BioMed Research International

BioMed Research International / 2019 / Article

Research Article | Open Access

Volume 2019 |Article ID 8048670 | 11 pages |

Molecular and Clinical Profiles of Human Pegivirus Type 1 Infection in Individuals Living with HIV-1 in the Extreme South of Brazil

Academic Editor: Lucia Lopalco
Received19 Feb 2019
Revised02 May 2019
Accepted16 May 2019
Published11 Jun 2019


Human pegivirus type 1 (HPgV-1) infection has been associated with a beneficial effect on the prognosis of human immunodeficiency virus type 1 (HIV-1)-coinfected individuals. However, the mechanisms involved in this protection are not yet fully elucidated. To date, circulating HPgV-1 genotypes in HIV-1-infected individuals have not yet been identified in the extreme south of Brazil. The present study aimed to determine the genotypic circulation of HPgV-1 and the influence of HPgV-1 status and persistence time on the evolution of HIV-1 infection. A retrospective cohort of 110 coinfected individuals was analyzed. Samples were subjected to viral RNA extraction, cDNA synthesis, nested PCR, and genotyping. Genotypes 1 (2.8%), 2 (47.9% of subtype 2a and 42.3% of subtype 2b), and 3 (7%) were identified. In antiretroviral treatment-naïve subjects HPgV-1 subtype 2b was associated with lower HIV-1 viral load (VL) rates (p = 0.04) and higher CD4+ T-cell counts (p = 0.03) than was subtype 2a, and the positivity for HPgV-1 was associated with higher CD4+ T-cell counts (p = 0.02). However, there was no significant difference in HIV-1 VL between HPgV-1-positive and HPgV-1-negative subjects ​​(p = 0.08). There was no significant association between the different groups in HPgV-1 persistence and median HIV-1 VL (p = 0.66) or CD4+ T-cell counts (p = 0.15). HPgV-1 subtype 2b is associated with better prognosis of HIV-1 infection. Although HPgV-1 infection is persistent, our data suggest that the time of infection does not influence HIV-1 VL or CD4+ T-cell counts in coinfected subjects.

1. Introduction

Human pegivirus type 1 (HPgV-1), formerly named GB virus type C (GBV-C), is an RNA virus of the Flaviviridae family and of the Pegivirus genus [1]. To date, seven HPgV-1 genotypes have been described which are distributed in different geographic regions [24]. Genotype 1 predominates in West Africa; genotype 2, in Europe, USA, South America, and North Africa; genotype 3, in Asian and Amerindian populations; genotype 4, in Southeast Asia and the Philippines; genotype 5, in South Africa; genotype 6, in Indonesia; and genotype 7, in China [3, 4]. HPgV-1 is found mainly in natural killer (NK) cells, T and B lymphocytes, and monocytes [5]. HPgV-1 is transmitted by parenteral, sexual, or maternal-infant routes [69]. The prevalence of HPgV-1 viremia in healthy blood donors ranges from 1% to 19% [10, 11].

Most studies involving HPgV-1 are related to its coinfection with HIV-1 [1215]. The presence of HPgV-1 RNA appears to be associated with increased survival and lower mortality of HIV-1-positive patients [12, 14]. In addition, HPgV-1 coinfection of hepatitis C virus (HCV) and HCV/HIV-1 carriers appears to decrease the severity of liver disease, and, in those coinfected with the Ebola virus, survival appears to be higher than that in monoinfected individuals [15, 16].

The mechanism by which HPgV-1 influences the progression of certain viral infections has not yet been fully elucidated. One of the hypotheses suggests that the presence of HPgV-1 reduces T-cell activation by modulating the immune system to better perform against viral agents [5, 17]. In addition, it has been suggested that this immune response occurs only in the presence of certain HPgV-1 genotypes [18, 19]. On the other hand, HPgV-1 has also recently been negatively associated with other diseases, such as non-Hodgkin’s lymphoma [20, 21], multiple sclerosis [22], and severe encephalitis [23].

The present study aimed to determine the genotypic circulation of HPgV-1 and the influence of HPgV-1 status and persistence time on the evolution of HIV-1 infection in a cohort of HIV-1/HPgV-1 coinfected patients followed up at a reference center in the southernmost part of Brazil.

