A Whole-genome Sequencing Analysis of


Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 13 08 2018
revised: 06 12 2018
accepted: 22 01 2019
entrez: 14 6 2019
pubmed: 14 6 2019
medline: 14 6 2019
Statut: epublish

Résumé

Tracking the spread of the We obtained clinical isolates and data from the China Gonococcal Resistance Surveillance Programme (China-GRSP) from 2012 to 2013. We sequenced the genomes of 435 clinical isolates of The most prevalent MLST STs in our gonococcal population were MLST ST7827 (n = 74), followed by ST7365 (n = 58), ST1600 (n = 38), ST7367 (n = 35), and ST7363 (n = 29). MLST ST1901 which was reported as the predominant ST in the US was not found in our population. A total of 2512 strains, including additional 2077 published NG strains, were further included for phylogenetic analysis. It generated two distinct lineages - lineage 1 and lineage 2. Analysis of MLST ST1901 in the database indicate that most of MLST ST1901 isolates in the lineage2.6 were Cfx-DS isolates while all isolates in the lineage 2.1 were sensitive to ceftriaxone (77/110 vs. 0/13; p < 0.001). ST1901/lineage 2.6 is a ceftriaxone resistant clone which cannot distinguished by MLST genotyping. In the isolates from our study, the MICs of ceftriaxone for ST7363/lineage 2.6 isolates ranged from 0.008-0.125 mg/L (mean ± SD; 0.054 ± 0.043 mg/L) while those for ST7363/lineage 2.8 isolates ranged from 0.032-0.250 mg/L (0.134 ± 0.085 mg/L). All ST7363/lineage 2.8 isolates contained To our knowledge, current study is the first WGS-based analysis of gonococcal population at national level in Asia. China harbors the different predominant clones associated with decreased susceptibility to ceftriaxone from those clones circulated in other regions. The findings from the study can be not only used as baseline data for future studies in China but also contributable to our understanding on spread of The Chinese Academy Medical Sciences (CAMS) Initiative for Innovative Medicine.

Sections du résumé

BACKGROUND BACKGROUND
Tracking the spread of the
METHODS METHODS
We obtained clinical isolates and data from the China Gonococcal Resistance Surveillance Programme (China-GRSP) from 2012 to 2013. We sequenced the genomes of 435 clinical isolates of
FINDINGS RESULTS
The most prevalent MLST STs in our gonococcal population were MLST ST7827 (n = 74), followed by ST7365 (n = 58), ST1600 (n = 38), ST7367 (n = 35), and ST7363 (n = 29). MLST ST1901 which was reported as the predominant ST in the US was not found in our population. A total of 2512 strains, including additional 2077 published NG strains, were further included for phylogenetic analysis. It generated two distinct lineages - lineage 1 and lineage 2. Analysis of MLST ST1901 in the database indicate that most of MLST ST1901 isolates in the lineage2.6 were Cfx-DS isolates while all isolates in the lineage 2.1 were sensitive to ceftriaxone (77/110 vs. 0/13; p < 0.001). ST1901/lineage 2.6 is a ceftriaxone resistant clone which cannot distinguished by MLST genotyping. In the isolates from our study, the MICs of ceftriaxone for ST7363/lineage 2.6 isolates ranged from 0.008-0.125 mg/L (mean ± SD; 0.054 ± 0.043 mg/L) while those for ST7363/lineage 2.8 isolates ranged from 0.032-0.250 mg/L (0.134 ± 0.085 mg/L). All ST7363/lineage 2.8 isolates contained
INTERPRETATION CONCLUSIONS
To our knowledge, current study is the first WGS-based analysis of gonococcal population at national level in Asia. China harbors the different predominant clones associated with decreased susceptibility to ceftriaxone from those clones circulated in other regions. The findings from the study can be not only used as baseline data for future studies in China but also contributable to our understanding on spread of
FUNDING BACKGROUND
The Chinese Academy Medical Sciences (CAMS) Initiative for Innovative Medicine.

Identifiants

pubmed: 31193648
doi: 10.1016/j.eclinm.2019.01.010
pii: S2589-5370(19)30015-X
pmc: PMC6537553
doi:

Types de publication

Journal Article

Langues

eng

Pagination

47-54

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Auteurs

Jun-Ping Peng (JP)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Yue-Ping Yin (YP)

Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China.
National Center for STD Control, Chinese Center for Disease Control and Prevention, Nanjing, China.

Shao-Chun Chen (SC)

Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China.
National Center for STD Control, Chinese Center for Disease Control and Prevention, Nanjing, China.

Jian Yang (J)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Xiu-Qin Dai (XQ)

Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China.
National Center for STD Control, Chinese Center for Disease Control and Prevention, Nanjing, China.

He-Ping Zheng (HP)

Dermatology Hospital, Southern Medical University, Guangzhou, China.
Guangdong Provincial Dermatology Hospital, Guangzhou, China.

Wei-Ming Gu (WM)

Shanghai Skin Disease Hospital, Shanghai, China.

Bang-Yong Zhu (BY)

Institute of Dermatology, Guangxi Autonomous Region, Nanning, China.

Gang Yong (G)

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Chengdu, China.

Na Zhong (N)

Hainan Provincial Center for STD/Skin Disease Control and Prevention, Haikou, China.

Li-Hua Hu (LH)

Zhejiang Provincial Institute of Dermatology, Deqing, China.

Wen-Ling Cao (WL)

Guangzhou Institute of Dermatology, Guangzhou, China.

Zhong-Jie Zheng (ZJ)

Tianjin Center for Disease Control and Prevention, Tianjin, China.

Feng Wang (F)

Shenzhen Center for Chronic Disease Control, Shenzhen, China.

Qi Zhi (Q)

Xinjiang Center for Disease Control and Prevention, Urumqi, China.

Chi Zhang (C)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Le-Shan Xiu (LS)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Bo Liu (B)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Jie Dong (J)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Li-Lian Sun (LL)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Ya-Fang Zhu (YF)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Xiang-Sheng Chen (XS)

Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, China.
National Center for STD Control, Chinese Center for Disease Control and Prevention, Nanjing, China.

Qi Jin (Q)

National Health Commission Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, P. R. China.

Classifications MeSH