Moran Robert A, Holt Kathryn E, Hall Ruth M
School of Life and Environmental Sciences, The University of Sydney, NSW, Australia.
Department of Biochemistry and Molecular Biology and Centre for Systems Genomics, University of Melbourne, VIC, Australia.
Plasmid. 2016 Mar-May;84-85:11-9. doi: 10.1016/j.plasmid.2016.02.002. Epub 2016 Feb 18.
The rare sulphonamide resistance gene sul3 was found in the commensal Escherichia coli ST95 strain 22.1-R1 that was isolated in 2010 from the faeces of a healthy Australian adult. The genome of 22.1-R1 was sequenced and a 144,344bp RepFII/FIB plasmid, pCERC3, carrying sul3 was assembled. The sul3 gene is part of a class 1 integron featuring a sul3-containing conserved segment (sul3-CS) that replaced the classic sul1-containing 3'-conserved segment (3'-CS) usually seen in class 1 integrons. The integron contained the cassette array dfrA12-orfF-aadA2-cmlA1-aadA1-qacH, conferring resistance to trimethoprim, streptomycin, spectinomycin, chloramphenicol and quaternary ammonium compound. Two additional antibiotic resistance genes, blaTEM (ampicillin resistance) and tetA(B) (tetracycline) were adjacent to the integron, forming a single resistance region. In pCERC3, the sul3-type class 1 integron was flanked by sequence derived from the tnp and mer modules of Tn21 and was in the same location as In2, the sul1-containing In5-type class 1 integron of Tn21. At one end the sequence extends into Tn2670-derived sequence and then into sequence derived from the plasmid NR1 (R100). Examination of the sequences of eleven more complete sul3-containing plasmids in GenBank confirmed the relationship between sul3-associated integrons and Tn21/Tn2670/NR1. This suggests that the events that formed sul3-associated class 1 integrons occurred within the Tn21/Tn2670 context, most likely in NR1 or a related plasmid. The backbone of pCERC3 is most closely related to the backbones of ColV virulence plasmids and contains a complete ColV operon as well as several virulence associated genes and gene clusters. Hence, pCERC3 is both an antibiotic resistance and virulence plasmid.
在一株共生大肠杆菌ST95菌株22.1-R1中发现了罕见的磺胺类耐药基因sul3,该菌株于2010年从一名健康澳大利亚成年人的粪便中分离得到。对22.1-R1的基因组进行了测序,并组装出了一个携带sul3的144,344bp的RepFII/FIB质粒pCERC3。sul3基因是1类整合子的一部分,其特征是含有sul3的保守片段(sul3-CS)取代了1类整合子中通常可见的经典含sul1的3'-保守片段(3'-CS)。该整合子包含盒式阵列dfrA12-orfF-aadA2-cmlA1-aadA1-qacH,赋予对甲氧苄啶、链霉素、壮观霉素、氯霉素和季铵化合物的抗性。另外两个抗生素耐药基因blaTEM(氨苄青霉素抗性)和tetA(B)(四环素抗性)与整合子相邻,形成一个单一的耐药区域。在pCERC3中,sul3型1类整合子两侧是来自Tn21的tnp和mer模块的序列,并且与Tn21的含sul1的In5型1类整合子In2位于同一位置。在一端,该序列延伸到Tn2670衍生的序列中,然后延伸到来自质粒NR1(R100)的序列中。对GenBank中另外11个完整的含sul3质粒的序列进行检查,证实了sul3相关整合子与Tn21/Tn2670/NR1之间的关系。这表明形成sul3相关1类整合子的事件发生在Tn21/Tn2670的背景下,最有可能发生在NR1或相关质粒中。pCERC3的主干与ColV毒力质粒的主干关系最为密切,并且包含一个完整的ColV操纵子以及几个毒力相关基因和基因簇。因此,pCERC3既是一个抗生素耐药性质粒,也是一个毒力质粒。