首页|基质辅助激光解吸电离飞行时间质谱仪检测耐碳青霉烯肺炎克雷伯菌的价值

基质辅助激光解吸电离飞行时间质谱仪检测耐碳青霉烯肺炎克雷伯菌的价值

The value of matrix-assisted laser desorption ionization time of flight mass spectrometry in detecting carbapenem resistant Klebsiella pneumoniae

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目的 评估基质辅助激光解吸电离飞行时间质谱仪(MALDI-TOF MS)检测耐碳青霉烯肺炎克雷伯菌(CRKP)的价值.方法 收集2020年1月至2023年1月我院住院患者分离的肺炎克雷伯菌108株,以亚胺培南或美罗培南卡片筛选出CRKP和碳青霉烯酶敏感肺炎克雷伯菌(CSKP),采用CLSIm100-S27标准判断CRKP的药敏,采用聚合酶链反应(PCR)检测CRKP的耐药基因序列,采用MALDI-TOF MS检测CRKP和CSKP特征峰.以同期收集的100株肺炎克雷伯菌,对CRKP和CSKP的特征峰进行验证.结果 108株肺炎克雷伯菌中25株CRKP和83株CSKP.25株CRKP均对碳青霉烯类、头孢菌素类氨曲南、喹诺酮类抗生素和氨基糖苷类抗生素存在不同程度的耐药性.83株CSKP几乎对所有类型的抗生素敏感.25株CRKP检出携带碳青霉烯酶基因25株,测序结果显示,携带blaKPC基因20株(80.0%),携带blaNDM基因3株(12.0%),携带 bla OXA-48 基因 2 株(8.00%),未检出 blaGES、blaIMP、blaNDM、blaVIM.CRKP 的特征峰分别为 4 159.5 m/z、8 369.7 m/z、10 808.0 m/z,CSKP 的特征峰分别为 3 599.6 m/z、10 087.5 m/z.将同期收集的100株肺炎克雷伯菌进行验证,30株CRKP中,MALDI-TOF MS检测出28株CRKP,70株CSKP中,MALDI-TOF MS检测68株CSKP,MALDI-TOF MS检出准确度为96.0%(96/100).结论 本地区CRKP的耐药基因多为 blaKPC,MALDI-TOF MS 可快速检测 CRKP,CRKP 的特征峰分别为 4 159.5 m/z、8 369.7 m/z、10 808.0 m/z.
Objective To evaluate the value of matrix assisted laser desorption ionization time of flight mass spectrometry(MALDI-TOF MS)in detecting carbapenem resistant Klebsiella pneumoniae(CRKP).Methods One hundred and eight strains of Klebsiella pneumoniae isolated from in-patients in our hospital from January 2020 to January 23 were collected.CRKP and carbapenem sensitive Klebsiella pneumoniae(CSKP)were screened out with imipenem or meropenem cards.The drug sensitivity of CRKP was judged by CLSI m100-S27,and the drug resistance gene sequence of CRKP was detected with polymerase chain reaction(PCR),the MALDI-TOF MS was used to detect characteristic peaks of CRKP and carbapenem sensitive Klebsiella pneumoniae(CSKP).The characteristic peaks of CRKP and CSKP was verified by 100 strains of Klebsiella pneumoniae collected at the same time.Results Among the 108 strains of Klebsiella pneumoniae,25 strains were CRKP and 83 strains were CSKP.All 25 strains of CRKP were resistant to carbapenems,cephalosporins,aztreonam,quinolones and aminoglycosides to varying degrees.Eighty-three strains of CSKP were sensitive to almost all types of antibiotics.Twenty-five CRKP strains were detected to carry carbapenemase genes.The sequencing results showed that 20 strains(80.0%)carried the blaKPC gene,3 strains(12.0%)carried the blaNDM gene and 2 strains(8.0%)carried the blaOXA-48 gene.No blaGES,blaIMP,blaNDM or blaVIM were detected.The characteristic peaks of CRKP were 4 159.5 m/z,8 369.7 m/z and 10 808.0 m/z,respectively,while the characteristic peaks of CSKP were 3599.6 m/z and 10 087.5 m/z,respectively.One hundred Klebsiella pneumoniae strains were collected and detected by characteristic peaks of CRKP and CSKP from MALDI-TOF MS.Among 100 Klebsiella pneumoniae strains,30 CRKPs were detected 28 CRKPs and 70 CSKPs were detected 68 CSKPs by MALDI-TOF MS,with an accuracy of 96.0%(96/100).Conclusion The resistance genes of CRKP in this region are mostly blaKPC,and MALDI-TOF MS can quickly detect CRKP.The characteristic peaks of CRKP are 4 159.5 m/z,8 369.7 m/z and 10 808.0 m/z,respectively.

Spectrometry,mass,matrix-assisted laser desorption-ionizationPolymerase Chain reactionCarbapenem-resistant Klebsiella pneumoniaeKlebsiella pneumoniae

吕辉、范明琴、陈美红、陈宇航、卢丹凤、蔡鹏威

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福建省立医院南院检验科,福州 350028

光谱法,质量,基质辅助激光解吸电离 聚合酶链反应 耐碳青霉烯类 肺炎克雷伯菌

2024

实用医技杂志
山西医药卫生传媒集团有限责任公司

实用医技杂志

影响因子:0.534
ISSN:1671-5098
年,卷(期):2024.31(6)