Shanghai Neisseria gonorrhoeae Isolates Exhibit Resistance to Extended-Spectrum Cephalosporins and Clonal Distribution.
Shanghai Neisseria gonorrhoeae Isolates Exhibit Resistance to Extended-Spectrum Cephalosporins and Clonal Distribution.
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DOI:
10.3389/fmicb.2020.580399
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发表时间:
2020
影响因子:
5.2
通讯作者:
Gu W
中科院分区:
文献类型:
--
作者:
Dong Y;Yang Y;Wang Y;Martin I;Demczuk W;Gu W
The emergence of Neisseria gonorrhoeae strains with resistance (R) to extended-spectrum cephalosporins (ESCsR) represents a public health threat of untreatable gonococcal infections. This study was designed to determine the prevalence and molecular mechanisms of ESCR of Shanghai N. gonorrhoeae isolates. A total of 366 N. gonorrhoeae isolates were collected in 2017 in Shanghai. Susceptibility to ceftriaxone (CRO), cefixime (CFM), azithromycin (AZM), ciprofloxacin (CIP), spectinomycin, penicillin, and tetracycline was determined using the agar dilution method. A subset of 124 isolates was subjected to phylogenetic analysis for nine antimicrobial resistance-associated genes, i.e., penA, porB, ponA, mtrR, 23S rRNA, gyrA, parC, 16S rRNA, and rpsE. Approximately 20.0% of the isolates exhibited CFMR [minimum inhibitory concentration (MIC) >0.125 mg/L], and 5.5% were CROR (MIC > 0.125 mg/L). In total, 72.7% of ESCR isolates were clonal and associated with mosaic penA 10 and 60 alleles. Non-mosaic penA 18 allele and substitutions of PenA A501T, G542S, and PorB1b G213S/Y were observed in non-clonal ESCR. Approximately 6.8% of the isolates showed AZM MIC above the epidemiological cutoff (ECOFF, 1 mg/L), were associated with 23S rRNA A2059G mutation, and did not exhibit clonal distribution. Almost all isolates were CIPR (resistance to ciprofloxacin) and associated with GyrA-91/92 and ParC-85/86/87/88/89/91 alterations. Isolates with ParC S88P substitution were clustered into the ESCR clade. The Shanghai isolates exhibited a high level of ESCR and distinct resistant patterns.
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影响因子:
3.2
作者:
Barry PM;Klausner JD
通讯作者:
Klausner JD
影响因子:
11.8
作者:
Lahra MM;Martin I;Demczuk W;Jennison AV;Lee KI;Nakayama SI;Lefebvre B;Longtin J;Ward A;Mulvey MR;Wi T;Ohnishi M;Whiley D
通讯作者:
Whiley D
DOI:
10.1093/bioinformatics/btx610
发表时间:
2018-01-15
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Hadfield J;Croucher NJ;Goater RJ;Abudahab K;Aanensen DM;Harris SR
通讯作者:
Harris SR
影响因子:
56.3
作者:
Grad, Yonatan H.;Kirkcaldy, Robert D.;Trees, David;Dordel, Janina;Harris, Simon R.;Goldstein, Edward;Weinstock, Hillard;Parkhill, Julian;Hanage, William P.;Bentley, Stephen;Lipsitch, Marc
通讯作者:
Lipsitch, Marc
影响因子:
5.2
作者:
Lee, Sang-Guk;Lee, Hyukmin;Lee, Kyungwon
通讯作者:
Lee, Kyungwon