Abstract

Type II toxin-antitoxin (TA) systems are highly prevalent in bacterial genomes and have been extensively studied. These modules involve in the formation of persistence cells, the biofilm formation, and stress resistance, which might play key roles in pathogen virulence. SezAT and yefM-yoeB TA modules in Streptococcus suis serotype 2 (S. suis 2) have been studied, although the other TA systems have not been identified. In this study, we investigated nine putative type II TA systems in the genome of S. suis 2 strain SC84 by bioinformatics analysis and identified three of them (two relBE loci and one parDE locus) that function as typical type II TA systems. Interestingly, we found that the introduction of the two RelBE TA systems into Escherichia coli or the induction of the ParE toxin led to cell filamentation. Promoter activity assays indicated that RelB1, RelB2, ParD, and ParDE negatively autoregulated the transcriptions of their respective TA operons, while RelBE2 positively autoregulated its TA operon transcription. Collectively, we identified three TA systems in S. suis 2, and our findings have laid an important foundation for further functional studies on these TA systems.

Highlights

  • Streptococcus suis (S. suis) is an important major swine and zoonotic pathogen that causes severe infection [1,2,3]

  • The putative type II TA loci in S. suis SC84 were predicted with TAfinder, a newly developed online tool in TADB (Toxin-Antitoxin Database, http://202.120.12.135/TADB2/Introduction.html#table_s2), which can quickly detect the TA prediction [12]

  • TA systems and the ID numbers of each putative toxin or antitoxin are included in the Figure S1

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Summary

Introduction

Streptococcus suis (S. suis) is an important major swine and zoonotic pathogen that causes severe infection [1,2,3]. It is associated with a variety of serious diseases, including arthritis, septicemia, pneumonia, endocarditis, and meningitis in pigs and leads to great economic losses worldwide [4,5]. TA_9 system or the toxin of the TA_9 system were toxin of the TA_7 system, and (C) the TA_9 system or the toxin of the TA_9 system were introduced into into pLysS pLysSwith cells andisopropyl were induced with 1 mM isopropyl

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