Suppr超能文献

耐庆大霉素猪鼻支原体的特性分析

Characterization of gentamicin-resistant Mycoplasma hyorhinis.

作者信息

Idowu Arit D, Celones Michelle C, Salgado Amparo E, Marquez Kristine M, Pleibel Nancy

机构信息

Quality Control Biology, Genentech, Inc., 73B, One, DNA Way, South San Francisco, CA 94080-4990, USA.

出版信息

Biologicals. 2003 Sep;31(3):175-9. doi: 10.1016/s1045-1056(03)00036-8.

Abstract

A study was conducted to determine if a gentamicin-resistant strain of mycoplasma could be developed for use in validating current mycoplasma detection methods for biologic product harvest cell culture fluid (CCF) containing gentamicin. A strain of gentamicin-resistant Mycoplasma hyorhinis was isolated and characterized. The study showed that this organism was similar to the wild-type strain in all ways examined except gentamicin resistance. Both strains of mycoplasma (the gentamicin resistant and the wild-type) exhibited comparable growth patterns and showed 100% homology based on DNA sequencing and analysis of a 464-bp PCR product. Also, analysis using species-specific antisera identified both strains as M. hyorhinis. Two commonly used lot release mycoplasma detection methods (culture and DNAF) consistently detected mycoplasmas in spiked biologic product harvest CCF containing gentamicin but not in unspiked samples. This study demonstrates the first isolation and characterization of a gentamicin-resistant M. hyorhinis that can be used to validate mycoplasma detection methods for biologic product harvest CCF containing gentamicin.

摘要

开展了一项研究,以确定是否可以培育出一种对庆大霉素耐药的支原体菌株,用于验证当前针对含有庆大霉素的生物制品收获细胞培养液(CCF)的支原体检测方法。分离并鉴定了一株对庆大霉素耐药的猪鼻支原体菌株。研究表明,除了对庆大霉素耐药外,该菌株在所有检测方面均与野生型菌株相似。两种支原体菌株(耐庆大霉素菌株和野生型菌株)呈现出相似的生长模式,并且基于对一段464bp的PCR产物进行DNA测序和分析显示二者具有100%的同源性。此外,使用种特异性抗血清进行的分析将两种菌株均鉴定为猪鼻支原体。两种常用的批放行支原体检测方法(培养法和DNA荧光染色法)能够持续检测出添加了庆大霉素的生物制品收获CCF中的支原体,但无法检测出未添加的样本中的支原体。本研究首次分离并鉴定了一种对庆大霉素耐药的猪鼻支原体,可用于验证针对含有庆大霉素的生物制品收获CCF的支原体检测方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验