• 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

应用吖啶橙单染定量 PCR 技术检测幽门螺杆菌的活性。

Viability determination of Helicobacter pylori using propidium monoazide quantitative PCR.

机构信息

Laboratori de Microbiologia Sanitària i Mediambiental (MSM Lab)-Aquasost, UNESCO Chair in Sustainability, Universitat Politècnica de Catalunya, 08222 Terrassa, Barcelona, Spain.

出版信息

Helicobacter. 2010 Oct;15(5):473-6. doi: 10.1111/j.1523-5378.2010.00794.x.

DOI:10.1111/j.1523-5378.2010.00794.x
PMID:21083754
Abstract

BACKGROUND

While Helicobacter pylori exists in a bacillary form in both the natural habitat and the human host, detrimental environmental circumstances have been observed to lead to the conversion of H. pylori from the bacillary to the coccoid form. However, the viability or nonviability of coccoid forms remains to be established in H. pylori. The aim of this study was to determine whether the quantitative PCR combined with propidium monoazide could be an alternative and good technique to determine H. pylori viability in environmental samples and, to contribute to understanding of the role of the H. pylori forms.

MATERIALS AND METHODS

Viability, morphological distribution, and the number of live H. pylori cells were determined using a propidium monoazide-based quantitative PCR method, at various time points.

RESULTS

Under adverse environmental conditions was observed the conversion of H. pylori from the bacillary to the coccoid form, and the decrease in amplification signal, in samples that were treated with propidium monoazide, over the time.

CONCLUSIONS

Incorporation of propidium monoazide indicates that there is an increase in H. pylori cells with the damaged membrane over the study, leading to the manifestation of cellular degeneration and death. Consequently, quantitative PCR combined with propidium monoazide contributes to our understanding of the role of H. pylori cells, under adverse environmental conditions.

摘要

背景

尽管幽门螺杆菌在自然栖息地和人类宿主中都以杆菌形式存在,但已观察到不利的环境情况会导致幽门螺杆菌从杆菌形式转化为球菌形式。然而,幽门螺杆菌球菌形式的生存能力或非生存能力仍有待确定。本研究旨在确定定量聚合酶链反应结合吖啶橙是否可以作为一种替代技术,用于确定环境样本中幽门螺杆菌的生存能力,并有助于了解幽门螺杆菌形态的作用。

材料和方法

使用基于吖啶橙的定量聚合酶链反应方法,在不同时间点确定生存能力、形态分布和活幽门螺杆菌细胞的数量。

结果

在不利的环境条件下,观察到幽门螺杆菌从杆菌形式向球菌形式的转化,并且在用吖啶橙处理的样本中,随着时间的推移,扩增信号减少。

结论

吖啶橙的结合表明,在研究过程中,细胞膜受损的幽门螺杆菌细胞数量增加,导致细胞退化和死亡的表现。因此,定量聚合酶链反应结合吖啶橙有助于我们了解幽门螺杆菌细胞在不利环境条件下的作用。

相似文献

1
Viability determination of Helicobacter pylori using propidium monoazide quantitative PCR.应用吖啶橙单染定量 PCR 技术检测幽门螺杆菌的活性。
Helicobacter. 2010 Oct;15(5):473-6. doi: 10.1111/j.1523-5378.2010.00794.x.
2
A filter-based propidium monoazide technique to distinguish live from membrane-compromised microorganisms using quantitative PCR.基于滤膜的碘化丙啶单染色法结合实时定量 PCR 技术检测活细胞与细胞膜损伤的微生物。
J Microbiol Methods. 2012 Apr;89(1):76-8. doi: 10.1016/j.mimet.2012.01.015. Epub 2012 Jan 31.
3
Selective detection of viable Helicobacter pylori using ethidium monoazide or propidium monoazide in combination with real-time polymerase chain reaction.采用吖啶橙或碘化丙啶单叠氮化物联合实时聚合酶链反应对活幽门螺杆菌的选择性检测。
Microbiol Immunol. 2011 Dec;55(12):841-6. doi: 10.1111/j.1348-0421.2011.00388.x.
4
Comparison of ethidium monoazide and propidium monoazide for the selective detection of viable Legionella cells.吖啶橙和碘化丙啶单染料法用于活嗜肺军团菌选择性检测的比较。
Jpn J Infect Dis. 2010 Mar;63(2):119-23.
5
Evaluation of propidium monoazide (PMA) treatment directly on membrane filter for the enumeration of viable but non cultivable Legionella by qPCR.采用膜过滤法直接对吖啶橙(PMA)处理后,通过 qPCR 对活但非可培养军团菌进行计数的评估。
J Microbiol Methods. 2012 Feb;88(2):319-21. doi: 10.1016/j.mimet.2011.12.010. Epub 2011 Dec 22.
6
A multicenter study of viable PCR using propidium monoazide to detect Legionella in water samples.一项使用单叠氮溴化丙锭进行实时荧光定量聚合酶链反应检测水样中军团菌的多中心研究。
Diagn Microbiol Infect Dis. 2016 Jul;85(3):283-288. doi: 10.1016/j.diagmicrobio.2016.04.009. Epub 2016 Apr 25.
7
Helicobacter pylori-coccoid forms and biofilm formation.幽门螺杆菌——球形形态与生物膜形成
FEMS Immunol Med Microbiol. 2009 Jul;56(2):112-5. doi: 10.1111/j.1574-695X.2009.00556.x. Epub 2009 Apr 27.
8
Use of propidium monoazide and increased amplicon length reduce false-positive signals in quantitative PCR for bioburden analysis.使用碘化丙啶单叠氮化物和增加扩增子长度可减少生物负载分析定量 PCR 中的假阳性信号。
Appl Microbiol Biotechnol. 2013 Mar;97(5):2153-62. doi: 10.1007/s00253-013-4711-6. Epub 2013 Jan 26.
9
Detection of Helicobacter pylori in sewage and water using a new quantitative PCR method with SYBR green.使用带有SYBR Green的新型定量PCR方法检测污水和水中的幽门螺杆菌。
J Appl Microbiol. 2007 Nov;103(5):1931-41. doi: 10.1111/j.1365-2672.2007.03435.x.
10
Selective PCR detection of viable Enterobacter sakazakii cells utilizing propidium monoazide or ethidium bromide monoazide.利用单叠氮化丙锭或单叠氮化溴化乙锭对阪崎肠杆菌活菌进行选择性PCR检测。
J Appl Microbiol. 2008 Oct;105(4):1178-85. doi: 10.1111/j.1365-2672.2008.03851.x. Epub 2008 Jul 8.

