鸭嘴兽(Ornithorhynchus anatinus)粪便细菌群落对圈养状态的反映--对保护和管理的启示。

IF 3.5 1区 生物学 Q1 ZOOLOGY
Ashley M. DUNGAN, Jessica L. THOMAS
{"title":"鸭嘴兽(Ornithorhynchus anatinus)粪便细菌群落对圈养状态的反映--对保护和管理的启示。","authors":"Ashley M. DUNGAN,&nbsp;Jessica L. THOMAS","doi":"10.1111/1749-4877.12865","DOIUrl":null,"url":null,"abstract":"<p>The duck-billed platypus (<i>Ornithorhynchus anatinus</i>) is currently listed as near-threatened. A key part of the conservation strategy for this species is its captive maintenance; however, captive animals often have dysbiotic gut bacterial microbiomes. Here, for the first time, we characterize the gut microbiome of wild platypus via fecal samples using high-throughput sequencing of the bacterial 16S rRNA gene and identify microbial biomarkers of captivity in this species. At the phylum level, Firmicutes (50.4%) predominated among all platypuses, followed by Proteobacteria (28.7%), Fusobacteria (13.4%), and Bacteroidota (6.9%), with 21 “core” bacteria identified. Captive individuals did not differ in their microbial α-diversity compared to wild platypus but had significantly different community composition (β-diversity) and exhibited higher abundances of <i>Enterococcus</i>, which are potential pathogenic bacteria. Four taxa were identified as biomarkers of wild platypus, including <i>Rickettsiella</i>, <i>Epulopiscium</i>, <i>Clostridium</i>, and <i>Cetobacterium</i>. This contrast in gut microbiome composition between wild and captive platypus is an essential insight for guiding conservation management, as the rewilding of captive animal microbiomes is a new and emerging tool to improve captive animal health, maximize captive breeding efforts, and give reintroduced or translocated animals the best chance of survival.</p>","PeriodicalId":13654,"journal":{"name":"Integrative zoology","volume":"19 6","pages":"1211-1223"},"PeriodicalIF":3.5000,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1749-4877.12865","citationCount":"0","resultStr":"{\"title\":\"Fecal bacterial communities of the platypus (Ornithorhynchus anatinus) reflect captivity status—Implications for conservation and management\",\"authors\":\"Ashley M. DUNGAN,&nbsp;Jessica L. THOMAS\",\"doi\":\"10.1111/1749-4877.12865\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The duck-billed platypus (<i>Ornithorhynchus anatinus</i>) is currently listed as near-threatened. A key part of the conservation strategy for this species is its captive maintenance; however, captive animals often have dysbiotic gut bacterial microbiomes. Here, for the first time, we characterize the gut microbiome of wild platypus via fecal samples using high-throughput sequencing of the bacterial 16S rRNA gene and identify microbial biomarkers of captivity in this species. At the phylum level, Firmicutes (50.4%) predominated among all platypuses, followed by Proteobacteria (28.7%), Fusobacteria (13.4%), and Bacteroidota (6.9%), with 21 “core” bacteria identified. Captive individuals did not differ in their microbial α-diversity compared to wild platypus but had significantly different community composition (β-diversity) and exhibited higher abundances of <i>Enterococcus</i>, which are potential pathogenic bacteria. Four taxa were identified as biomarkers of wild platypus, including <i>Rickettsiella</i>, <i>Epulopiscium</i>, <i>Clostridium</i>, and <i>Cetobacterium</i>. This contrast in gut microbiome composition between wild and captive platypus is an essential insight for guiding conservation management, as the rewilding of captive animal microbiomes is a new and emerging tool to improve captive animal health, maximize captive breeding efforts, and give reintroduced or translocated animals the best chance of survival.</p>\",\"PeriodicalId\":13654,\"journal\":{\"name\":\"Integrative zoology\",\"volume\":\"19 6\",\"pages\":\"1211-1223\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/1749-4877.12865\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Integrative zoology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/1749-4877.12865\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ZOOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative zoology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/1749-4877.12865","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

