The course of hepatitis E virus infection in pigs after contact-infection and intravenous inoculation
<p>Abstract</p> <p>Background</p> <p>Worldwide, hepatitis E virus (HEV) genotype 3 is observed in pigs and transmission to humans is implied. To be able to estimate public health risks from <it>e.g</it>. contact with pigs or consumption of pork products, the...
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doaj-068e93b4568247678754d7b92b5edb9a2020-11-24T22:36:36ZengBMCBMC Veterinary Research1746-61482009-02-0151710.1186/1746-6148-5-7The course of hepatitis E virus infection in pigs after contact-infection and intravenous inoculationde Jong Mart CMFrankena KlaasStockhofe-Zurwieden NorbertReusken Chantal BEMRutjes Saskia ABouwknegt Martijnde Roda Husman Ana Mariavan der Poel Wim HM<p>Abstract</p> <p>Background</p> <p>Worldwide, hepatitis E virus (HEV) genotype 3 is observed in pigs and transmission to humans is implied. To be able to estimate public health risks from <it>e.g</it>. contact with pigs or consumption of pork products, the transmission routes and dynamics of infection should be identified. Hence, the course of HEV-infection in naturally infected pigs should be studied.</p> <p>Results</p> <p>To resemble natural transmission, 24 HEV-susceptible pigs were infected either by one-to-one exposure to intravenously inoculated pigs (C1-pigs; n = 10), by one-to-one exposure to contact-infected pigs (C2-pigs: n = 7; C3-pigs: n = 5) or due to an unknown non-intravenous infection route (one C2-pig and one C3-pig). The course of HEV-infection for contact-infected pigs was characterized by: faecal HEV RNA excretion that started at day 7 (95% confidence interval: 5–10) postexposure and lasted 23 (19–28) days; viremia that started after 13 (8–17) days of faecal HEV RNA excretion and lasted 11 (8–13) days; antibody development that was detected after 13 (10–16) days of faecal HEV RNA excretion. The time until onset of faecal HEV RNA excretion and onset of viremia was significantly shorter for <it>iv</it>-pigs compared to contact-infected pigs, whereas the duration of faecal HEV RNA excretion was significantly longer. At 28 days postinfection HEV RNA was detected less frequently in organs of contact-infected pigs compared to <it>iv</it>-pigs. For contact-infected pigs, HEV RNA was detected in 20 of 39 muscle samples that were proxies for pork at retail and in 4 of 7 urine samples.</p> <p>Conclusion</p> <p>The course of infection differed between infection routes, suggesting that contact-infection could be a better model for natural transmission than <it>iv </it>inoculation. Urine and meat were identified as possible HEV-sources for pig-to-pig and pig-to-human HEV transmission.</p> http://www.biomedcentral.com/1746-6148/5/7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
de Jong Mart CM Frankena Klaas Stockhofe-Zurwieden Norbert Reusken Chantal BEM Rutjes Saskia A Bouwknegt Martijn de Roda Husman Ana Maria van der Poel Wim HM |
spellingShingle |
de Jong Mart CM Frankena Klaas Stockhofe-Zurwieden Norbert Reusken Chantal BEM Rutjes Saskia A Bouwknegt Martijn de Roda Husman Ana Maria van der Poel Wim HM The course of hepatitis E virus infection in pigs after contact-infection and intravenous inoculation BMC Veterinary Research |
author_facet |
de Jong Mart CM Frankena Klaas Stockhofe-Zurwieden Norbert Reusken Chantal BEM Rutjes Saskia A Bouwknegt Martijn de Roda Husman Ana Maria van der Poel Wim HM |
author_sort |
de Jong Mart CM |
title |
The course of hepatitis E virus infection in pigs after contact-infection and intravenous inoculation |
title_short |
The course of hepatitis E virus infection in pigs after contact-infection and intravenous inoculation |
title_full |
The course of hepatitis E virus infection in pigs after contact-infection and intravenous inoculation |
title_fullStr |
The course of hepatitis E virus infection in pigs after contact-infection and intravenous inoculation |
title_full_unstemmed |
The course of hepatitis E virus infection in pigs after contact-infection and intravenous inoculation |
title_sort |
course of hepatitis e virus infection in pigs after contact-infection and intravenous inoculation |
publisher |
BMC |
series |
BMC Veterinary Research |
issn |
1746-6148 |
publishDate |
2009-02-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Worldwide, hepatitis E virus (HEV) genotype 3 is observed in pigs and transmission to humans is implied. To be able to estimate public health risks from <it>e.g</it>. contact with pigs or consumption of pork products, the transmission routes and dynamics of infection should be identified. Hence, the course of HEV-infection in naturally infected pigs should be studied.</p> <p>Results</p> <p>To resemble natural transmission, 24 HEV-susceptible pigs were infected either by one-to-one exposure to intravenously inoculated pigs (C1-pigs; n = 10), by one-to-one exposure to contact-infected pigs (C2-pigs: n = 7; C3-pigs: n = 5) or due to an unknown non-intravenous infection route (one C2-pig and one C3-pig). The course of HEV-infection for contact-infected pigs was characterized by: faecal HEV RNA excretion that started at day 7 (95% confidence interval: 5–10) postexposure and lasted 23 (19–28) days; viremia that started after 13 (8–17) days of faecal HEV RNA excretion and lasted 11 (8–13) days; antibody development that was detected after 13 (10–16) days of faecal HEV RNA excretion. The time until onset of faecal HEV RNA excretion and onset of viremia was significantly shorter for <it>iv</it>-pigs compared to contact-infected pigs, whereas the duration of faecal HEV RNA excretion was significantly longer. At 28 days postinfection HEV RNA was detected less frequently in organs of contact-infected pigs compared to <it>iv</it>-pigs. For contact-infected pigs, HEV RNA was detected in 20 of 39 muscle samples that were proxies for pork at retail and in 4 of 7 urine samples.</p> <p>Conclusion</p> <p>The course of infection differed between infection routes, suggesting that contact-infection could be a better model for natural transmission than <it>iv </it>inoculation. Urine and meat were identified as possible HEV-sources for pig-to-pig and pig-to-human HEV transmission.</p> |
url |
http://www.biomedcentral.com/1746-6148/5/7 |
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