Volume 24, Number 11—November 2018
Detection and Characterization of Human Pegivirus 2, Vietnam
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|EID||Anh N, Hong N, Nhu L, Thanh T, Anscombe C, Chau L, et al. Detection and Characterization of Human Pegivirus 2, Vietnam. Emerg Infect Dis. 2018;24(11):2063-2067. https://dx.doi.org/10.3201/eid2411.180668|
|AMA||Anh N, Hong N, Nhu L, et al. Detection and Characterization of Human Pegivirus 2, Vietnam. Emerging Infectious Diseases. 2018;24(11):2063-2067. doi:10.3201/eid2411.180668.|
|APA||Anh, N., Hong, N., Nhu, L., Thanh, T., Anscombe, C., Chau, L....Van Tan, L. (2018). Detection and Characterization of Human Pegivirus 2, Vietnam. Emerging Infectious Diseases, 24(11), 2063-2067. https://dx.doi.org/10.3201/eid2411.180668.|
We report human pegivirus 2 (HPgV-2) infection in Vietnam. We detected HPgV-2 in some patients with hepatitis C virus/HIV co-infection but not in patients with HIV or hepatitis A, B, or C virus infection, nor in healthy controls. HPgV-2 strains in Vietnam are phylogenetically related to global strains.
Human pegivirus 2 (HPgV-2), also known as human hepegivirus 1, is a recently discovered bloodborne flavivirus (1,2). Existing evidence suggests that HPgV-2 is more frequently detected in patients with hepatitis C virus (HCV) infection, particularly HCV and HIV co-infection, although detection rates vary between studies and patient groups. In the United States, HPgV-2 was detected in 1.2% (12/983) of patients with active HCV infections (1), whereas in China, the reported detection rates of HPgV-2 RNA were 0.29% (7/2440) among HCV monoinfected patients and from 3% (8/270) to 5.7% (4/70) among HCV/HIV co-infected patients (3,4). HPgV-2 RNA was detected in 10.9% (17/156) of injection drug users in the United States, and there was a strong association between HPgV-2 and other infections such as HCV and SEN virus D (5).
Given the high burden of HCV and HIV infections worldwide and the potential clinical significance of HPgV-2, we investigated the geographic distribution and genetic diversity of this virus to help prioritize the development and implementation of appropriate intervention strategies. The studies were approved by the corresponding institutional review boards of the local hospitals in Vietnam where patients were enrolled and the Oxford Tropical Research Ethics Committee. We obtained written informed consent from each participant or from the participant’s parent or legal guardian.
Patient information and clinical samples were derived from a multilocation observational study designed to evaluate the causes of community-acquired infection in Southeast Asia (6). We included all 493 samples (384 plasma, 92 pooled nasal and throat swabs, 10 stool, and 7 cerebrospinal fluid [CSF]) from 386 patients in Vietnam with community-acquired infection of unknown origin after extensive diagnostic workup for viral metagenomic analysis (7).
Analysis of metagenomic data revealed that, in 1 plasma sample, of 98,344 obtained reads, 5,342 reads were of HCV sequences, 430 of HIV sequences, and 273 of HPgV-2 sequences; we confirmed all reads by corresponding virus-specific reverse transcription PCR (RT-PCR). HPgV-2 sequence screening and HPgV-2 RT-PCR testing did not detect HPgV-2 in any of the remaining samples of the patients included in metagenomic analysis.
To explore the prevalence of HPgV-2 in HCV-infected patients in Vietnam, we used a reference-based mapping strategy to screen for HPgV-2 sequences in additional viral metagenomic datasets (Table 1). We detected HPgV-2 sequences in 5/79 HIV/HCV co-infected patients who participated in a trial evaluating the hepatic safety of raltegravir/efavirenz-based therapies in antiretroviral-naive HIV-infected subjects co-infected with HCV. We did not detect HPgV-2 sequences in 394 HCV-infected patients with clinically diagnosed hepatitis who participated in molecular epidemiologic studies of hepatitis viruses (Table 1).
