• 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

比较培养法和 qPCR 检测非慢性感染囊性纤维化患者的铜绿假单胞菌。

Comparison of culture and qPCR for the detection of Pseudomonas aeruginosa in not chronically infected cystic fibrosis patients.

机构信息

Laboratory for Bacteriology Research, Ghent University Hospital, Ghent University, Ghent, Belgium.

出版信息

BMC Microbiol. 2010 Sep 24;10:245. doi: 10.1186/1471-2180-10-245.

DOI:10.1186/1471-2180-10-245
PMID:20868481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2949703/
Abstract

BACKGROUND

Pseudomonas aeruginosa is the major respiratory pathogen causing severe lung infections among CF patients, leading to high morbidity and mortality. Once infection is established, early antibiotic treatment is able to postpone the transition to chronic lung infection. In order to optimize the early detection, we compared the sensitivity of microbiological culture and quantitative PCR (qPCR) for the detection of P. aeruginosa in respiratory samples of not chronically infected CF patients.

RESULTS

In this national study, we followed CF patients during periods between 1 to 15 months. For a total of 852 samples, 729 (86%) remained P. aeruginosa negative by both culture and qPCR, whereas 89 samples (10%) were positive by both culture and qPCR.Twenty-six samples were negative by culture but positive by qPCR, and 10 samples were positive by culture but remained negative by qPCR. Five of the 26 patients with a culture negative, qPCR positive sample became later P. aeruginosa positive both by culture and qPCR.

CONCLUSION

Based on the results of this study, it can be concluded that qPCR may have a predictive value for impending P. aeruginosa infection for only a limited number of patients.

摘要

背景

铜绿假单胞菌是引起 CF 患者严重肺部感染的主要呼吸道病原体,导致高发病率和死亡率。一旦发生感染,早期抗生素治疗能够延缓向慢性肺部感染的转变。为了优化早期检测,我们比较了微生物培养和定量 PCR(qPCR)检测非慢性感染 CF 患者呼吸道样本中铜绿假单胞菌的敏感性。

结果

在这项全国性研究中,我们在 1 至 15 个月的时间段内对 CF 患者进行了随访。共 852 个样本中,729 个(86%)通过培养和 qPCR 均为阴性,而 89 个样本(10%)通过培养和 qPCR 均为阳性。26 个样本培养阴性但 qPCR 阳性,10 个样本培养阳性但 qPCR 仍为阴性。26 个培养阴性、qPCR 阳性样本中的 5 个后来通过培养和 qPCR 均为铜绿假单胞菌阳性。

结论

根据这项研究的结果,可以得出结论,qPCR 可能对少数即将发生铜绿假单胞菌感染的患者具有预测价值。

相似文献

1
Comparison of culture and qPCR for the detection of Pseudomonas aeruginosa in not chronically infected cystic fibrosis patients.比较培养法和 qPCR 检测非慢性感染囊性纤维化患者的铜绿假单胞菌。
BMC Microbiol. 2010 Sep 24;10:245. doi: 10.1186/1471-2180-10-245.
2
One time quantitative PCR detection of Pseudomonas aeruginosa to discriminate intermittent from chronic infection in cystic fibrosis.一次实时定量 PCR 检测铜绿假单胞菌,以区分囊性纤维化患者的间歇性感染和慢性感染。
J Cyst Fibros. 2018 May;17(3):348-355. doi: 10.1016/j.jcf.2017.12.007. Epub 2018 Jan 12.
3
Proposal of a quantitative PCR-based protocol for an optimal Pseudomonas aeruginosa detection in patients with cystic fibrosis.提出一种基于定量 PCR 的方案,以优化囊性纤维化患者中铜绿假单胞菌的检测。
BMC Microbiol. 2013 Jun 21;13:143. doi: 10.1186/1471-2180-13-143.
4
Application of quantitative PCR to the diagnosis and monitoring of Pseudomonas aeruginosa colonization in 5-18-year-old cystic fibrosis patients.定量 PCR 在诊断和监测 5-18 岁囊性纤维化患者铜绿假单胞菌定植中的应用。
J Med Microbiol. 2011 Feb;60(Pt 2):157-161. doi: 10.1099/jmm.0.023838-0. Epub 2010 Oct 14.
5
Evaluation of quantitative PCR for early diagnosis of Pseudomonas aeruginosa infection in cystic fibrosis: a prospective cohort study.定量 PCR 对囊性纤维化患者铜绿假单胞菌感染早期诊断的评价:一项前瞻性队列研究。
Clin Microbiol Infect. 2017 Mar;23(3):203-207. doi: 10.1016/j.cmi.2016.11.016. Epub 2016 Nov 27.
6
Detection of viable but non-culturable Pseudomonas aeruginosa in cystic fibrosis by qPCR: a validation study.qPCR 检测囊性纤维化中存活但不可培养的铜绿假单胞菌:一项验证研究。
BMC Infect Dis. 2018 Dec 27;18(1):701. doi: 10.1186/s12879-018-3612-9.
7
Evaluation of the efficacy of real-time polymerase chain reaction for the routine early detection of Pseudomonas aeruginosa in cystic fibrosis sputum and throat swab specimens.评价实时聚合酶链反应在常规早期检测囊性纤维化患者痰和咽喉拭子标本中产铜绿假单胞菌中的疗效。
Diagn Microbiol Infect Dis. 2010 Dec;68(4):358-65. doi: 10.1016/j.diagmicrobio.2010.07.012. Epub 2010 Sep 29.
8
Bacterial Culture Underestimates Lung Pathogen Detection and Infection Status in Cystic Fibrosis.细菌培养低估了囊性纤维化患者肺部病原体的检测和感染状态。
Microbiol Spectr. 2022 Oct 26;10(5):e0041922. doi: 10.1128/spectrum.00419-22. Epub 2022 Aug 16.
9
The combination of PCR and serology increases the diagnosis of Pseudomonas aeruginosa colonization/infection in cystic fibrosis.聚合酶链反应(PCR)与血清学检测相结合可提高囊性纤维化患者铜绿假单胞菌定植/感染的诊断率。
Pediatr Pulmonol. 2007 Oct;42(10):938-44. doi: 10.1002/ppul.20686.
10
PCR and the detection of Pseudomonas aeruginosa in respiratory samples of CF patients. A literature review.PCR 技术与呼吸道样本中产铜绿假单胞菌的检测:文献综述。
J Cyst Fibros. 2011 Sep;10(5):293-7. doi: 10.1016/j.jcf.2011.05.004.

