Cargando…
Genetics and immunity of Anopheles response to the entomopathogenic fungus Metarhizium anisopliae overlap with immunity to Plasmodium
Entomopathogenic fungi have been explored as a potential biopesticide to counteract the insecticide resistance issue in mosquitoes. However, little is known about the possibility that genetic resistance to fungal biopesticides could evolve in mosquito populations. Here, we detected an important gene...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012835/ https://www.ncbi.nlm.nih.gov/pubmed/35428783 http://dx.doi.org/10.1038/s41598-022-10190-3 |
_version_ | 1784687875006136320 |
---|---|
author | Bukhari, Tullu Aimanianda, Vishukumar Bischoff, Emmanuel Brito-Fravallo, Emma Eiglmeier, Karin Riehle, Michelle M. Vernick, Kenneth D. Mitri, Christian |
author_facet | Bukhari, Tullu Aimanianda, Vishukumar Bischoff, Emmanuel Brito-Fravallo, Emma Eiglmeier, Karin Riehle, Michelle M. Vernick, Kenneth D. Mitri, Christian |
author_sort | Bukhari, Tullu |
collection | PubMed |
description | Entomopathogenic fungi have been explored as a potential biopesticide to counteract the insecticide resistance issue in mosquitoes. However, little is known about the possibility that genetic resistance to fungal biopesticides could evolve in mosquito populations. Here, we detected an important genetic component underlying Anopheles coluzzii survival after exposure to the entomopathogenic fungus Metarhizium anisopliae. A familiality study detected variation for survival among wild mosquito isofemale pedigrees, and genetic mapping identified two loci that significantly influence mosquito survival after fungus exposure. One locus overlaps with a previously reported locus for Anopheles susceptibility to the human malaria parasite Plasmodium falciparum. Candidate gene studies revealed that two LRR proteins encoded by APL1C and LRIM1 genes in this newly mapped locus are required for protection of female A. coluzzii from M. anisopliae, as is the complement-like factor Tep1. These results indicate that natural Anopheles populations already segregate frequent genetic variation for differential mosquito survival after fungal challenge and suggest a similarity in Anopheles protective responses against fungus and Plasmodium. However, this immune similarity raises the possibility that fungus-resistant mosquitoes could also display enhanced resistance to Plasmodium, suggesting an advantage of selecting for fungus resistance in vector populations to promote naturally diminished malaria vector competence. |
format | Online Article Text |
id | pubmed-9012835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90128352022-04-18 Genetics and immunity of Anopheles response to the entomopathogenic fungus Metarhizium anisopliae overlap with immunity to Plasmodium Bukhari, Tullu Aimanianda, Vishukumar Bischoff, Emmanuel Brito-Fravallo, Emma Eiglmeier, Karin Riehle, Michelle M. Vernick, Kenneth D. Mitri, Christian Sci Rep Article Entomopathogenic fungi have been explored as a potential biopesticide to counteract the insecticide resistance issue in mosquitoes. However, little is known about the possibility that genetic resistance to fungal biopesticides could evolve in mosquito populations. Here, we detected an important genetic component underlying Anopheles coluzzii survival after exposure to the entomopathogenic fungus Metarhizium anisopliae. A familiality study detected variation for survival among wild mosquito isofemale pedigrees, and genetic mapping identified two loci that significantly influence mosquito survival after fungus exposure. One locus overlaps with a previously reported locus for Anopheles susceptibility to the human malaria parasite Plasmodium falciparum. Candidate gene studies revealed that two LRR proteins encoded by APL1C and LRIM1 genes in this newly mapped locus are required for protection of female A. coluzzii from M. anisopliae, as is the complement-like factor Tep1. These results indicate that natural Anopheles populations already segregate frequent genetic variation for differential mosquito survival after fungal challenge and suggest a similarity in Anopheles protective responses against fungus and Plasmodium. However, this immune similarity raises the possibility that fungus-resistant mosquitoes could also display enhanced resistance to Plasmodium, suggesting an advantage of selecting for fungus resistance in vector populations to promote naturally diminished malaria vector competence. Nature Publishing Group UK 2022-04-15 /pmc/articles/PMC9012835/ /pubmed/35428783 http://dx.doi.org/10.1038/s41598-022-10190-3 Text en © The Author(s) 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bukhari, Tullu Aimanianda, Vishukumar Bischoff, Emmanuel Brito-Fravallo, Emma Eiglmeier, Karin Riehle, Michelle M. Vernick, Kenneth D. Mitri, Christian Genetics and immunity of Anopheles response to the entomopathogenic fungus Metarhizium anisopliae overlap with immunity to Plasmodium |
title | Genetics and immunity of Anopheles response to the entomopathogenic fungus Metarhizium anisopliae overlap with immunity to Plasmodium |
title_full | Genetics and immunity of Anopheles response to the entomopathogenic fungus Metarhizium anisopliae overlap with immunity to Plasmodium |
title_fullStr | Genetics and immunity of Anopheles response to the entomopathogenic fungus Metarhizium anisopliae overlap with immunity to Plasmodium |
title_full_unstemmed | Genetics and immunity of Anopheles response to the entomopathogenic fungus Metarhizium anisopliae overlap with immunity to Plasmodium |
title_short | Genetics and immunity of Anopheles response to the entomopathogenic fungus Metarhizium anisopliae overlap with immunity to Plasmodium |
title_sort | genetics and immunity of anopheles response to the entomopathogenic fungus metarhizium anisopliae overlap with immunity to plasmodium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012835/ https://www.ncbi.nlm.nih.gov/pubmed/35428783 http://dx.doi.org/10.1038/s41598-022-10190-3 |
work_keys_str_mv | AT bukharitullu geneticsandimmunityofanophelesresponsetotheentomopathogenicfungusmetarhiziumanisopliaeoverlapwithimmunitytoplasmodium AT aimaniandavishukumar geneticsandimmunityofanophelesresponsetotheentomopathogenicfungusmetarhiziumanisopliaeoverlapwithimmunitytoplasmodium AT bischoffemmanuel geneticsandimmunityofanophelesresponsetotheentomopathogenicfungusmetarhiziumanisopliaeoverlapwithimmunitytoplasmodium AT britofravalloemma geneticsandimmunityofanophelesresponsetotheentomopathogenicfungusmetarhiziumanisopliaeoverlapwithimmunitytoplasmodium AT eiglmeierkarin geneticsandimmunityofanophelesresponsetotheentomopathogenicfungusmetarhiziumanisopliaeoverlapwithimmunitytoplasmodium AT riehlemichellem geneticsandimmunityofanophelesresponsetotheentomopathogenicfungusmetarhiziumanisopliaeoverlapwithimmunitytoplasmodium AT vernickkennethd geneticsandimmunityofanophelesresponsetotheentomopathogenicfungusmetarhiziumanisopliaeoverlapwithimmunitytoplasmodium AT mitrichristian geneticsandimmunityofanophelesresponsetotheentomopathogenicfungusmetarhiziumanisopliaeoverlapwithimmunitytoplasmodium |