We subsequently confirmed the result of this reference-mapping approach by HPgV-2 multiplex RT-PCR (8) testing of the extracted RNA from original samples. We conducted multiplex RT-PCR screening for HPgV-2 RNA in plasma samples of matched controls (78 HIV-infected patients and 80 healthy volunteers) of the 79 HCV/HIV co-infected patients; we found no evidence of HPgV-2 (Table 1). In addition, we did not detect HPgV-2 RNA in any plasma samples from patients with HAV (n = 71) and HBV (n = 103) infection (Table 1).
HPgV-2 RNA was detectable for <18 months in 3/5 patients with HCV/HIV co-infection (Table 2). We did not detect HPgV-2 RNA in the available follow-up serum sample collected 14 days after enrollment from the patient with community-acquired infection (Table 2).
All 5 HCV/HIV co-infected patients had CD4 counts >200 cells/µL at baseline and at 6-, 12-, and 18-month follow-up (Table 2), but none received specific anti-HCV drugs, which was attributed to drug unavailability or unaffordability during the study period. During follow-up, hepatitis and splenic abnormalities were detected in 4/5 patients, which were likely attributable to HCV infection (Table 2). The patient with community-acquired infection was recorded as surviving to 28 days of follow-up (Table 2).
Using deep sequencing and a combination of overlapping PCRs and Sanger sequencing of PCR amplicons (primer sequences available upon request), we obtained 5 nearly complete genomes (coverage of >92%) and another partial genome (coverage of ≈69.1%). Pairwise comparison of HPgV-2 coding regions obtained in this study and previously reported HPgV-2 sequences showed overall sequence identities at the nucleotide level of >94.6% and at the amino acid level of >95.3% (data not shown). Phylogenetic analyses revealed a tight cluster between viruses from Vietnam and global strains (Figure). We submitted the HPgV-2 sequences we generated to GenBank (accession nos. MH194408–13).
Of the 5 HPgV-2 genome sequences we recovered, we generated 2 by deep sequencing. The results were above the proposed sequencing-depth threshold of >5 for sequences generated by next-generation sequencing (9) and sufficient for intrahost diversity investigation. One sequence we generated had mean coverage of 2,049 (range 12–9,912), with a total of 26 (10 [38%] nonsynonymous) positions carrying minor variations detected in the corresponding dataset (data not shown). For the other sequence, mean coverage was 32,531 (range 13–138,383), with a total of 37 (13 [35%] nonsynonymous) positions carrying minor variations in its dataset (data not shown).
We report the detection and genetic characterization of HPgV-2 in Vietnam and describe the observed demographic and clinical characteristics of patients with HPgV-2 infection. Together with reports from China, Iran, and the United States (1–4,8,10), our findings further emphasize the strong association between HPgV-2 and HCV, especially HCV/HIV co-infection. The absence of HPgV-2 in 394 HCV-infected patients may have been attributed to the small sample size and the fact that the reported prevalence of HIV among HCV-infected patients was <6.5% (11,12). Of note, HPgV-2 was detected in only 0.29% of HCV-monoinfected patients in China.
Previous reports showed that HPgV-2 viremia can be transient or persistent. Likewise, in our study, HPgV-2 RNA became undetectable after 14 days in a HCV/HIV co-infected patient with community-acquired infection of unknown origin, but remained detectable in other HCV/HIV co-infected patients through up to 18 months of follow-up.
The pathogenic potential of HPgV-2 remains unknown. Its role in HCV/HIV co-infection and response to treatment warrants further research, given its low detection rates in blood donors in the United States and China (1,3) and its absence in healthy persons (this study) but close association with HCV/HIV co-infection.
In the era of sequence-based virus discovery, a key question is whether the detected genome represents live virus or a non–replication competent genome. Addressing this question would require recovery of virus in cell culture. However, our detection of minor variations across 2 HPgV-2 genomes suggests that viral replication had occurred in the infected patients. Phylogenetically, the close relatedness between HPgV-2 strains from Vietnam and global strains suggests HPgV-2 has a wide geographic distribution.
