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首页> 外文期刊>Veterinary Microbiology >Quadruple or quintuple conversion of hlb, sak, sea (or sep), scn, and chp genes by bacteriophages in non-beta-hemolysin-producing bovine isolates of Staphylococcus aureus
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Quadruple or quintuple conversion of hlb, sak, sea (or sep), scn, and chp genes by bacteriophages in non-beta-hemolysin-producing bovine isolates of Staphylococcus aureus

机译:产非β-溶血素的金黄色葡萄球菌分离株中噬菌体对hlb,sak,sea(或sep),scn和chp基因进行四倍或五倍转换

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摘要

In 13 of 43 non-beta-hemolysin-producing bovine isolates of Staphylococcus aureus, two truncated beta-hemolysin (hlb) genes were demonstrated by PCR and sequencing, and one truncated hlb gene was located beside the integrase (int) gene of phage origin. The staphylokinase (sak) gene was detected in all 13 isolates in which the truncated hlb genes were detected by PCR. Enterotoxin A (sea) and enterotoxin P (sep) genes were also detected in 5 and 2 of the 13 isolates, respectively. Moreover, the scn and chp genes encoding staphylococcal complement inhibitor (SCIN) and chemotaxis inhibitory protein of S. aureus (CHIPS) were detected in 13 and 4 of the 13 isolates, respectively. The bacteriophage induced by mitomycin C treatment was able to lysogenize one beta-hemolysin-producing isolate of S. aureus, and the sak and scn genes were detected from the lysogenized isolate. These results suggest quadruple or quintuple conversion of hlb, sak, sea (or sep), scn, and chp genes by bacteriophages among non-beta-hemolysin-producing bovine isolates of S. aureus.
机译:在43个非β-溶血素的金黄色葡萄球菌产牛分离株中,有13个通过PCR和测序证实了两个截短的β-溶血素(hlb)基因,一个截短的hlb基因位于噬菌体来源的整合酶(int)基因旁边。在通过PCR检测到截短的hlb基因的所有13个分离物中均检测到葡萄球菌激酶(sak)基因。还分别在13个分离株中的5个和2个中检测到肠毒素A(海)和肠毒素P(sep)基因。此外,分别在13个分离株中的13个和4个中检测到编码葡萄球菌补体抑制剂(SCIN)和金黄色葡萄球菌趋化抑制蛋白(CHIPS)的scn和chp基因。通过丝裂霉素C处理诱导的噬菌体能够溶血一种产金黄色葡萄球菌的β-溶血素的分离株,并且从该溶源分离株中检测到sak和scn基因。这些结果表明,在产非β-溶血素的金黄色葡萄球菌中,噬菌体可将hlb,sak,sea(或sep),scn和chp基因进行四倍或五倍转换。

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