{"title":"Surviving in the fast lane: No increased mortality, but faster growth for pathogen-exposed larvae of a family living beetle.","authors":"Leon Müller, Sandra Steiger, Maximilian Körner","doi":"10.1093/jeb/voaf068","DOIUrl":null,"url":null,"abstract":"<p><p>Animal taxa exhibiting post-hatching care can be found throughout the animal kingdom. During this period, parents aggregate with their offspring and allow them to invest their resources into growth and development as parents take over energy consuming tasks. For instance, studies show that food provisioning and social immunity by parents can alleviate the costs of an offspring's immune response to pathogen exposure. However, this issue has rarely been explored in offspring of species showing plasticity in their dependency on parental care. Here, we raise the question of how offspring are affected by pathogen exposure if they have access to social immunity through a caring parent. Parents of Nicrophorus vespilloides, a species exhibiting facultative post-hatching care, control the carcass microbiome by coating it with their antimicrobial exudates, stopping further decay and protecting their offspring from potential pathogens. We exposed N. vespilloides offspring to a generalist entomopathogenic fungus, Beauveria bassiana, while manipulating presence or absence of post-hatching parental care. We monitored offspring performance parameters throughout their development and found, curiously, larvae showed an increase in mean weight and growth rate after being exposed to the pathogen, while their survival and adult immunity were unaffected. These effects of pathogen exposure occurred regardless of parental care. Simultaneously, our results indicate that females invest fewer resources into their offspring if they have been exposed to the pathogen. Overall, we show that offspring of facultative subsocial species may not respond differently to pathogen exposure depending on their parents' aid. Additionally, our results indicate that offspring of facultatively subsocial species may adjust their growth rate in response to pathogen exposure in the nest.</p>","PeriodicalId":50198,"journal":{"name":"Journal of Evolutionary Biology","volume":" ","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Evolutionary Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jeb/voaf068","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Animal taxa exhibiting post-hatching care can be found throughout the animal kingdom. During this period, parents aggregate with their offspring and allow them to invest their resources into growth and development as parents take over energy consuming tasks. For instance, studies show that food provisioning and social immunity by parents can alleviate the costs of an offspring's immune response to pathogen exposure. However, this issue has rarely been explored in offspring of species showing plasticity in their dependency on parental care. Here, we raise the question of how offspring are affected by pathogen exposure if they have access to social immunity through a caring parent. Parents of Nicrophorus vespilloides, a species exhibiting facultative post-hatching care, control the carcass microbiome by coating it with their antimicrobial exudates, stopping further decay and protecting their offspring from potential pathogens. We exposed N. vespilloides offspring to a generalist entomopathogenic fungus, Beauveria bassiana, while manipulating presence or absence of post-hatching parental care. We monitored offspring performance parameters throughout their development and found, curiously, larvae showed an increase in mean weight and growth rate after being exposed to the pathogen, while their survival and adult immunity were unaffected. These effects of pathogen exposure occurred regardless of parental care. Simultaneously, our results indicate that females invest fewer resources into their offspring if they have been exposed to the pathogen. Overall, we show that offspring of facultative subsocial species may not respond differently to pathogen exposure depending on their parents' aid. Additionally, our results indicate that offspring of facultatively subsocial species may adjust their growth rate in response to pathogen exposure in the nest.
期刊介绍:
It covers both micro- and macro-evolution of all types of organisms. The aim of the Journal is to integrate perspectives across molecular and microbial evolution, behaviour, genetics, ecology, life histories, development, palaeontology, systematics and morphology.