scholarly journals Zebra-borne neurotropic equid herpesvirus 1 meningoencephalitis in a Thomson’s gazelle (Eudorcas thomsonii)

2017 ◽  
Vol 29 (4) ◽  
pp. 548-556 ◽  
Author(s):  
Kanako Sakaguchi ◽  
Kenneth Kim ◽  
Ingeborg Langohr ◽  
Annabel G. Wise ◽  
Roger K. Maes ◽  
...  

We describe the histopathologic, immunohistochemical, and molecular features of a case of meningoencephalitis in a Thomson’s gazelle ( Eudorcas thomsonii) naturally infected with zebra-borne equid herpesvirus 1 (EHV-1) and the implications for the molecular detection of zebra-borne EHV-1. A 4-y-old female Thomson’s gazelle was submitted for postmortem examination; no gross abnormalities were noted except for meningeal congestion. Microscopic evaluation demonstrated multifocal nonsuppurative meningoencephalitis with intranuclear eosinophilic and amphophilic inclusion bodies and EHV-9 antigen in neurons. PCR demonstrated the presence of a herpesvirus with a nucleotide sequence 99–100% identical to the corresponding sequences of zebra-borne EHV-1 and of EHV-9 strains. To determine whether EHV-1 or EHV-9 was involved, a PCR with a specific primer set for EHV-9 ORF59/60 was used. The sequence was identical to that of 3 recognized zebra-borne EHV-1 strains and 91% similar to that of EHV-9. This isolate was designated as strain LM2014. The partial glycoprotein G ( gG) gene sequence of LM2014 was also identical to the sequence of 2 zebra-borne EHV-1 strains (T-529 isolated from an onager, 94-137 from a Thomson’s gazelle). The histologic lesions of encephalitis and antigen localization in this gazelle indicate prominent viral neurotropism, and lesions were very similar to those seen in EHV-1– and EHV-9–infected non-equid species. Histologic lesions caused by EHV-9 and zebra-borne EHV-1 are therefore indistinguishable.

2001 ◽  
Vol 82 (1) ◽  
pp. 227-232 ◽  
Author(s):  
Hong Li ◽  
Janice Keller ◽  
Donald P. Knowles ◽  
Timothy B. Crawford

A novel gammaherpesvirus in goats that is herein tentatively designated as caprine herpesvirus-2 was identified based on the sequence of a fragment from the herpesvirus DNA polymerase gene. Sequence alignment analysis revealed that the virus sequence isolated from goats was 67% identical to the homologous sequence from alcelaphine herpesvirus-1, 71% identical to ovine herpesvirus-2 and 73% identical to a recently recognized herpesvirus causing malignant catarrhal fever in white-tailed deer. Combined serological and PCR-survey data demonstrated that this virus is endemic in goats and its transmission pattern may be similar to that of ovine herpesvirus-2 in sheep.


1991 ◽  
Vol 53 (1) ◽  
pp. 133-135
Author(s):  
Nobuo KOIZUMI ◽  
Eiichi HONDA ◽  
Tetsuo KUMAGAI ◽  
Katsunori OKAZAKI

2021 ◽  
Vol 49 (06) ◽  
pp. 462-467
Author(s):  
Lisa Schüler ◽  
Pierre Picquet ◽  
Christoph Leineweber ◽  
Janosch Dietz ◽  
Elisabeth Müller ◽  
...  

AbstractIn spring 2020, a severe disease outbreak with high morbidity and mortality was observed in a collection of 15 Horsfield’s tortoises (Testudo horsfieldii). Affected tortoises showed upper respiratory- and gastrointestinal tract signs, including rhinitis and stomatitis. Testudinid herpesvirus 1 (TeHV1) and Mycoplasma spp. were detected by PCR in oral swabs of affected animals. Histological examination of one deceased animal showed intranuclear inclusion bodies typical for herpesvirus infections in liver, spleen and oesophagus. The virus was likely introduced into the collection 2 years earlier by a clinically healthy Horsfield’s tortoise that was tested positive for TeHV1 by PCR.


2019 ◽  
Vol 67 (3) ◽  
pp. 463-476
Author(s):  
Hakan Işidan ◽  
Turhan Turan ◽  
Mustafa Ozan Atasoy ◽  
Ibrahim Sözdutmaz ◽  
Bünyamin Irehan

The involvement of picornaviruses in calf diarrhoea was evaluated by the analysis of 127 faecal samples collected from diarrhoeic calves during 2014–2016. Virus detections were carried out by PCR using generic or specific primer pairs. One-third of the faecal samples (33.86%) were found to be positive for one or more of the studied viruses. Bovine kobuvirus was detected in 22.83%, bovine hungarovirus in 11.02%, while bovine enterovirus 1 in 5.51% of the samples. The sequences of the PCR products indicated the existence of novel variants in all the three virus species. When comparing the partial sequences, the nucleotide sequence identities between our newly detected viruses and those previously deposited to the GenBank ranged between 76 and 99%. Phylogenetic analyses revealed a novel lineage within the species Hunnivirus A. Our findings suggest that these viruses should be regarded as possible aetiological agents of calf diarrhoea. Based on the newly determined sequences, we designed and tested a new generic PCR primer set for the more reliable detection of bovine hungaroviruses. This is the first report on the molecular detection of the presence of bovine hungarovirus, bovine kobuvirus and bovine enterovirus 1 in the faecal samples of diarrhoeic calves in Turkey.


1993 ◽  
Vol 55 (1) ◽  
pp. 119-121 ◽  
Author(s):  
Mamiko INAZU ◽  
Osamu TSUHA ◽  
Rikio KIRISAWA ◽  
Yoshimi KAWAKAMI ◽  
Hiroshi IWAI

1996 ◽  
Vol 115 (4) ◽  
pp. 385-397 ◽  
Author(s):  
J.P. Tearle ◽  
K.C. Smith ◽  
M.S. Boyle ◽  
M.M. Binns ◽  
G.J. Livesay ◽  
...  

1984 ◽  
Vol 114 (15) ◽  
pp. 369-374 ◽  
Author(s):  
R. Burrows ◽  
D. Goodridge ◽  
M. Denyer

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