Elizabeth A Kleeman,Carolina Gubert,Sonali N Reisinger,Kathryn C Davidson,Da Lu,Merle Dayton,Liana Mackiewicz,Bethany A Masson,Pranav Adithya,Alexandra L Garnham,Gemma Stathatos,Moira K O'Bryan,Rikeish R Muralitharan,Francine Z Marques,Shanshan Li,Huan Liao,Shae McLaughlin,Emmet T Keough,Michelle Y Wheeler,Pamudika Kiridena,Marcel Doerflinger,Marc Pellegrini,Anthony J Hannan
{"title":"父本SARS-CoV-2感染影响精子小非编码rna,并以性别依赖的方式增加后代的焦虑。","authors":"Elizabeth A Kleeman,Carolina Gubert,Sonali N Reisinger,Kathryn C Davidson,Da Lu,Merle Dayton,Liana Mackiewicz,Bethany A Masson,Pranav Adithya,Alexandra L Garnham,Gemma Stathatos,Moira K O'Bryan,Rikeish R Muralitharan,Francine Z Marques,Shanshan Li,Huan Liao,Shae McLaughlin,Emmet T Keough,Michelle Y Wheeler,Pamudika Kiridena,Marcel Doerflinger,Marc Pellegrini,Anthony J Hannan","doi":"10.1038/s41467-025-64473-0","DOIUrl":null,"url":null,"abstract":"Given that the SARS-CoV-2 virus, and the COVID-19 pandemic, constitutes a major environmental challenge faced by billions of people worldwide, we investigated whether paternal pre-conceptual SARS-CoV-2 infection has impacts on sperm RNA content, and intergenerational (F1) and transgenerational (F2) effects on offspring phenotypes. Using an established mouse-adapted SARS-CoV-2 (P21) preclinical model, we infected adult male mice with the virus, or performed a mock control infection, and bred them with naïve female mice four weeks later, when males were no longer infectious. Here we show that offspring of infected sires display increased anxiety-like behaviors. Additionally, the F1 offspring have significant transcriptomic changes in their hippocampus. Various sperm small noncoding RNAs, including PIWI-interacting RNAs, transfer-derived RNAs and microRNAs, are differentially altered by prior paternal SARS-CoV-2 infection. Microinjection of RNA from the sperm of SARS-CoV-2 infected males into fertilized oocytes leads to a phenotype resembling that of the naturally born F1 offspring, supporting the interpretation that sperm RNAs are contributing to the outcomes of our paternal SARS-CoV-2 model. Therefore, this study provides evidence that paternal SARS-CoV-2 infection impacts sperm and affects offspring phenotypes. These findings have public-health implications and inform further research in males affected by COVID-19, and their offspring.","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"339 1","pages":"9045"},"PeriodicalIF":15.7000,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Paternal SARS-CoV-2 infection impacts sperm small noncoding RNAs and increases anxiety in offspring in a sex-dependent manner.\",\"authors\":\"Elizabeth A Kleeman,Carolina Gubert,Sonali N Reisinger,Kathryn C Davidson,Da Lu,Merle Dayton,Liana Mackiewicz,Bethany A Masson,Pranav Adithya,Alexandra L Garnham,Gemma Stathatos,Moira K O'Bryan,Rikeish R Muralitharan,Francine Z Marques,Shanshan Li,Huan Liao,Shae McLaughlin,Emmet T Keough,Michelle Y Wheeler,Pamudika Kiridena,Marcel Doerflinger,Marc Pellegrini,Anthony J Hannan\",\"doi\":\"10.1038/s41467-025-64473-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Given that the SARS-CoV-2 virus, and the COVID-19 pandemic, constitutes a major environmental challenge faced by billions of people worldwide, we investigated whether paternal pre-conceptual SARS-CoV-2 infection has impacts on sperm RNA content, and intergenerational (F1) and transgenerational (F2) effects on offspring phenotypes. Using an established mouse-adapted SARS-CoV-2 (P21) preclinical model, we infected adult male mice with the virus, or performed a mock control infection, and bred them with naïve female mice four weeks later, when males were no longer infectious. Here we show that offspring of infected sires display increased anxiety-like behaviors. Additionally, the F1 offspring have significant transcriptomic changes in their hippocampus. Various sperm small noncoding RNAs, including PIWI-interacting RNAs, transfer-derived RNAs and microRNAs, are differentially altered by prior paternal SARS-CoV-2 infection. Microinjection of RNA from the sperm of SARS-CoV-2 infected males into fertilized oocytes leads to a phenotype resembling that of the naturally born F1 offspring, supporting the interpretation that sperm RNAs are contributing to the outcomes of our paternal SARS-CoV-2 model. Therefore, this study provides evidence that paternal SARS-CoV-2 infection impacts sperm and affects offspring phenotypes. 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Paternal SARS-CoV-2 infection impacts sperm small noncoding RNAs and increases anxiety in offspring in a sex-dependent manner.
Given that the SARS-CoV-2 virus, and the COVID-19 pandemic, constitutes a major environmental challenge faced by billions of people worldwide, we investigated whether paternal pre-conceptual SARS-CoV-2 infection has impacts on sperm RNA content, and intergenerational (F1) and transgenerational (F2) effects on offspring phenotypes. Using an established mouse-adapted SARS-CoV-2 (P21) preclinical model, we infected adult male mice with the virus, or performed a mock control infection, and bred them with naïve female mice four weeks later, when males were no longer infectious. Here we show that offspring of infected sires display increased anxiety-like behaviors. Additionally, the F1 offspring have significant transcriptomic changes in their hippocampus. Various sperm small noncoding RNAs, including PIWI-interacting RNAs, transfer-derived RNAs and microRNAs, are differentially altered by prior paternal SARS-CoV-2 infection. Microinjection of RNA from the sperm of SARS-CoV-2 infected males into fertilized oocytes leads to a phenotype resembling that of the naturally born F1 offspring, supporting the interpretation that sperm RNAs are contributing to the outcomes of our paternal SARS-CoV-2 model. Therefore, this study provides evidence that paternal SARS-CoV-2 infection impacts sperm and affects offspring phenotypes. These findings have public-health implications and inform further research in males affected by COVID-19, and their offspring.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.