引用本文的文献

1
Veterinary Clinics as Reservoirs for : A Neglected Pathway in One Health Surveillance.作为储存宿主的兽医诊所:“同一健康”监测中一条被忽视的途径
Antibiotics (Basel). 2025 Jul 17;14(7):720. doi: 10.3390/antibiotics14070720.
2
The airway microbiome of persons with cystic fibrosis correlates with acquisition and microbiological outcomes of incident infection.囊性纤维化患者的气道微生物群与新发感染的获得及微生物学结果相关。
Front Microbiol. 2024 Apr 16;15:1353145. doi: 10.3389/fmicb.2024.1353145. eCollection 2024.
3
AtbFinder Diagnostic Test System Improves Optimal Selection of Antibiotic Therapy in Persons with Cystic Fibrosis.AtbFinder 诊断测试系统有助于优化囊性纤维化患者的抗生素治疗选择。
J Clin Microbiol. 2023 Jan 26;61(1):e0155822. doi: 10.1128/jcm.01558-22. Epub 2023 Jan 5.
4
Repeated isolation of an antibiotic-dependent and temperature-sensitive mutant of Pseudomonas aeruginosa from a cystic fibrosis patient.从一名囊性纤维化患者体内反复分离出铜绿假单胞菌的一种抗生素依赖且温度敏感的突变体。
J Antimicrob Chemother. 2021 Feb 11;76(3):616-625. doi: 10.1093/jac/dkaa482.
5
Effects of Propidium Monoazide (PMA) Treatment on Mycobiome and Bacteriome Analysis of Cystic Fibrosis Airways during Exacerbation.单叠氮碘化丙啶(PMA)处理对囊性纤维化气道急性加重期真菌群落和细菌群落分析的影响
PLoS One. 2016 Dec 28;11(12):e0168860. doi: 10.1371/journal.pone.0168860. eCollection 2016.
6
Detection of algD, oprL and exoA Genes by New Specific Primers as an Efficient, Rapid and Accurate Procedure for Direct Diagnosis of Pseudomonas aeruginosa Strains in Clinical Samples.利用新型特异性引物检测algD、oprL和exoA基因作为临床样本中铜绿假单胞菌菌株直接诊断的高效、快速且准确的方法
Jundishapur J Microbiol. 2014 Oct;7(10):e13583. doi: 10.5812/jjm.13583. Epub 2014 Oct 1.
7
A novel multiplex PCR for detection of Pseudomonas aeruginosa: A major cause of wound infections.一种用于检测铜绿假单胞菌的新型多重 PCR:一种主要的伤口感染病原体。
Pak J Med Sci. 2013 Jul;29(4):957-61. doi: 10.12669/pjms.294.3652.
8
Is the improvement of CF patients, hospitalized for pulmonary exacerbation, correlated to a decrease in bacterial load?因肺部恶化而住院的 CF 患者的改善情况是否与细菌负荷的降低有关?
PLoS One. 2013 Nov 29;8(11):e79010. doi: 10.1371/journal.pone.0079010. eCollection 2013.
9
Diagnostic performance and therapeutic impact of LightCycler SeptiFast assay in patients with suspected sepsis.LightCycler SeptiFast检测法对疑似脓毒症患者的诊断效能及治疗影响
Eur J Microbiol Immunol (Bp). 2013 Mar;3(1):68-76. doi: 10.1556/EuJMI.3.2013.1.10. Epub 2013 Mar 13.
10
Proposal of a quantitative PCR-based protocol for an optimal Pseudomonas aeruginosa detection in patients with cystic fibrosis.提出一种基于定量 PCR 的方案,以优化囊性纤维化患者中铜绿假单胞菌的检测。
BMC Microbiol. 2013 Jun 21;13:143. doi: 10.1186/1471-2180-13-143.

