Comparative In vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin-resistant Staphylococcus aureus blood isolates in Taiwan

Abstract Background Nemonoxacin is a new quinolone with an antibacterial efficacy against methicillin-resistant Staphylococcus aureus (MRSA). Certain sequence types (STs) have been emerging in Taiwan, including fluoroquinolone-resistant ST8/USA300. It’s an urgent need to determine nemonoxacin suscep...

Full description

Saved in:
Bibliographic Details
Main Authors: Pao -Yu Chen, Mao-Wang Ho, Po-Liang Lu, Hung-Jen Tang, Cheng Len Sy, Jann-Tay Wang, Taiwan Staphylococcus aureus Consortium (TSAC)
Format: Article
Language:English
Published: BMC 2025-01-01
Series:Annals of Clinical Microbiology and Antimicrobials
Subjects:
Online Access:https://doi.org/10.1186/s12941-024-00772-6
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832594908510158848
author Pao -Yu Chen
Mao-Wang Ho
Po-Liang Lu
Hung-Jen Tang
Cheng Len Sy
Jann-Tay Wang
Taiwan Staphylococcus aureus Consortium (TSAC)
author_facet Pao -Yu Chen
Mao-Wang Ho
Po-Liang Lu
Hung-Jen Tang
Cheng Len Sy
Jann-Tay Wang
Taiwan Staphylococcus aureus Consortium (TSAC)
author_sort Pao -Yu Chen
collection DOAJ
description Abstract Background Nemonoxacin is a new quinolone with an antibacterial efficacy against methicillin-resistant Staphylococcus aureus (MRSA). Certain sequence types (STs) have been emerging in Taiwan, including fluoroquinolone-resistant ST8/USA300. It’s an urgent need to determine nemonoxacin susceptibility against ST8/USA300 and other emerging lineages, if any. Additionally, molecular characterization of nemonoxacin resistance among different lineages has yet to be defined. Methods Non-duplicated MRSA blood isolates from five hospitals during 2019–2020 were collected and genotyped by pulsed-field gel electrophoresis, and further correlated to their STs. Antimicrobial susceptibility testing for all antibiotics was performing by using Sensititre standard panel, except nemonoxacin by using agar dilution method. Selected isolates with nemonoxacin MICs ≥ 0.5 mg/mL were sequenced for quinolone resistance-determining regions (QRDRs). Results Overall, 915 MRSA isolates belonged to four major lineages, ST8 (34.2%), ST59 (23.5%), ST239 (13.9%), and clonal complex 45 (13.7%). Two-thirds of tested isolates were non-susceptible to moxifloxacin, especially ST8/USA300 and ST239. Of them, proportions of nemonoxacin non-susceptibility by a tentative clinical breakpoint (tCBP) of 1 µg/mL among four major lineages appeared to be different (P = 0.06) and highest in ST239 (22.2%), followed by ST8/USA300 (13.5%). Among 89 isolates sequenced, 44.1% of ST8 and all ST239 isolates had ≥ 3 amino acid substitutions (AAS) in gyrA/parC (group A) or 2 AAS in gyrA/parC with additional AAS in gyrB/parE (group B). Compared to other AAS patterns, isolates in group A had the greatest non-susceptible proportions to nemonoxacin (86.9%; overall/pair-wised comparisons, P < 0.05). Conclusions Our study confirmed ST8/USA300 MRSA has disseminated in Taiwan. Using a tCBP defined by a higher parenteral daily dosage, nemonoxacin retained potency against moxifloxacin non-susceptible isolates. Patterns of AAS in QRDRs among different lineages may contribute to difference of nemonoxacin susceptibility.
format Article
id doaj-art-73b6ca0949b3420da2d0d84e7af863ce
institution Kabale University
issn 1476-0711
language English
publishDate 2025-01-01
publisher BMC
record_format Article
series Annals of Clinical Microbiology and Antimicrobials
spelling doaj-art-73b6ca0949b3420da2d0d84e7af863ce2025-01-19T12:13:29ZengBMCAnnals of Clinical Microbiology and Antimicrobials1476-07112025-01-0124111010.1186/s12941-024-00772-6Comparative In vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin-resistant Staphylococcus aureus blood isolates in TaiwanPao -Yu Chen0Mao-Wang Ho1Po-Liang Lu2Hung-Jen Tang3Cheng Len Sy4Jann-Tay Wang5Taiwan Staphylococcus aureus Consortium (TSAC)Division of Infectious Diseases, Department of Internal Medicine, National Taiwan University HospitalDivision of Infectious Diseases, Department of Internal Medicine, China Medical University HospitalDivision of Infectious Diseases, Department of Internal Medicine, Kaohsiung Medical University HospitalDivision of Infectious Diseases, Department of Internal Medicine, Chi Mei Medical CenterDivision of Infectious Diseases, Department of Internal Medicine, Kaohsiung Veteran General HospitalDivision of Infectious Diseases, Department of Internal Medicine, National Taiwan University HospitalAbstract Background Nemonoxacin is a new quinolone with an antibacterial efficacy against methicillin-resistant Staphylococcus aureus (MRSA). Certain sequence types (STs) have been emerging in Taiwan, including fluoroquinolone-resistant ST8/USA300. It’s an urgent need to determine nemonoxacin susceptibility against