{"title":"采用微量肉汤稀释、微量检测和VITEK质谱法评价耐碳青霉烯鲍曼不动杆菌对粘菌素的敏感性。","authors":"Fatih Mehmet Akıllı, Arzu İlki","doi":"10.1002/mbo3.70046","DOIUrl":null,"url":null,"abstract":"<p><p>We aimed to analyze the colistin susceptibility using broth microdilution (BMD) and commercially available MICRONAUT-MIC-Strip (MMS) test and VITEK MS in carbapenem-resistant Acinetobacter baumannii (CRAB) isolates. Colistin susceptibility of 194 CRAB isolated from various clinical specimens between December 2020 and 2022 was determined by BMD and commercial MMS method. Minimum inhibitory concentrations of the commercial method were compared with the standard BMD. In the second part of the study, colistin susceptibility of the isolates was tested using the MALDIxin method, which detects modified lipid A, by VITEK MS, MALDI-TOF MS (bioMérieux, France). The presence of mcr-1-5 genes in resistant isolates was investigated using in-house multiplex polymerase chain reaction. Of these, 23 (11.8%) were found to be colistin resistant, whereas 171 (88.2%) isolates were susceptible. MMS categorical agreement was found to be 98.9% and essential agreement was 96.3%. The major error was found to be 1.03%, whereas a very major error was not detected. The MALDIxin test developed according to VITEK MS did not detect mutations responsible for lipopolysaccharide-induced colistin resistance in our isolates (expected peak at 1935-2033 m/z). The mcr-1-5 genes were not detected in our isolates. The MMS test is a reliable alternative method for the detection of colistin susceptibility in CRAB. Colistin resistance of the isolates used in our study was not associated with lipid A modification. Alternative mechanisms, such as efflux pumps, are a possibility. To our knowledge, this is the first VITEK MS-based method that enables rapid detection of colistin resistance in negative ion mode, and further studies are needed to determine colistin resistance in this way.</p>","PeriodicalId":18573,"journal":{"name":"MicrobiologyOpen","volume":"14 4","pages":"e70046"},"PeriodicalIF":4.6000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12332535/pdf/","citationCount":"0","resultStr":"{\"title\":\"Evaluation of Colistin Susceptibility in Carbapenem-Resistant Acinetobacter baumannii Isolates Using Broth Microdilution, MICRONAUT-MIC-Strip, and VITEK MS.\",\"authors\":\"Fatih Mehmet Akıllı, Arzu İlki\",\"doi\":\"10.1002/mbo3.70046\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We aimed to analyze the colistin susceptibility using broth microdilution (BMD) and commercially available MICRONAUT-MIC-Strip (MMS) test and VITEK MS in carbapenem-resistant Acinetobacter baumannii (CRAB) isolates. Colistin susceptibility of 194 CRAB isolated from various clinical specimens between December 2020 and 2022 was determined by BMD and commercial MMS method. Minimum inhibitory concentrations of the commercial method were compared with the standard BMD. In the second part of the study, colistin susceptibility of the isolates was tested using the MALDIxin method, which detects modified lipid A, by VITEK MS, MALDI-TOF MS (bioMérieux, France). The presence of mcr-1-5 genes in resistant isolates was investigated using in-house multiplex polymerase chain reaction. Of these, 23 (11.8%) were found to be colistin resistant, whereas 171 (88.2%) isolates were susceptible. MMS categorical agreement was found to be 98.9% and essential agreement was 96.3%. The major error was found to be 1.03%, whereas a very major error was not detected. 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引用次数: 0
摘要
采用微量肉汤稀释法(BMD)、市售的微质谱法(MMS)和VITEK质谱法对耐碳青霉烯鲍曼不动杆菌(CRAB)分离株的粘菌素敏感性进行分析。采用BMD法和商用MMS法对2020年12月~ 2022年12月从不同临床标本分离的194例CRAB进行粘菌素敏感性检测。将商业方法的最低抑菌浓度与标准BMD进行比较。在研究的第二部分,使用MALDIxin方法检测了分离株的粘菌素敏感性,该方法检测了修饰脂质A,采用VITEK MS, MALDI-TOF MS (biomrieux, France)。采用多重聚合酶链反应研究耐药菌株中mcr-1-5基因的存在。其中23株(11.8%)耐粘菌素,171株(88.2%)敏感。MMS的绝对一致性为98.9%,基本一致性为96.3%。发现主要错误为1.03%,而没有检测到非常严重的错误。根据VITEK MS开发的MALDIxin试验在我们的分离株中未检测到导致脂多糖诱导的粘菌素耐药的突变(预计峰值在1935-2033 m/z)。分离株中未检出mcr-1-5基因。MMS试验是检测螃蟹黏菌素敏感性的可靠替代方法。在我们的研究中使用的分离株粘菌素耐药性与脂质A修饰无关。替代机制,如外排泵,是一种可能性。据我们所知,这是首个能够在负离子模式下快速检测粘菌素耐药性的基于VITEK质谱的方法,需要进一步研究以这种方式确定粘菌素耐药性。
Evaluation of Colistin Susceptibility in Carbapenem-Resistant Acinetobacter baumannii Isolates Using Broth Microdilution, MICRONAUT-MIC-Strip, and VITEK MS.
We aimed to analyze the colistin susceptibility using broth microdilution (BMD) and commercially available MICRONAUT-MIC-Strip (MMS) test and VITEK MS in carbapenem-resistant Acinetobacter baumannii (CRAB) isolates. Colistin susceptibility of 194 CRAB isolated from various clinical specimens between December 2020 and 2022 was determined by BMD and commercial MMS method. Minimum inhibitory concentrations of the commercial method were compared with the standard BMD. In the second part of the study, colistin susceptibility of the isolates was tested using the MALDIxin method, which detects modified lipid A, by VITEK MS, MALDI-TOF MS (bioMérieux, France). The presence of mcr-1-5 genes in resistant isolates was investigated using in-house multiplex polymerase chain reaction. Of these, 23 (11.8%) were found to be colistin resistant, whereas 171 (88.2%) isolates were susceptible. MMS categorical agreement was found to be 98.9% and essential agreement was 96.3%. The major error was found to be 1.03%, whereas a very major error was not detected. The MALDIxin test developed according to VITEK MS did not detect mutations responsible for lipopolysaccharide-induced colistin resistance in our isolates (expected peak at 1935-2033 m/z). The mcr-1-5 genes were not detected in our isolates. The MMS test is a reliable alternative method for the detection of colistin susceptibility in CRAB. Colistin resistance of the isolates used in our study was not associated with lipid A modification. Alternative mechanisms, such as efflux pumps, are a possibility. To our knowledge, this is the first VITEK MS-based method that enables rapid detection of colistin resistance in negative ion mode, and further studies are needed to determine colistin resistance in this way.
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