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199. Fast Detection of Ceftazidime-avibactam-resistant Enterobacterales with VITEK-MS(TM) Incorporating a Direct-on-target Microdroplet Growth Assay

BACKGROUND: The direct-on-target microdroplet growth assay (DOT-MGA) was evaluated for its ability to rapidly detect ceftazidime-avibactam resistant Enterobacterales. METHODS: In this study, 47 non-duplicate CRE isolates were used to determine unequivocally the performance of ceftazidime-avibatam re...

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Autores principales: haung, Shenglei, qin, Chengfeng, Pu, Bingchun, Zhou, Chunmei, ma, Yan, Wang, Beili, Pan, Baishen, Hu, Bijie, Guo, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679129/
http://dx.doi.org/10.1093/ofid/ofad500.272
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author haung, Shenglei
qin, Chengfeng
Pu, Bingchun
Zhou, Chunmei
ma, Yan
Wang, Beili
Pan, Baishen
Hu, Bijie
Guo, Wei
author_facet haung, Shenglei
qin, Chengfeng
Pu, Bingchun
Zhou, Chunmei
ma, Yan
Wang, Beili
Pan, Baishen
Hu, Bijie
Guo, Wei
author_sort haung, Shenglei
collection PubMed
description BACKGROUND: The direct-on-target microdroplet growth assay (DOT-MGA) was evaluated for its ability to rapidly detect ceftazidime-avibactam resistant Enterobacterales. METHODS: In this study, 47 non-duplicate CRE isolates were used to determine unequivocally the performance of ceftazidime-avibatam resistance detection of 7 organisms found in clinical isolates. The isolates were incubated for 3 to 6 h in the presence and absence of 8 µg/mL ceftazidime-avibatam in the broth applied as microdroplets directly on to the matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) target spots. Following the incubation period, broth was separated from the microbes by pipette. MALDI-TOF MS was employed to evaluate the growth of isolates in each spot and to identify the microbes simultaneously. The micro-broth dilution method, recommended by EUCAST was used as a reference method. A PCR-based assay was carried out to evaluate the carbapenem resistance mechanisms by screening for the presence of various β-lactamase-encoding genes. RESULTS: It was found that a 3 h incubation time was insufficient for MS to identify isolates. At this time-point, the identification of valid results of the growth control was only 25.0%. Therefore, the study of 3 h incubation times was not continued. For ceftazidime-avibactam-resistant Enterobacter strains, 83.7% of growth controls were successfully detected after the 4 h-time-point of incubation when the sensitivity and specificity of drug resistance detection were both 100%. Following incubation for 5 h, the rate of growth controls, sensitivity and specificity were 98.0%, 100% and 100%. When the incubation was extended to 6 h, the rate of growth controls, sensitivity and specificity reached an ideal 100%. CONCLUSION: The VITEK MS-based DOT-MGA is a fast, convenient and accurate in detecting Enterobacterales that is resistant to ceftazidime-avibatam within 5 to 6 h. The assay can also determine the resistance status of an isolate and the potential novel resistant mechanisms involved. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106791292023-11-27 199. Fast Detection of Ceftazidime-avibactam-resistant Enterobacterales with VITEK-MS(TM) Incorporating a Direct-on-target Microdroplet Growth Assay haung, Shenglei qin, Chengfeng Pu, Bingchun Zhou, Chunmei ma, Yan Wang, Beili Pan, Baishen Hu, Bijie Guo, Wei Open Forum Infect Dis Abstract BACKGROUND: The direct-on-target microdroplet growth assay (DOT-MGA) was evaluated for its ability to rapidly detect ceftazidime-avibactam resistant Enterobacterales. METHODS: In this study, 47 non-duplicate CRE isolates were used to determine unequivocally the performance of ceftazidime-avibatam resistance detection of 7 organisms found in clinical isolates. The isolates were incubated for 3 to 6 h in the presence and absence of 8 µg/mL ceftazidime-avibatam in the broth applied as microdroplets directly on to the matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) target spots. Following the incubation period, broth was separated from the microbes by pipette. MALDI-TOF MS was employed to evaluate the growth of isolates in each spot and to identify the microbes simultaneously. The micro-broth dilution method, recommended by EUCAST was used as a reference method. A PCR-based assay was carried out to evaluate the carbapenem resistance mechanisms by screening for the presence of various β-lactamase-encoding genes. RESULTS: It was found that a 3 h incubation time was insufficient for MS to identify isolates. At this time-point, the identification of valid results of the growth control was only 25.0%. Therefore, the study of 3 h incubation times was not continued. For ceftazidime-avibactam-resistant Enterobacter strains, 83.7% of growth controls were successfully detected after the 4 h-time-point of incubation when the sensitivity and specificity of drug resistance detection were both 100%. Following incubation for 5 h, the rate of growth controls, sensitivity and specificity were 98.0%, 100% and 100%. When the incubation was extended to 6 h, the rate of growth controls, sensitivity and specificity reached an ideal 100%. CONCLUSION: The VITEK MS-based DOT-MGA is a fast, convenient and accurate in detecting Enterobacterales that is resistant to ceftazidime-avibatam within 5 to 6 h. The assay can also determine the resistance status of an isolate and the potential novel resistant mechanisms involved. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10679129/ http://dx.doi.org/10.1093/ofid/ofad500.272 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
haung, Shenglei
qin, Chengfeng
Pu, Bingchun
Zhou, Chunmei
ma, Yan
Wang, Beili
Pan, Baishen
Hu, Bijie
Guo, Wei
199. Fast Detection of Ceftazidime-avibactam-resistant Enterobacterales with VITEK-MS(TM) Incorporating a Direct-on-target Microdroplet Growth Assay
title 199. Fast Detection of Ceftazidime-avibactam-resistant Enterobacterales with VITEK-MS(TM) Incorporating a Direct-on-target Microdroplet Growth Assay
title_full 199. Fast Detection of Ceftazidime-avibactam-resistant Enterobacterales with VITEK-MS(TM) Incorporating a Direct-on-target Microdroplet Growth Assay
title_fullStr 199. Fast Detection of Ceftazidime-avibactam-resistant Enterobacterales with VITEK-MS(TM) Incorporating a Direct-on-target Microdroplet Growth Assay
title_full_unstemmed 199. Fast Detection of Ceftazidime-avibactam-resistant Enterobacterales with VITEK-MS(TM) Incorporating a Direct-on-target Microdroplet Growth Assay
title_short 199. Fast Detection of Ceftazidime-avibactam-resistant Enterobacterales with VITEK-MS(TM) Incorporating a Direct-on-target Microdroplet Growth Assay
title_sort 199. fast detection of ceftazidime-avibactam-resistant enterobacterales with vitek-ms(tm) incorporating a direct-on-target microdroplet growth assay
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679129/
http://dx.doi.org/10.1093/ofid/ofad500.272
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