ST8/USA300 and other emerging lineages, if any. Additionally, molecular characterization of nemonoxacin resistance among different lineages has yet to be defined. Methods Non-duplicated MRSA blood isolates from five hospitals during 2019–2020 were collected and genotyped by pulsed-field gel electrophoresis, and further correlated to their STs. Antimicrobial susceptibility testing for all antibiotics was performing by using Sensititre standard panel, except nemonoxacin by using agar dilution method. Selected isolates with nemonoxacin MICs ≥ 0.5 mg/mL were sequenced for quinolone resistance-determining regions (QRDRs). Results Overall, 915 MRSA isolates belonged to four major lineages, ST8 (34.2%), ST59 (23.5%), ST239 (13.9%), and clonal complex 45 (13.7%). Two-thirds of tested isolates were non-susceptible to moxifloxacin, especially ST8/USA300 and ST239. Of them, proportions of nemonoxacin non-susceptibility by a tentative clinical breakpoint (tCBP) of 1 µg/mL among four major lineages appeared to be different (P = 0.06) and highest in ST239 (22.2%), followed by ST8/USA300 (13.5%). Among 89 isolates sequenced, 44.1% of ST8 and all ST239 isolates had ≥ 3 amino acid substitutions (AAS) in gyrA/parC (group A) or 2 AAS in gyrA/parC with additional AAS in gyrB/parE (group B). Compared to other AAS patterns, isolates in group A had the greatest non-susceptible proportions to nemonoxacin (86.9%; overall/pair-wised comparisons, P < 0.05). Conclusions Our study confirmed ST8/USA300 MRSA has disseminated in Taiwan. Using a tCBP defined by a higher parenteral daily dosage, nemonoxacin retained potency against moxifloxacin non-susceptible isolates. Patterns of AAS in QRDRs among different lineages may contribute to difference of nemonoxacin susceptibility.https://doi.org/10.1186/s12941-024-00772-6MoxifloxacinLevofloxacinCiprofloxacinQuinolone resistance determination regionsSequence type 8
spellingShingle Pao -Yu Chen
Mao-Wang Ho
Po-Liang Lu
Hung-Jen Tang
Cheng Len Sy
Jann-Tay Wang
Taiwan Staphylococcus aureus Consortium (TSAC)
Comparative In vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin-resistant Staphylococcus aureus blood isolates in Taiwan
Annals of Clinical Microbiology and Antimicrobials
Moxifloxacin
Levofloxacin
Ciprofloxacin
Quinolone resistance determination regions
Sequence type 8
title Comparative In vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin-resistant Staphylococcus aureus blood isolates in Taiwan
title_full Comparative In vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin-resistant Staphylococcus aureus blood isolates in Taiwan
title_fullStr Comparative In vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin-resistant Staphylococcus aureus blood isolates in Taiwan
title_full_unstemmed Comparative In vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin-resistant Staphylococcus aureus blood isolates in Taiwan
title_short Comparative In vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin-resistant Staphylococcus aureus blood isolates in Taiwan
title_sort comparative in vitro antibacterial activity of nemonoxacin and other fluoroquinolones in correlation with resistant mechanisms in contemporary methicillin resistant staphylococcus aureus blood isolates in taiwan
topic Moxifloxacin
Levofloxacin
Ciprofloxacin
Quinolone resistance determination regions
Sequence type 8
url https://doi.org/10.1186/s12941-024-00772-6
work_keys_str_mv AT paoyuchen comparativeinvitroantibacterialactivityofnemonoxacinandotherfluoroquinolonesincorrelationwithresistantmechanismsincontemporarymethicillinresistantstaphylococcusaureusbloodisolatesintaiwan
AT maowangho comparativeinvitroantibacterialactivityofnemonoxacinandotherfluoroquinolonesincorrelationwithresistantmechanismsincontemporarymethicillinresistantstaphylococcusaureusbloodisolatesintaiwan
AT polianglu comparativeinvitroantibacterialactivityofnemonoxacinandotherfluoroquinolonesincorrelationwithresistantmechanismsincontemporarymethicillinresistantstaphylococcusaureusbloodisolatesintaiwan
AT hungjentang comparativeinvitroantibacterialactivityofnemonoxacinandotherfluoroquinolonesincorrelationwithresistantmechanismsincontemporarymethicillinresistantstaphylococcusaureusbloodisolatesintaiwan
AT chenglensy comparativeinvitroantibacterialactivityofnemonoxacinandotherfluoroquinolonesincorrelationwithresistantmechanismsincontemporarymethicillinresistantstaphylococcusaureusbloodisolatesintaiwan
AT janntaywang comparativeinvitroantibacterialactivityofnemonoxacinandotherfluoroquinolonesincorrelationwithresistantmechanismsincontemporarymethicillinresistantstaphylococcusaureusbloodisolatesintaiwan
AT taiwanstaphylococcusaureusconsortiumtsac comparativeinvitroantibacterialactivityofnemonoxacinandotherfluoroquinolonesincorrelationwithresistantmechanismsincontemporarymethicillinresistantstaphylococcusaureusbloodisolatesintaiwan