引用本文的文献

1
Viability discrimination of bacterial microbiomes in home kitchen dish sponges using propidium monoazide treatment.利用吖啶橙单染法对家庭厨房洗碗海绵中的细菌微生物群落进行活性判别。
Environ Microbiol Rep. 2024 Oct;16(5):e70006. doi: 10.1111/1758-2229.70006.
2
Subtracting the background by reducing cell-free DNA's confounding effects on Mycobacterium tuberculosis quantitation and the sputum microbiome.通过降低无细胞 DNA 对结核分枝杆菌定量和痰微生物组的干扰作用来扣除背景。
Sci Rep. 2024 Sep 27;14(1):22350. doi: 10.1038/s41598-024-73497-3.
3
Can qPCR replace the standard plaque assay in the ASTM F1671 to assess personal protective equipment barrier performance?
定量聚合酶链反应(qPCR)能否取代美国材料与试验协会(ASTM)F1671标准中的噬斑测定法来评估个人防护装备的屏障性能?
Int J Cloth Sci Technol. 2024;36(3):385-392. doi: 10.1108/ijcst-06-2024-208.
4
A putative amino acid transporter localizes to the plant-like vacuolar compartment and controls parasite extracellular survival and stage differentiation.一个假定的氨基酸转运蛋白定位于类似植物的液泡隔室,并控制寄生虫的细胞外存活和阶段分化。
mSphere. 2024 Jan 30;9(1):e0059723. doi: 10.1128/msphere.00597-23. Epub 2023 Dec 5.
5
Development of a propidium monoazide-polymerase chain reaction assay for detection of viable Lactobacillus brevis in beer.一种用于检测啤酒中活性短乳杆菌的单叠氮碘化丙啶-聚合酶链反应检测方法的开发。
Braz J Microbiol. 2017 Oct-Dec;48(4):740-746. doi: 10.1016/j.bjm.2016.11.012. Epub 2017 Jun 3.
6
Advances and Challenges in Viability Detection of Foodborne Pathogens.食源性病原体生存力检测的进展与挑战
Front Microbiol. 2016 Nov 22;7:1833. doi: 10.3389/fmicb.2016.01833. eCollection 2016.
7
Microbial succession in an inflated lunar/Mars analog habitat during a 30-day human occupation.在为期 30 天的人类居住期间,充气式月球/火星模拟栖息地中的微生物演替。
Microbiome. 2016 Jun 2;4(1):22. doi: 10.1186/s40168-016-0167-0.
8
Detection and Quantification of Viable and Nonviable Trypanosoma cruzi Parasites by a Propidium Monoazide Real-Time Polymerase Chain Reaction Assay.通过单叠氮碘化丙啶实时聚合酶链反应检测和定量活的和非活的克氏锥虫寄生虫
Am J Trop Med Hyg. 2016 Jun 1;94(6):1282-9. doi: 10.4269/ajtmh.15-0693. Epub 2016 May 2.
9
Experimental design for the optimization of propidium monoazide treatment to quantify viable and non-viable bacteria in piggery effluents.用于优化单叠氮碘化丙啶处理以定量猪场废水中活细菌和非活细菌的实验设计。
BMC Microbiol. 2015 Aug 16;15:164. doi: 10.1186/s12866-015-0505-6.
10
Exploring preterm birth as a polymicrobial disease: an overview of the uterine microbiome.将早产视为一种多微生物疾病进行探索:子宫微生物组概述
Front Immunol. 2014 Nov 27;5:595. doi: 10.3389/fimmu.2014.00595. eCollection 2014.