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1.
Transbound Emerg Dis ; 64(3): 1001-1007, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-26671034

RESUMO

A number of contemporary outbreaks of Newcastle disease (ND) in Israel, Turkey, Georgia and Bulgaria have all been caused by a very similar viruses related to lineage 5a (genotype VIIa). Comparison with published ND virus (NDV) sequences suggests that this virus strain originated in South-East Asia and on introduction has circulated widely in backyard poultry in the Middle East and into Eastern Europe. An intracerebral pathogenicity index of 1.9 was obtained for a representative isolate from Bulgaria. In addition, the International Reference Laboratory for ND has characterized a molecular epidemiologically linked virus that has been reported to have caused disease in well-vaccinated broiler chickens in Pakistan. In the 1990s, another strain from the 5a lineage NDV was introduced into Europe and spread across the continent causing numerous outbreaks up to 1999. Despite improved controls, including good diagnostic tests and widespread vaccination, in commercial poultry, the novel circulating NDV strains described here have been established widely in the region and represent an increased risk for similar disease outbreak events to reoccur within the EU.


Assuntos
Doenças Transmissíveis Emergentes/virologia , Surtos de Doenças/veterinária , Doença de Newcastle/virologia , Vírus da Doença de Newcastle/patogenicidade , Animais , Galinhas , Doenças Transmissíveis Emergentes/epidemiologia , Doenças Transmissíveis Emergentes/transmissão , Europa Oriental/epidemiologia , Genótipo , Epidemiologia Molecular , Doença de Newcastle/epidemiologia , Doença de Newcastle/transmissão , Vírus da Doença de Newcastle/genética , Vírus da Doença de Newcastle/imunologia , Filogenia , Aves Domésticas , Doenças das Aves Domésticas/epidemiologia , Doenças das Aves Domésticas/virologia , RNA Viral/química , RNA Viral/isolamento & purificação , Vacinas Virais , Virulência
2.
Virology ; 440(1): 84-8, 2013 May 25.
Artigo em Inglês | MEDLINE | ID: mdl-23507452

RESUMO

Several viruses of the family of Adenoviridae are associated with disease in birds. Here we report the detection of a novel adenovirus in the cloacal bursa of herring gulls (Larus argentatus) and lesser black-backed gulls (Larus fuscus) that were found dead in the Netherlands in 2001. Histopathological analysis of the cloacal bursa revealed cytomegaly and karyomegaly with basophilic intranuclear inclusions typical for adenovirus infection. The presence of an adenovirus was confirmed by electron microscopy. By random PCR in combination with deep sequencing, sequences were detected that had the best hit with known adenoviruses. Phylogenetic analysis of complete coding sequences of the hexon, penton and polymerase genes indicates that this novel virus, tentatively named Gull adenovirus, belongs to the genus Aviadenovirus. The present study demonstrates that birds of the Laridae family are infected by family-specific adenoviruses that differ from known adenoviruses in other bird species.


Assuntos
Infecções por Adenoviridae/veterinária , Adenoviridae/classificação , Adenoviridae/isolamento & purificação , Doenças das Aves/virologia , Charadriiformes , Adenoviridae/genética , Infecções por Adenoviridae/epidemiologia , Infecções por Adenoviridae/virologia , Animais , Doenças das Aves/epidemiologia , Bolsa de Fabricius/ultraestrutura , Bolsa de Fabricius/virologia , Cloaca/patologia , Cloaca/virologia , Genoma Viral , Microscopia Eletrônica de Transmissão/veterinária , Países Baixos/epidemiologia , Filogenia , Especificidade da Espécie
3.
Euro Surveill ; 17(39)2012 Sep 27.
Artigo em Inglês | MEDLINE | ID: mdl-23041020

RESUMO

We present two real-time reverse-transcription polymerase chain reaction assays for a novel human coronavirus (CoV), targeting regions upstream of the E gene (upE) or within open reading frame (ORF)1b, respectively. Sensitivity for upE is 3.4 copies per reaction (95% confidence interval (CI): 2.5­6.9 copies) or 291 copies/mL of sample. No cross-reactivity was observed with coronaviruses OC43, NL63, 229E, SARS-CoV, nor with 92 clinical specimens containing common human respiratory viruses. We recommend using upE for screening and ORF1b for confirmation.


Assuntos
Infecções por Coronavirus/virologia , Reação em Cadeia da Polimerase em Tempo Real/métodos , Coronavírus Relacionado à Síndrome Respiratória Aguda Grave/genética , Coronavírus Relacionado à Síndrome Respiratória Aguda Grave/isolamento & purificação , Coronavirus Humano 229E/genética , Coronavirus Humano 229E/isolamento & purificação , Infecções por Coronavirus/diagnóstico , Infecções por Coronavirus/genética , Coronavirus Humano NL63/genética , Coronavirus Humano NL63/isolamento & purificação , Coronavirus Humano OC43/genética , Coronavirus Humano OC43/isolamento & purificação , Humanos , Fases de Leitura Aberta , Arábia Saudita , Sensibilidade e Especificidade , Viagem , Proteínas do Envelope Viral , Proteínas Viroporinas
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