鸭嘴兽(Ornithorhynchus anatinus)目前被列为濒危物种。该物种保护策略的一个关键部分是圈养;然而,圈养动物的肠道细菌微生物组通常存在菌群失调。在这里,我们首次利用细菌 16S rRNA 基因的高通量测序技术,通过粪便样本描述了野生鸭嘴兽肠道微生物组的特征,并确定了该物种圈养的微生物生物标志物。在所有鸭嘴兽的肠道细菌门中,固着菌门(50.4%)占主导地位,其次是变形菌门(28.7%)、镰刀菌门(13.4%)和类杆菌门(6.9%),共鉴定出 21 种 "核心 "细菌。与野生鸭嘴兽相比,人工饲养个体的微生物α-多样性并无差异,但群落组成(β-多样性)却有显著不同,并表现出较高的肠球菌丰度,而肠球菌是潜在的致病菌。有四个类群被确定为野生鸭嘴兽的生物标志物,包括立克次体、表粘菌、梭菌和鲸杆菌。野生鸭嘴兽与人工饲养鸭嘴兽肠道微生物组组成的这种反差是指导保护管理的重要依据,因为人工饲养动物微生物组的野化是一种新兴的工具,可以改善人工饲养动物的健康状况,最大限度地提高人工饲养动物的繁殖率,并为重新引进或转移的动物提供最好的生存机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fecal bacterial communities of the platypus (Ornithorhynchus anatinus) reflect captivity status—Implications for conservation and management

Fecal bacterial communities of the platypus (Ornithorhynchus anatinus) reflect captivity status—Implications for conservation and management

The duck-billed platypus (Ornithorhynchus anatinus) is currently listed as near-threatened. A key part of the conservation strategy for this species is its captive maintenance; however, captive animals often have dysbiotic gut bacterial microbiomes. Here, for the first time, we characterize the gut microbiome of wild platypus via fecal samples using high-throughput sequencing of the bacterial 16S rRNA gene and identify microbial biomarkers of captivity in this species. At the phylum level, Firmicutes (50.4%) predominated among all platypuses, followed by Proteobacteria (28.7%), Fusobacteria (13.4%), and Bacteroidota (6.9%), with 21 “core” bacteria identified. Captive individuals did not differ in their microbial α-diversity compared to wild platypus but had significantly different community composition (β-diversity) and exhibited higher abundances of Enterococcus, which are potential pathogenic bacteria. Four taxa were identified as biomarkers of wild platypus, including Rickettsiella, Epulopiscium, Clostridium, and Cetobacterium. This contrast in gut microbiome composition between wild and captive platypus is an essential insight for guiding conservation management, as the rewilding of captive animal microbiomes is a new and emerging tool to improve captive animal health, maximize captive breeding efforts, and give reintroduced or translocated animals the best chance of survival.

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
CiteScore
6.40
自引率
12.10%
发文量
81
审稿时长
>12 weeks
期刊介绍: The official journal of the International Society of Zoological Sciences focuses on zoology as an integrative discipline encompassing all aspects of animal life. It presents a broader perspective of many levels of zoological inquiry, both spatial and temporal, and encourages cooperation between zoology and other disciplines including, but not limited to, physics, computer science, social science, ethics, teaching, paleontology, molecular biology, physiology, behavior, ecology and the built environment. It also looks at the animal-human interaction through exploring animal-plant interactions, microbe/pathogen effects and global changes on the environment and human society. Integrative topics of greatest interest to INZ include: (1) Animals & climate change (2) Animals & pollution (3) Animals & infectious diseases (4) Animals & biological invasions (5) Animal-plant interactions (6) Zoogeography & paleontology (7) Neurons, genes & behavior (8) Molecular ecology & evolution (9) Physiological adaptations
×
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