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Spiroplasma as facultative bacterial symbionts of stinkbugs

Many insects are associated with facultative symbiotic bacteria, and their infection prevalence provides an important clue to understand the biological impact of such microbial associates. Here we surveyed diverse stinkbugs representing 13 families, 69 genera, 97 species and 468 individuals for Spir...

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Autores principales: Kakizawa, Shigeyuki, Hosokawa, Takahiro, Oguchi, Kohei, Miyakoshi, Kaori, Fukatsu, Takema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638005/
https://www.ncbi.nlm.nih.gov/pubmed/36353457
http://dx.doi.org/10.3389/fmicb.2022.1044771
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author Kakizawa, Shigeyuki
Hosokawa, Takahiro
Oguchi, Kohei
Miyakoshi, Kaori
Fukatsu, Takema
author_facet Kakizawa, Shigeyuki
Hosokawa, Takahiro
Oguchi, Kohei
Miyakoshi, Kaori
Fukatsu, Takema
author_sort Kakizawa, Shigeyuki
collection PubMed
description Many insects are associated with facultative symbiotic bacteria, and their infection prevalence provides an important clue to understand the biological impact of such microbial associates. Here we surveyed diverse stinkbugs representing 13 families, 69 genera, 97 species and 468 individuals for Spiroplasma infection. Diagnostic PCR detection revealed that 4 families (30.8%), 7 genera (10.1%), 11 species (11.3%) and 21 individuals (4.5%) were Spiroplasma positive. All the 21 stinkbug samples with Spiroplasma infection were subjected to PCR amplification and sequencing of Spiroplasma’s 16S rRNA gene. Molecular phylogenetic analysis uncovered that the stinkbug-associated Spiroplasma symbionts were placed in three distinct clades in the Spiroplasmataceae, highlighting multiple evolutionary origins of the stinkbug-Spiroplasma associations. The Spiroplasma phylogeny did not reflect the host stinkbug phylogeny, indicating the absence of host-symbiont co-speciation. On the other hand, the Spiroplasma symbionts associated with the same stinkbug family tended to be related to each other, suggesting the possibility of certain levels of host-symbiont specificity and/or ecological symbiont sharing. Amplicon sequencing analysis targeting bacterial 16S rRNA gene, FISH visualization of the symbiotic bacteria, and rearing experiments of the host stinkbugs uncovered that the Spiroplasma symbionts are generally much less abundant in comparison with the primary gut symbiotic bacteria, localized to various tissues and organs at relatively low densities, and vertically transmitted to the offspring. On the basis of these results, we conclude that the Spiroplasma symbionts are, in general, facultative bacterial associates of low infection prevalence that are not essential but rather commensalistic for the host stinkbugs, like the Spiroplasma symbionts of fruit flies and aphids, although their impact on the host phenotypes should be evaluated in future studies.
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spelling pubmed-96380052022-11-08 Spiroplasma as facultative bacterial symbionts of stinkbugs Kakizawa, Shigeyuki Hosokawa, Takahiro Oguchi, Kohei Miyakoshi, Kaori Fukatsu, Takema Front Microbiol Microbiology Many insects are associated with facultative symbiotic bacteria, and their infection prevalence provides an important clue to understand the biological impact of such microbial associates. Here we surveyed diverse stinkbugs representing 13 families, 69 genera, 97 species and 468 individuals for Spiroplasma infection. Diagnostic PCR detection revealed that 4 families (30.8%), 7 genera (10.1%), 11 species (11.3%) and 21 individuals (4.5%) were Spiroplasma positive. All the 21 stinkbug samples with Spiroplasma infection were subjected to PCR amplification and sequencing of Spiroplasma’s 16S rRNA gene. Molecular phylogenetic analysis uncovered that the stinkbug-associated Spiroplasma symbionts were placed in three distinct clades in the Spiroplasmataceae, highlighting multiple evolutionary origins of the stinkbug-Spiroplasma associations. The Spiroplasma phylogeny did not reflect the host stinkbug phylogeny, indicating the absence of host-symbiont co-speciation. On the other hand, the Spiroplasma symbionts associated with the same stinkbug family tended to be related to each other, suggesting the possibility of certain levels of host-symbiont specificity and/or ecological symbiont sharing. Amplicon sequencing analysis targeting bacterial 16S rRNA gene, FISH visualization of the symbiotic bacteria, and rearing experiments of the host stinkbugs uncovered that the Spiroplasma symbionts are generally much less abundant in comparison with the primary gut symbiotic bacteria, localized to various tissues and organs at relatively low densities, and vertically transmitted to the offspring. On the basis of these results, we conclude that the Spiroplasma symbionts are, in general, facultative bacterial associates of low infection prevalence that are not essential but rather commensalistic for the host stinkbugs, like the Spiroplasma symbionts of fruit flies and aphids, although their impact on the host phenotypes should be evaluated in future studies. Frontiers Media S.A. 2022-10-24 /pmc/articles/PMC9638005/ /pubmed/36353457 http://dx.doi.org/10.3389/fmicb.2022.1044771 Text en Copyright © 2022 Kakizawa, Hosokawa, Oguchi, Miyakoshi and Fukatsu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Kakizawa, Shigeyuki
Hosokawa, Takahiro
Oguchi, Kohei
Miyakoshi, Kaori
Fukatsu, Takema
Spiroplasma as facultative bacterial symbionts of stinkbugs
title Spiroplasma as facultative bacterial symbionts of stinkbugs
title_full Spiroplasma as facultative bacterial symbionts of stinkbugs
title_fullStr Spiroplasma as facultative bacterial symbionts of stinkbugs
title_full_unstemmed Spiroplasma as facultative bacterial symbionts of stinkbugs
title_short Spiroplasma as facultative bacterial symbionts of stinkbugs
title_sort spiroplasma as facultative bacterial symbionts of stinkbugs
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638005/
https://www.ncbi.nlm.nih.gov/pubmed/36353457
http://dx.doi.org/10.3389/fmicb.2022.1044771
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