Rap-protein paralogs ofB. thuringiensis: a multifunctional and redundant regulatory repertoire for the control of collective functions

Author:

Gastélum GabrielaORCID,de la Torre Mayra,Rocha JorgeORCID

Abstract

AbstractQuorum Sensing (QS) are mechanisms of synthesis and detection of signaling molecules to regulate gene expression and coordinate behaviors in bacterial populations. InBacillus subtilis(Bs), multiple paralog Rap-Phr QS systems (receptor-signaling peptide) are highly redundant and multifunctional, interconnecting the regulation of differentiation processes such as sporulation and competence. However, their functions in theB. cereusgroup are largely unknown. We evaluated the diversification of Rap-Phr systems in theB. cereusgroup as well as their functions, usingBacillus thuringiensisBt8741 as model. Bt8741 codes for eight Rap-Phr systems; these were overexpressed to study their participation in sporulation, biofilm formation, extracellular proteolytic activity and spreading. Our results show that five Rap-Phr systems (RapC, K, F, I and RapLike) inhibit sporulation, two of which (RapK and RapF) probably dephosphorylate of Spo0F from the Spo0A phosphorelay; these two Rap proteins also inhibit biofilm formation. Five systems (RapC, F, F2, I1 and RapLike) decrease extracellular proteolytic activity; finally, four systems (RapC, F1, F2 and RapLike) participate in spreading inhibition. Our bioinformatic analyses showed that Rap proteins from theB. cereusgroup diversified into five pherogroups, and we foresee that functions performed by Rap proteins of Bt8741 could also be carried out by Rap homologs in other species within the group. These results indicate that Rap-Phr systems constitute a highly multifunctional and redundant regulatory repertoire that enables bacteria from theB. cereusgroup to efficiently regulate collective functions during the bacterial life cycle, in the face of changing environments.ImportanceTheBacillus cereusgroup of bacteria includes species of high economic, clinical, biological warfare and biotechnological interest, e.g.B. anthracisin bioterrorism,B. cereusin food intoxications andB. thuringiensisin biocontrol. Knowledge on the ecology of these bacteria is hindered due to our limited understanding about the regulatory circuits that control differentiation and specialization processes. Here, we uncover the participation of eight Rap quorum-sensing receptors in collective functions ofB. thuringiensis. These proteins are highly multifunctional and redundant in their functions, linking ecologically relevant processes such as sporulation, biofilm formation, extracellular proteolytic activity, spreading, and probably other additional functions in species from theB. cereusgroup.

Publisher

Cold Spring Harbor Laboratory

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

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