从蝙蝠中分离的一种耐寒酵母。

IF 9.5 1区 生物学 Q1 MYCOLOGY Persoonia Pub Date : 2018-12-01 Epub Date: 2018-02-05 DOI:10.3767/persoonia.2018.41.04
J M Lorch, J M Palmer, K J Vanderwolf, K Z Schmidt, M L Verant, T J Weller, D S Blehert
{"title":"从蝙蝠中分离的一种耐寒酵母。","authors":"J M Lorch,&nbsp;J M Palmer,&nbsp;K J Vanderwolf,&nbsp;K Z Schmidt,&nbsp;M L Verant,&nbsp;T J Weller,&nbsp;D S Blehert","doi":"10.3767/persoonia.2018.41.04","DOIUrl":null,"url":null,"abstract":"<p><p><i>Malassezia</i> is a genus of medically-important, lipid-dependent yeasts that live on the skin of warm-blooded animals. The 17 described species have been documented primarily on humans and domestic animals, but few studies have examined <i>Malassezia</i> species associated with more diverse host groups such as wildlife. While investigating the skin mycobiota of healthy bats, we isolated a <i>Malassezia</i> sp. that exhibited only up to 92% identity with other known species in the genus for the portion of the DNA sequence of the internal transcribed spacer region that could be confidently aligned. The <i>Malassezia</i> sp. was cultured from the skin of nine species of bats in the subfamily <i>Myotinae</i>; isolates originated from bats sampled in both the eastern and western United States. Physiological features and molecular characterisation at seven additional loci (D1/D2 region of 26S rDNA, 18S rDNA, chitin synthase, second largest subunit of RNA polymerase II, β-tubulin, translation elongation factor EF-1α, and minichromosome maintenance complex component 7) indicated that all of the bat <i>Malassezia</i> isolates likely represented a single species distinct from other named taxa. Of particular note was the ability of the <i>Malassezia</i> sp. to grow over a broad range of temperatures (7-40 °C), with optimal growth occurring at 24 °C. These thermal growth ranges, unique among the described <i>Malassezia</i>, may be an adaptation by the fungus to survive on bats during both the host's hibernation and active seasons. The combination of genetic and physiological differences provided compelling evidence that this lipid-dependent yeast represents a novel species described herein as <i>Malassezia vespertilionis</i> sp. nov. Whole genome sequencing placed the new species as a basal member of the clade containing the species <i>M. furfur</i>, <i>M. japonica</i>, <i>M. obtusa</i>, and <i>M. yamatoensis</i>. The genetic and physiological uniqueness of <i>Malassezia vespertilionis</i> among its closest relatives may make it important in future research to better understand the evolution, life history, and pathogenicity of the <i>Malassezia</i> yeasts.</p>","PeriodicalId":20014,"journal":{"name":"Persoonia","volume":"41 ","pages":"56-70"},"PeriodicalIF":9.5000,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3767/persoonia.2018.41.04","citationCount":"68","resultStr":"{\"title\":\"<i>Malassezia vespertilionis</i> sp. nov.: a new cold-tolerant species of yeast isolated from bats.\",\"authors\":\"J M Lorch,&nbsp;J M Palmer,&nbsp;K J Vanderwolf,&nbsp;K Z Schmidt,&nbsp;M L Verant,&nbsp;T J Weller,&nbsp;D S Blehert\",\"doi\":\"10.3767/persoonia.2018.41.04\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Malassezia</i> is a genus of medically-important, lipid-dependent yeasts that live on the skin of warm-blooded animals. The 17 described species have been documented primarily on humans and domestic animals, but few studies have examined <i>Malassezia</i> species associated with more diverse host groups such as wildlife. While investigating the skin mycobiota of healthy bats, we isolated a <i>Malassezia</i> sp. that exhibited only up to 92% identity with other known species in the genus for the portion of the DNA sequence of the internal transcribed spacer region that could be confidently aligned. The <i>Malassezia</i> sp. was cultured from the skin of nine species of bats in the subfamily <i>Myotinae</i>; isolates originated from bats sampled in both the eastern and western United States. Physiological features and molecular characterisation at seven additional loci (D1/D2 region of 26S rDNA, 18S rDNA, chitin synthase, second largest subunit of RNA polymerase II, β-tubulin, translation elongation factor EF-1α, and minichromosome maintenance complex component 7) indicated that all of the bat <i>Malassezia</i> isolates likely represented a single species distinct from other named taxa. Of particular note was the ability of the <i>Malassezia</i> sp. to grow over a broad range of temperatures (7-40 °C), with optimal growth occurring at 24 °C. These thermal growth ranges, unique among the described <i>Malassezia</i>, may be an adaptation by the fungus to survive on bats during both the host's hibernation and active seasons. The combination of genetic and physiological differences provided compelling evidence that this lipid-dependent yeast represents a novel species described herein as <i>Malassezia vespertilionis</i> sp. nov. Whole genome sequencing placed the new species as a basal member of the clade containing the species <i>M. furfur</i>, <i>M. japonica</i>, <i>M. obtusa</i>, and <i>M. yamatoensis</i>. The genetic and physiological uniqueness of <i>Malassezia vespertilionis</i> among its closest relatives may make it important in future research to better understand the evolution, life history, and pathogenicity of the <i>Malassezia</i> yeasts.</p>\",\"PeriodicalId\":20014,\"journal\":{\"name\":\"Persoonia\",\"volume\":\"41 \",\"pages\":\"56-70\"},\"PeriodicalIF\":9.5000,\"publicationDate\":\"2018-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.3767/persoonia.2018.41.04\",\"citationCount\":\"68\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Persoonia\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3767/persoonia.2018.41.04\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2018/2/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"MYCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Persoonia","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3767/persoonia.2018.41.04","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/2/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MYCOLOGY","Score":null,"Total":0}
引用次数: 68

