Comparative genomics ofMycoplasma feriruminatoris, a fast-growing pathogen of wildCaprinae

Author:

Baby VincentORCID,Ambroset ChloéORCID,Gaurivaud PatriceORCID,Falquet LaurentORCID,Boury Christophe,Guichoux ErwanORCID,Jores JoergORCID,Lartigue CaroleORCID,Tardy FlorenceORCID,Sirand-Pugnet PascalORCID

Abstract

AbstractMycoplasma feriruminatorisis a fast-growingMycoplasmaspecies isolated from wildCaprinaeand first described in 2013.M. feriruminatorisisolates have been associated with arthritis, keratoconjunctivitis, pneumonia and septicemia, but were also recovered from apparently healthy animals. To better understand what defines this species, we performed a genomic survey on 14 strains collected from free-ranging or zoo-housed animals between 1987 and 2017. The average chromosome size of theM. feriruminatorisstrains was 1,040 ± 0,024 kbp, with 24% G+C and 852 ± 31 CDS. The core genome and pan-genome of theM. feriruminatorisspecies contained 628 and 1,312 protein families, respectively. TheM. feriruminatorisstrains displayed a relatively closed pan-genome, with many features and putative virulence factors shared with species from theM. mycoidescluster, including the MIB-MIP Ig cleavage system, a repertoire of DUF285 surface proteins and a complete biosynthetic pathway for galactan.M. feriruminatorisgenomes were found to be mostly syntenic, although repertoires of mobile genetic elements, including Mycoplasma Integrative and Conjugative Elements, insertion sequences, and a single plasmid varied. Phylogenetic- and gene content analyzes confirmed thatM. feriruminatoriswas closer to theM. mycoidescluster than to the ruminant speciesM. yeatsiiandM. putrefaciens. Ancestral genome reconstruction showed that the emergence of theM. feriruminatorisspecies was associated with the gain of 17 gene families, some of which encode defense enzymes and surface proteins, and the loss of 25 others, some of which are involved in sugar transport and metabolism. This comparative study suggests that theM. mycoidescluster could be extended to includeM. feriruminatoris. We also find evidence that the specific organization and structure of the DnaA boxes around theoriCofM. feriruminatorismay contribute to drive the remarkable fast growth of this minimal bacterium.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3