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- Open Access
Acute and chronic infections with nonprimate hepacivirus in young horses
Veterinary Research volume 47, Article number: 97 (2016)
The recently discovered nonprimate hepacivirus (NPHV) naturally infects horses and is the closest known homolog of hepatitis C virus to date. Within a follow-up study acute field infections were monitored in four young Thoroughbred horses until the ages of 12–13 months. Serum samples were analyzed for the presence of NPHV RNA and anti-NPHV NS3 antibodies and liver specific parameters were evaluated. The four young horses were not able to clear infection, but remained chronically infected for the entire monitored time period despite the presence of NPHV specific antibodies.
Nonprimate hepacivirus (NPHV) was described to infect horses in several countries worldwide and represents a new member within the family Flaviviridae, genus Hepacivirus [1, 2]. Among all hepaciviruses, NPHV is the closest known homolog of hepatitis C virus (HCV) to date. HCV is a major human pathogen with approximately 146 million people infected worldwide . In 75–85% of acutely infected patients progression to chronic disease occurs, which can lead to hepatic fibrosis, cirrhosis and carcinoma . In recent years, similar as well as distinct features between HCV and NPHV have been described. NPHV is highly prevalent in horses with 30–40% seropositivity and 3% viremia [1, 5–10]. However, disease association remains uncertain although several studies reported subclinical hepatitis in infected horses. A mild elevation of serum liver enzymes was observed at seroconversion in some affected horses, although in most horses serum liver enzymes remained within the reference range [7, 11, 12]. Single reports exist about NPHV infected horses suffering from severe hepatitis. Yet, a causative relationship still needs to be confirmed [12, 13]. Comparable to HCV infection, hepatotropism has been confirmed for NPHV [11, 14]. Nevertheless, the routes of NPHV transmission remain mostly unclear. Similar to HCV a parenteral infection route via direct blood–blood contact has been described in horses by experimental inoculation with infectious plasma containing NPHV . In a recent study, we investigated twenty mare-foal pairs at parturition until 6 months postpartum and could show the occurrence of vertical transmission of NPHV at parturition . Moreover, we observed transmission of NPHV isolates within the respective pasture herds indicating the possibility of a direct transmission between horses. Interestingly, we could show that several foals became viremic within the first 6 months of life . To shed some light on the course of naturally acquired NPHV infection of the young horses, we aimed to perform a follow-up study by monitoring four foals (foal # 9, # 10, # 17 and # 19) until the age of 12–13 months.
Materials, methods and results
Blood samples were taken from these four foals at indicated time points (Figure 1; Table 1). All samples were obtained with full owner consent as part of routine health management. Additionally, a general examination of the foals was conducted at all investigated time points. Next, sera was analyzed for the presence of NPHV RNA and anti-NPHV NS3 antibodies by a SYBR Green based quantitative real-time PCR (qRT-PCR) and luciferase immunoprecipitation assay (LIPS), respectively, as described earlier [1, 11, 15]. As shown in Figure 1, NPHV RNA was detected in the serum of all foals 6 months after birth. From the initial virus detection onwards the four acutely infected young horses remained viremic with high viral loads during the entire monitored 7 months and none of them eliminated the virus until the last sampling at the age of 12–13 months (Figure 1A–D). For the foals # 9, # 10 and # 19 anti-NPHV NS3 antibodies were detected at the time point of birth, decreased until 6 months postpartum below or close to the cut-off of the assay and NPHV specific antibodies appeared again after NPHV RNA was detected in the serum (Figure 1A, B and D). Of note, foal # 17 was the only foal not receiving maternal anti-NPHV NS3 antibodies after foaling and became newly infected at a similar age as the remaining foals and production of anti-NPHV NS3 antibodies was observed from the age of 10 months onwards (Figure 1C). In Table 1 details on the NPHV RNA and anti-NPHV NS3 antibody status of the follow-up samples of the four horses are given (Table 1).
To investigate the clinical relevance of NPHV infection for liver disease, the horses were clinically examined and blood was analyzed for the liver specific enzymes glutamate dehydrogenase (GLDH), γ-glutamyl-transferase (GGT) and aspartate aminotransferase (AST) in the laboratory of the small animal clinic at the University of Veterinary Medicine Hannover, Foundation. Results for each sampling time point are shown in Figure 1, lower panels. A mild elevation of liver enzymes was observed at the age of 12–13 months for foals # 9, # 17, and # 19. However, values of all other time points remained within the reference range and no clinical signs indicating liver disease were found at any sampling time point.
