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携带基因菌株的抗性及……的遗传环境 (原文中“the Genetic Environment of ”后面似乎缺少具体内容)

Resistance of Strains Carrying Gene and the Genetic Environment of .

作者信息

Xiang Tianxin, Chen Chuanhui, Wen Jiangxiong, Liu Yang, Zhang Qi, Cheng Na, Wu Xiaoping, Zhang Wei

机构信息

Department of Hospital Infection Control, The First Affiliated Hospital of Nanchang University, Nanchang, China.

Department of Respiratory and Critical Care, The First Affiliated Hospital of Nanchang University, Nanchang, China.

出版信息

Front Microbiol. 2020 Apr 30;11:700. doi: 10.3389/fmicb.2020.00700. eCollection 2020.

Abstract

OBJECTIVE

Regional dissemination is the major cause of the widespread prevalence of a plasmid-encoding NDM-1 enzyme. We investigated the drug resistance, joint efficiency, and gene environment of a strain carrying gene.

MATERIALS AND METHODS

Carbapenem-non-susceptible strains were analyzed using the VITEK 2 Compact. Strains carrying were identified using polymerase chain reaction and sequencing. Antimicrobial susceptibility testing and plasmid conjugation experiments were then conducted. Strains carrying were subjected to Southern blot analysis. After the gene mapping of , library construction, and sequencing, plasmids were subsequently spliced and genotyped using the software Glimmer 3.0, and then analyzed using Mauve software.

RESULTS

Among 1735 carbapenem-non-susceptible strains, 54 strains of -positive bacteria were identified, which consisted of 44 strains of , 8 strains of and 2 strains of . Strains carrying had a resistance rate of more than 50% in most antibiotics. Plasmid conjugation between strains carrying and strain J53 had a success rate of 50%. Southern blot analysis indicated that each strain had multiple plasmids containing . Among the five plasmids containing in for sequencing, two plasmids with complete sequences were obtained. The findings were as follows: (i) The p11106 and p12 plasmids were highly similar to pNDM-BTR; (ii) the p11106 and p12 plasmids showed differences in the 20-30 kb region (orf00032-orf00043) from the other six plasmids; and (iii) was located at orf00037, while was found at orf00038. Two genes were located in the upstream region, and orf00052 () in the 36 kb region was in the downstream sequence.

CONCLUSION

-containing bacteria exhibit multidrug resistance, which rapidly spreads and is transferred through efficient plasmid conjugation; the multidrug resistance of these bacteria may be determined by analyzing their drug-resistant plasmids. The presence of and genes suggests a possible hypothesis that originates from , which is retained in over a long period by transposition of mobile elements.

摘要

目的

区域传播是编码NDM-1酶的质粒广泛流行的主要原因。我们研究了携带该基因的菌株的耐药性、接合效率及基因环境。

材料与方法

使用VITEK 2 Compact对碳青霉烯不敏感菌株进行分析。通过聚合酶链反应和测序鉴定携带该基因的菌株。随后进行药敏试验和质粒接合实验。对携带该基因的菌株进行Southern印迹分析。在对该基因进行定位、文库构建和测序后,使用Glimmer 3.0软件对质粒进行拼接和基因分型,然后用Mauve软件进行分析。

结果

在1735株碳青霉烯不敏感菌株中,鉴定出54株该基因阳性菌,其中包括44株肺炎克雷伯菌、8株大肠埃希菌和2株产气肠杆菌。携带该基因的菌株对大多数抗生素的耐药率超过50%。携带该基因的菌株与J53菌株之间的质粒接合成功率为50%。Southern印迹分析表明,每株菌都有多个含该基因的质粒。在用于测序的5个含该基因的质粒中,获得了2个序列完整的质粒。结果如下:(i)p11106和p12质粒与pNDM-BTR高度相似;(ii)p11106和p12质粒在20 - 30 kb区域(orf00032 - orf00043)与其他6个质粒存在差异;(iii)blaNDM-1位于orf00037,而blaOXA-1位于orf00038。两个IS26基因位于上游区域,36 kb区域的orf00052(aadA)位于下游序列。

结论

含该基因的细菌表现出多重耐药性,可通过高效的质粒接合迅速传播和转移;分析这些细菌的耐药质粒可能有助于确定其多重耐药性。blaNDM-1和blaOXA-1基因的存在提示了一种可能的假说,即blaNDM-1起源于blaOXA-1,通过移动元件的转座在blaNDM-1中长时间保留。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7e3/7203411/b3ef5865f7db/fmicb-11-00700-g001.jpg

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