A molecular phylogenetics-based approach for identifying recent hepatitis C virus transmission events

被引:21
|
作者
Olmstead, Andrea D. [1 ,2 ]
Joy, Jeffrey B. [3 ]
Montoya, Vincent [1 ,2 ]
Luo, Iris [2 ]
Poon, Art F. Y. [3 ]
Jacka, Brendan [4 ]
Lamoury, Francois [4 ]
Applegate, Tanya [4 ]
Montaner, Julio [2 ,3 ]
Khudyakov, Yury [5 ]
Grebely, Jason [4 ]
Cook, Darrel [1 ]
Harrigan, P. Richard [3 ]
Krajden, Mel [1 ,2 ]
机构
[1] BC Ctr Dis Control, Vancouver, BC, Canada
[2] Univ British Columbia, Vancouver, BC V5Z 4R4, Canada
[3] St Pauls Hosp, BC Ctr Excellence HIV AIDS, Vancouver, BC V6Z 1Y6, Canada
[4] UNSW Australia, Kirby Inst, Sydney, NSW, Australia
[5] Ctr Dis Control & Prevent, Atlanta, GA USA
关键词
Hepatitis C virus; Recent transmission clusters; British Columbia; Epidemiology; Sequencing; Phylogenetics; Surveillance; Seroconversion; INJECT DRUGS; IATROGENIC TRANSMISSION; SEQUENCE EVOLUTION; HIV TRANSMISSION; EPIDEMIOLOGY; HCV; INFECTION; PEOPLE; IDENTIFICATION; PREVENTION;
D O I
10.1016/j.meegid.2015.04.017
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Improved surveillance methods are needed to better understand the current hepatitis C virus (HCV) disease burden and to monitor the impact of prevention and treatment interventions on HCV transmission dynamics. Sanger sequencing (HCV NS5B, HVR1 and Core-E1-HVR1) and phylogenetics were applied to samples from individuals diagnosed with HCV in British Columbia, Canada in 2011. This included individuals with two or three sequential samples collected <1 year apart. Patristic distances between sequential samples were used to set cutoffs to identify recent transmission clusters. Factors associated with transmission clustering were analyzed using logistic regression. From 618 individuals, 646 sequences were obtained. Depending on the cutoff used, 63 (10%) to 92 (15%) unique individuals were identified within transmission clusters of predicted recent origin. Clustered individuals were more likely to be <40 years old (Adjusted Odds Ratio (AOR) 2.12, 95% CI 1.21-3.73), infected with genotype la (AOR 6.60, 95% CI 1.98-41.0), and to be seroconverters with estimated infection duration of <1 year (AOR 3.13, 95% CI 1.29-7.36) or >1 year (AOR 2.19, 95% CI1.22-3.97). Conclusion: Systematic application of molecular phylogenetics may be used to enhance traditional surveillance methods through identification of recent transmission clusters. (C) 2015 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:101 / 109
页数:9
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