Exfoliative toxin production by Staphylococcus aureus strains isolated from animals and human beings in Nigeria.

Microbiologica Pub Date : 1991-10-01
A A Adesiyun, W Lenz, K P Schaal
{"title":"Exfoliative toxin production by Staphylococcus aureus strains isolated from animals and human beings in Nigeria.","authors":"A A Adesiyun,&nbsp;W Lenz,&nbsp;K P Schaal","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Strains of Staphylococcus aureus isolated from lesions and apparently healthy animals, human diarrhoea and wounds in Nigeria were phage typed and tested for exfoliative toxin (ET) production using the modified Ouchterlony double diffusion test. Thirty-four (4.0%) of 860 strains tested produced exfoliative toxins A (ETA), B (ETB) or a combination. ETA was produced singly by 91.1% of the toxigenic strains. Twenty-six (3.9%) of 666 animal strains were toxigenic compared to 8 (4.4%) of 194 strains from human beings. Overall, a majority of ET-producing strains were non-typable (58.8%), followed by phage group II strains (17.7%). The detection of a similar frequency of production of ET by strains of S. aureus from animals and non-scalded skin syndrome cases indicates that animals may serve as a reservoir for human infection.</p>","PeriodicalId":77264,"journal":{"name":"Microbiologica","volume":"14 4","pages":"357-62"},"PeriodicalIF":0.0000,"publicationDate":"1991-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiologica","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Strains of Staphylococcus aureus isolated from lesions and apparently healthy animals, human diarrhoea and wounds in Nigeria were phage typed and tested for exfoliative toxin (ET) production using the modified Ouchterlony double diffusion test. Thirty-four (4.0%) of 860 strains tested produced exfoliative toxins A (ETA), B (ETB) or a combination. ETA was produced singly by 91.1% of the toxigenic strains. Twenty-six (3.9%) of 666 animal strains were toxigenic compared to 8 (4.4%) of 194 strains from human beings. Overall, a majority of ET-producing strains were non-typable (58.8%), followed by phage group II strains (17.7%). The detection of a similar frequency of production of ET by strains of S. aureus from animals and non-scalded skin syndrome cases indicates that animals may serve as a reservoir for human infection.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
从尼日利亚动物和人类分离的金黄色葡萄球菌菌株产生剥脱性毒素。
从尼日利亚的病变和明显健康的动物、人腹泻和伤口中分离的金黄色葡萄球菌菌株被噬菌体分型,并使用改进的Ouchterlony双重扩散试验检测剥离毒素(ET)的产生。860株中34株(4.0%)产生剥脱性毒素A (ETA)、B (ETB)或两者的组合。91.1%的产毒菌株产生ETA。666株动物毒株中26株(3.9%)产毒,194株人毒株中8株(4.4%)产毒。总的来说,大多数产生et的菌株是不可分型的(58.8%),其次是噬菌体II组菌株(17.7%)。从动物和非烫伤皮肤综合征病例中发现的金黄色葡萄球菌菌株产生ET的频率相似,这表明动物可能是人类感染的宿主。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Methisoprinol-effect on the replication cycle of human hepatitis A virus. Absence of HTLV-I/II infection in blood donors with positive and inconclusive HTLV-I/II serology. Role of phospholipids in BK virus infection and haemagglutination. The response of pregnant gilts previously given an inactivated preparation of porcine parvovirus (PPV) to challenge infection with a fully virulent PPV. A mechanism involved in the plaque enhancement effect of sodium thiosulfate for foot-and-mouth disease viruses.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1