Evolution rates of in vivo and horizontal transmission of HCV 1b subtype
XU Ru1,2, HUANG Jie-ting1,2, WANG Min1,2, LIAO Qiao1,2, RONG Xia1,2, FU Yong-shui1,2
1.Guangzhou Blood Center, Guanzhou, Guangdong 510095, China; 2.Guangzhou Key Laboratory of Medicine (Key Laboratory of Blood Safety), Guanzhou, Guangdong 510095, China
Abstract:Objective To obtain the evolution rates of in vivo and horizontal transmission of HCV 1b subtype and its biodiversity. Methods Samples collected from two blood donors infected with HCV in Guangdong region were followed up every 6 months. The next-generation sequencing technology and bioinformatics analysis method were used to obtain the whole mitochondrial genome sequence. Mega 7.0 software was employed to determine HCV genotype. The evolution rates of in vivo and horizontal transmission of HCV 1b subtype and its biodiversity were analyzed by using Markov Chain Monte Carlo (MCMC) method in Beast package. Results We obtained 6 HCV full-length sequences in three samples collected from two HCV-infected patients, with the average depth of 2,486. The 6 specimen sequences could basically cover the HCV whole genome, all of which were HCV 1b subtype. The evolution rate of in vivotransmission in the sample 1 was higher than that in the sample 2 under the relaxed lognormal model, while the evolution rates of in vivo transmission in samples 1 and 2 were both higher than those of horizontal transmission under relaxed lognormal and strict models. In addition, the recent common ancestor of HCV 1b in China originated in 1,938. The number of HCV-infected cases in China during 1986-1998 increased logarithmically, but there was a gradually decreasing trend after 1998. Conclusions The evolution rate of in vivo transmission of HCV 1b subtype is higher than that of horizontal transmission, and the evolution rates of different individuals are dissimilar.
[1] Perales C. Quasispecies dynamics and clinical significance of hepatitis C virus (HCV) antiviral resistance[J]. Int J Antimicrob Agents, 2018, S0924-8579(18):30297-30298. [2] Smith DB, Bukh J, Kuiken C, et al. Expanded classification of hepatitis C virus into 7 genotypes and 67 subtypes: updated criteria and genotype assignment web resource[J]. Hepatology, 2014, 59(1):318-327. [3] Herring BL, Tsui R, Peddada L, et al. Wide range of quasispecies diversity during primary hepatitis C virus infection[J]. J Virol, 2005,79(7):4340-4346. [4] Huang K, Chen J, Xu R, et al. Molecular evolution of hepatitis C virus in China: a nationwide study[J]. Virology, 2018, 516:210-218. [5] 范公忍,闻炜,韩聚强,等. 蒙古国人丙型肝炎患者HCV RNA 检测及基因型的研究[J]. 实用预防医学, 2012, 19(12):1867-1869. [6] 戴俊斌,王芳宇,邹潇白,等.湖南省美沙酮门诊就诊者感染丙型肝炎病毒基因型特征分析[J].实用预防医学,2019,4(26):500-502. [7] Wertheim JO, Kosakovsky Pond SL. Purifying selection can obscure the ancient age of viral lineages[J]. Mol Biol Evol, 2011, 28(12):3355-3365. [8] Wymant C, Hall M, Ratmann O, et al. PHYLOSCANNER: inferring transmission from within- and between-host pathogen genetic diversity[J]. Mol Biol Evol, 2018,35(3):719-733. [9] Powdrill MH, Tchesnokov EP, Kozak RA, et al. Contribution of a mutational bias in hepatitis C virus replication to the genetic barrier in the development of drug resistance[J]. Proc Nati Acad Sci USA,2011,108(51):20509-20513. [10] Sanjuan R, Nebot MR, Chirico N, et al. Viral mutation rates[J]. J Virol,2010, 84(19):9733-9748. [11] Gray RR, Parker J, Lemey P,et al. The mode and tempo of hepatitis C virus evolution within and among hosts[J]. BMC Evol Biol, 2011, 11:131. [12] Romero-Severson EO, Bulla I, Leitner T. Phylogenetically resolving epidemiologic linkage[J]. Proc Natl Acad Sci USA, 2016, 113(10):2690-2695. [13] Pybus OG, Rambaut A. Evolutionary analysis of the dynamics of viral infectious disease[J]. Nat Rev Genet, 2009, 10(8):540-550. [14] Bartolini B, Lionetti R, Giombini E, et al. Dynamics of HCV genotype 4 resistance-associated variants during virologic escape with pIFN/RBV+daclatasvir: a case study using ultra deep pyrosequencing[J]. J Clin Virol, 2015, 66:38-43. [15] Henquell C, Guglielmini J, Verbeeck J, et al. Evolutionary history of hepatitis C virus genotype 5a in France, a multicenter ANRS study[J]. Infect Genet Evol, 2011, 11(2):496-503. [16] Zhou X, Chan PK, Tam JS, et al. A possible geographic origin of endemic hepatitis C virus 6a in Hong Kong: evidences for the association with Vietnamese immigration[J]. PLoS One, 2011, 6(9):e24889. [17] Choudhary MC, Natarajan V, Pandey P, et al. Identification of Indian sub-continent as hotspot for HCV genotype 3a origin by Bayesian evolutionary reconstruction[J]. Infect Genet Evol, 2014, 28:87-94. [18] Thomson E, Ip CL, Badhan A, et al. Comparison of next-generation sequencing technologies for comprehensive assessment of full-length hepatitis C viral genomes[J]. J Clin Microbiol, 2016, 54(10):2470-2484. [19] Saleem S, Ali A, Khubaib B, et al. Genetic diversity of hepatitis C virus in Pakistan using next generation sequencing[J]. J Clin Virol, 2018, 108:26-31. [20] Raghwani J, Wu CH, Ho CKY, et al. High resolution evolutionary analysis of within-host hepatitis C virus infection[J]. J Infect Dis, 2019, 219(11):1722-1729. [21] Iles JC, Raghwani J, Harrison GLA, et al. Phylogeography and epidemic history of hepatitis C virus genotype 4 in Africa[J]. Virology, 2014, 464-465:233-243. [22] Ling Lu, Tong W, Lin Gu, et al. The current hepatitis C virus prevalence in China may have resulted mainly from an officially encouraged plasma campaign in the 1990s: a coalescence inference with genetic sequences[J]. J Virol, 2013, 87:12041-12050.