Our study has some limitations. First, we only retrospectively tested available archived samples without formal sample size estimation, which may have explained the absence of HPgV-2 in the remaining 394 HCV patients. Second, we did not employ a serologic assay to screen for HPgV-2 antibodies in patients’ plasma. Third, we used only multiplex PCR with primers based on a limited number of available HPgV-2 sequences. Therefore, we may have missed genetically diverse HPgV-2 strains, and we may have underestimated the prevalence of HPgV-2 infections in Vietnam.
Our findings contribute expanded data about geographic distribution, demographics, and genetic diversity of HPgV-2. Because HCV and HIV infections are global public health issues, the extent to which HPgV-2 interacts with HCV and HIV in co-infected patients and the possible clinical consequences warrant further research.
Ms. Nguyen is a PhD student in life science at Open University, Milton Keynes, United Kingdom. Her research interests are virus discovery and evolution of emerging pathogens such as enteroviruses.
We thank Le Kim Thanh for her logistic support. We thank the patients for their participation in this study.
This study was funded by National Institute of Allergy and Infectious Diseases, US National Institutes of Health, and the Wellcome Trust of Great Britain (106680/B/14/Z and 204904/Z/16/Z). X.D. and E.D. were supported by the Blood Systems Research Institute and National Heart, Lung, and Blood Institute (grant no. R01 HL105770).
Members of the Southeast Asia Infectious Disease Clinical Research Network: Pratiwi Sudarmono (Cipto Mangunkusumo Hospital, Jakarta, Indonesia); Abu Tholib Aman (Sardjito Hospital, Yogyakarta, Indonesia); Mansyur Arif (Wahidin Soedirohusodo Hospital, Makassar, Indonesia); Armaji Kamaludi Syarif, Herman Kosasih, and Muhammad Karyana (National Institute of Health Research and Development, Jakarta); Tawee Chotpitayasunondh and Warunee Punpanich Vandepitte (Queen Sirikit National Institute of Child Health, Bangkok, Thailand); Adiratha Boonyasiri, Keswadee Lapphra, Kulkanya Chokephaibulkit, Pinyo Rattanaumpawan, and Visanu Thamlikitkul (Siriraj Hospital, Bangkok, Thailand); Direk Limmathurotsakul, Janjira Thaipadungpanit, Stuart Blacksell, and Nicholas Day (Mahidol-Oxford Tropical Medicine Research Unit, Bangkok); Achara Laongnualpanich (Chiang Rai Prachanukroh Hospital, Chiang Rai, Thailand); Prapit Teparrakkul and Pramot Srisamang (Sappasithiprasong Hospital, Ubon Ratchathani, Thailand); Claire Ling (Shoklo Malaria Research Unit, Mae Sot, Thailand); Phan Huu Phuc and Le Thanh Hai (National Hospital of Pediatrics, Hanoi, Vietnam); Nguyen Van Kinh (National Hospital of Tropical Diseases, Hanoi); Bui Duc Phu (Hue Central Hospital, Hue, Vietnam); Nguyen Thanh Hung and Tang Chi Thuong (Children’s Hospital 1, Ho Chi Minh City, Vietnam); Ha Manh Tuan (Children’s Hospital 2, Ho Chi Minh City); Lam Minh Yen and Nguyen Van Vinh Chau (Hospital for Tropical Diseases, Ho Chi Minh City); Guy Thwaites, Heiman Wertheim, Le Van Tan, Motiur Rahman, and H. Rogier van Doorn (Oxford University Clinical Research Unit, Ho Chi Minh City); and Chuen-Yen Lau (National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA).
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TablesCite This Article
Original Publication Date: 9/27/2018
1Members of the Southeast Asia Infectious Disease Clinical Research Network are listed at the end of this article.
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