A Longitudinal Study of Hematology and Stress Biomarker Profiles in Young Asian Elephants (Elephas Maximus) in Relation to Elephant Endotheliotropic Herpesvirus (EEHV) in Thailand
Elephant endotheliotropic herpesvirus hemorrhagic disease (EEHV-HD) is a virulent disease that causes severe hemorrhage and sudden death in Asian elephant calves. A change in hematology profiles is one indicator of infection before clinical signs appear; however, to be effective, individual baseline...
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Published in | Animals (Basel) Vol. 11; no. 9; p. 2530 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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28.08.2021
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ISSN | 2076-2615 2076-2615 |
DOI | 10.3390/ani11092530 |
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Abstract | Elephant endotheliotropic herpesvirus hemorrhagic disease (EEHV-HD) is a virulent disease that causes severe hemorrhage and sudden death in Asian elephant calves. A change in hematology profiles is one indicator of infection before clinical signs appear; however, to be effective, individual baselines and age-matched reference values are needed. Stress has been speculated to be a factor in clinical EEHV cases, but relationships have not been demonstrated empirically. This study evaluated blood hematology and several stress response markers—salivary cortisol, fecal glucocorticoid metabolites (FGM), salivary Immunoglobulin A (SIgA), and fecal IgA (FIgA) in samples collected for 1 year from three healthy calves with no EEHV history (non-EEHV), and six that had previously been infected, developed clinical signs and survived (prior-EEHV). Hematology values between non-EEHV and prior-EEHV elephants were not different and within published reference ranges. Concentrations of salivary cortisol, FGM, SIgA, and FIgA also were variable and showed seasonal differences, but no relationships to prior EEHV status. One of the prior EEHV calves became re-infected, developed hemorrhagic disease (HD), and died during the study period. That calf exhibited lymphocytopenia, monocytopenia, and thrombocytopenia. Additionally, all stress biomarker concentrations were lower in the 12 days before viremia was observed. Thus, as in other studies, changes in hematology occur with EEHV infection, while preliminary data in one calf suggests that stress-response measures might also be informative and should be studied further. |
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AbstractList | Elephant endotheliotropic herpesvirus hemorrhagic disease (EEHV-HD) is a virulent disease that causes severe hemorrhage and sudden death in Asian elephant calves. A change in hematology profiles is one indicator of infection before clinical signs appear; however, to be effective, individual baselines and age-matched reference values are needed. Stress has been speculated to be a factor in clinical EEHV cases, but relationships have not been demonstrated empirically. This study evaluated blood hematology and several stress response markers—salivary cortisol, fecal glucocorticoid metabolites (FGM), salivary Immunoglobulin A (SIgA), and fecal IgA (FIgA) in samples collected for 1 year from three healthy calves with no EEHV history (non-EEHV), and six that had previously been infected, developed clinical signs and survived (prior-EEHV). Hematology values between non-EEHV and prior-EEHV elephants were not different and within published reference ranges. Concentrations of salivary cortisol, FGM, SIgA, and FIgA also were variable and showed seasonal differences, but no relationships to prior EEHV status. One of the prior EEHV calves became re-infected, developed hemorrhagic disease (HD), and died during the study period. That calf exhibited lymphocytopenia, monocytopenia, and thrombocytopenia. Additionally, all stress biomarker concentrations were lower in the 12 days before viremia was observed. Thus, as in other studies, changes in hematology occur with EEHV infection, while preliminary data in one calf suggests that stress-response measures might also be informative and should be studied further. Elephant endotheliotropic herpesvirus hemorrhagic disease (EEHV-HD) is a virulent disease that causes severe hemorrhage and sudden death in Asian elephant calves. A change in hematology profiles is one indicator of infection before clinical signs appear; however, to be effective, individual baselines and age-matched reference values are needed. Stress has been speculated to be a factor in clinical EEHV cases, but relationships have not been demonstrated empirically. This study evaluated blood hematology and several stress response markers-salivary cortisol, fecal glucocorticoid metabolites (FGM), salivary Immunoglobulin