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Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance

Heritable symbionts play an essential role in many aspects of host ecology in a temperature-dependent manner. However, how temperature impacts the host and their interaction with endosymbionts remains largely unknown. Here, we investigated the impact of moderate (20°C) and high (30 and 35°C) tempera...

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Autores principales: Zhu, Yu-Xi, Song, Zhang-Rong, Zhang, Yi-Yin, Hoffmann, Ary A., Hong, Xiao-Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292952/
https://www.ncbi.nlm.nih.gov/pubmed/34305877
http://dx.doi.org/10.3389/fmicb.2021.706321
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author Zhu, Yu-Xi
Song, Zhang-Rong
Zhang, Yi-Yin
Hoffmann, Ary A.
Hong, Xiao-Yue
author_facet Zhu, Yu-Xi
Song, Zhang-Rong
Zhang, Yi-Yin
Hoffmann, Ary A.
Hong, Xiao-Yue
author_sort Zhu, Yu-Xi
collection PubMed
description Heritable symbionts play an essential role in many aspects of host ecology in a temperature-dependent manner. However, how temperature impacts the host and their interaction with endosymbionts remains largely unknown. Here, we investigated the impact of moderate (20°C) and high (30 and 35°C) temperatures on symbioses between the spider mite Tetranychus truncatus and two maternally inherited endosymbionts (Wolbachia and Spiroplasma). We found that the thermal tolerance of mites (as measured by survival after heat exposure) was lower for mites that were singly infected with either Wolbachia or Spiroplasma than it was for co-infected or uninfected mites. Although a relatively high temperature (30°C) is thought to promote bacterial replication, rearing at high temperature (35°C) resulted in losses of Wolbachia and particularly Spiroplasma. Exposing the mites to 20°C reduced the density and transmission of Spiroplasma but not Wolbachia. The four spider mite strains tested differed in the numbers of heat shock genes (Hsps) induced under moderate or high temperature exposure. In thermal preference (Tp) assays, the two Wolbachia-infected spider mite strains preferred a lower temperature than strains without Wolbachia. Our results show that endosymbiont-mediated spider mite responses to temperature stress are complex, involving a combination of changing endosymbiont infection patterns, altered thermoregulatory behavior, and transcription responses.
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spelling pubmed-82929522021-07-22 Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance Zhu, Yu-Xi Song, Zhang-Rong Zhang, Yi-Yin Hoffmann, Ary A. Hong, Xiao-Yue Front Microbiol Microbiology Heritable symbionts play an essential role in many aspects of host ecology in a temperature-dependent manner. However, how temperature impacts the host and their interaction with endosymbionts remains largely unknown. Here, we investigated the impact of moderate (20°C) and high (30 and 35°C) temperatures on symbioses between the spider mite Tetranychus truncatus and two maternally inherited endosymbionts (Wolbachia and Spiroplasma). We found that the thermal tolerance of mites (as measured by survival after heat exposure) was lower for mites that were singly infected with either Wolbachia or Spiroplasma than it was for co-infected or uninfected mites. Although a relatively high temperature (30°C) is thought to promote bacterial replication, rearing at high temperature (35°C) resulted in losses of Wolbachia and particularly Spiroplasma. Exposing the mites to 20°C reduced the density and transmission of Spiroplasma but not Wolbachia. The four spider mite strains tested differed in the numbers of heat shock genes (Hsps) induced under moderate or high temperature exposure. In thermal preference (Tp) assays, the two Wolbachia-infected spider mite strains preferred a lower temperature than strains without Wolbachia. Our results show that endosymbiont-mediated spider mite responses to temperature stress are complex, involving a combination of changing endosymbiont infection patterns, altered thermoregulatory behavior, and transcription responses. Frontiers Media S.A. 2021-07-07 /pmc/articles/PMC8292952/ /pubmed/34305877 http://dx.doi.org/10.3389/fmicb.2021.706321 Text en Copyright © 2021 Zhu, Song, Zhang, Hoffmann and Hong. 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
Zhu, Yu-Xi
Song, Zhang-Rong
Zhang, Yi-Yin
Hoffmann, Ary A.
Hong, Xiao-Yue
Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance
title Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance
title_full Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance
title_fullStr Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance
title_full_unstemmed Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance
title_short Spider Mites Singly Infected With Either Wolbachia or Spiroplasma Have Reduced Thermal Tolerance
title_sort spider mites singly infected with either wolbachia or spiroplasma have reduced thermal tolerance
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8292952/
https://www.ncbi.nlm.nih.gov/pubmed/34305877
http://dx.doi.org/10.3389/fmicb.2021.706321
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