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从泌乳奶牛乳样中分离出的多重耐药葡萄球菌属中红霉素抗性甲基化酶基因的鉴定

Characterization of erythromycin-resistant methylase genes from multiple antibiotic resistant Staphylococcus spp isolated from milk samples of lactating cows.

作者信息

Khan S A, Nawaz M S, Khan A A, Steele R S, Cerniglia C E

机构信息

Division of Microbiology, The National Center for Toxicological Research, United States Food and Drug Administration, Jefferson, AR 72079, USA.

出版信息

Am J Vet Res. 2000 Sep;61(9):1128-32. doi: 10.2460/ajvr.2000.61.1128.

Abstract

OBJECTIVE

To isolate and characterize erythromycin-resistant methylase genes in multiple-antibiotic resistant staphylococci isolated from milk samples.

ANIMALS

300 lactating cows.

PROCEDURE

23 erythromycin-resistant staphylococci were isolated from milk samples of 300 lactating cows. The prevalence of erythromycin-resistant methylase (erm) genes, ermC and ermA genes, and the multicomponent macrolide efflux pump in staphylococci msrA genes were identified and characterized by use of multiplex polymerase chain reaction (PCR), Southern hybridization, restricted fragment length polymorphism (RFLP) analysis, and dot-blot hybridization.

RESULTS

Biochemical characterization indicated that 3 of 23 (13%) isolates were coagulase-positive Staphylococcus aureus, and the rest were coagulase-negative. Multiplex PCR resulted in amplification of a 520-base pair (bp) region of the ermC gene from the cell lysates of a strain of S simulans M-21 and S sciuri M-28. The ermC gene in both isolates was found on a 3-kilobase plasmid. The ermA gene was found on the chromosome of 21 isolates, and 6 RFLP patterns were observed. None of the isolates harbored the msrA gene.

CONCLUSIONS

Erythromycin-resistant Staphylococcus spp isolated from milk samples of lactating cows may serve as reservoirs of erm genes homologous to those described in human isolates. However, the chromosomal insert patterns and prevalence of these genes, the sizes of plasmids harboring the genes, and the number of inserts of the genes (copy number) may differ from that of human isolates.

摘要

目的

从牛奶样本中分离出的多重耐药葡萄球菌中分离并鉴定耐红霉素甲基化酶基因。

动物

300头泌乳奶牛。

方法

从300头泌乳奶牛的牛奶样本中分离出23株耐红霉素葡萄球菌。通过多重聚合酶链反应(PCR)、Southern杂交、限制性片段长度多态性(RFLP)分析和点杂交,鉴定并表征葡萄球菌中耐红霉素甲基化酶(erm)基因、ermC和ermA基因以及多组分大环内酯外排泵msrA基因的流行情况。

结果

生化特性表明,23株分离株中有3株(13%)为凝固酶阳性金黄色葡萄球菌,其余为凝固酶阴性。多重PCR从一株模仿葡萄球菌M-21和松鼠葡萄球菌M-28的细胞裂解物中扩增出ermC基因的一个520碱基对(bp)区域。在两个分离株中,ermC基因均位于一个3千碱基的质粒上。在21株分离株的染色体上发现了ermA基因,并观察到6种RFLP模式。没有分离株携带msrA基因。

结论

从泌乳奶牛牛奶样本中分离出的耐红霉素葡萄球菌属可能是与人类分离株中描述的erm基因同源的基因库。然而,这些基因的染色体插入模式和流行情况、携带这些基因的质粒大小以及基因的插入数量(拷贝数)可能与人类分离株不同。

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