[Development and Evaluation of a New Selective Culture Medium, KBM Anaero RS-GNR, for Detection of Anaerobic Gram Negative Rods].

Taeko Narita, Kyohei Kato, Hiroki Hanaiwa, Tetsuhiro Harada, Yumiko Funashima, Makoto Akiwa, Jun-Ichiro Sekiguchi, Zenzo Nagasawa, Tsukuru Umemura
{"title":"[Development and Evaluation of a New Selective Culture Medium, KBM Anaero RS-GNR, for Detection of Anaerobic Gram Negative Rods].","authors":"Taeko Narita,&nbsp;Kyohei Kato,&nbsp;Hiroki Hanaiwa,&nbsp;Tetsuhiro Harada,&nbsp;Yumiko Funashima,&nbsp;Makoto Akiwa,&nbsp;Jun-Ichiro Sekiguchi,&nbsp;Zenzo Nagasawa,&nbsp;Tsukuru Umemura","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The laboratory culture methods for isolating drug-resistant pathogens has been the gold standard in medical microbiology, and play pivotal roles in the overall management of infectious diseases. Recently, several reports have emphasized the development of antibiotics-resistance among anaerobic gram-negative rods, especially Genus <i>Bacteroides</i> and <i>Prevotella</i>. Therefore, a selective culture method to detect these pathogens is needed. We developed here the new selective culture medium, termed \"KBM Anaero RS-GNR,\" for detecting anaerobic Gram-negative rods. Growth capability and selectivity of the agar medium were assessed by using the pure culture suspensions of more than 100 bacterial strains as well as the 13 samples experimentally contaminated with these bacterial strains. This new medium, \"KBM Anaero RS-GNR,\" successfully showed the selective isolation of anaerobic Gram-negative rods. Compared with commercially available medium, \"PV Brucella HK Agar, \" which is also designed to detect anaerobic Gram-negative rods, there was no significant difference of the overall detection efficiency between two media. However, \"KBM Anaero RS-GNR\" showed superior to selectivity for anaerobic Gram-negative rods, especially from the samples contaminated with <i>Candida</i> species. Thus, the culture method using KBM Anaero RS-GNR is relevant for isolation of anaerobic Gram-negative rods especially from clinical specimens.</p>","PeriodicalId":74740,"journal":{"name":"Rinsho Biseibutsu Jinsoku Shindan Kenkyukai shi = JARMAM : Journal of the Association for Rapid Method and Automation in Microbiology","volume":"27 1","pages":"15-23"},"PeriodicalIF":0.0000,"publicationDate":"2017-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rinsho Biseibutsu Jinsoku Shindan Kenkyukai shi = JARMAM : Journal of the Association for Rapid Method and Automation in Microbiology","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

The laboratory culture methods for isolating drug-resistant pathogens has been the gold standard in medical microbiology, and play pivotal roles in the overall management of infectious diseases. Recently, several reports have emphasized the development of antibiotics-resistance among anaerobic gram-negative rods, especially Genus Bacteroides and Prevotella. Therefore, a selective culture method to detect these pathogens is needed. We developed here the new selective culture medium, termed "KBM Anaero RS-GNR," for detecting anaerobic Gram-negative rods. Growth capability and selectivity of the agar medium were assessed by using the pure culture suspensions of more than 100 bacterial strains as well as the 13 samples experimentally contaminated with these bacterial strains. This new medium, "KBM Anaero RS-GNR," successfully showed the selective isolation of anaerobic Gram-negative rods. Compared with commercially available medium, "PV Brucella HK Agar, " which is also designed to detect anaerobic Gram-negative rods, there was no significant difference of the overall detection efficiency between two media. However, "KBM Anaero RS-GNR" showed superior to selectivity for anaerobic Gram-negative rods, especially from the samples contaminated with Candida species. Thus, the culture method using KBM Anaero RS-GNR is relevant for isolation of anaerobic Gram-negative rods especially from clinical specimens.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[一种检测厌氧革兰氏阴性棒的新型选择性培养基KBM Anaero RS-GNR的开发与评价]。
实验室培养分离耐药病原菌的方法已成为医学微生物学的金标准,在传染病的整体管理中起着举足轻重的作用。最近,一些报道强调了厌氧革兰氏阴性棒中抗生素耐药性的发展,特别是拟杆菌属和普雷沃氏菌。因此,需要一种选择性培养方法来检测这些病原体。我们在这里开发了新的选择性培养基,称为“KBM Anaero RS-GNR”,用于检测厌氧革兰氏阴性棒。利用100余株细菌的纯培养悬浮液和13个被这些细菌污染的实验样品,评估了琼脂培养基的生长能力和选择性。这种新的培养基,“KBM Anaero RS-GNR”,成功地展示了厌氧革兰氏阴性棒的选择性分离。与同样用于检测厌氧革兰氏阴性棒的市售培养基“PV Brucella HK琼脂”相比,两种培养基的总体检测效率没有显著差异。然而,“KBM Anaero RS-GNR”对厌氧革兰氏阴性棒的选择性较好,特别是对念珠菌污染的样品。因此,KBM Anaero RS-GNR培养方法适用于革兰氏阴性棒的厌氧分离,特别是从临床标本中。
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
A Japanese Case of COVID-19 Caused by Omicron Strain with Y453F Substitution. [Evaluation of Methicillin Resistance Determination Time for MRSA Using Fully Automated Rapid Identification Susceptibility testing system RAISAS S4]. [Evaluation of the Clinical Validity of the Clostridioides difficile Nucleic Acid Detection Kit "Smart Gene® CD ToxinB"]. [Relationship between Serotypes and Biotypes of Yersinia enterocolitica and the Names of Identified Bacteria in the Microbial Identification and Susceptibility Testing Devices]. Comparison of Microorganism Detection, Time to Positivity, and Time-Dependent Shift in Viable Bacterial Count from VersaTREK and BacT/ALERT 3D Blood Culture Systems.
×
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