2. Materials and Methods

2.1. Study Design and Population

This is a retrospective cohort study that evaluated the HPgV-1/HIV-1 coinfection of 110 patients, all of whom were followed up at the Infectious Diseases Department of Dr. Miguel Riet Corrêa Jr. University Hospital (HU-FURG) in the city of Rio Grande, RS, in the extreme south of Brazil. Sociodemographic, economic, and behavioral information was obtained from the study database previously assembled [6]. Clinical and laboratory data were obtained after review of medical records. The evolution of HIV-1 infection was estimated through HIV viral load and CD4+ T-cell count trajectories. Plasma samples were collected by the Laboratory of HIV Viral Load and CD4+ T-cell counts (BioLab) of HU-FURG between 2002 and 2016. An aliquot of each sample was stored in the BioLab Biorepository at −70°C and made available for the present study. The protocol of this study has been approved by the Ethics and Health Research Committee (CEPAS) of the Federal University of Rio Grande (FURG) (#103/2012).

2.2. Inclusion Criteria

Initially, we included HPgV-1/HIV-1 coinfected individuals (n = 118) (Figure 1(a)). Of those, we selected subjects followed for at least six months at HU-FURG (n = 110) (Figure 1(b)). In addition, those subjects had at least six biological samples available at BioLab, obtained through collections at intervals of at least one month (n = 110) (Figure 1(c)). All enrolled patients were tested for hepatitises B (HBsAg) and C (anti-HCV). These individuals were recruited to HU-FURG and invited to participate in the study. All subjects signed a free and informed consent form.

To assess whether persistence time of HPgV-1 infection modifies the evolution of HIV-1 infection, individuals with persistent HPgV-1 infection were selected (n = 109) (Figure 1(d)). A persistent infection was defined if the virus was detected for more than six months. This definition was based on the time criterion for establishing chronicity for HCV [24]. The time period evaluated in each patient was at least 6 months, varying further according to the availability of the samples. The persistence time was grouped into 3 categories (Figure 1(e)) to allow a more robust comparison between the groups. For each patient, the median values of HIV-1 viral load and CD4+ T cell counts, corresponding to the positivity period for HPgV-1, were estimated.

To assess the effect of HPgV-1 and its subtypes 2a and 2b on the progression of HIV-1 infection, subjects who were naive to antiretroviral therapy (ART) were studied to assess the patients’ natural history. Of the 109 patients recruited to evaluate HPgV-1 persistence, 70 had samples without the influence of ART (Figure 1(f)), and, of those, 40 comprised subtype 2a (n = 19) or 2b (n = 21) (Figure 1(g)). HIV-1 viral load, CD4+ T cell counts, and HPgV subtypes were obtained from the same sample tested for HPgV-1.

2.3. Pilot Study

A pilot study was performed with approximately 10% (n = 10) of the initial population (10/110). Subjects were randomly selected, and each had one sample per year (2002 to 2016) tested for HPgV-1 RNA positivity. A pattern was observed in the molecular behavior of HPgV-1 since only one period of positivity occurred in each individual, with no indication of reinfection (Figure 2(a)).

Following these observations, we chose to define a standard protocol for subsequent HPgV-1 molecular tests. It was established that we would start by testing the oldest (closest to 2002) and the most recent (closest to 2016) sample of each participant. If a given result was negative, the test would proceed to the following (or previous) sample, according to the directions shown by the red arrows in Figure 2(a). This direction was followed until finding the HPgV-1 positive interval for each subject (blue line in Figure 2(b)). This period was considered the time of HPgV-1infection per subject. By establishing this methodology, it was also considered that other studies identified only one period of infection by HPgV-1 [8, 13, 25, 26]. For quality control of the established standard testing strategy, two samples contained in the HPgV-1 positivity range were also processed per patient. In addition, every 10 patients had a representative sample per year tested. Figure 2(b) shows the results of the pilot study. Their different colors indicate which samples would have been tested if the standard test criteria were used for them.

2.4. Molecular Tests
2.4.1. Viral RNA Extraction and cDNA Synthesis

Viral RNA was extracted from 140 μL of plasma using the QIAamp Viral RNA Extraction Kit (QIAGEN), according to the manufacturer’s protocol. Ten microliters of the extracted RNA was added to 300 ng of random oligonucleotides (2 μL of 150 ng/solution, N6, Life Technologies, Itapevi, Brazil) and denatured at 70°C for 10 minutes. For cDNA synthesis, 200 U of Superscript reverse transcriptase (Thermo Fisher Scientific, Pittsburgh, PA), 0.1 M DTT, 5 U of RNaseOUT® (Life Technologies, Forster City, CA), and 0.5 mM of each deoxynucleotide were added. The cDNA reaction was conducted at 42°C for 1.5h in a final volume of 20 μL.

