Discovery of a Novel Human Pegivirus in Blood Associated with Hepatitis C Virus Co-Infection

被引:74
作者
Berg, Michael G. [1 ]
Lee, Deanna [2 ,3 ]
Coller, Kelly [1 ]
Frankel, Matthew [1 ]
Aronsohn, Andrew [4 ]
Cheng, Kevin [1 ]
Forberg, Kenn [1 ]
Marcinkus, Marilee [1 ]
Naccache, Samia N. [2 ,3 ]
Dawson, George [1 ]
Brennan, Catherine [1 ]
Jensen, Donald M. [4 ]
Hackett, John, Jr. [1 ]
Chiu, Charles Y. [2 ,3 ,5 ]
机构
[1] Abbott Labs, Abbott Pk, IL 60064 USA
[2] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Abbott Viral Diagnost & Discovery Ctr, San Francisco, CA 94143 USA
[4] Univ Chicago, Ctr Liver Dis, Med Ctr, Chicago, IL 60637 USA
[5] Univ Calif San Francisco, Dept Med, Div Infect Dis, San Francisco, CA 94143 USA
关键词
GBV-C; IDENTIFICATION; INFECTION; RNA; SEROPREVALENCE; HEPACIVIRUSES; PREVALENCE; ALIGNMENT; SOFTWARE; DISEASE;
D O I
10.1371/journal.ppat.1005325
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis C virus (HCV) and human pegivirus (HPgV), formerly GBV-C, are the only known human viruses in the Hepacivirus and Pegivirus genera, respectively, of the family Flaviviridae. We present the discovery of a second pegivirus, provisionally designated human pegivirus 2 (HPgV-2), by next-generation sequencing of plasma from an HCV-infected patient with multiple bloodborne exposures who died from sepsis of unknown etiology. HPgV-2 is highly divergent, situated on a deep phylogenetic branch in a clade that includes rodent and bat pegiviruses, with which it shares < 32% amino acid identity. Molecular and serological tools were developed and validated for high-throughput screening of plasma samples, and a panel of 3 independent serological markers strongly correlated antibody responses with viral RNA positivity (99.9% negative predictive value). Discovery of 11 additional RNA-positive samples from a total of 2440 screened (0.45%) revealed 93-94% nucleotide identity between HPgV-2 strains. All 12 HPgV-2 RNA-positive cases were identified in individuals also testing positive for HCV RNA (12 of 983; 1.22%), including 2 samples co-infected with HIV, but HPgV-2 RNA was not detected in non-HCV-infected individuals (p < 0.0001), including those singly infected by HIV (p = 0.0075) or HBV (p = 0.0077), nor in volunteer blood donors (p = 0.0082). Nine of the 12 (75%) HPgV-2 RNA positive samples were reactive for antibodies to viral serologic markers, whereas only 28 of 2,429 (1.15%) HPgV-2 RNA negative samples were seropositive. Longitudinal sampling in two individuals revealed that active HPgV-2 infection can persist in blood for at least 7 weeks, despite the presence of virus-specific antibodies. One individual harboring both HPgV-2 and HCV RNA was found to be seronegative for both viruses, suggesting a high likelihood of simultaneous acquisition of HCV and HPgV-2 infection from an acute co-transmission event. Taken together, our results indicate that HPgV-2 is a novel bloodborne infectious virus of humans and likely transmitted via the parenteral route.
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页数:18
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