摘要

马拉色菌是一种在医学上很重要的、依赖于脂质的酵母菌属,生活在温血动物的皮肤上。所描述的17个物种主要记录在人类和家畜身上,但很少有研究调查与野生动物等更多样化的寄主群体有关的马拉色菌物种。在调查健康蝙蝠的皮肤真菌群时,我们分离出一种马拉色菌属,由于其内部转录间隔区DNA序列的一部分可以自信地排列,它与该属其他已知物种的一致性仅为92%。从蝙蝠亚科9种蝙蝠皮肤中培养马拉色菌;分离株起源于美国东部和西部取样的蝙蝠。另外7个位点(26S rDNA的D1/D2区、18S rDNA、几丁质合成酶、RNA聚合酶II的第二大亚基、β-微管蛋白、翻译延伸因子EF-1α和小染色体维持复合体组分7)的生理特征和分子特征表明,所有分离的马拉色菌可能代表一个不同于其他已命名分类群的单一物种。特别值得注意的是马拉色菌的生长温度范围很广(7-40°C),最佳生长温度为24°C。这些热生长范围在所描述的马拉色菌中是独特的,可能是真菌在蝙蝠的冬眠和活动季节生存的一种适应。遗传和生理差异的结合提供了令人信服的证据,证明这种脂质依赖性酵母代表了一种新物种,本文将其描述为Malassezia vespertilionis sp. 11 .全基因组测序将该新物种定位为包含M. furfur, M. japonica, M. obtusa和M. yamatoensis的分支的基础成员。马拉色菌在其近亲中的遗传和生理独特性,可能对今后研究马拉色菌的进化、生活史和致病性具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Malassezia vespertilionis sp. nov.: a new cold-tolerant species of yeast isolated from bats.

Malassezia is a genus of medically-important, lipid-dependent yeasts that live on the skin of warm-blooded animals. The 17 described species have been documented primarily on humans and domestic animals, but few studies have examined Malassezia species associated with more diverse host groups such as wildlife. While investigating the skin mycobiota of healthy bats, we isolated a Malassezia sp. that exhibited only up to 92% identity with other known species in the genus for the portion of the DNA sequence of the internal transcribed spacer region that could be confidently aligned. The Malassezia sp. was cultured from the skin of nine species of bats in the subfamily Myotinae; isolates originated from bats sampled in both the eastern and western United States. Physiological features and molecular characterisation at seven additional loci (D1/D2 region of 26S rDNA, 18S rDNA, chitin synthase, second largest subunit of RNA polymerase II, β-tubulin, translation elongation factor EF-1α, and minichromosome maintenance complex component 7) indicated that all of the bat Malassezia isolates likely represented a single species distinct from other named taxa. Of particular note was the ability of the Malassezia sp. to grow over a broad range of temperatures (7-40 °C), with optimal growth occurring at 24 °C. These thermal growth ranges, unique among the described Malassezia, may be an adaptation by the fungus to survive on bats during both the host's hibernation and active seasons. The combination of genetic and physiological differences provided compelling evidence that this lipid-dependent yeast represents a novel species described herein as Malassezia vespertilionis sp. nov. Whole genome sequencing placed the new species as a basal member of the clade containing the species M. furfur, M. japonica, M. obtusa, and M. yamatoensis. The genetic and physiological uniqueness of Malassezia vespertilionis among its closest relatives may make it important in future research to better understand the evolution, life history, and pathogenicity of the Malassezia yeasts.

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
Persoonia
Persoonia MYCOLOGY-
CiteScore
17.70
自引率
5.50%
发文量
10
审稿时长
3 months
期刊介绍: Persoonia aspires to publish papers focusing on the molecular systematics and evolution of fungi. Additionally, it seeks to advance fungal taxonomy by employing a polythetic approach to elucidate the genuine phylogeny and relationships within the kingdom Fungi. The journal is dedicated to disseminating high-quality papers that unravel both known and novel fungal taxa at the DNA level. Moreover, it endeavors to provide fresh insights into evolutionary processes and relationships. The scope of papers considered encompasses research articles, along with topical and book reviews.
期刊最新文献
A comprehensive molecular phylogeny of Cephalotrichum and Microascus provides novel insights into their systematics and evolutionary history Single host plant species may harbour more than one species of Peronospora – a case study on Peronospora infecting Plantag Phylogenomic analysis of the Candida auris- Candida haemuli clade and related taxa in the Metschnikowiaceae, and proposal of thirteen new genera, fifty-five new combinations and nine new species Endless forms most frustrating: disentangling species boundaries in the Ramalina decipiens group (Lecanoromycetes, Ascomycota), with the description of six new species and a key to the group Saccharomycetaceae: delineation of fungal genera based on phylogenomic analyses, genomic relatedness indices and genomics-based synapomorphies
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1