2.4.2. Nested-PCR for HPgV-1 Detection

After obtaining the cDNA, a nested polymerase chain reaction (nested-PCR) was used to detect HPgV-1. The virus noncoding genomic region (5′NCR) was amplified by adapting a PCR protocol described by Jarvis et al. [27]. The first round was performed with 5 μL of the obtained cDNA and the second with 5 μL of the product of the first PCR. Both reactions used 1x PCR Buffer, 2 mM MgCl2, 0.5 mM dNTPs, 1U of recombinant Taq DNA polymerase enzyme (Invitrogen, Carlsbad, CA), Milli-Q water q.s.p. to a final volume of 50 μL, and 0.5 μM of primers HGV1 and HGV2 (first round) or HGV3 and HGV4 (second round). Primer sequences were as follows: HGV1 forward 5′-AGGTGGTGGATGGGTGAT3′; HGV2 reverse 5′-TGCCACCCGCCCTCACCCGAA-3′; HGV3 forward 5′-TGGTAGGTCGTAAATCCCGGT-3′; HGV4 reverse 5′- GGAGCTGGGTGGCCCCATGCAT-3′. PCRs were performed in a thermocycler with the following cycling: initial denaturation at 95°C for 10 min, followed by 40 cycles of 94°C for 30 sec, 55°C for 30 sec, and 72°C for 30 sec, and a final extension stage at 72°C for 2 min. PCR products from the second round were electrophoresed on a 1.5% agarose gel. For this, 5 μL of the PCR product from each sample was mixed with 1 μL of Blue Green Loading Dye (LGC Biotecnologia, São Paulo, Brazil). Gels were visualized on a UV transilluminator and images were captured. A positive control for HPgV-1 (providing a PCR band of 344 bp), confirmed by direct sequencing of the PCR product, and an HPgV-1-negative sample were used, in addition to a blank reaction containing no DNA sample.

2.4.3. HPgV-1 Genotyping and Phylogenetic Analysis

For the genotyping and phylogenetic analysis, PCR products were purified with the GFX PCR DNA and TM-Gel Band Purification kit (GE Healthcare, São Paulo, Brazil) and subjected to sequencing using the BigDye™ ABI PRISM 1 kit (Life Technologies). Afterwards, samples were sequenced on an ABI 3130xl Genetic Analyzer (Life Technologies) and the chromatograms obtained were edited manually in the SeqMan program (DNASTAR, Madison, WI). Sequence alignment was performed using the CLUSTALW algorithm implemented in the BioEdit package [28]. The obtained sequences were converted to FASTA format and were aligned with sequences representative of each HPgV-1 genotype. From the alignment, sequences were subjected to phylogenetic analysis by the neighbor-joining distance method (NJ). This algorithm provided the corrected genetic distances based on the evolutionary model of Kimura two-parameter (K2P). The confidence test of the generated topology was determined by the calculation of bootstrap values ​​and those ​​greater than 75% were considered significant. A total of 1000 replicates were performed in MEGA 7. The NJ method of phylogenetic reconstruction was chosen because of the greater computational speed. All sequences generated in this study were submitted to GenBank and were assigned the access numbers MH782477-MH782547.

2.4.4. Statistical Analysis

Sociodemographic, behavioral, clinical, and laboratorial variables were analyzed in the statistical software SPSS for Windows v. 21 (IBM Corp., Armonk, NY). The population studied, the positivity for HPgV-1 in ART-naïve samples, the minimum time of HPgV-1 persistence, and the virus circulating genotypes were described using proportions and means. The prevalence of the HPgV-1 and subtypes 2a and 2b in the ART-naïve subjects were compared in relation to the HIV-1 VL and CD4+ T-cell counts with the Mann-Whitney U-Test. The low frequency of HPgV-1 genotypes 1 and 3 prevented their inclusion in the statistical analyses. In order to analyze the influence of HPgV-1 persistence time on the evolution of HIV-1 infection, three categories were created: 0 to 4 years (n = 42), 5 to 8 years (n = 36), and 9 or more years (n = 31). In this case, the analysis of variance (ANOVA) and the Tukey test were used. p-values ≤ 0.05 were considered statistically significant.

3. Results

3.1. General Characteristics of the Study Population

The initial population studied was composed of 110 patients coinfected with HPgV-1/HIV-1. A summary of the sociodemographic and clinical characteristics of the study population can be seen in Table 1. Seventy-five subjects (68.2%) self-declared to be white, 61 (55.5%) were male, 79 (71.8%) were single or without a fixed partner, the mean age was 40.4 years (SD ± 10.4), the average schooling was 7 years (SD ± 3.9), and average monthly income was R$ 1,007.89 (SD ± 885.40). Among the behavioral variables, 97 (88.2%) never used injecting drugs, 67 (60.9%) never used inhaled drugs, 71 (64.5%) had no tattoos, 85 (77.3%) never received transfusion blood, and the average number of partners was 2.6 per year (SD ± 4.1). Regarding clinical and laboratory variables, 91 never had hepatitis, and, among the 19 who had declared previous hepatitis, HCV was the known triggering agent in 10 and HBV in one. The minimum time of HIV-1 diagnosis was on average 8.2 years. The HIV-1 subtypes identified were subtype B (10%), subtype C (25.5%), subtype F1 (1.8%), and recombinant forms (13.6%). The remainder (49.1%) had no previously documented HIV-1 subtyping done.

