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Rapid detection and surveillance of cfiA-positive Bacteroides fragilis using matrix-assisted laser desorption ionization time-of-flight mass spectrometry.
Kawamoto, Yasuhide; Kosai, Kosuke; Ota, Kenji; Uno, Naoki; Sakamoto, Kei; Hasegawa, Hiroo; Izumikawa, Koichi; Mukae, Hiroshi; Yanagihara, Katsunori.
Afiliação
  • Kawamoto Y; Department of Laboratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Kosai K; Department of Laboratory Medicine, Nagasaki University Hospital, Nagasaki, Japan. Electronic address: k-kosai@nagasaki-u.ac.jp.
  • Ota K; Department of Laboratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Uno N; Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Sakamoto K; Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Hasegawa H; Department of Laboratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Izumikawa K; Department of Infectious Diseases, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Mukae H; Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Yanagihara K; Department of Laboratory Medicine, Nagasaki University Hospital, Nagasaki, Japan; Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Anaerobe ; 72: 102448, 2021 Dec.
Article em En | MEDLINE | ID: mdl-34537378
OBJECTIVES: To perform surveillance of cfiA-positive Bacteroides fragilis using new subtyping software module, MALDI Biotyper Subtyping Module (MBT Subtyping Module), on MALDI-TOF MS system, and to evaluate the detection ability of the module. METHODS: cfiA-positive strains were presumed using the module against B. fragilis isolated between 2006 and 2019. The cfiA gene was confirmed using PCR. In cfiA-positive B. fragilis, the insertion sequence (IS) elements were examined and the MBT STAR-BL assay was performed to examine meropenem hydrolysis activity. RESULTS: Of the 396 B. fragilis strains included, the MBT Subtyping Module detected 33 presumptive cfiA-positive strains (8.3%), of which 32 harbored the cfiA gene. The sensitivity and specificity of the MBT Subtyping Module for detecting cfiA-positive B. fragilis were 100.0% and 99.7%, respectively. Of the 32 strains harboring the cfiA gene, seven strains possessed IS elements, which were thought to induce high cfiA expression. Meropenem hydrolysis was detected in all seven strains that were positive for both cfiA and IS elements, and they exhibited resistance to meropenem and imipenem. The overall non-susceptibility rates to meropenem and imipenem were 84.8% and 36.4%, respectively, in the 33 presumptive cfiA-positive strains. CONCLUSION: The MBT Subtyping Module can detect cfiA-positive B. fragilis rapidly and accurately, supporting its use for surveillance of cfiA-positive B. fragilis in clinical settings.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Bacteroides fragilis / Infecções por Bacteroides / Beta-Lactamases / Técnicas de Tipagem Bacteriana / Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Anaerobe Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Bactérias / Bacteroides fragilis / Infecções por Bacteroides / Beta-Lactamases / Técnicas de Tipagem Bacteriana / Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Anaerobe Ano de publicação: 2021 Tipo de documento: Article