• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

两种分型方法(hsp65 PRA和ITS测序)的比较研究揭示了堪萨斯分枝杆菌I型和II型分离株之间可能存在的进化联系。

Comparative study of two typing methods, hsp65 PRA and ITS sequencing, revealed a possible evolutionary link between Mycobacterium kansasii type I and II isolates.

作者信息

Iwamoto Tomotada, Saito Hajime

机构信息

Department of Microbiology, Kobe Institute of Health, Kobe, Japan.

出版信息

FEMS Microbiol Lett. 2006 Jan;254(1):129-33. doi: 10.1111/j.1574-6968.2005.00013.x.

DOI:10.1111/j.1574-6968.2005.00013.x
PMID:16451190
Abstract

One hundred and ninety-eight clinical isolates of Mycobacterium kansasii collected between 2003 and 2004 in Japan were genotyped by PCR and restriction enzyme analysis (PRA) and 16S-23S internal transcribed spacer (ITS) sequencing. The results demonstrated that clinical isolates of M. kansasii in Japan are almost exclusively of the type I PRA genotype, as is the case in other countries. Although the results of subtyping using the 16S-23S ITS sequence were generally consistent with subtyping using hsp65 PRA, four strains showed a discrepancy between the two methods. Sequence analysis of the hsp65, gyrB and 16S rRNA genes and the ITS sequence of the four strains suggests that they branched from type II and could be considered an ancestral strain of the type I strain. The newly recognized strains were designated as intermediate type I.

摘要

2003年至2004年期间在日本收集的198株堪萨斯分枝杆菌临床分离株,通过聚合酶链反应(PCR)和限制性内切酶分析(PRA)以及16S - 23S内部转录间隔区(ITS)测序进行基因分型。结果表明,日本的堪萨斯分枝杆菌临床分离株几乎均为I型PRA基因型,其他国家的情况也是如此。虽然使用16S - 23S ITS序列进行亚型分析的结果与使用hsp65 PRA进行亚型分析的结果总体一致,但有4株菌株在两种方法之间存在差异。对这4株菌株的hsp65、gyrB和16S rRNA基因以及ITS序列进行分析表明,它们从II型分支出来,可被视为I型菌株的祖先菌株。新识别出的菌株被指定为中间I型。

相似文献

1
Comparative study of two typing methods, hsp65 PRA and ITS sequencing, revealed a possible evolutionary link between Mycobacterium kansasii type I and II isolates.两种分型方法(hsp65 PRA和ITS测序)的比较研究揭示了堪萨斯分枝杆菌I型和II型分离株之间可能存在的进化联系。
FEMS Microbiol Lett. 2006 Jan;254(1):129-33. doi: 10.1111/j.1574-6968.2005.00013.x.
2
Intra- and interpatient variability of the hsp65 and 16S-23S intergenic gene region in Mycobacterium abscessus strains from patients with cystic fibrosis.囊性纤维化患者脓肿分枝杆菌菌株中hsp65和16S-23S基因间隔区在患者内和患者间的变异性。
J Clin Microbiol. 2005 Jul;43(7):3500-3. doi: 10.1128/JCM.43.7.3500-3503.2005.
3
[Molecular epidemiological analysis of Mycobacterium kansasii isolates].堪萨斯分枝杆菌分离株的分子流行病学分析
Kekkaku. 2007 Feb;82(2):103-10.
4
hsp65 PCR-restriction analysis (PRA) with capillary electrophoresis for species identification and differentiation of Mycobacterium kansasii and Mycobacterium chelonae-Mycobacterium abscessus group.hsp65 PCR-限制性分析 (PRA) 联合毛细管电泳用于堪萨斯分枝杆菌和脓肿分枝杆菌-龟分枝杆菌复合群的种属鉴定和区分。
Int J Infect Dis. 2012 Mar;16(3):e193-7. doi: 10.1016/j.ijid.2011.11.011. Epub 2012 Jan 11.
5
Mycobacterium insubricum sp. nov.新种隐秘分枝杆菌
Int J Syst Evol Microbiol. 2009 Jun;59(Pt 6):1518-23. doi: 10.1099/ijs.0.003459-0.
6
Rapid identification of Mycobacteria to the species level using INNO-LiPA Mycobacteria, a reverse hybridization assay.使用INNO-LiPA分枝杆菌(一种反向杂交检测法)对分枝杆菌进行快速种水平鉴定。
J Clin Microbiol. 2001 Dec;39(12):4477-82. doi: 10.1128/JCM.39.12.4477-4482.2001.
7
Mycobacterium noviomagense sp. nov.; clinical relevance evaluated in 17 patients.新诺马根分枝杆菌新种;对17例患者的临床相关性进行了评估。
Int J Syst Evol Microbiol. 2009 Apr;59(Pt 4):845-9. doi: 10.1099/ijs.0.001511-0.
8
Mycobacterium sherrisii isolation from a patient with pulmonary disease.从一名肺部疾病患者中分离出谢里斯分枝杆菌。
Diagn Microbiol Infect Dis. 2007 Feb;57(2):221-3. doi: 10.1016/j.diagmicrobio.2006.06.021. Epub 2006 Aug 23.
9
Application of four molecular typing methods for analysis of Mycobacterium fortuitum group strains causing post-mammaplasty infections.应用四种分子分型方法分析引起隆胸术后感染的偶然分枝杆菌菌群菌株
Clin Microbiol Infect. 2006 Feb;12(2):142-9. doi: 10.1111/j.1469-0691.2005.01312.x.
10
Identification of Mycobacterium kansasii by using a DNA probe (AccuProbe) and molecular techniques.使用DNA探针(AccuProbe)和分子技术鉴定堪萨斯分枝杆菌。
J Clin Microbiol. 1999 Apr;37(4):964-70. doi: 10.1128/JCM.37.4.964-970.1999.