Variable/categoryN (%)Mean (± SD)

Skin color
 Non-white35 (31.8)-
 White75 (68.2)-
 Female49 (44.5)-
 Male61 (55.5)-
Age (yr) -40.4 (±10.4)
Schooling (yr)-7 (±3.9)
Monthly income-1,007.89 (±885.4)
Marital status
 Married / with a fixed partner31 (28.2)-
 Single / without a fixed partner79 (71.8)-
Number of sexual partners -2.6 (±4.1)
Injecting drug user
 No97 (88.2)-
 Yes13 (11.8)-
Inhaled drug user
 No67 (60.9)-
 Yes43 (39.1)-
 No71 (64.5)-
 Yes39 (35.5)-
Blood transfusion
 No85 (77.3)-
 Yes25 (22.7)-
Hepatitis C virus (anti-HCV+)
 No100 (90.9)-
 Yes10 (9.1)-
Hepatitis B virus (HBsAg+)
 No109 (99.1)-
 Yes1 (0.9)-
Time since HIV-1 diagnosis8.2 (±5.2)
HIV-1 infecting subtype
 B11 (10.0)-
 C28 (25.5)-
 F12 (1.8)-
 Recombinants forms15 (13.6)-
 ND54 (49.1)-

SD, standard deviation; ND, not done.
According to the classification of the Brazilian Institute of Geography and Statistics.
Income in Brazilian reais (R$).
3.2. Molecular Tests

A total of 797 samples were submitted to molecular testing by PCR-nested for HPgV-1. A total of 130 tests were performed during the pilot study and 292 after the pilot study, following the standard strategy established for the tests. Two hundred samples were tested for internal quality control of the positivity range; 105, for quality control for every 10 patients; and 70 tests for the samples from ART-naïve subjects.

3.3. HPgV-1 Genotype Circulation and the Influence on HIV-1 Infection

HPgV-1 genotypes were determined in 71 (64.5%) of the 110 subjects studied. For the remaining 39 subjects, sequence quality was not adequate for phylogenetic analysis. Genotypes 1 (2; 2.8%), 2 (64; 90.1%), and 3 (5; 7%) were found. With respect to genotype 2, 34 (47.9%) were of subtype 2a and 30 (42.3%) were of subtype 2b. Figure 3 illustrates the phylogenetic tree containing the genotypic circulation of the HPgV-1 in the HIV-1 positive population of southerner most Brazil. We observed that individuals infected with HPgV-1 subtype 2b had higher CD4+ T-cell counts (Mann-Whitney U-Test, p = 0.03) and lower HIV-1 VL (Mann-Whitney U-Test, p = 0.04) relative to subtype 2a (Table 2). Figure 4(a) shows the distribution of HIV-1 VL and CD4+ T-cell counts between subjects infected with HPgV-1 subtypes 2a and 2b.

People living with HIV-1Variables
HIV-1 VL CD4+ cell counts
(copies/ml) (cells/mm3)
NMean pMeanp

subtype 2a
subtype 2b


Mann-Whitney U-Test. Mean ranks.
#Statistically significant results are indicated in bold.
3.4. HPgV-1 in ART-Naïve Individuals and the Evolution of HIV-1 Infection

Of the 110 subjects recruited, 70 had samples available while being still ART-naïve. Of these, 40 (57.1%) were positive and 30 (42.9%) were negative for HPgV-1. Molecular positivity was significantly associated with higher CD4+ T-cell counts (Mann-Whitney U-Test, p = 0.02). However, there was no significant difference between groups with respect to mean HIV-1 VL (Mann-Whitney U-Test, p = 0.08) (Table 2). Figure 4(b) shows the distribution of the HIV-1 VL and CD4+ T-cell counts between HPgV-1-positive and negative ART-naïve subjects.

3.5. Time of HPgV-1 Infection and Evolution of HIV-1 Infection

Of the 110 study participants, 109 had a persistent infection, all with a period over 1 year and a mean of 5.93 years (SD ± 3.54). There was no significant difference in the mean HIV-1 VL (ANOVA, p = 0.66) and CD4+ T-cell counts (ANOVA, p = 0.15) among the different groups of HPgV-1 persistence time. Figure 4(c) depicts the distribution of HIV-1 VL and CD4+ T-cell counts between the different groups.

