Zhang Anyun, Xu Changwen, Wang Hongning, Lei Changwei, Liu Bihui, Guan Zhongbin, Yang Chunmei, Yang Yongqiang, Peng Linyao
Key Laboratory of Bio-Resources and Eco-Environment, Ministry of Education, College of Life science, Sichuan University, Chengdu, Sichuan 610064, PR China; Animal Disease Prevention and Food Safety Key Laboratory of Sichuan Province, Chengdu, Sichuan 610064, PR China.
Key Laboratory of Bio-Resources and Eco-Environment, Ministry of Education, College of Life science, Sichuan University, Chengdu, Sichuan 610064, PR China; Animal Disease Prevention and Food Safety Key Laboratory of Sichuan Province, Chengdu, Sichuan 610064, PR China; "985 Project" Science Innovative Platform for Resource and environment Protection of Southwestern, Sichuan University, Chengdu, Sichuan 610064, PR China.
Vet Microbiol. 2015 May 15;177(1-2):162-7. doi: 10.1016/j.vetmic.2015.02.014. Epub 2015 Feb 25.
Erysipelothrix rhusiopathiae is a Gram-positive bacillus that causes erysipelas in swine. In recent years, erysipelas infection among swine in China has been increasing. A combined resistance phenotype to pleuromutilins, lincosamides, and streptogramin A (PLSA phenotype) was found in some E. rhusiopathiae isolates. The aim of this study was to identify the resistance genes responsible for the PLSA phenotype in E. rhusiopathiae strains and to map the genetic environment of the identified resistance gene. A total of 46 E. rhusiopathiae isolates from 31 pig farms in China were studied. Minimum inhibitory concentrations (MICs) of 11 antimicrobial agents were determined by broth microdilution method. Seven were highly resistant to tiamulin (MICs 32 μg/ml) and clindamycin (MICs 64 μg/ml). Resistance genes responsible for the PLSA phenotype were screened by PCR. The lsa(E), spw, lnu(B), aadE and aphA3 genes were detected in strains had the PLSA phenotype, whereas none was detected in susceptible strains. The genetic environment of lsa(E) gene was determined by whole-genome sequencing and overlapping PCR assays. A novel multiresistance gene cluster, orf1-aadE-apt-spw-lsa(E)-lnu(B)-rec-orf2-orf1-aadE-sat4-aphA3, was found. Horizontal gene transfer experiments and whole-genome sequencing suggested that the lsa(E)-carrying multiresistance gene cluster was located in the chromosome. This is the first molecular characterization of PLSA resistance in E. rhusiopathiae. The lsa(E), spw and lnu(B) genes were found in E. rhusiopathiae for the first time. A novel lsa(E)-carrying multiresistance gene cluster was found. The location of lsa(E) in different gene cluster facilitates its persistence and dissemination.
猪红斑丹毒丝菌是一种革兰氏阳性杆菌,可引起猪丹毒。近年来,中国猪群中的丹毒感染呈上升趋势。在一些猪红斑丹毒丝菌分离株中发现了对截短侧耳素类、林可酰胺类和链阳菌素A的联合耐药表型(PLSA表型)。本研究的目的是鉴定猪红斑丹毒丝菌菌株中导致PLSA表型的耐药基因,并绘制已鉴定耐药基因的遗传环境图谱。对来自中国31个猪场的46株猪红斑丹毒丝菌分离株进行了研究。采用肉汤微量稀释法测定11种抗菌药物的最低抑菌浓度(MIC)。其中7株对泰妙菌素(MIC为32μg/ml)和克林霉素(MIC为64μg/ml)高度耐药。通过PCR筛选导致PLSA表型的耐药基因。在具有PLSA表型的菌株中检测到lsa(E)、spw、lnu(B)、aadE和aphA3基因,而在敏感菌株中未检测到。通过全基因组测序和重叠PCR分析确定了lsa(E)基因的遗传环境。发现了一个新的多耐药基因簇,即orf1-aadE-apt-spw-lsa(E)-lnu(B)-rec-orf2-orf1-aadE-sat4-aphA3。水平基因转移实验和全基因组测序表明,携带lsa(E)的多耐药基因簇位于染色体上。这是猪红斑丹毒丝菌中PLSA耐药性的首次分子特征分析。首次在猪红斑丹毒丝菌中发现lsa(E)、spw和lnu(B)基因。发现了一个新的携带lsa(E)的多耐药基因簇。lsa(E)在不同基因簇中的位置促进了其持久性和传播。