本文引用的文献

1
Comparison of the sensitivity of culture, PCR and quantitative real-time PCR for the detection of Pseudomonas aeruginosa in sputum of cystic fibrosis patients.比较培养、PCR 和实时荧光定量 PCR 检测囊性纤维化患者痰液中铜绿假单胞菌的敏感性。
BMC Microbiol. 2009 Nov 29;9:244. doi: 10.1186/1471-2180-9-244.
2
Antibody response to Pseudomonas aeruginosa in children with cystic fibrosis.囊性纤维化患儿对铜绿假单胞菌的抗体反应。
Pediatr Pulmonol. 2009 Apr;44(4):392-401. doi: 10.1002/ppul.21022.
3
Cystic fibrosis and innate immunity: how chloride channel mutations provoke lung disease.囊性纤维化与先天免疫:氯离子通道突变如何引发肺部疾病
Cell Microbiol. 2009 Feb;11(2):208-16. doi: 10.1111/j.1462-5822.2008.01271.x. Epub 2008 Dec 2.
4
Validation criteria for nucleic acid amplification techniques for bacterial infections.用于细菌感染的核酸扩增技术的验证标准。
Clin Chem Lab Med. 2008;46(7):909-18. doi: 10.1515/CCLM.2008.152.
5
Development and optimization of quantitative PCR for the diagnosis of invasive aspergillosis with bronchoalveolar lavage fluid.用于支气管肺泡灌洗液体侵袭性曲霉病诊断的定量PCR的开发与优化
BMC Infect Dis. 2008 May 29;8:73. doi: 10.1186/1471-2334-8-73.
6
Quantitative detection of metallo-beta-lactamase of blaIMP-cluster-producing Pseudomonas aeruginosa by real-time polymerase chain reaction with melting curve analysis for rapid diagnosis and treatment of nosocomial infection.通过实时聚合酶链反应结合熔解曲线分析对产blaIMP基因簇的铜绿假单胞菌金属β-内酰胺酶进行定量检测,以快速诊断和治疗医院感染。
Diagn Microbiol Infect Dis. 2008 Jun;61(2):222-6. doi: 10.1016/j.diagmicrobio.2008.01.018. Epub 2008 Mar 17.
7
Pseudomonas aeruginosa in the home environment of newly infected cystic fibrosis patients.新感染囊性纤维化患者家庭环境中的铜绿假单胞菌。
Eur Respir J. 2008 Apr;31(4):822-9. doi: 10.1183/09031936.00088907. Epub 2007 Dec 19.
8
The combination of PCR and serology increases the diagnosis of Pseudomonas aeruginosa colonization/infection in cystic fibrosis.聚合酶链反应(PCR)与血清学检测相结合可提高囊性纤维化患者铜绿假单胞菌定植/感染的诊断率。
Pediatr Pulmonol. 2007 Oct;42(10):938-44. doi: 10.1002/ppul.20686.
9
Improved reliability of Pseudomonas aeruginosa PCR detection by the use of the species-specific ecfX gene target.通过使用物种特异性的ecfX基因靶点提高铜绿假单胞菌PCR检测的可靠性。
J Microbiol Methods. 2007 Jul;70(1):20-9. doi: 10.1016/j.mimet.2007.03.008. Epub 2007 Mar 30.
10
Rapid and accurate detection of Pseudomonas aeruginosa by real-time polymerase chain reaction with melting curve analysis targeting gyrB gene.通过针对gyrB基因进行熔解曲线分析的实时聚合酶链反应快速准确地检测铜绿假单胞菌。
Diagn Microbiol Infect Dis. 2007 May;58(1):53-8. doi: 10.1016/j.diagmicrobio.2006.11.007. Epub 2007 Mar 26.