4. Discussion

The present study was the first to determine the genotypic circulation of HPgV-1 in HIV-1-positive individuals at an HIV/AIDS reference center in the extreme south of Brazil. In addition, the HPgV-1 persistence time and its influence on the evolution of HIV-1 infection were estimated.

The results of the phylogenetic analysis revealed the predominance of genotype 2 (subtypes 2a and 2b) in the population studied, while genotypes 1 and 3 were less frequently observed. These findings were similar to those found in other regions of Brazil, which detected the same genotypes in the HIV-1-infected population [10, 29, 30]. Another important observation in this study is that the five individuals coinfected with genotype 3 were infected with HIV-1 subtype C. In addition, in these individuals, HIV-1 infection preceded HPgV-1 infection. Thus, the possibility of HIV-1 subtype C strains acting as a facilitating agent to HPgV-1 genotype 3 infection should be further evaluated. With respect to genotype 2, subtype 2b was associated with an improvement in the prognosis of HIV-1 patients compared to subtype 2a. The median HIV-1 viral load in those infected with HPgV-1 subtype 2b was significantly lower, as were the higher CD4+ T-cell counts. The fact that some HPgV-1 strains influence the clinical course of HIV-1 infection more than others has already been suggested [19, 3133]. Subtype 2b and genotype 5 were already related to higher rates of CD4+ T-cells compared to subtype 2a and genotype 1 [19, 33], and genotype 7 has already been associated with slower progression to AIDS [34]. It is thought that the different HPgV-1 genotypes have different tropisms to the CXCR4 and CCR5 coreceptors used by HIV-1 for entry into host cells, which would be determinant in the evolution of HIV-1 infection [35]. The competition for these coreceptors has also been suggested [36], since both viruses present cell tropism to CD4+ T-cells [37]. Blocking of these coreceptors was also proposed, which would be dependent on the production of cytokines stimulated by HPgV-1 viremia [38, 39].

The present study demonstrated that HPgV-1 establishes a persistent infection in individuals living with HIV-1. Some studies have associated persistent viremia of HPgV-1 with an improvement in the evolution of HIV-1 infection [12, 40]. However, the present study found that persistence does not appear to influence the evolution of HIV-1 infection, since there was no significant difference between median HIV-1 VL and CD4+ T-cell counts in the different groups of HPgV-1 persistence time.

Antiretroviral-naïve HPgV-1/HIV-1-coinfected subjects had higher CD4+ T-cell counts compared to HIV-1-monoinfected individuals. However, after ART initiation, this study did not observe an association between HPgV-1 and the median HIV-1 VL or CD4+ T-cell counts. Some studies have indicated that HPgV-1 may act to reduce T-cell activation [4143], benefiting coinfected individuals even after the introduction of therapy, with a likely synergy between both viruses [15, 42]. The beneficial effects of HPgV-1 have already been associated with other viral infections, such as those with HCV [44] and Ebola [16]. Studying the effects of this viral agent in different populations and understanding its mechanisms of action may be useful in developing novel antiviral therapies.

5. Conclusions

The present study showed that human pegivirus type 1 is a persistent infection in individuals living with HIV-1. It is suggested that the active infection influences the CD4+ T-cell counts of ART-naïve individuals, which could explain the improvement in the prognosis of HIV-1-infected individuals. The data from the present study also suggest that HPgV-1 subtype 2b may be directly related to a better prognosis. In addition, HIV-1 subtype C strains may act as facilitators of genotype 3 HPgV-1 infection. However, further studies are needed to clarify the mechanisms that HPgV-1 uses during infection, whether related to host or viral factors.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Additional Points

Study Limitations. The present study suffers from some important limitations. First, due to the low sample size of HPgV-1 genotypes 1 and 3 present in our study, statistical analysis associations with coinfecting HIV-1 subtype or with modified HIV-1 disease course could not be performed with all HPgV-1 genotypes found. Also, we cannot exclude the possibility that our lack of association between time of HPgV-1 persistence and HIV laboratory markers of disease progression was due to small number of patients when breaking them down into three groups. Studies with larger cohorts may be able to tease out such effect. Finally, we were not able to measure cytokine/chemokine and their receptor levels, which are suggested to explain the effect of HPgV-1 coinfection in HIV+ subjects.

Conflicts of Interest

The authors do not have any conflicts of interest to report.


The authors wish to thank the Infectious Diseases Service and Laboratory of HIV Viral Load and CD4+ T-cells count of HU-FURG for having allowed and approved the conduction of this study and the INCA Oncovirology Program for laboratory support. Financial support was provided by CAPES/CNPq (552361/2011-9 to Ana M. B. Martínez).


