Attempt to Isolate Elephant Endotheliotropic Herpesvirus (EEHV) Using a Continuous Cell Culture System

Elephant endotheliotropic herpesvirus (EEHV) infection is known to cause acute fatal hemorrhagic disease, which has killed many young Asian elephants (<i>Elephas maximus</i>). Until recently, in vitro isolation and propagation of the virus have not been successful. This study aimed to is...

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Main Authors: Kornravee Photichai, Thunyamas Guntawang, Tidaratt Sittisak, Varankpicha Kochagul, Phongsakorn Chuammitri, Chatchote Thitaram, Hathairat Thananchai, Teera Chewonarin, Korawan Sringarm, Kidsadagon Pringproa
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:Animals
Subjects:
Online Access:https://www.mdpi.com/2076-2615/10/12/2328
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spelling doaj-02e8f204e2c649b6bc5d4e0f03082fec2020-12-08T00:04:57ZengMDPI AGAnimals2076-26152020-12-01102328232810.3390/ani10122328Attempt to Isolate Elephant Endotheliotropic Herpesvirus (EEHV) Using a Continuous Cell Culture SystemKornravee Photichai0Thunyamas Guntawang1Tidaratt Sittisak2Varankpicha Kochagul3Phongsakorn Chuammitri4Chatchote Thitaram5Hathairat Thananchai6Teera Chewonarin7Korawan Sringarm8Kidsadagon Pringproa9Department of Veterinary Biosciences and Veterinary Public Health, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, ThailandDepartment of Veterinary Biosciences and Veterinary Public Health, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, ThailandDepartment of Veterinary Biosciences and Veterinary Public Health, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, ThailandVeterinary Diagnostic Laboratory, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, ThailandDepartment of Veterinary Biosciences and Veterinary Public Health, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, ThailandDepartment of Companion Animals and Wildlife Clinics, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, ThailandDepartment of Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Animal and Aquatic Sciences, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Veterinary Biosciences and Veterinary Public Health, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, ThailandElephant endotheliotropic herpesvirus (EEHV) infection is known to cause acute fatal hemorrhagic disease, which has killed many young Asian elephants (<i>Elephas maximus</i>). Until recently, in vitro isolation and propagation of the virus have not been successful. This study aimed to isolate and propagate EEHV using continuous cell lines derived from human and/or animal origins. Human cell lines, including EA. hy926, A549, U937, RKO, SW620, HCT-116 and HT-29, and animal cell lines, including CT26.CL25 and sp2/0-Ag14, were investigated in this study. Mixed frozen tissue samples of the heart, lung, liver, spleen and kidney obtained from fatal EEHV1A- or EEHV4-infected cases were homogenized and used for cell inoculation. At 6, 24, 48 and 72 h post infection (hpi), EEHV-inoculated cells were observed for cytopathic effects (CPEs) or were assessed for EEHV infection by immunoperoxidase monolayer assay (IPMA) or quantitative PCR. The results were then compared to those of the mock-infected controls. Replication of EEHV in the tested cells was further determined by immunohistochemistry of cell pellets using anti-EEHV DNA polymerase antibodies or re-inoculated cells with supernatants obtained from passages 2 or 3 of the culture medium. The results reveal that no CPEs were observed in the tested cells, while immunolabeling for EEHV gB was observed in only U937 human myeloid leukemia cells. However, quantitation values of the EEHV terminase gene, as well as those of the EEHV gB or EEHV DNA polymerase proteins in U937 cells, gradually declined from passage 1 to passage 3. The findings of this study indicate that despite poor adaptation in U937 cells, this cell line displays promise and potential to be used for the isolation of EEHV1 and EEHV4 in vitro.https://www.mdpi.com/2076-2615/10/12/2328elephant endotheliotropic herpesvirusisolationcell culturein vitro
collection DOAJ
language English
format Article
sources DOAJ
author Kornravee Photichai
Thunyamas Guntawang
Tidaratt Sittisak
Varankpicha Kochagul
Phongsakorn Chuammitri
Chatchote Thitaram
Hathairat Thananchai
Teera Chewonarin
Korawan Sringarm
Kidsadagon Pringproa
spellingShingle Kornravee Photichai
Thunyamas Guntawang
Tidaratt Sittisak
Varankpicha Kochagul
Phongsakorn Chuammitri
Chatchote Thitaram
Hathairat Thananchai
Teera Chewonarin
Korawan Sringarm
Kidsadagon Pringproa
Attempt to Isolate Elephant Endotheliotropic Herpesvirus (EEHV) Using a Continuous Cell Culture System
Animals
elephant endotheliotropic herpesvirus
isolation
cell culture
in vitro
author_facet Kornravee Photichai
Thunyamas Guntawang
Tidaratt Sittisak
Varankpicha Kochagul
Phongsakorn Chuammitri
Chatchote Thitaram
Hathairat Thananchai
Teera Chewonarin
Korawan Sringarm
Kidsadagon Pringproa
author_sort Kornravee Photichai
title Attempt to Isolate Elephant Endotheliotropic Herpesvirus (EEHV) Using a Continuous Cell Culture System
title_short Attempt to Isolate Elephant Endotheliotropic Herpesvirus (EEHV) Using a Continuous Cell Culture System
title_full Attempt to Isolate Elephant Endotheliotropic Herpesvirus (EEHV) Using a Continuous Cell Culture System
title_fullStr Attempt to Isolate Elephant Endotheliotropic Herpesvirus (EEHV) Using a Continuous Cell Culture System
title_full_unstemmed Attempt to Isolate Elephant Endotheliotropic Herpesvirus (EEHV) Using a Continuous Cell Culture System
title_sort attempt to isolate elephant endotheliotropic herpesvirus (eehv) using a continuous cell culture system
publisher MDPI AG
series Animals
issn 2076-2615
publishDate 2020-12-01
description Elephant endotheliotropic herpesvirus (EEHV) infection is known to cause acute fatal hemorrhagic disease, which has killed many young Asian elephants (<i>Elephas maximus</i>). Until recently, in vitro isolation and propagation of the virus have not been successful. This study aimed to isolate and propagate EEHV using continuous cell lines derived from human and/or animal origins. Human cell lines, including EA. hy926, A549, U937, RKO, SW620, HCT-116 and HT-29, and animal cell lines, including CT26.CL25 and sp2/0-Ag14, were investigated in this study. Mixed frozen tissue samples of the heart, lung, liver, spleen and kidney obtained from fatal EEHV1A- or EEHV4-infected cases were homogenized and used for cell inoculation. At 6, 24, 48 and 72 h post infection (hpi), EEHV-inoculated cells were observed for cytopathic effects (CPEs) or were assessed for EEHV infection by immunoperoxidase monolayer assay (IPMA) or quantitative PCR. The results were then compared to those of the mock-infected controls. Replication of EEHV in the tested cells was further determined by immunohistochemistry of cell pellets using anti-EEHV DNA polymerase antibodies or re-inoculated cells with supernatants obtained from passages 2 or 3 of the culture medium. The results reveal that no CPEs were observed in the tested cells, while immunolabeling for EEHV gB was observed in only U937 human myeloid leukemia cells. However, quantitation values of the EEHV terminase gene, as well as those of the EEHV gB or EEHV DNA polymerase proteins in U937 cells, gradually declined from passage 1 to passage 3. The findings of this study indicate that despite poor adaptation in U937 cells, this cell line displays promise and potential to be used for the isolation of EEHV1 and EEHV4 in vitro.
topic elephant endotheliotropic herpesvirus
isolation
cell culture
in vitro
url https://www.mdpi.com/2076-2615/10/12/2328
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