Cargando…

Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy

BACKGROUND: Elephant Endotheliotropic Herpesviruses (EEHVs) can cause acute haemorrhagic disease in young Asian elephants (Elephas maximus) and clinical EEHV infections account for the majority of their fatalities. The anti-herpesviral drug famciclovir (FCV) has been used routinely to treat viraemic...

Descripción completa

Detalles Bibliográficos
Autores principales: Dastjerdi, Akbar, Seilern-Moy, Katharina, Darpel, Karin, Steinbach, Falko, Molenaar, Fieke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002104/
https://www.ncbi.nlm.nih.gov/pubmed/27567895
http://dx.doi.org/10.1186/s12917-016-0806-5
_version_ 1782450514686902272
author Dastjerdi, Akbar
Seilern-Moy, Katharina
Darpel, Karin
Steinbach, Falko
Molenaar, Fieke
author_facet Dastjerdi, Akbar
Seilern-Moy, Katharina
Darpel, Karin
Steinbach, Falko
Molenaar, Fieke
author_sort Dastjerdi, Akbar
collection PubMed
description BACKGROUND: Elephant Endotheliotropic Herpesviruses (EEHVs) can cause acute haemorrhagic disease in young Asian elephants (Elephas maximus) and clinical EEHV infections account for the majority of their fatalities. The anti-herpesviral drug famciclovir (FCV) has been used routinely to treat viraemic at-risk elephants, but thus far without proven efficacy. This paper presents clinical and virological investigations of two EEHV-1A infected elephants treated with FCV, and discusses anti-herpesvirus therapies of viraemic elephants. CASES PRESENTATIONS: Two 1.5 year old male Asian elephants at a zoological collection in the UK developed clinical EEHV-1A infections. Case 1 showed signs of myalgia for the duration of 24 hours before returning back to normal. EEHV-1A DNAemia was confirmed on the day of clinical signs and continued to be present for 18 days in total. Trunk shedding of the virus commenced 10 days after detection of initial DNAemia. Case 2 tested positive for EEHV-1A DNAemia in a routine blood screening sample in the absence of clinical signs. The blood viral load increased exponentially leading up to fatal clinical disease seven days after initial detection of DNAemia. Both calves were treated with 15 mg/kg FCV per rectum on detection of DNAemia and penciclovir, the FCV metabolite, could be detected in the blood at assumed therapeutic levels. The early indicators for clinical disease were a marked absolute and relative drop in white blood cells, particularly monocytes prior to the detection of viraemia. The most prognostic haematological parameter at later stages of the disease was the platelet count showing a continuous sharp decline throughout, followed by a dramatic drop at the time of death. CONCLUSIONS: The EEHV-1A viraemic animals investigated here further highlight the ongoing threat posed by these viruses to juvenile Asian elephants. The findings call into question the efficacy of rectal FCV in clinical cases and direct towards the use of alternative anti-herpesvirus drugs and complementary treatments such as plasma infusions if no improvement in either viral load or the above-mentioned blood parameters are observed in the initial days of viraemia despite anti-herpesvirus therapy.
format Online
Article
Text
id pubmed-5002104
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-50021042016-08-28 Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy Dastjerdi, Akbar Seilern-Moy, Katharina Darpel, Karin Steinbach, Falko Molenaar, Fieke BMC Vet Res Case Report BACKGROUND: Elephant Endotheliotropic Herpesviruses (EEHVs) can cause acute haemorrhagic disease in young Asian elephants (Elephas maximus) and clinical EEHV infections account for the majority of their fatalities. The anti-herpesviral drug famciclovir (FCV) has been used routinely to treat viraemic at-risk elephants, but thus far without proven efficacy. This paper presents clinical and virological investigations of two EEHV-1A infected elephants treated with FCV, and discusses anti-herpesvirus therapies of viraemic elephants. CASES PRESENTATIONS: Two 1.5 year old male Asian elephants at a zoological collection in the UK developed clinical EEHV-1A infections. Case 1 showed signs of myalgia for the duration of 24 hours before returning back to normal. EEHV-1A DNAemia was confirmed on the day of clinical signs and continued to be present for 18 days in total. Trunk shedding of the virus commenced 10 days after detection of initial DNAemia. Case 2 tested positive for EEHV-1A DNAemia in a routine blood screening sample in the absence of clinical signs. The blood viral load increased exponentially leading up to fatal clinical disease seven days after initial detection of DNAemia. Both calves were treated with 15 mg/kg FCV per rectum on detection of DNAemia and penciclovir, the FCV metabolite, could be detected in the blood at assumed therapeutic levels. The early indicators for clinical disease were a marked absolute and relative drop in white blood cells, particularly monocytes prior to the detection of viraemia. The most prognostic haematological parameter at later stages of the disease was the platelet count showing a continuous sharp decline throughout, followed by a dramatic drop at the time of death. CONCLUSIONS: The EEHV-1A viraemic animals investigated here further highlight the ongoing threat posed by these viruses to juvenile Asian elephants. The findings call into question the efficacy of rectal FCV in clinical cases and direct towards the use of alternative anti-herpesvirus drugs and complementary treatments such as plasma infusions if no improvement in either viral load or the above-mentioned blood parameters are observed in the initial days of viraemia despite anti-herpesvirus therapy. BioMed Central 2016-08-27 /pmc/articles/PMC5002104/ /pubmed/27567895 http://dx.doi.org/10.1186/s12917-016-0806-5 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Dastjerdi, Akbar
Seilern-Moy, Katharina
Darpel, Karin
Steinbach, Falko
Molenaar, Fieke
Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy
title Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy
title_full Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy
title_fullStr Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy
title_full_unstemmed Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy
title_short Surviving and fatal Elephant Endotheliotropic Herpesvirus-1A infections in juvenile Asian elephants – lessons learned and recommendations on anti-herpesviral therapy
title_sort surviving and fatal elephant endotheliotropic herpesvirus-1a infections in juvenile asian elephants – lessons learned and recommendations on anti-herpesviral therapy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5002104/
https://www.ncbi.nlm.nih.gov/pubmed/27567895
http://dx.doi.org/10.1186/s12917-016-0806-5
work_keys_str_mv AT dastjerdiakbar survivingandfatalelephantendotheliotropicherpesvirus1ainfectionsinjuvenileasianelephantslessonslearnedandrecommendationsonantiherpesviraltherapy
AT seilernmoykatharina survivingandfatalelephantendotheliotropicherpesvirus1ainfectionsinjuvenileasianelephantslessonslearnedandrecommendationsonantiherpesviraltherapy
AT darpelkarin survivingandfatalelephantendotheliotropicherpesvirus1ainfectionsinjuvenileasianelephantslessonslearnedandrecommendationsonantiherpesviraltherapy
AT steinbachfalko survivingandfatalelephantendotheliotropicherpesvirus1ainfectionsinjuvenileasianelephantslessonslearnedandrecommendationsonantiherpesviraltherapy
AT molenaarfieke survivingandfatalelephantendotheliotropicherpesvirus1ainfectionsinjuvenileasianelephantslessonslearnedandrecommendationsonantiherpesviraltherapy