  1. M. J. Adams, A. M. Q. King, and E. B. Carstens, “Ratification vote on taxonomic proposals to the International Committee on Taxonomy of Viruses (2013),” Archives of Virology, vol. 158, no. 9, pp. 2023–2030, 2013. View at: Publisher Site | Google Scholar
  2. A. Pavesi, “Origin and evolution of GBV-C/hepatitis G virus and relationships with ancient human migrations,” Journal of Molecular Evolution, vol. 53, no. 2, pp. 104–113, 2001. View at: Publisher Site | Google Scholar
  3. Y. Feng, W. Zhao, Y. Feng et al., “A novel genotype of GB Virus C: its identification and predominance among injecting drug users in Yunnan, China,” PLoS ONE, vol. 6, no. 10, p. e21151, 2011. View at: Publisher Site | Google Scholar
  4. S. Tracy, K. Höfling, S. Pirruccello, P. H. Lane, S. M. Reyna, and C. J. Gauntt, “GBV-C/HGV genotypes: Proposed nomenclature for genotypes 1-5,” Journal of Medical Virology, vol. 62, no. 1, pp. 82-83, 2000. View at: Publisher Site | Google Scholar
  5. E. T. Chivero and J. T. Stapleton, “Tropism of human pegivirus (Formerly known as GB virus C/hepatitis G virus) and host immunomodulation: Insights into a highly successful viral infection,” Journal of General Virology, vol. 96, no. 7, pp. 1521–1532, 2015. View at: Publisher Site | Google Scholar
  6. L. D. Da Mota, A. S. Nishiya, F. Finger-Jardim et al., “Prevalence of human pegivirus (HPgV) infection in patients carrying HIV-1C or non-C in southern Brazil,” Journal of Medical Virology, vol. 88, no. 12, pp. 2106–2114, 2016. View at: Publisher Site | Google Scholar
  7. L. M. Santos, R. C. Lobato, M. F. M. Barral, C. V. Gonçalves, V. P. da Hora, and A. M. B. Martinez, “Prevalence and vertical transmission of human pegivirus among pregnant women infected with HIV,” International Journal of Gynecology and Obstetrics, vol. 138, no. 1, pp. 113–118, 2017. View at: Publisher Site | Google Scholar
  8. H.-H. Feucht, B. Zollner, S. Polywka et al., “Prevalence of hepatitis G viremia among healthy subjects, individuals with liver disease, and persons at risk for parenteral transmission,” Journal of Clinical Microbiology, vol. 35, no. 3, pp. 767-768, 1997. View at: Google Scholar
  9. S. Ramia, J. Mokhbat, A. Sibai, S. Klayme, and R. Naman, “Exposure rates to hepatitis C and G virus infections among HIV-infected patients: Evidence of efficient transmission of HGV by the sexual route,” International Journal of STD & AIDS, vol. 15, no. 7, pp. 463–466, 2004. View at: Publisher Site | Google Scholar
  10. L. A. Oliveira, R. M. Martins, M. A. Carneiro et al., “Prevalence and genotypes of GB Virus C/Hepatitis G virus among blood donors in central Brazil,” Memórias do Instituto Oswaldo Cruz, vol. 97, no. 7, pp. 953–957, 2002. View at: Publisher Site | Google Scholar
  11. L. D. Da Mota, F. Finger-Jardim, C. M. Silva et al., “High prevalence and autochtonous transmission of human pegivirus (HPgV-1) in blood donors in the extreme southern of Brazil,” Journal of Medical Virology, vol. 91, no. 1, pp. 31–37, 2019. View at: Publisher Site | Google Scholar
  12. E. L. Mohr and J. T. Stapleton, “GB virus type C interactions with HIV: The role of envelope glycoproteins,” Journal of Viral Hepatitis, vol. 16, no. 11, pp. 757–768, 2009. View at: Publisher Site | Google Scholar
  13. G. Horemheb-Rubio, P. Ramos-Cervantes, H. Arroyo-Figueroa et al., “High HPgV replication is associated with improved surrogate markers of HIV progression,” PLoS ONE, vol. 12, no. 9, p. e0184494, 2017. View at: Publisher Site | Google Scholar
  14. F. Vahidnia, M. Petersen, G. Rutherford et al., “Transmission of GB virus type C via transfusion in a cohort of HIV-infected patients,” The Journal of Infectious Diseases, vol. 205, no. 9, pp. 1436–1442, 2012. View at: Publisher Site | Google Scholar
