• 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

建立和应用 VITEK 质谱技术检测产碳青霉烯酶的方法。

Methodology Establishment and Application of VITEK Mass Spectrometry to Detect Carbapenemase-Producing .

机构信息

Department of Clinical Laboratory, Shenzhen People's Hospital (The Second Clinical Medical College, Jinan University; The First Affiliated Hospital, Southern University of Science and Technology), Shenzhen, China.

出版信息

Front Cell Infect Microbiol. 2022 Feb 11;12:761328. doi: 10.3389/fcimb.2022.761328. eCollection 2022.

DOI:10.3389/fcimb.2022.761328
PMID:35223536
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8873529/
Abstract

The ability of VITEK mass spectrometry (MS) in detection of bacterial resistance is currently under exploration and evaluation. In this study, we developed and validated a VITEK MS method to rapidly test carbapenemase-producing (CPKP). Solvents, antibiotic concentrations, crystal conditions and times, centrifugation speeds, and other factors were optimized to design a rapid sample pretreatment process for CPKP detection by VITEK MS. The related parameters of the mass spectrum were adjusted on the instrument to establish an CPKP detection mode. 133 clinically isolated strains of CPKP in the microbiology laboratory at the Shenzhen People's Hospital from 2004 to 2017 were selected for accuracy evaluation. The fresh suspected strains from the microbiology laboratory in 2020 were used to complete the clinical verification. Two antibiotics, meropenem (MEM) and imipenem (IPM), were used as substrates. These two substrates were incubated with suspected CPKP, and the results were obtained by VITEK MS detection. Using this method, different types of CPKP showed different detection results and all the CPKP strains producing KPC-2 and IMP-4 carbapenemase were detected by VITEK MS. Thus, VITEK MS can be used for rapid detection of CPKP, especially for some common types of CPKP. This method provides high accuracy and speed of detection. Combined with its cost advantages, it can be intensely valuable in clinical microbiology laboratories after the standard operating procedures are determined.

摘要

VITEK 质谱(MS)在检测细菌耐药性方面的能力目前正在探索和评估中。在这项研究中,我们开发并验证了一种 VITEK MS 方法,用于快速检测产碳青霉烯酶的 (CPKP)。优化了溶剂、抗生素浓度、晶体条件和时间、离心速度等因素,以设计一种快速的 VITEK MS 检测 CPKP 的样品预处理方法。调整仪器上的质谱相关参数,建立 CPKP 检测模式。选择 2004 年至 2017 年深圳市人民医院微生物实验室分离的 133 株临床分离的 CPKP 菌株进行准确性评估。2020 年从微生物实验室采集新鲜疑似菌株进行临床验证。使用两种抗生素,美罗培南(MEM)和亚胺培南(IPM)作为底物。将这两种底物与疑似 CPKP 孵育,通过 VITEK MS 检测获得结果。使用该方法,不同类型的 CPKP 显示出不同的检测结果,所有产 KPC-2 和 IMP-4 碳青霉烯酶的 CPKP 菌株均通过 VITEK MS 检测到。因此,VITEK MS 可用于快速检测 CPKP,尤其是一些常见类型的 CPKP。该方法具有较高的检测准确性和速度。结合其成本优势,在确定标准操作程序后,它在临床微生物学实验室中具有很高的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/daa47ca1e5e0/fcimb-12-761328-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/4e0f7e731ef6/fcimb-12-761328-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/ee742fe724df/fcimb-12-761328-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/80f99b00d95e/fcimb-12-761328-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/daa47ca1e5e0/fcimb-12-761328-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/4e0f7e731ef6/fcimb-12-761328-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/ee742fe724df/fcimb-12-761328-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/80f99b00d95e/fcimb-12-761328-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8873529/daa47ca1e5e0/fcimb-12-761328-g004.jpg