引用本文的文献

1
Genomic-based genotype and drug susceptibility profile of in China.中国基于基因组的基因型和药物敏感性概况。
Front Microbiol. 2025 Apr 29;16:1573448. doi: 10.3389/fmicb.2025.1573448. eCollection 2025.
2
Clinical and Microbiological Characteristics of Mycobacterium kansasii Pulmonary Infections in China.中国堪萨斯分枝杆菌肺部感染的临床和微生物学特征。
Microbiol Spectr. 2022 Feb 23;10(1):e0147521. doi: 10.1128/spectrum.01475-21. Epub 2022 Jan 12.
3
Molecular Identification, and Characterization of Strains Isolated from Four Tuberculosis Regional Reference Laboratories in Iran During 2016-2018.
2016 - 2018年期间从伊朗四个结核病区域参考实验室分离出的菌株的分子鉴定与特征分析
Infect Drug Resist. 2020 Jul 7;13:2171-2180. doi: 10.2147/IDR.S245295. eCollection 2020.
4
Genomic Insights Into the Complex: An Update.关于该复合体的基因组学见解:最新进展
Front Microbiol. 2020 Jan 15;10:2918. doi: 10.3389/fmicb.2019.02918. eCollection 2019.
5
Disseminated mycobacteriosis caused by Mycobacterium kansasii in a pot-bellied pig.一只大肚猪感染堪萨斯分枝杆菌引起的播散性分枝杆菌病。
J Vet Diagn Invest. 2018 Jul;30(4):646-650. doi: 10.1177/1040638718780189. Epub 2018 Jun 1.
6
Molecular typing of Mycobacterium kansasii using pulsed-field gel electrophoresis and a newly designed variable-number tandem repeat analysis.应用脉冲场凝胶电泳和新设计的可变数目串联重复序列分析对堪萨斯分枝杆菌进行分子分型。
Sci Rep. 2018 Mar 13;8(1):4462. doi: 10.1038/s41598-018-21562-z.
7
Drug Susceptibility Profiling and Genetic Determinants of Drug Resistance in Mycobacterium kansasii.堪萨斯分枝杆菌的药物敏感性分析及耐药基因的遗传决定因素。
Antimicrob Agents Chemother. 2018 Mar 27;62(4). doi: 10.1128/AAC.01788-17. Print 2018 Apr.
8
Rapid and accurate identification of Mycobacterium tuberculosis complex and common non-tuberculous mycobacteria by multiplex real-time PCR targeting different housekeeping genes.采用多重实时 PCR 靶向不同管家基因快速准确鉴定结核分枝杆菌复合群和常见非结核分枝杆菌。
Curr Microbiol. 2012 Nov;65(5):493-9. doi: 10.1007/s00284-012-0188-2. Epub 2012 Jul 14.