  15. D. Ernst, M. Greer, R. Akmatova et al., “Impact of GB virus C viraemia on clinical outcome in HIV-1-infected patients: A 20-year follow-up study,” HIV Medicine, vol. 15, no. 4, pp. 245–250, 2014. View at: Publisher Site | Google Scholar
  16. M. Lauck, A. L. Bailey, K. G. Andersen, T. L. Goldberg, P. C. Sabeti, and D. H. O'Connora, “GB virus C coinfections in West African Ebola patients,” Journal of Virology, vol. 89, no. 4, pp. 2425–2429, 2015. View at: Publisher Site | Google Scholar
  17. M. D. Berzsenyi, D. S. Bowden, H. A. Kelly et al., “Reduction in Hepatitis C-Related Liver Disease Associated With GB Virus C in Human Immunodeficiency Virus Coinfection,” Gastroenterology, vol. 133, no. 6, pp. 1821–1830, 2007. View at: Publisher Site | Google Scholar
  18. R. T. Rydze, N. Bhattarai, and J. T. Stapletone, “GB virus C infection is associated with a reduced rate of reactivation of latent HIV and protection against activation-induced T-cell death,” Antiviral Therapy, vol. 17, no. 7, pp. 1271–1279, 2012. View at: Publisher Site | Google Scholar
  19. A. S. Muerhoff, H. L. Tillmann, M. P. Manns, G. J. Dawson, and S. M. Desai, “GB virus C genotype determination in GB virus-C/HIV co-infected individuals,” Journal of Medical Virology, vol. 70, no. 1, pp. 141–149, 2003. View at: Publisher Site | Google Scholar
  20. A. Fama, J. Xiang, B. K. Link et al., “Human Pegivirus infection and lymphoma risk and prognosis: a North American study,” British Journal of Haematology, vol. 182, no. 5, pp. 644–653, 2018. View at: Publisher Site | Google Scholar
  21. J. C. Arroyave-Ospina, M. F. Caicedo, M. C. Navas, and F. M. Cortés-Mancera, “Human Pegivirus: Pathogenic potential and non-hodgkin lymphoma development risk,” Revista Chilena de Infectologia, vol. 35, no. 2, pp. 164–175, 2018. View at: Publisher Site | Google Scholar
  22. J. D. Kriesel, M. R. Hobbs, B. B. Jones, B. Milash, R. M. Nagra, and K. F. Fischer, “Deep sequencing for the detection of virus-like sequences in the brains of patients with multiple sclerosis: Detection of GBV-C in human brain,” PLoS ONE, vol. 7, no. 3, Article ID e31886, 2012. View at: Google Scholar
  23. H. Fridholm, L. Østergaard Sørensen, M. W. Rosenstierne et al., “Human pegivirus detected in a patient with severe encephalitis using a metagenomic pan-virus array,” Journal of Clinical Virology, vol. 77, pp. 5–8, 2016. View at: Publisher Site | Google Scholar
  24. Brazil, Ministry of Health, Epidemiological Bulletin of Viral Hepatitis, 2017.
  25. H. L. Tillmann and M. P. Manns, “GB virus-C infection in patients infected with the human immunodeficiency virus,” Antiviral Research, vol. 52, no. 2, pp. 83–90, 2001. View at: Publisher Site | Google Scholar
  26. J. T. Stapleton, “GB virus type C/hepatitis G virus,” Seminars in Liver Disease, vol. 23, no. 2, pp. 137–148, 2003. View at: Publisher Site | Google Scholar
  27. L. M. Jarvis, F. Davidson, J. P. Hanley, P. L. Yap, C. A. Ludlam, and P. Simmonds, “Infection with hepatitis G virus among recipients of plasma products,” The Lancet, vol. 348, no. 9038, pp. 1352–1355, 1996. View at: Publisher Site | Google Scholar
  28. T. A. Hall, “BioEdit: a user-friendly biological sequence alignmente ditor and analysis program for windows 95/98/NT,” Nucleic Acids Symposium Series, vol. 41, pp. 95–98, 1999. View at: Google Scholar
  29. M. T. Giret, J. L. Miraglia, M. C. Sucupira et al., “Prevalence, incidence density, and genotype distribution of GB virus C infection in a cohort of recently HIV-1-infected subjects in Sao Paulo, Brazil,” PLoS ONE, vol. 6, no. 4, p. e18407, 2011. View at: Publisher Site | Google Scholar
  30. S. N. Slavov, R. M. Silveira, E. S. Rodrigues et al., “Human pegivirus-1 (HPgV-1, GBV-C) RNA prevalence and genotype diversity among volunteer blood donors from an intra-hospital hemotherapy service in southern Brazil,” Transfusion and Apheresis Science, vol. 58, no. 2, pp. 174–178, 2019. View at: Publisher Site | Google Scholar
