In vitro induction and selection of fluoroquinolone-resistant mutants in Elizabethkingia anophelis

Ching Chi Lee; Chung Hsu Lai; Shang Yi Lin; Nan Yao Lee; Po Yu Liu; Chih Hui Yang; Yi Han Huang; Jiun Nong Lin

doi:10.1016/j.jmii.2024.05.011

In vitro induction and selection of fluoroquinolone-resistant mutants in Elizabethkingia anophelis

Ching Chi Lee, Chung Hsu Lai, Shang Yi Lin, Nan Yao Lee, Po Yu Liu, Chih Hui Yang, Yi Han Huang, Jiun Nong Lin

內科學科

研究成果: Article › 同行評審

摘要

For 29 parent strains, recognized by pulsed-field gel electrophoresis, the MICs multiplied significantly in the ciprofloxacin group than levofloxacin group, following the first and third induction cycle. Ser83Arg in GyrA was the most common site of mutations. No mutation in ParC nor ParE was identified in the selected mutants.

原文	English
頁（從 - 到）	822-826
頁數	5
期刊	Journal of Microbiology, Immunology and Infection
卷	57
發行號	5
DOIs	https://doi.org/10.1016/j.jmii.2024.05.011
出版狀態	Published - 2024 10月

All Science Journal Classification (ASJC) codes

免疫學和過敏
一般免疫學和微生物學
微生物學（醫學）
傳染性疾病

UN SDG

此研究成果有助於以下永續發展目標

存取文件

10.1016/j.jmii.2024.05.011

其它文件與鏈接

引用此

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abstract = "For 29 parent strains, recognized by pulsed-field gel electrophoresis, the MICs multiplied significantly in the ciprofloxacin group than levofloxacin group, following the first and third induction cycle. Ser83Arg in GyrA was the most common site of mutations. No mutation in ParC nor ParE was identified in the selected mutants.",

author = "Lee, {Ching Chi} and Lai, {Chung Hsu} and Lin, {Shang Yi} and Lee, {Nan Yao} and Liu, {Po Yu} and Yang, {Chih Hui} and Huang, {Yi Han} and Lin, {Jiun Nong}",

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AU - Lee, Ching Chi

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AU - Lee, Nan Yao

AU - Liu, Po Yu

AU - Yang, Chih Hui

AU - Huang, Yi Han

AU - Lin, Jiun Nong

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AB - For 29 parent strains, recognized by pulsed-field gel electrophoresis, the MICs multiplied significantly in the ciprofloxacin group than levofloxacin group, following the first and third induction cycle. Ser83Arg in GyrA was the most common site of mutations. No mutation in ParC nor ParE was identified in the selected mutants.

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