雄性海马怀孕期间育儿袋生殖微生物组的变化(海马腹部)。

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Reproduction Pub Date : 2025-03-10 Print Date: 2025-04-01 DOI:10.1530/REP-24-0159
Jenny Wang, Zoe M G Skalkos, Catherine E Grueber, Camilla M Whittington
{"title":"雄性海马怀孕期间育儿袋生殖微生物组的变化(海马腹部)。","authors":"Jenny Wang, Zoe M G Skalkos, Catherine E Grueber, Camilla M Whittington","doi":"10.1530/REP-24-0159","DOIUrl":null,"url":null,"abstract":"<p><strong>In brief: </strong>Reproductive microbiomes contribute to the successful embryogenesis of offspring but are poorly studied in non-mammalian species that exhibit pregnancy. This study characterises the male pregnant seahorse brood pouch microbiome and identifies potential microbial maternal contributions to the pouch, providing insights into the sources and adaptive value of the embryonic microbial environment.</p><p><strong>Abstract: </strong>Seahorses demonstrate an unusual reproductive strategy, in which males incubate embryos inside a complex 'brood pouch' until parturition, analogous to mammalian viviparity. In many species, a 'normal' reproductive microbiome ensures successful embryogenesis and enables parents (usually mothers) to provide their offspring with their initial microbiome. In male-pregnant seahorses, embryos may receive microbiomes from both parents: from the paternal brood pouch and from the maternal eggs. Using the pot-bellied seahorse (Hippocampus abdominalis), we employed 16S rRNA sequencing to explore the reproductive microbiome. We aimed to compare the microbiome of the male pregnant pouch to the male non-pregnant pouch and external skin, and to identify bacterial taxa found exclusively in the pregnant pouch that could be derived maternally from the microbiome of eggs. Our findings demonstrate that the pregnant brood pouch microbiome is compositionally distinct from the non-pregnant pouch and external skin. The pouch microbiome also has characteristics of resistance to colonisation by pathogens, including a low species richness, high species evenness and diversity and very low abundance of Vibrio, a genus that includes fish skin pathogens. Thirteen bacterial taxa appear exclusively in the pregnant pouch, relative to the non-pregnant pouch, and seven of these overlapped with taxa present in or on the eggs. The possible supplementation of brood pouch microbiome with egg-associated micro-organisms hints at a maternal microbial contribution to male pregnancy. This characterisation of the pregnant seahorse pouch microbiome provides a platform for further research into its function and possible adaptive value during male pregnancy.</p>","PeriodicalId":21127,"journal":{"name":"Reproduction","volume":" ","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11906128/pdf/","citationCount":"0","resultStr":"{\"title\":\"Changes to the reproductive microbiome of the brood pouch during male pregnancy in seahorses (Hippocampus abdominalis).\",\"authors\":\"Jenny Wang, Zoe M G Skalkos, Catherine E Grueber, Camilla M Whittington\",\"doi\":\"10.1530/REP-24-0159\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>In brief: </strong>Reproductive microbiomes contribute to the successful embryogenesis of offspring but are poorly studied in non-mammalian species that exhibit pregnancy. This study characterises the male pregnant seahorse brood pouch microbiome and identifies potential microbial maternal contributions to the pouch, providing insights into the sources and adaptive value of the embryonic microbial environment.</p><p><strong>Abstract: </strong>Seahorses demonstrate an unusual reproductive strategy, in which males incubate embryos inside a complex 'brood pouch' until parturition, analogous to mammalian viviparity. In many species, a 'normal' reproductive microbiome ensures successful embryogenesis and enables parents (usually mothers) to provide their offspring with their initial microbiome. In male-pregnant seahorses, embryos may receive microbiomes from both parents: from the paternal brood pouch and from the maternal eggs. Using the pot-bellied seahorse (Hippocampus abdominalis), we employed 16S rRNA sequencing to explore the reproductive microbiome. We aimed to compare the microbiome of the male pregnant pouch to the male non-pregnant pouch and external skin, and to identify bacterial taxa found exclusively in the pregnant pouch that could be derived maternally from the microbiome of eggs. Our findings demonstrate that the pregnant brood pouch microbiome is compositionally distinct from the non-pregnant pouch and external skin. The pouch microbiome also has characteristics of resistance to colonisation by pathogens, including a low species richness, high species evenness and diversity and very low abundance of Vibrio, a genus that includes fish skin pathogens. Thirteen bacterial taxa appear exclusively in the pregnant pouch, relative to the non-pregnant pouch, and seven of these overlapped with taxa present in or on the eggs. The possible supplementation of brood pouch microbiome with egg-associated micro-organisms hints at a maternal microbial contribution to male pregnancy. This characterisation of the pregnant seahorse pouch microbiome provides a platform for further research into its function and possible adaptive value during male pregnancy.</p>\",\"PeriodicalId\":21127,\"journal\":{\"name\":\"Reproduction\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-03-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11906128/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reproduction\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1530/REP-24-0159\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/4/1 0:00:00\",\"PubModel\":\"Print\",\"JCR\":\"Q1\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reproduction","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1530/REP-24-0159","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/1 0:00:00","PubModel":"Print","JCR":"Q1","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

