransferases, are significantly expanded in B. tabaci. Other expanded gene families, including cathepsins, large clusters of tandemly duplicated B. tabaci-specific genes, and phosphatidylethanolamine-binding proteins (PEBPs), were found to be associated with virus acquisition and transmission and/or insecticide resistance, likely contributing to the global invasiveness and efficient virus transmission capacity of B. tabaci. The presence of 142 horizontally transferred genes from bacteria or fungi in the B. tabaci genome, including genes encoding hopanoid/sterol synthesis and xenobiotic detoxification enzymes that are not present in other insects, offers novel insights into the unique biological adaptations of this insect such as polyphagy and insecticide resistance. Interestingly, two adjacent bacterial pantothenate biosynthesis genes, panB and panC, have been co-transferred into B. tabaci and fused into a single gene that has acquired introns during its evolution.

conclusionsThe B. tabaci genome contains numerous genetic novelties, including expansions in gene families associated with insecticide resistance, detoxification and virus transmission, as well as numerous horizontally transferred genes from bacteria and fungi. We believe these novelties likely have shaped B. tabaci as a highly invasive polyphagous crop pest and efficient vector of plant viruses. The genome serves as a reference for resolving the B. tabaci cryptic species complex, understanding fundamental biological novelties, and providing valuable genetic information to assist the development of novel strategies for controlling whiteflies and the viruses they transmit.

Indexed as

AnimalsGenome, InsectHemipteraInsecticide ResistanceInsect ProteinsPlant VirusesInsect ProteinsBemisia tabaciDraft genomeInsecticide resistancePolyphagyVirus transmissionWhitefly

Identifiers

PMID27974049
PMCPMC5157087

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.