  31. C. Schwarze-Zander, J. T. Blackard, H. Zheng et al., “GB virus C (GBV-C) infection in hepatitis C virus (HCY)/HIV-coinfected patients receiving HCV treatment: Importance of the GBV-C genotype,” The Journal of Infectious Diseases, vol. 194, no. 4, pp. 410–419, 2006. View at: Publisher Site | Google Scholar
  32. Q. Chang, J. H. McLinden, J. T. Stapleton, M. A. Sathar, and J. Xiang, “Expression of GB virus C NS5A protein from genotypes 1, 2, 3 and 5 and a 30 aa NS5A fragment inhibit human immunodeficiency virus type 1 replication in a CD4+ T-lymphocyte cell line,” Journal of General Virology, vol. 88, no. 12, pp. 3341–3346, 2007. View at: Publisher Site | Google Scholar
  33. K. F. N’Guessan, M. Anderson, B. Phinius et al., “The impact of human pegivirus on CD4 cell count in HIV-positive persons in Botswana,” Open Forum Infectious Diseases, vol. 4, no. 4, p. ofx222, 2017. View at: Publisher Site | Google Scholar
  34. Z. Miao, L. Gao, Y. Song et al., “Prevalence and clinical impact of human pegivirus-1 infection in HIV-1-infected individuals in Yunnan, China,” Viruses, vol. 9, no. 2, 2017. View at: Google Scholar
  35. T. Ruegamer, R. Hoffmann, A. Rohrhofer et al., “Inhibition of HIV-1 infection by HPgV-1 derived peptides is affected by HPgV-1 genotype and HIV-1 coreceptor tropism,” AIDS, 2018. View at: Publisher Site | Google Scholar
  36. J. Xiang, S. Wunschmann, D. J. Diekema et al., “Effect of coinfection with GB virus C on survival among patients with HIV infection,” The New England Journal of Medicine, vol. 345, no. 10, pp. 707–714, 2001. View at: Publisher Site | Google Scholar
  37. E. T. Chivero, N. Bhattarai, J. H. McLinden, J. Xiang, and J. T. Stapleton, “Human Pegivirus (HPgV; formerly known as GBV-C) inhibits IL-12 dependent natural killer cell function,” Virology, vol. 485, pp. 116–127, 2015. View at: Publisher Site | Google Scholar
  38. J. Nattermann, H.-D. Nischalke, B. Kupfer et al., “Regulation of CC chemokine receptor 5 in hepatitis G virus infection,” AIDS, vol. 17, no. 10, pp. 1457–1462, 2003. View at: Publisher Site | Google Scholar
  39. J. Xiang, S. L. George, S. Wünschmann, Q. Chang, D. Klinzman, and J. T. Stapleton, “Inhibition of HIV-1 replication by GB virus C infection through increases in RANTES, MIP-1α, MIP-1β, and SDF-1,” The Lancet, vol. 363, no. 9426, pp. 2040–2046, 2004. View at: Publisher Site | Google Scholar
  40. M. T. Maidana Giret and E. G. Kallas, “GBV-C: State of the art and future prospects,” Current HIV/AIDS Reports, vol. 9, no. 1, pp. 26–33, 2012. View at: Publisher Site | Google Scholar
  41. M. Moenkemeyer, R. E. Schmidt, H. Wedemeyer, H. L. Tillmann, and H. Heiken, “GBV-C coinfection is negatively correlated to Fas expression and Fas-mediated apoptosis in HIV-1 infected patients,” Journal of Medical Virology, vol. 80, no. 11, pp. 1933–1940, 2008. View at: Publisher Site | Google Scholar
  42. J. T. Stapleton, K. Chaloner, J. A. Martenson et al., “GB Virus C infection is associated with altered lymphocyte subset distribution and reduced t cell activation and proliferation in hiv-infected individuals,” PLoS ONE, vol. 7, no. 11, Article ID e50563, 2012. View at: Publisher Site | Google Scholar
  43. B. K. B. de Miranda, K. S. G. de Sá, A. N. R. da Silva et al., “GBV-C/HIV-1 coinfection is associated with low HIV-1 viral load and high CD4+ T lymphocyte count,” Archives of Virology, vol. 162, no. 11, pp. 3431–3438, 2017. View at: Publisher Site | Google Scholar
  44. Y. Feng, L. Liu, Y. M. Feng et al., “GB virus C infection in patients with HIV/hepatitis C virus coinfection: improvement of the liver function in chronic hepatitis C,” Hepatitis Monthly, vol. 14, no. 3, Article ID e14169, 2014. View at: Publisher Site | Google Scholar

Copyright © 2019 Luísa D. Da Mota et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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