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使用单分子实时测序对从多重耐药性纽波特沙门氏菌中分离出的IncA/C和IncI1质粒进行序列分析。

Sequence Analysis of IncA/C and IncI1 Plasmids Isolated from Multidrug-Resistant Salmonella Newport Using Single-Molecule Real-Time Sequencing.

作者信息

Cao Guojie, Allard Marc, Hoffmann Maria, Muruvanda Tim, Luo Yan, Payne Justin, Meng Kevin, Zhao Shaohua, McDermott Patrick, Brown Eric, Meng Jianghong

机构信息

1 Department of Nutrition and Food Science, Joint Institute for Food Safety and Applied Nutrition, University of Maryland , College Park, Maryland.

2 Center for Food Safety and Applied Nutrition , U.S. Food and Drug Administration, College Park, Maryland.

出版信息

Foodborne Pathog Dis. 2018 Jun;15(6):361-371. doi: 10.1089/fpd.2017.2385. Epub 2018 Apr 5.

Abstract

Multidrug-resistant (MDR) plasmids play an important role in disseminating antimicrobial resistance genes. To elucidate the antimicrobial resistance gene compositions in A/C incompatibility complex (IncA/C) plasmids carried by animal-derived MDR Salmonella Newport, and to investigate the spread mechanism of IncA/C plasmids, this study characterizes the complete nucleotide sequences of IncA/C plasmids by comparative analysis. Complete nucleotide sequencing of plasmids and chromosomes of six MDR Salmonella Newport strains was performed using PacBio RSII. Open reading frames were assigned using prokaryotic genome annotation pipeline (PGAP). To understand genomic diversity and evolutionary relationships among Salmonella Newport IncA/C plasmids, we included three complete IncA/C plasmid sequences with similar backbones from Salmonella Newport and Escherichia coli: pSN254, pAM04528, and peH4H, and additional 200 draft chromosomes. With the exception of canine isolate CVM22462, which contained an additional IncI1 plasmid, each of the six MDR Salmonella Newport strains contained only the IncA/C plasmid. These IncA/C plasmids (including references) ranged in size from 80.1 (pCVM21538) to 176.5 kb (pSN254) and carried various resistance genes. Resistance genes floR, tetA, tetR, strA, strB, sul, and mer were identified in all IncA/C plasmids. Additionally, bla and sugE were present in all IncA/C plasmids, excepting pCVM21538. Plasmid pCVM22462 was capable of being transferred by conjugation. The IncI1 plasmid pCVM22462b in CVM22462 carried bla and sugE. Our data showed that MDR Salmonella Newport strains carrying similar IncA/C plasmids clustered together in the phylogenetic tree using chromosome sequences and the IncA/C plasmids from animal-derived Salmonella Newport contained diverse resistance genes. In the current study, we analyzed genomic diversities and phylogenetic relationships among MDR Salmonella Newport using complete plasmids and chromosome sequences and provided possible spread mechanism of IncA/C plasmids in Salmonella Newport Lineage II.

摘要

多重耐药(MDR)质粒在传播抗菌药物耐药基因方面发挥着重要作用。为阐明动物源多重耐药纽波特沙门氏菌携带的A/C不相容复合体(IncA/C)质粒中的抗菌药物耐药基因组成,并研究IncA/C质粒的传播机制,本研究通过比较分析对IncA/C质粒的完整核苷酸序列进行了表征。使用PacBio RSII对6株多重耐药纽波特沙门氏菌菌株的质粒和染色体进行了完整核苷酸测序。使用原核生物基因组注释管道(PGAP)对开放阅读框进行了注释。为了解纽波特沙门氏菌IncA/C质粒之间的基因组多样性和进化关系,我们纳入了来自纽波特沙门氏菌和大肠杆菌的3个具有相似骨架的完整IncA/C质粒序列:pSN254、pAM04528和peH4H,以及另外200个草图染色体。除犬源分离株CVM22462含有一个额外的IncI1质粒外,6株多重耐药纽波特沙门氏菌菌株中的每一株仅含有IncA/C质粒。这些IncA/C质粒(包括参考质粒)大小从80.1(pCVM21538)到176.5 kb(pSN254)不等,并携带各种耐药基因。在所有IncA/C质粒中均鉴定出耐药基因floR、tetA、tetR、strA、strB、sul和mer。此外,除pCVM21538外,所有IncA/C质粒中均存在bla和sugE。质粒pCVM22462能够通过接合进行转移。CVM22462中的IncI1质粒pCVM22462b携带bla和sugE。我们的数据表明,携带相似IncA/C质粒的多重耐药纽波特沙门氏菌菌株在使用染色体序列构建的系统发育树中聚集在一起,并且来自动物源纽波特沙门氏菌的IncA/C质粒含有多种耐药基因。在本研究中,我们使用完整的质粒和染色体序列分析了多重耐药纽波特沙门氏菌之间的基因组多样性和系统发育关系,并提供了IncA/C质粒在纽波特沙门氏菌谱系II中的可能传播机制。

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