相似文献

1
Methodology Establishment and Application of VITEK Mass Spectrometry to Detect Carbapenemase-Producing .建立和应用 VITEK 质谱技术检测产碳青霉烯酶的方法。
Front Cell Infect Microbiol. 2022 Feb 11;12:761328. doi: 10.3389/fcimb.2022.761328. eCollection 2022.
2
Investigation of the presence of carbapenemases in carbapenem-resistant Klebsiella pneumoniae strains by MALDI-TOF MS (matrix-assisted laser desorption ionization-time of flight mass spectrometry) and comparison with real-time PCR method.采用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)检测耐碳青霉烯类肺炎克雷伯菌菌株中碳青霉烯酶的存在,并与实时荧光定量PCR方法进行比较。
Indian J Med Microbiol. 2021 Jul;39(3):300-305. doi: 10.1016/j.ijmmb.2021.03.013. Epub 2021 Apr 3.
3
Comparison of performance of MALDI-TOF MS and MLST for biotyping carbapenemase-producing Klebsiella pneumoniae sequence types ST11 and ST101 isolates.碳青霉烯酶产生肺炎克雷伯菌 ST11 和 ST101 分离株的 MALDI-TOF MS 和 MLST 生物分型性能比较。
Enferm Infecc Microbiol Clin (Engl Ed). 2022 Apr;40(4):172-178. doi: 10.1016/j.eimce.2020.10.011.
4
Rapid detection of carbapenemase-producing Klebsiella pneumoniae strains derived from blood cultures by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS).通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)快速检测源自血培养的产碳青霉烯酶肺炎克雷伯菌菌株。
BMC Microbiol. 2017 Mar 8;17(1):54. doi: 10.1186/s12866-017-0952-3.
5
Carbapenemase producing : implication on future therapeutic strategies.产碳青霉烯酶:对未来治疗策略的影响
Expert Rev Anti Infect Ther. 2022 Jan;20(1):53-69. doi: 10.1080/14787210.2021.1935237. Epub 2021 Jun 3.
6
Rapid detection of carbapenemase activity of Enterobacteriaceae isolated from positive blood cultures by MALDI-TOF MS.MALDI-TOF MS 快速检测血培养阳性的肠杆菌科中产碳青霉烯酶活性。
Ann Clin Microbiol Antimicrob. 2018 May 18;17(1):22. doi: 10.1186/s12941-018-0274-9.
7
[Comparison of phenotypic methods and polymerase chain reaction for the detection of carbapenemase production in clinical Klebsiella pneumoniae isolates].[临床肺炎克雷伯菌分离株中碳青霉烯酶产生检测的表型方法与聚合酶链反应的比较]
Mikrobiyol Bul. 2017 Jul;51(3):269-276. doi: 10.5578/mb.57333.
8
Genomic and clinical characterisation of multidrug-resistant carbapenemase-producing ST231 and ST16 Klebsiella pneumoniae isolates colonising patients at Siriraj hospital, Bangkok, Thailand from 2015 to 2017.2015 年至 2017 年间,泰国曼谷诗里拉吉医院定植患者的产多药耐药碳青霉烯酶 ST231 和 ST16 肺炎克雷伯菌的基因组和临床特征。
BMC Infect Dis. 2021 Feb 4;21(1):142. doi: 10.1186/s12879-021-05790-9.
9
Evaluation of different pretreatment protocols to detect accurately clinical carbapenemase-producing Enterobacteriaceae by MALDI-TOF.通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)准确检测临床产碳青霉烯酶肠杆菌科细菌的不同预处理方案的评估
J Antimicrob Chemother. 2016 Oct;71(10):2856-67. doi: 10.1093/jac/dkw208. Epub 2016 Jun 10.
10
Rapid detection method of carbapenemase-producing Enterobacteriaceae by MALDI-TOF MS with imipenem/cilastatin (KB) disc and zinc sulfate solution.MALDI-TOF MS 法结合亚胺培南/西司他丁(KB)纸片和硫酸锌溶液快速检测产碳青霉烯酶肠杆菌科。
J Infect Chemother. 2021 Feb;27(2):205-210. doi: 10.1016/j.jiac.2020.09.013. Epub 2020 Sep 29.

