Experimental Infections of Pigs with Japanese Encephalitis Virus Genotype 4

The emergence of Japanese encephalitis virus (JEV) in eastern Australia in 2022 caused extensive reproductive disease in pigs and is a threat to public health. Groups of weaned piglets were experimentally infected with the Australian outbreak strain of JEV (genotype 4). All pigs challenged at 5 week...

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Main Authors: Paul M. Hick, Deborah S. Finlaison, Kate Parrish, Xingnian Gu, Philip Hayton, Tiffany O’Connor, Andrew Read, Jing Zhang, Zoe B. Spiers, Pedro Pinczowski, Angel L. Ngo, Peter D. Kirkland
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Language:English
Published: MDPI AG 2024-10-01
Series:Microorganisms
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Online Access:https://www.mdpi.com/2076-2607/12/11/2163
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author Paul M. Hick
Deborah S. Finlaison
Kate Parrish
Xingnian Gu
Philip Hayton
Tiffany O’Connor
Andrew Read
Jing Zhang
Zoe B. Spiers
Pedro Pinczowski
Angel L. Ngo
Peter D. Kirkland
author_facet Paul M. Hick
Deborah S. Finlaison
Kate Parrish
Xingnian Gu
Philip Hayton
Tiffany O’Connor
Andrew Read
Jing Zhang
Zoe B. Spiers
Pedro Pinczowski
Angel L. Ngo
Peter D. Kirkland
author_sort Paul M. Hick
collection DOAJ
description The emergence of Japanese encephalitis virus (JEV) in eastern Australia in 2022 caused extensive reproductive disease in pigs and is a threat to public health. Groups of weaned piglets were experimentally infected with the Australian outbreak strain of JEV (genotype 4). All pigs challenged at 5 weeks of age were infected after an intradermal injection of 1 × 10<sup>5.5</sup> (<i>n</i> = 4) or 1 × 10<sup>4.5</sup> TCID<sub>50</sub>/pig (<i>n</i> = 5). Intranasal instillation was less effective at this age, infecting 3/4 pigs with the same higher dose and 1/5 with the lower dose. Intradermal injection using 1 × 10<sup>5.0</sup> TCID<sub>50</sub>/pig also infected 9/9 pigs at 11 weeks of age. Infection in all cases was confirmed by qRT-PCR of blood samples, which identified a viremia peak at 3–4 days and detected JEV-specific antibodies as early as 5 days after the challenge. The detection of JEV in oral and nasal swabs and in saliva from chew ropes was less consistent. JEV was detected in the tonsils of 21/22 infected pigs and was isolated from the tonsils of 9/9 pigs sampled 19 days after the challenge at 11 weeks of age. The infected pigs showed no clinical signs other than pyrexia on Days 4–6. Histopathology consistent with JEV infection was evident in the nervous tissues of all but two pigs sampled 28 days after the challenge and was characterized by meningitis, encephalitis and gliosis throughout the brain. Serological studies showed extensive cross-reactivity between JEV and Murray Valley encephalitis virus using blocking ELISAs. However, the determination of limiting-dilution titres allowed for the identification of the infecting virus. This in vivo infection model will be useful in evaluating JEV vaccines and for comparative pathogenesis studies with other JEV genotypes.
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spelling doaj-art-4a04e1dcfe4c45f2800d8dd4cb17aec22025-08-20T01:53:57ZengMDPI AGMicroorganisms2076-26072024-10-011211216310.3390/microorganisms12112163Experimental Infections of Pigs with Japanese Encephalitis Virus Genotype 4Paul M. Hick0Deborah S. Finlaison1Kate Parrish2Xingnian Gu3Philip Hayton4Tiffany O’Connor5Andrew Read6Jing Zhang7Zoe B. Spiers8Pedro Pinczowski9Angel L. Ngo10Peter D. Kirkland11Virology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaVirology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaVirology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaVirology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaVirology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaVirology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaVirology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaVirology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaVeterinary Pathology Services, Elizabeth Macarthur Agriculture Institute, Menangle, NSW 2568, AustraliaVeterinary Pathology Services, Elizabeth Macarthur Agriculture Institute, Menangle, NSW 2568, AustraliaVeterinary Pathology Services, Elizabeth Macarthur Agriculture Institute, Menangle, NSW 2568, AustraliaVirology Laboratory, Elizabeth Macarthur Agriculture Institute, New South Wales Department of Primary Industries and Regional Development, Menangle, NSW 2568, AustraliaThe emergence of Japanese encephalitis virus (JEV) in eastern Australia in 2022 caused extensive reproductive disease in pigs and is a threat to public health. Groups of weaned piglets were experimentally infected with the Australian outbreak strain of JEV (genotype 4). All pigs challenged at 5 weeks of age were infected after an intradermal injection of 1 × 10<sup>5.5</sup> (<i>n</i> = 4) or 1 × 10<sup>4.5</sup> TCID<sub>50</sub>/pig (<i>n</i> = 5). Intranasal instillation was less effective at this age, infecting 3/4 pigs with the same higher dose and 1/5 with the lower dose. Intradermal injection using 1 × 10<sup>5.0</sup> TCID<sub>50</sub>/pig also infected 9/9 pigs at 11 weeks of age. Infection in all cases was confirmed by qRT-PCR of blood samples, which identified a viremia peak at 3–4 days and detected JEV-specific antibodies as early as 5 days after the challenge. The detection of JEV in oral and nasal swabs and in saliva from chew ropes was less consistent. JEV was detected in the tonsils of 21/22 infected pigs and was isolated from the tonsils of 9/9 pigs sampled 19 days after the challenge at 11 weeks of age. The infected pigs showed no clinical signs other than pyrexia on Days 4–6. Histopathology consistent with JEV infection was evident in the nervous tissues of all but two pigs sampled 28 days after the challenge and was characterized by meningitis, encephalitis and gliosis throughout the brain. Serological studies showed extensive cross-reactivity between JEV and Murray Valley encephalitis virus using blocking ELISAs. However, the determination of limiting-dilution titres allowed for the identification of the infecting virus. This in vivo infection model will be useful in evaluating JEV vaccines and for comparative pathogenesis studies with other JEV genotypes.https://www.mdpi.com/2076-2607/12/11/2163Japanese encephalitis virus genotype 4viremiaserologyinfection modelswinepathogenesis
spellingShingle Paul M. Hick
Deborah S. Finlaison
Kate Parrish
Xingnian Gu
Philip Hayton
Tiffany O’Connor
Andrew Read
Jing Zhang
Zoe B. Spiers
Pedro Pinczowski
Angel L. Ngo
Peter D. Kirkland
Experimental Infections of Pigs with Japanese Encephalitis Virus Genotype 4
Microorganisms
Japanese encephalitis virus genotype 4
viremia
serology
infection model
swine
pathogenesis
title Experimental Infections of Pigs with Japanese Encephalitis Virus Genotype 4
title_full Experimental Infections of Pigs with Japanese Encephalitis Virus Genotype 4
title_fullStr Experimental Infections of Pigs with Japanese Encephalitis Virus Genotype 4
title_full_unstemmed Experimental Infections of Pigs with Japanese Encephalitis Virus Genotype 4
title_short Experimental Infections of Pigs with Japanese Encephalitis Virus Genotype 4
title_sort experimental infections of pigs with japanese encephalitis virus genotype 4
topic Japanese encephalitis virus genotype 4
viremia
serology
infection model
swine
pathogenesis
url https://www.mdpi.com/2076-2607/12/11/2163
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