Evolving origin-of-transfer sequences on staphylococcal conjugative and mobilizable plasmids—who’s mimicking whom?

Author:

Yui Eto Karina123,Kwong Stephen M4,LaBreck Patrick T5,Crow Jade E23,Traore Daouda A K6789,Parahitiyawa Nipuna2,Fairhurst Heather M2,Merrell D Scott5,Firth Neville4,Bond Charles S1,Ramsay Joshua P321ORCID

Affiliation:

1. School of Molecular Sciences, University of Western Australia, Perth, WA 6009, Australia

2. Curtin Medical School, Curtin University, Perth, WA 6102, Australia

3. Curtin Health Innovation Research Institute, Curtin University, Perth, WA 6102, Australia

4. School of Life and Environmental Sciences, University of Sydney, Sydney, NSW 2006, Australia

5. Department of Microbiology and Immunology, Uniformed Services University of the Health Sciences, Bethesda, Maryland, MD 20814, USA

6. Department of Biochemistry and Molecular Biology, Infection and Immunity Program, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia

7. Faculty of Natural Sciences, School of Life Sciences, Keele University, Staffordshire ST5 5BG, UK

8. Life Sciences Group, Institut Laue Langevin, Grenoble 38000, France

9. Faculté des Sciences et Techniques, Université des Sciences, des Techniques et des Technologies de Bamako (USTTB), Bamako BP E423, Mali

Abstract

Abstract In Staphylococcus aureus, most multiresistance plasmids lack conjugation or mobilization genes for horizontal transfer. However, most are mobilizable due to carriage of origin-of-transfer (oriT) sequences mimicking those of conjugative plasmids related to pWBG749. pWBG749-family plasmids have diverged to carry five distinct oriT subtypes and non-conjugative plasmids have been identified that contain mimics of each. The relaxasome accessory factor SmpO, encoded by each conjugative plasmid, determines specificity for its cognate oriT. Here we characterized the binding of SmpO proteins to each oriT. SmpO proteins predominantly formed tetramers in solution and bound 5′-GNNNNC-3′ sites within each oriT. Four of the five SmpO proteins specifically bound their cognate oriT. An F7K substitution in pWBG749 SmpO switched oriT-binding specificity in vitro. In vivo, the F7K substitution reduced but did not abolish self-transfer of pWBG749. Notably, the substitution broadened the oriT subtypes that were mobilized. Thus, this substitution represents a potential evolutionary intermediate with promiscuous DNA-binding specificity that could facilitate a switch between oriT specificities. Phylogenetic analysis suggests pWBG749-family plasmids have switched oriT specificity more than once during evolution. We hypothesize the convergent evolution of oriT specificity in distinct branches of the pWBG749-family phylogeny reflects indirect selection pressure to mobilize plasmids carrying non-cognate oriT-mimics.

Funder

National Health and Medical Research Council

Australian Research Council

University of Western Australia

U.S. Department of Defense Program

Military Infectious Diseases Research Program award

Publisher

Oxford University Press (OUP)

Subject

Genetics

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