A (SIgA), and fecal IgA (FIgA) in samples collected for 1 year from three healthy calves with no EEHV history (non-EEHV), and six that had previously been infected, developed clinical signs and survived (prior-EEHV). Hematology values between non-EEHV and prior-EEHV elephants were not different and within published reference ranges. Concentrations of salivary cortisol, FGM, SIgA, and FIgA also were variable and showed seasonal differences, but no relationships to prior EEHV status. One of the prior EEHV calves became re-infected, developed hemorrhagic disease (HD), and died during the study period. That calf exhibited lymphocytopenia, monocytopenia, and thrombocytopenia. Additionally, all stress biomarker concentrations were lower in the 12 days before viremia was observed. Thus, as in other studies, changes in hematology occur with EEHV infection, while preliminary data in one calf suggests that stress-response measures might also be informative and should be studied further.Elephant endotheliotropic herpesvirus hemorrhagic disease (EEHV-HD) is a virulent disease that causes severe hemorrhage and sudden death in Asian elephant calves. A change in hematology profiles is one indicator of infection before clinical signs appear; however, to be effective, individual baselines and age-matched reference values are needed. Stress has been speculated to be a factor in clinical EEHV cases, but relationships have not been demonstrated empirically. This study evaluated blood hematology and several stress response markers-salivary cortisol, fecal glucocorticoid metabolites (FGM), salivary Immunoglobulin A (SIgA), and fecal IgA (FIgA) in samples collected for 1 year from three healthy calves with no EEHV history (non-EEHV), and six that had previously been infected, developed clinical signs and survived (prior-EEHV). Hematology values between non-EEHV and prior-EEHV elephants were not different and within published reference ranges. Concentrations of salivary cortisol, FGM, SIgA, and FIgA also were variable and showed seasonal differences, but no relationships to prior EEHV status. One of the prior EEHV calves became re-infected, developed hemorrhagic disease (HD), and died during the study period. That calf exhibited lymphocytopenia, monocytopenia, and thrombocytopenia. Additionally, all stress biomarker concentrations were lower in the 12 days before viremia was observed. Thus, as in other studies, changes in hematology occur with EEHV infection, while preliminary data in one calf suggests that stress-response measures might also be informative and should be studied further. Simple SummaryA change in hematology profiles is one indicator of EEHV infection before clinical signs appear; however, to be effective, individual baselines and age-matched reference values are needed. A longitudinal investigation of viremia, hematology values, and stress biomarkers was performed in three non-EEHV and six prior infected EEHV calves to better understand EEHV-HD-associated factors. Blood, saliva, and feces were collected for 1 year for analysis of complete blood count (CBC), viral load, glucocorticoids (GCs), and Immunoglobulin A (IgA). Results did not differ between the groups, except for one elephant that presented with EEHV-HD during the study and exhibited high viremia, altered hematology profiles, and decreased stress biomarker concentrations. Thus, as in other studies, hematology changes were associated with EEHV infection, while preliminary data in one calf suggests that stress-response measures might also be informative and warrant further investigation.AbstractElephant endotheliotropic herpesvirus hemorrhagic disease (EEHV-HD) is a virulent disease that causes severe hemorrhage and sudden death in Asian elephant calves. A change in hematology profiles is one indicator of infection before clinical signs appear; however, to be effective, individual baselines and age-matched reference values are needed. Stress has been speculated to be a factor in clinical EEHV cases, but relationships have not been demonstrated empirically. This study evaluated blood hematology and several stress response markers—salivary cortisol, fecal glucocorticoid metabolites (FGM), salivary Immunoglobulin A (SIgA), and fecal IgA (FIgA) in samples collected for 1 year from three healthy calves with no EEHV history (non-EEHV), and six that had previously been infected, developed clinical signs and survived (prior-EEHV). Hematology values between non-EEHV and prior-EEHV elephants were not different and within published reference ranges. Concentrations of salivary cortisol, FGM, SIgA, and FIgA also were variable and showed seasonal differences, but no relationships to prior EEHV status. One of the prior EEHV calves became re-infected, developed hemorrhagic disease (HD), and died during the study period. That calf exhibited lymphocytopenia, monocytopenia, and thrombocytopenia. Additionally, all stress biomarker concentrations were lower in the 12 days before viremia was observed. Thus, as in other studies, changes in hematology occur with EEHV infection, while preliminary data in one calf suggests that stress-response measures might also be informative and should be studied further. |