In conclusion, four acutely infected foals developed chronic infection and remained viremic with high viral loads during the entire monitored 7 months. Despite the presence of anti-NPHV NS3 antibodies, the four young horses were not able to clear the infection within the monitored time period.
This study provides the first description of the clinical course of naturally acquired NPHV infection in young horses. This follow-up study was conducted in the context of a previous study investigating the occurrence of vertical transmission of NPHV in a horse cohort, where we monitored twenty Thoroughbred broodmares and their foals from parturition until 6 months after foaling . Here, we monitored four of these foals for another 7 months. These foals became NPHV RNA positive at the age of 6 months and stayed viremic for another 7 months with the concurrent detection of anti-NPHV NS3 antibodies. The activity of liver specific enzymes increased in three foals at the ages of 12–13 months. The mild elevation of enzyme activity could indicate a subclinical hepatitis due to the persistent NPHV infection. For reliable diagnosis liver biopsies would be required, since the elevation of liver enzymes might have had an unrelated reason.
In a retrospective study Matsuu et al. also detected NPHV infections in 5 out of 7 young horses aged between 4 and 6 months and 2 years , supporting the time of infection in our foals. In three foals (foal # 9, # 10, and # 19) maternal anti-NPHV NS3 antibodies were detected after birth until three to 6 months postpartum (Figures 1A, B and D). One could speculate that after degradation of maternal antibodies, the foals are more susceptible to a NPHV infection. However, foal # 17 did not receive protection by maternal antibodies, yet it became infected at the same age as the three other foals. Moreover, it is not clear whether the maternal antibodies protect against a NPHV infection. So far, the course of infection for NPHV in young horses has only been described by Ramsay et al. who experimentally infected two foals at the age of 2–4 weeks and monitored them for more than 1 year post-infection . These foals became viremic shortly after inoculation and remained persistently infected for the entire monitored 63 weeks. Anti-NPHV antibodies were detected from the age of approximately 8 weeks onwards and peaked 23 weeks post-infection. In the following weeks, the detection of antibodies decreased in parallel with the viral loads that sharply declined from 40 weeks post-infection onwards. Interestingly, in our study four naturally infected foals also remained persistently infected during the entire monitored time with high viral loads and were not able to clear the infection despite the presence of antibodies from the age of 7 to 9 months onwards. The reason for the inability of the four young horses to eliminate NPHV remains unclear. The development of the immune system of young horses is only partially understood. It is known, that the onset of the adaptive immune response is delayed and antibody responses of type IgG4, IgG7 and IgE as well as T cell and cytokine responses slowly evolve within the first year of life . However, to understand the complex interaction of NPHV and the equine immune system, further research is required. It has been shown, that adult horses are often able to clear NPHV infection within 2 months after acute infection although persistently infected horses have also been described analogous to chronic HCV infection in humans [11, 12].
In conclusion, in four young horses the NPHV field infection progressed from acute to chronic infection. The four horses were not able to clear NPHV until the ages of 12–13 months despite the presence of antibodies for several months.
aspartate amino transferase
hepatitis C virus
luciferase immunoprecipitation system
- NS 3:
nonstructural protein 3
relative light units
quantitative real-time polymerase chain reaction
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The authors declare that they have no competing interests.
All authors participated in the design of the study. TG conducted the experiments, analyzed the data and prepared the manuscript. SW, SP, DT, KF, ES and JMVC have revised the manuscript and coordinated the research. All authors read and approved the final manuscript.
We are grateful to Stiftung Gestüt Fährhof, especially to Stefan Ullrich and David Sachs, for their great support of our study. We also thank Peter D. Burbelo (NIH, Maryland, USA) for providing the Renilla-luciferase-NS3 fusion plasmid and all members of the Institute of Experimental Virology, Twincore, for helpful suggestions and discussions. We are also thankful to Anja Seemann-Jensen and Christiane Richter for technical support.
ES was supported by the Helmholtz Centre for Infection Research and TG received financial support from a stipend of the Clinic for Horses, University of Veterinary Medicine Hannover.
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Gather, T., Walter, S., Pfaender, S. et al. Acute and chronic infections with nonprimate hepacivirus in young horses. Vet Res 47, 97 (2016). https://doi.org/10.1186/s13567-016-0381-6
- High Viral Load
- Sampling Time Point
- Maternal Antibody
- Mild Elevation
- Field Infection