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Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector
Wolbachia, a maternally inherited intracellular bacterial species, can manipulate host insect reproduction by cytoplasmic incompatibility (CI), which results in embryo lethality in crosses between infected males and uninfected females. CI is encoded by two prophage genes, cifA and cifB. Wolbachia, c...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612931/ https://www.ncbi.nlm.nih.gov/pubmed/34819638 http://dx.doi.org/10.1038/s41564-021-00998-6 |
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author | Adams, Kelsey L. Abernathy, Daniel G. Willett, Bailey C. Selland, Emily K. Itoe, Maurice A. Catteruccia, Flaminia |
author_facet | Adams, Kelsey L. Abernathy, Daniel G. Willett, Bailey C. Selland, Emily K. Itoe, Maurice A. Catteruccia, Flaminia |
author_sort | Adams, Kelsey L. |
collection | PubMed |
description | Wolbachia, a maternally inherited intracellular bacterial species, can manipulate host insect reproduction by cytoplasmic incompatibility (CI), which results in embryo lethality in crosses between infected males and uninfected females. CI is encoded by two prophage genes, cifA and cifB. Wolbachia, coupled with the sterile insect technique, has been used in field trials to control populations of the dengue vector Aedes albopictus, but CI-inducing strains are not known to infect the malaria vector Anopheles gambiae. Here we show that cifA and cifB can induce conditional sterility in the malaria vector An. gambiae. We used transgenic expression of these Wolbachia-derived genes in the An. gambiae germline to show that cifB is sufficient to cause embryonic lethality and that cifB-induced sterility is rescued by cifA expression in females. When we co-expressed cifA and cifB in male mosquitoes, the CI phenotype was attenuated. In female mosquitoes, cifB impaired fertility, which was overcome by co-expression of cifA. Our findings pave the way towards using CI to control malaria mosquito vectors. |
format | Online Article Text |
id | pubmed-8612931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86129312021-12-10 Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector Adams, Kelsey L. Abernathy, Daniel G. Willett, Bailey C. Selland, Emily K. Itoe, Maurice A. Catteruccia, Flaminia Nat Microbiol Article Wolbachia, a maternally inherited intracellular bacterial species, can manipulate host insect reproduction by cytoplasmic incompatibility (CI), which results in embryo lethality in crosses between infected males and uninfected females. CI is encoded by two prophage genes, cifA and cifB. Wolbachia, coupled with the sterile insect technique, has been used in field trials to control populations of the dengue vector Aedes albopictus, but CI-inducing strains are not known to infect the malaria vector Anopheles gambiae. Here we show that cifA and cifB can induce conditional sterility in the malaria vector An. gambiae. We used transgenic expression of these Wolbachia-derived genes in the An. gambiae germline to show that cifB is sufficient to cause embryonic lethality and that cifB-induced sterility is rescued by cifA expression in females. When we co-expressed cifA and cifB in male mosquitoes, the CI phenotype was attenuated. In female mosquitoes, cifB impaired fertility, which was overcome by co-expression of cifA. Our findings pave the way towards using CI to control malaria mosquito vectors. Nature Publishing Group UK 2021-11-24 2021 /pmc/articles/PMC8612931/ /pubmed/34819638 http://dx.doi.org/10.1038/s41564-021-00998-6 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Adams, Kelsey L. Abernathy, Daniel G. Willett, Bailey C. Selland, Emily K. Itoe, Maurice A. Catteruccia, Flaminia Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector |
title | Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector |
title_full | Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector |
title_fullStr | Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector |
title_full_unstemmed | Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector |
title_short | Wolbachia cifB induces cytoplasmic incompatibility in the malaria mosquito vector |
title_sort | wolbachia cifb induces cytoplasmic incompatibility in the malaria mosquito vector |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612931/ https://www.ncbi.nlm.nih.gov/pubmed/34819638 http://dx.doi.org/10.1038/s41564-021-00998-6 |
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