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Microbial interactions in the mosquito gut determine Serratia colonization and blood-feeding propensity

How microbe–microbe interactions dictate microbial complexity in the mosquito gut is unclear. Previously we found that, Serratia, a gut symbiont that alters vector competence and is being considered for vector control, poorly colonized Aedes aegypti yet was abundant in Culex quinquefasciatus reared...

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Autores principales: Kozlova, Elena V., Hegde, Shivanand, Roundy, Christopher M., Golovko, George, Saldaña, Miguel A., Hart, Charles E., Anderson, Enyia R., Hornett, Emily A., Khanipov, Kamil, Popov, Vsevolod L., Pimenova, Maria, Zhou, Yiyang, Fovanov, Yuriy, Weaver, Scott C., Routh, Andrew L., Heinz, Eva, Hughes, Grant L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852612/
https://www.ncbi.nlm.nih.gov/pubmed/32895494
http://dx.doi.org/10.1038/s41396-020-00763-3
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author Kozlova, Elena V.
Hegde, Shivanand
Roundy, Christopher M.
Golovko, George
Saldaña, Miguel A.
Hart, Charles E.
Anderson, Enyia R.
Hornett, Emily A.
Khanipov, Kamil
Popov, Vsevolod L.
Pimenova, Maria
Zhou, Yiyang
Fovanov, Yuriy
Weaver, Scott C.
Routh, Andrew L.
Heinz, Eva
Hughes, Grant L.
author_facet Kozlova, Elena V.
Hegde, Shivanand
Roundy, Christopher M.
Golovko, George
Saldaña, Miguel A.
Hart, Charles E.
Anderson, Enyia R.
Hornett, Emily A.
Khanipov, Kamil
Popov, Vsevolod L.
Pimenova, Maria
Zhou, Yiyang
Fovanov, Yuriy
Weaver, Scott C.
Routh, Andrew L.
Heinz, Eva
Hughes, Grant L.
author_sort Kozlova, Elena V.
collection PubMed
description How microbe–microbe interactions dictate microbial complexity in the mosquito gut is unclear. Previously we found that, Serratia, a gut symbiont that alters vector competence and is being considered for vector control, poorly colonized Aedes aegypti yet was abundant in Culex quinquefasciatus reared under identical conditions. To investigate the incompatibility between Serratia and Ae. aegypti, we characterized two distinct strains of Serratia marcescens from Cx. quinquefasciatus and examined their ability to infect Ae. aegypti. Both Serratia strains poorly infected Ae. aegypti, but when microbiome homeostasis was disrupted, the prevalence and titers of Serratia were similar to the infection in its native host. Examination of multiple genetically diverse Ae. aegypti lines found microbial interference to S. marcescens was commonplace, however, one line of Ae. aegypti was susceptible to infection. Microbiome analysis of resistant and susceptible lines indicated an inverse correlation between Enterobacteriaceae bacteria and Serratia, and experimental co-infections in a gnotobiotic system recapitulated the interference phenotype. Furthermore, we observed an effect on host behavior; Serratia exposure to Ae. aegypti disrupted their feeding behavior, and this phenotype was also reliant on interactions with their native microbiota. Our work highlights the complexity of host–microbe interactions and provides evidence that microbial interactions influence mosquito behavior.
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spelling pubmed-78526122021-02-08 Microbial interactions in the mosquito gut determine Serratia colonization and blood-feeding propensity Kozlova, Elena V. Hegde, Shivanand Roundy, Christopher M. Golovko, George Saldaña, Miguel A. Hart, Charles E. Anderson, Enyia R. Hornett, Emily A. Khanipov, Kamil Popov, Vsevolod L. Pimenova, Maria Zhou, Yiyang Fovanov, Yuriy Weaver, Scott C. Routh, Andrew L. Heinz, Eva Hughes, Grant L. ISME J Article How microbe–microbe interactions dictate microbial complexity in the mosquito gut is unclear. Previously we found that, Serratia, a gut symbiont that alters vector competence and is being considered for vector control, poorly colonized Aedes aegypti yet was abundant in Culex quinquefasciatus reared under identical conditions. To investigate the incompatibility between Serratia and Ae. aegypti, we characterized two distinct strains of Serratia marcescens from Cx. quinquefasciatus and examined their ability to infect Ae. aegypti. Both Serratia strains poorly infected Ae. aegypti, but when microbiome homeostasis was disrupted, the prevalence and titers of Serratia were similar to the infection in its native host. Examination of multiple genetically diverse Ae. aegypti lines found microbial interference to S. marcescens was commonplace, however, one line of Ae. aegypti was susceptible to infection. Microbiome analysis of resistant and susceptible lines indicated an inverse correlation between Enterobacteriaceae bacteria and Serratia, and experimental co-infections in a gnotobiotic system recapitulated the interference phenotype. Furthermore, we observed an effect on host behavior; Serratia exposure to Ae. aegypti disrupted their feeding behavior, and this phenotype was also reliant on interactions with their native microbiota. Our work highlights the complexity of host–microbe interactions and provides evidence that microbial interactions influence mosquito behavior. Nature Publishing Group UK 2020-09-07 2021-01 /pmc/articles/PMC7852612/ /pubmed/32895494 http://dx.doi.org/10.1038/s41396-020-00763-3 Text en © The Author(s) 2020 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/.
spellingShingle Article
Kozlova, Elena V.
Hegde, Shivanand
Roundy, Christopher M.
Golovko, George
Saldaña, Miguel A.
Hart, Charles E.
Anderson, Enyia R.
Hornett, Emily A.
Khanipov, Kamil
Popov, Vsevolod L.
Pimenova, Maria
Zhou, Yiyang
Fovanov, Yuriy
Weaver, Scott C.
Routh, Andrew L.
Heinz, Eva
Hughes, Grant L.
Microbial interactions in the mosquito gut determine Serratia colonization and blood-feeding propensity
title Microbial interactions in the mosquito gut determine Serratia colonization and blood-feeding propensity
title_full Microbial interactions in the mosquito gut determine Serratia colonization and blood-feeding propensity
title_fullStr Microbial interactions in the mosquito gut determine Serratia colonization and blood-feeding propensity
title_full_unstemmed Microbial interactions in the mosquito gut determine Serratia colonization and blood-feeding propensity
title_short Microbial interactions in the mosquito gut determine Serratia colonization and blood-feeding propensity
title_sort microbial interactions in the mosquito gut determine serratia colonization and blood-feeding propensity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852612/
https://www.ncbi.nlm.nih.gov/pubmed/32895494
http://dx.doi.org/10.1038/s41396-020-00763-3
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