Show simple item record

dc.contributor.authorLe, Wenjing
dc.contributor.authorSu, Xiaohong
dc.contributor.authorLou, Xiangdi
dc.contributor.authorLi, Xuechun
dc.contributor.authorGong, Xiangdong
dc.contributor.authorWang, Baoxi
dc.contributor.authorGenco, Caroline A.
dc.contributor.authorMueller, John P.
dc.contributor.authorRice, Peter A
dc.date2022-08-11T08:09:58.000
dc.date.accessioned2022-08-23T16:50:39Z
dc.date.available2022-08-23T16:50:39Z
dc.date.issued2020-12-14
dc.date.submitted2021-01-28
dc.identifier.citation<p>Le W, Su X, Lou X, Li X, Gong X, Wang B, Genco CA, Mueller JP, Rice PA. Susceptibility trends of zoliflodacin against multidrug-resistant <em>Neisseria gonorrhoeae</em> clinical isolates in Nanjing, China (2014-2018). Antimicrob Agents Chemother. 2020 Dec 14:AAC.00863-20. doi: 10.1128/AAC.00863-20. Epub ahead of print. PMID: 33318010. <a href="https://doi.org/10.1128/AAC.00863-20">Link to article on publisher's site</a></p>
dc.identifier.issn0066-4804 (Linking)
dc.identifier.doi10.1128/AAC.00863-20
dc.identifier.pmid33318010
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41698
dc.description.abstractPreviously, we reported potent activity of a novel spiropyrimidinetrione, zoliflodacin, against N. gonorrhoeae isolates from symptomatic men in Nanjing, China, collected in 2013. Here, we investigated trends of susceptibilities of zoliflodacin in 986 isolates collected from men between 2014 and 2018. N. gonorrhoeae isolates were tested for susceptibility to zoliflodacin and seven other antibiotics. Mutations in gyrA, gyrB, parC, parE and mtrR genes were determined by PCR and sequencing. The MICs of zoliflodacin ranged from < /=0.002 to 0.25 mg/L; the overall MIC50s and MIC90s were 0.06 mg/L and 0.125mg/L in 2018, increasing two-fold from 2014. However, the percent of isolates with lower zoliflodacin MICs declined in each year sequentially while the percent with higher MICs increased yearly (P < /=0.00001). All isolates were susceptible to spectinomycin but resistant to ciprofloxacin (MIC > /=1 mg/L); 21.2% (209/986) were resistant to azithromycin ( > /=1 mg/L), 43.4% (428/986) were penicillinase-producing (PPNG), 26.9% (265/986) tetracycline-resistant (TRNG) and 19.4% (191/986) were multi-drug resistant (MDR) isolates. Among 202 isolates tested, all were quinolone resistant with double or triple mutations in gyrA; One hundred ninety three (193/202; 95.5%) also had mutations in parC There were no D429N/A and/or K450T mutations in GyrB identified in the 143 isolates with higher zoliflodacin MICs; a S467N mutation in GyrB was identified in one isolate. We report that zoliflodacin continues to have excellent in vitro activity against clinical gonococcal isolates, including those with high-level resistance to ciprofloxacin, azithromycin and extended spectrum cephalosporins.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=33318010&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright © 2020 Le et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectN. gonorrhoeae
dc.subjectDNA gyrase
dc.subjectzoliflodacin
dc.subjectsusceptibility
dc.subjectBacterial Infections and Mycoses
dc.subjectMicrobiology
dc.titleSusceptibility trends of zoliflodacin against multidrug-resistant Neisseria gonorrhoeae clinical isolates in Nanjing, China (2014-2018)
dc.typeAccepted Manuscript
dc.source.journaltitleAntimicrobial agents and chemotherapy
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5518&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/4488
dc.identifier.contextkey21308496
refterms.dateFOA2022-08-23T16:50:39Z
html.description.abstract<p>Previously, we reported potent activity of a novel spiropyrimidinetrione, zoliflodacin, against N. gonorrhoeae isolates from symptomatic men in Nanjing, China, collected in 2013. Here, we investigated trends of susceptibilities of zoliflodacin in 986 isolates collected from men between 2014 and 2018. N. gonorrhoeae isolates were tested for susceptibility to zoliflodacin and seven other antibiotics. Mutations in gyrA, gyrB, parC, parE and mtrR genes were determined by PCR and sequencing. The MICs of zoliflodacin ranged from < /=0.002 to 0.25 mg/L; the overall MIC50s and MIC90s were 0.06 mg/L and 0.125mg/L in 2018, increasing two-fold from 2014. However, the percent of isolates with lower zoliflodacin MICs declined in each year sequentially while the percent with higher MICs increased yearly (P < /=0.00001). All isolates were susceptible to spectinomycin but resistant to ciprofloxacin (MIC > /=1 mg/L); 21.2% (209/986) were resistant to azithromycin ( > /=1 mg/L), 43.4% (428/986) were penicillinase-producing (PPNG), 26.9% (265/986) tetracycline-resistant (TRNG) and 19.4% (191/986) were multi-drug resistant (MDR) isolates. Among 202 isolates tested, all were quinolone resistant with double or triple mutations in gyrA; One hundred ninety three (193/202; 95.5%) also had mutations in parC There were no D429N/A and/or K450T mutations in GyrB identified in the 143 isolates with higher zoliflodacin MICs; a S467N mutation in GyrB was identified in one isolate. We report that zoliflodacin continues to have excellent in vitro activity against clinical gonococcal isolates, including those with high-level resistance to ciprofloxacin, azithromycin and extended spectrum cephalosporins.</p>
dc.identifier.submissionpathoapubs/4488
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology


Files in this item

Thumbnail
Name:
Antimicrobial_Agents_and_Chemo ...
Size:
603.2Kb
Format:
PDF

This item appears in the following Collection(s)

Show simple item record

Copyright © 2020 Le et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
Except where otherwise noted, this item's license is described as Copyright © 2020 Le et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.