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Evolution and Diversity of the Antimicrobial Resistance Associated Mobilome in Streptococcus suis: A Probable Mobile Genetic Elements Reservoir for Other Streptococci
被引:92
作者:
Huang, Jinhu
[1
]
Ma, Jiale
[1
]
Shang, Kexin
[1
]
Hu, Xiao
[2
]
Liang, Yuan
[1
]
Li, Daiwei
[2
,3
]
Wu, Zuowei
[2
]
Dai, Lei
[2
]
Chen, Li
[1
]
Wang, Liping
[1
]
机构:
[1] Nanjing Agr Univ, Coll Vet Med, Lab Vet Pharmacol & Toxicol, Nanjing, Jiangsu, Peoples R China
[2] Iowa State Univ, Dept Vet Microbiol & Prevent Med, Ames, IA USA
[3] Dalian Med Univ, Hosp 2, Dept Pharm, Dalian, Peoples R China
基金:
中国国家自然科学基金;
关键词:
antimicrobial resistance;
mobilome;
ICEs;
MGEs;
prophages;
Streptococcus;
evolution;
COMPARATIVE GENOMIC ANALYSIS;
EMERGING ZOONOTIC PATHOGEN;
GROUP-A STREPTOCOCCUS;
TOXIC-SHOCK-SYNDROME;
CONJUGATIVE ELEMENTS;
ENTEROCOCCUS-FAECALIS;
SEQUENCE;
SEROTYPE-2;
AGALACTIAE;
ISLANDS;
D O I:
10.3389/fcimb.2016.00118
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Streptococcus suis is a previously neglected, newly emerging multidrug-resistant zoonotic pathogen. Mobile genetic elements (MGEs) play a key role in intra- and interspecies horizontal transfer of antimicrobial resistance (AMR) determinants. Although, previous studies showed the presence of several MGEs, a comprehensive analysis of AMR-associated mobilome as well as their interaction and evolution has not been performed. In this study, we presented the AMR-associated mobilome and their insertion hotspots in S. suis. Integrative conjugative elements (ICEs), prophages and tandem MGEs were located at different insertion sites, while 86% of the AMR-associated MGEs were inserted at rpIL and rum loci. Comprehensive analysis of insertions at rplL and rum loci among four pathogenic Streptococcus species (Streptococcus agalactiae, Streptococcus pneumoniae, Streptococcus pyogenes, and S. suis) revealed the existence of different groups of MGEs, including Tn5252, ICESp1108, and TnGBS2 groups ICEs, Phi m46.1 group prophage, ICE_ICE and ICE_prophage tandem MGEs. Comparative ICE genomics of ICESa2603 family revealed that module exchange and acquisition/deletion were the main mechanisms in MGEs' expansion and evolution. Furthermore, the observation of tandem MGEs reflected a novel mechanism for MGE diversity. Moreover, an in vitro competition assay showed no visible fitness cost was observed between different MGE-carrying isolates and a conjugation assay revealed the transferability of ICESa2603 family of ICEs. Our statistics further indicated that the prevalence and diversity of MGEs in S. suis is much greater than in other three species which prompted our hypothesis that S. suis is probably a MGEs reservoir for other streptococci. In conclusion, our results showed that acquisition of MGEs confers S. suis not only its capability as a multidrug resistance pathogen, but also represents a paradigm to study the modular evolution and matryoshkas of MGEs.
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