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The Genetic Basis of Natural Variation in Drosophila melanogaster Immune Defense against Enterococcus faecalis
Dissecting the genetic basis of natural variation in disease response in hosts provides insights into the coevolutionary dynamics of host-pathogen interactions. Here, a genome-wide association study of Drosophila melanogaster survival after infection with the Gram-positive entomopathogenic bacterium...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074548/ https://www.ncbi.nlm.nih.gov/pubmed/32098395 http://dx.doi.org/10.3390/genes11020234 |
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author | Chapman, Joanne R Dowell, Maureen A Chan, Rosanna Unckless, Robert L |
author_facet | Chapman, Joanne R Dowell, Maureen A Chan, Rosanna Unckless, Robert L |
author_sort | Chapman, Joanne R |
collection | PubMed |
description | Dissecting the genetic basis of natural variation in disease response in hosts provides insights into the coevolutionary dynamics of host-pathogen interactions. Here, a genome-wide association study of Drosophila melanogaster survival after infection with the Gram-positive entomopathogenic bacterium Enterococcus faecalis is reported. There was considerable variation in defense against E. faecalis infection among inbred lines of the Drosophila Genetics Reference Panel. We identified single nucleotide polymorphisms associated with six genes with a significant (p < 10(−08), corresponding to a false discovery rate of 2.4%) association with survival, none of which were canonical immune genes. To validate the role of these genes in immune defense, their expression was knocked-down using RNAi and survival of infected hosts was followed, which confirmed a role for the genes krishah and S6k in immune defense. We further identified a putative role for the Bomanin gene BomBc1 (also known as IM23), in E. faecalis infection response. This study adds to the growing set of association studies for infection in Drosophila melanogaster and suggests that the genetic causes of variation in immune defense differ for different pathogens. |
format | Online Article Text |
id | pubmed-7074548 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70745482020-03-20 The Genetic Basis of Natural Variation in Drosophila melanogaster Immune Defense against Enterococcus faecalis Chapman, Joanne R Dowell, Maureen A Chan, Rosanna Unckless, Robert L Genes (Basel) Article Dissecting the genetic basis of natural variation in disease response in hosts provides insights into the coevolutionary dynamics of host-pathogen interactions. Here, a genome-wide association study of Drosophila melanogaster survival after infection with the Gram-positive entomopathogenic bacterium Enterococcus faecalis is reported. There was considerable variation in defense against E. faecalis infection among inbred lines of the Drosophila Genetics Reference Panel. We identified single nucleotide polymorphisms associated with six genes with a significant (p < 10(−08), corresponding to a false discovery rate of 2.4%) association with survival, none of which were canonical immune genes. To validate the role of these genes in immune defense, their expression was knocked-down using RNAi and survival of infected hosts was followed, which confirmed a role for the genes krishah and S6k in immune defense. We further identified a putative role for the Bomanin gene BomBc1 (also known as IM23), in E. faecalis infection response. This study adds to the growing set of association studies for infection in Drosophila melanogaster and suggests that the genetic causes of variation in immune defense differ for different pathogens. MDPI 2020-02-22 /pmc/articles/PMC7074548/ /pubmed/32098395 http://dx.doi.org/10.3390/genes11020234 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chapman, Joanne R Dowell, Maureen A Chan, Rosanna Unckless, Robert L The Genetic Basis of Natural Variation in Drosophila melanogaster Immune Defense against Enterococcus faecalis |
title | The Genetic Basis of Natural Variation in Drosophila melanogaster Immune Defense against Enterococcus faecalis |
title_full | The Genetic Basis of Natural Variation in Drosophila melanogaster Immune Defense against Enterococcus faecalis |
title_fullStr | The Genetic Basis of Natural Variation in Drosophila melanogaster Immune Defense against Enterococcus faecalis |
title_full_unstemmed | The Genetic Basis of Natural Variation in Drosophila melanogaster Immune Defense against Enterococcus faecalis |
title_short | The Genetic Basis of Natural Variation in Drosophila melanogaster Immune Defense against Enterococcus faecalis |
title_sort | genetic basis of natural variation in drosophila melanogaster immune defense against enterococcus faecalis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074548/ https://www.ncbi.nlm.nih.gov/pubmed/32098395 http://dx.doi.org/10.3390/genes11020234 |
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