{"title":"Overwintering Does Not Affect Microbiota Diversity in Halyomorpha halys: Implications for Its Ecology and Management","authors":"Riccardo Piccinno, Giulio Galla, Gerardo Roselli, Mirco Rodeghiero, Valerio Mazzoni, Lloyd Stringer, Heidi Christine Hauffe, Gianfranco Anfora, Omar Rota-Stabelli","doi":"10.1111/1758-2229.70116","DOIUrl":null,"url":null,"abstract":"<p>Host-associated microbial communities play an important role in regulating many aspects of insect biology, but changes in this microbiota during diapause and overwintering are still largely unknown. <i>Halyomorpha halys</i> is an invasive agricultural pest characterised by a unique overwintering strategy where individuals aggregate and enter a state of dormancy, making it an excellent model to study the relationship between microbiota and diapause. We investigated the bacterial diversity of wild <i>H. halys</i> specimens before and after dormancy using 16S rRNA gene amplicon-sequencing. We found that microbiota varies between geographically neighbouring sampling locations, but there were no significant differences in microbial diversity or composition between populations sampled before and after diapause, despite stressful overwintering conditions. Such stability may relate to the highly specific taxa that dominate the stinkbug-associated microbial community. In addition, we did not detect any strong association of stink bugs with phytopathogens, but we found that two populations harboured <i>Nosema maddoxi</i>, a microsporidian pathogen of stink bugs. Our results are relevant to the assessment of accidental spillovers of microorganisms in newly invaded areas and to the implementation of the sterile insect technique based on mass trapping, irradiation, shipping and release after diapause of wild individuals.</p>","PeriodicalId":163,"journal":{"name":"Environmental Microbiology Reports","volume":"17 3","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1758-2229.70116","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Microbiology Reports","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1758-2229.70116","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Host-associated microbial communities play an important role in regulating many aspects of insect biology, but changes in this microbiota during diapause and overwintering are still largely unknown. Halyomorpha halys is an invasive agricultural pest characterised by a unique overwintering strategy where individuals aggregate and enter a state of dormancy, making it an excellent model to study the relationship between microbiota and diapause. We investigated the bacterial diversity of wild H. halys specimens before and after dormancy using 16S rRNA gene amplicon-sequencing. We found that microbiota varies between geographically neighbouring sampling locations, but there were no significant differences in microbial diversity or composition between populations sampled before and after diapause, despite stressful overwintering conditions. Such stability may relate to the highly specific taxa that dominate the stinkbug-associated microbial community. In addition, we did not detect any strong association of stink bugs with phytopathogens, but we found that two populations harboured Nosema maddoxi, a microsporidian pathogen of stink bugs. Our results are relevant to the assessment of accidental spillovers of microorganisms in newly invaded areas and to the implementation of the sterile insect technique based on mass trapping, irradiation, shipping and release after diapause of wild individuals.
期刊介绍:
The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side.
Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.