| Literature DB >> 26582955 |
David S Campo1, Guo-Liang Xia1, Zoya Dimitrova1, Yulin Lin1, Joseph C Forbi1, Lilia Ganova-Raeva1, Lili Punkova1, Sumathi Ramachandran1, Hong Thai1, Pavel Skums1, Seth Sims1, Inna Rytsareva1, Gilberto Vaughan1, Ha-Jung Roh1, Michael A Purdy1, Amanda Sue1, Yury Khudyakov1.
Abstract
Hepatitis C is a major public health problem in the United States and worldwide. Outbreaks of hepatitis C virus (HCV) infections are associated with unsafe injection practices, drug diversion, and other exposures to blood and are difficult to detect and investigate. Here, we developed and validated a simple approach for molecular detection of HCV transmissions in outbreak settings. We obtained sequences from the HCV hypervariable region 1 (HVR1), using end-point limiting-dilution (EPLD) technique, from 127 cases involved in 32 epidemiologically defined HCV outbreaks and 193 individuals with unrelated HCV strains. We compared several types of genetic distances and calculated a threshold, using minimal Hamming distances, that identifies transmission clusters in all tested outbreaks with 100% accuracy. The approach was also validated on sequences obtained using next-generation sequencing from HCV strains recovered from 239 individuals, and findings showed the same accuracy as that for EPLD. On average, the nucleotide diversity of the intrahost population was 6.2 times greater in the source case than in any incident case, allowing the correct detection of transmission direction in 8 outbreaks for which source cases were known. A simple and accurate distance-based approach developed here for detecting HCV transmissions streamlines molecular investigation of outbreaks, thus improving the public health capacity for rapid and effective control of hepatitis C. Published by Oxford University Press for the Infectious Diseases Society of America 2015. This work is written by (a) US Government employee(s) and is in the public domain in the US.Entities:
Keywords: HCV; NGS; hamming distance; nucleotide diversity; outbreak; phylogenetic analysis; threshold; transmission networks
Mesh:
Year: 2015 PMID: 26582955 PMCID: PMC5119477 DOI: 10.1093/infdis/jiv542
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226