Author | Thitaram, Chatchote Yun, Yaoprapa Kosaruk, Worapong Tankaew, Pallop Muanghong, Panida Janyamathakul, Thittaya Punyapornwithaya, Veerasak Boonprasert, Khajohnpat Brown, Janine L. Towiboon, Patcharapa Somgird, Chaleamchat |
AuthorAffiliation | 6 Center for Species Survival, Smithsonian Conservation Biology Institute, Front Royal, VA 22630, USA 4 Pattara Elephant Farm, Chiang Mai 50100, Thailand; thittayavet68@gmail.com 2 Department of Food Animal Clinic, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand; pveerasak.r@gmail.com 3 Veterinary Public Health Centre and Food Safety for Asia Pacific (VPHCAP), Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand 7 Department of Companion Animal and Wildlife Clinics, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand 1 Center of Elephant and Wildlife Research, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand; khajohnpat@gmail.com (K.B.); yaoprapam@gmail.com (Y.Y.); woraph.kosa@gmail.com (W.K.); towiboon@gmail.com (P.T.); pallop_off@hotmail.com (P.T.); BrownJan@si.edu (J.L.B.); cthitaram@gmail.com (C.T.) 5 Mae Taeng Elephant Park and Clinic, Mae Thang, Chiang Mai 50150 |
AuthorAffiliation_xml | – name: 7 Department of Companion Animal and Wildlife Clinics, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand – name: 5 Mae Taeng Elephant Park and Clinic, Mae Thang, Chiang Mai 50150, Thailand; panida.vet72@hotmail.com – name: 6 Center for Species Survival, Smithsonian Conservation Biology Institute, Front Royal, VA 22630, USA – name: 3 Veterinary Public Health Centre and Food Safety for Asia Pacific (VPHCAP), Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand – name: 1 Center of Elephant and Wildlife Research, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand; khajohnpat@gmail.com (K.B.); yaoprapam@gmail.com (Y.Y.); woraph.kosa@gmail.com (W.K.); towiboon@gmail.com (P.T.); pallop_off@hotmail.com (P.T.); BrownJan@si.edu (J.L.B.); cthitaram@gmail.com (C.T.) – name: 4 Pattara Elephant Farm, Chiang Mai 50100, Thailand; thittayavet68@gmail.com – name: 2 Department of Food Animal Clinic, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand; pveerasak.r@gmail.com |
Author_xml | – sequence: 1 givenname: Khajohnpat surname: Boonprasert fullname: Boonprasert, Khajohnpat – sequence: 2 givenname: Yaoprapa surname: Yun fullname: Yun, Yaoprapa – sequence: 3 givenname: Worapong orcidid: 0000-0002-1706-2684 surname: Kosaruk fullname: Kosaruk, Worapong – sequence: 4 givenname: Patcharapa surname: Towiboon fullname: Towiboon, Patcharapa – sequence: 5 givenname: Pallop surname: Tankaew fullname: Tankaew, Pallop – sequence: 6 givenname: Veerasak orcidid: 0000-0001-9870-7773 surname: Punyapornwithaya fullname: Punyapornwithaya, Veerasak – sequence: 7 givenname: Thittaya surname: Janyamathakul fullname: Janyamathakul, Thittaya – sequence: 8 givenname: Panida surname: Muanghong fullname: Muanghong, Panida – sequence: 9 givenname: Janine L. orcidid: 0000-0003-3898-7755 surname: Brown fullname: Brown, Janine L. – sequence: 10 givenname: Chatchote surname: Thitaram fullname: Thitaram, Chatchote – sequence: 11 givenname: Chaleamchat surname: Somgird fullname: Somgird, Chaleamchat |
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Snippet | Elephant endotheliotropic herpesvirus hemorrhagic disease (EEHV-HD) is a virulent disease that causes severe hemorrhage and sudden death in Asian elephant... Simple SummaryA change in hematology profiles is one indicator of EEHV infection before clinical signs appear; however, to be effective, individual baselines... |
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SubjectTerms | Age Antibodies Asian elephant Biomarkers Blood calves cortisol death elephant endotheliotropic herpesvirus Elephantid betaherpesvirus 1 Elephants Elephas maximus Feces Genetic testing Genomes glucocorticoids Hematology hematology parameters hemorrhage Hormones immunoglobulin A Infections Longitudinal studies Medical prognosis metabolites Physiology stress indicators stress response Thailand thrombocytopenia Veterinary medicine viremia virulence Weaning |
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Title | A Longitudinal Study of Hematology and Stress Biomarker Profiles in Young Asian Elephants (Elephas Maximus) in Relation to Elephant Endotheliotropic Herpesvirus (EEHV) in Thailand |
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