海马表现出一种不同寻常的繁殖策略,雄性海马在一个复杂的“育儿袋”里孵化胚胎,直到分娩,类似于哺乳动物的胎生。在许多物种中,“正常”的生殖微生物群确保胚胎发育成功,并使父母(通常是母亲)能够为后代提供初始的微生物群。在雄性怀孕的海马中,胚胎可能接受来自父母双方的微生物组:来自父亲的育儿袋和母亲的卵子。以大肚海马(Hippocampus abdominalis)为研究对象,采用16S rRNA测序技术对其生殖微生物组进行了研究。我们的目的是比较雄性怀孕育儿袋与雄性非怀孕育儿袋和外部皮肤的微生物组,并从卵子的微生物组中鉴定出仅存在于怀孕育儿袋中的细菌分类群。我们的研究结果表明,怀孕育儿袋微生物组在组成上不同于非怀孕育儿袋和外部皮肤。袋微生物组还具有抵抗病原体定植的特征,包括物种丰富度低,物种均匀性和多样性高,弧菌丰度非常低,弧菌属包括鱼皮病原体。13个细菌分类群只出现在怀孕的育儿袋中,相对于未怀孕的育儿袋,其中7个与存在于卵内或卵上的分类群重叠。可能补充育儿袋微生物组与卵子相关的微生物暗示了母体微生物对男性怀孕的贡献。怀孕海马育儿袋微生物组的特征为进一步研究其在雄性怀孕期间的功能和可能的适应价值提供了一个平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes to the reproductive microbiome of the brood pouch during male pregnancy in seahorses (Hippocampus abdominalis).

In brief: Reproductive microbiomes contribute to the successful embryogenesis of offspring but are poorly studied in non-mammalian species that exhibit pregnancy. This study characterises the male pregnant seahorse brood pouch microbiome and identifies potential microbial maternal contributions to the pouch, providing insights into the sources and adaptive value of the embryonic microbial environment.

Abstract: Seahorses demonstrate an unusual reproductive strategy, in which males incubate embryos inside a complex 'brood pouch' until parturition, analogous to mammalian viviparity. In many species, a 'normal' reproductive microbiome ensures successful embryogenesis and enables parents (usually mothers) to provide their offspring with their initial microbiome. In male-pregnant seahorses, embryos may receive microbiomes from both parents: from the paternal brood pouch and from the maternal eggs. Using the pot-bellied seahorse (Hippocampus abdominalis), we employed 16S rRNA sequencing to explore the reproductive microbiome. We aimed to compare the microbiome of the male pregnant pouch to the male non-pregnant pouch and external skin, and to identify bacterial taxa found exclusively in the pregnant pouch that could be derived maternally from the microbiome of eggs. Our findings demonstrate that the pregnant brood pouch microbiome is compositionally distinct from the non-pregnant pouch and external skin. The pouch microbiome also has characteristics of resistance to colonisation by pathogens, including a low species richness, high species evenness and diversity and very low abundance of Vibrio, a genus that includes fish skin pathogens. Thirteen bacterial taxa appear exclusively in the pregnant pouch, relative to the non-pregnant pouch, and seven of these overlapped with taxa present in or on the eggs. The possible supplementation of brood pouch microbiome with egg-associated micro-organisms hints at a maternal microbial contribution to male pregnancy. This characterisation of the pregnant seahorse pouch microbiome provides a platform for further research into its function and possible adaptive value during male pregnancy.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信