本文引用的文献

1
Application of a multiplex immunochromatographic assay for rapid identification of carbapenemases in a clinical microbiology laboratory: performance and turn-around-time evaluation of NG-test Carba 5.多重免疫层析法在临床微生物实验室快速鉴定碳青霉烯酶的应用:NG-test Carba 5 的性能和周转时间评估。
BMC Microbiol. 2021 Sep 29;21(1):260. doi: 10.1186/s12866-021-02309-9.
2
A Rapid Antimicrobial Susceptibility Test for Using a Broth Micro-Dilution Combined with MALDI TOF MS.一种使用肉汤微量稀释法与基质辅助激光解吸电离飞行时间质谱联用的快速抗菌药敏试验。
Infect Drug Resist. 2021 May 14;14:1823-1831. doi: 10.2147/IDR.S305280. eCollection 2021.
3
Occurrence of the Gene in the -Harboring Plasmids: Adverse Clinical Impact for Direct Tracking of KPC-Producing by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry.
该基因在携带质粒中的出现:对通过基质辅助激光解吸电离飞行时间质谱直接追踪产KPC菌的临床不良影响。
J Clin Microbiol. 2021 Jul 19;59(8):e0023821. doi: 10.1128/JCM.00238-21.
4
Applications of stable isotopes in MALDI imaging: current approaches and an eye on the future.稳定同位素在 MALDI 成像中的应用:当前方法及未来展望。
Anal Bioanal Chem. 2021 Apr;413(10):2637-2653. doi: 10.1007/s00216-021-03189-8. Epub 2021 Feb 2.
5
Evaluation of the Immunochromatographic NG-Test Carba 5, RESIST-5 O.O.K.N.V., and IMP -SeT for Rapid Detection of KPC-, NDM-, IMP-, VIM-type, and OXA-48-like Carbapenemase Among .免疫层析法NG-Test Carba 5、RESIST-5 O.O.K.N.V.和IMP-SeT用于快速检测KPC型、NDM型、IMP型、VIM型和OXA-48样碳青霉烯酶的评估
Front Microbiol. 2021 Jan 15;11:609856. doi: 10.3389/fmicb.2020.609856. eCollection 2020.
6
Rapid detection method of carbapenemase-producing Enterobacteriaceae by MALDI-TOF MS with imipenem/cilastatin (KB) disc and zinc sulfate solution.MALDI-TOF MS 法结合亚胺培南/西司他丁(KB)纸片和硫酸锌溶液快速检测产碳青霉烯酶肠杆菌科。
J Infect Chemother. 2021 Feb;27(2):205-210. doi: 10.1016/j.jiac.2020.09.013. Epub 2020 Sep 29.
7
A large-scale investigation and identification of methicillin-resistant Staphylococcus aureus based on peaks binning of matrix-assisted laser desorption ionization-time of flight MS spectra.基于基质辅助激光解吸电离飞行时间质谱峰聚类分析的耐甲氧西林金黄色葡萄球菌的大规模调查与鉴定。
Brief Bioinform. 2021 May 20;22(3). doi: 10.1093/bib/bbaa138.
8
Insufficient repeatability and reproducibility of MALDI-TOF MS-based identification of MRSA.基质辅助激光解吸电离飞行时间质谱法鉴定耐甲氧西林金黄色葡萄球菌的重复性和重现性不足。
Folia Microbiol (Praha). 2020 Oct;65(5):895-900. doi: 10.1007/s12223-020-00799-0. Epub 2020 Jul 2.
9
Detection of Colistin Resistance in Using MALDIxin Test on the Routine MALDI Biotyper Sirius Mass Spectrometer.在常规基质辅助激光解吸电离生物分型仪Sirius质谱仪上使用MALDIxin测试检测对黏菌素的耐药性。
Front Microbiol. 2020 Jun 3;11:1141. doi: 10.3389/fmicb.2020.01141. eCollection 2020.
10
Rapid qualitative antibiotic resistance characterization using VITEK MS.采用 VITEK MS 快速定性抗生素耐药性特征分析。
Diagn Microbiol Infect Dis. 2020 Aug;97(4):115093. doi: 10.1016/j.diagmicrobio.2020.115093. Epub 2020 May 24.