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1.
PLoS One ; 19(5): e0300862, 2024.
Article in English | MEDLINE | ID: mdl-38739614

ABSTRACT

Influenza A viruses of the H2 subtype represent a zoonotic and pandemic threat to humans due to a lack of widespread specific immunity. Although A(H2) viruses that circulate in wild bird reservoirs are distinct from the 1957 pandemic A(H2N2) viruses, there is concern that they could impact animal and public health. There is limited information on AIVs in Latin America, and next to nothing about H2 subtypes in Brazil. In the present study, we report the occurrence and genomic sequences of two influenza A viruses isolated from wild-caught white-rumped sandpipers (Calidris fuscicollis). One virus, identified as A(H2N1), was isolated from a bird captured in Restinga de Jurubatiba National Park (PNRJ, Rio de Janeiro), while the other, identified as A(H2N2), was isolated from a bird captured in Lagoa do Peixe National Park (PNLP, Rio Grande do Sul). DNA sequencing and phylogenetic analysis of the obtained sequences revealed that each virus belonged to distinct subtypes. Furthermore, the phylogenetic analysis indicated that the genomic sequence of the A(H2N1) virus isolated from PNRJ was most closely related to other A(H2N1) viruses isolated from North American birds. On the other hand, the A(H2N2) virus genome recovered from the PNLP-captured bird exhibited a more diverse origin, with some sequences closely related to viruses from Iceland and North America, and others showing similarity to virus sequences recovered from birds in South America. Viral genes of diverse origins were identified in one of the viruses, indicating local reassortment. This suggests that the extreme South of Brazil may serve as an environment conducive to reassortment between avian influenza virus lineages from North and South America, potentially contributing to an increase in overall viral diversity.


Subject(s)
Charadriiformes , Influenza A virus , Influenza in Birds , Phylogeny , Reassortant Viruses , Animals , Brazil , Influenza in Birds/virology , Influenza in Birds/epidemiology , Influenza A virus/genetics , Influenza A virus/isolation & purification , Reassortant Viruses/genetics , Reassortant Viruses/isolation & purification , Charadriiformes/virology , Genome, Viral , Birds/virology
2.
Emerg Infect Dis ; 30(3): 619-621, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38290826

ABSTRACT

We report 4 highly pathogenic avian influenza A(H5N1) clade 2.3.4.4.b viruses in samples collected during June 2023 from Royal terns and Cabot's terns in Brazil. Phylodynamic analysis revealed viral movement from Peru to Brazil, indicating a concerning spread of this clade along the Atlantic Americas migratory bird flyway.


Subject(s)
Charadriiformes , Influenza A Virus, H5N1 Subtype , Influenza in Birds , Influenza, Human , Animals , Humans , Influenza in Birds/epidemiology , Animals, Wild , Brazil/epidemiology , Birds , Phylogeny
3.
Arch Virol ; 167(11): 2319-2324, 2022 Nov.
Article in English | MEDLINE | ID: mdl-35962822

ABSTRACT

This study describes a case report in captive rose-ringed parakeets (Psittacula krameri) that developed clinical signs and eventually died after introducing new birds without quarantine. Bronchopneumonia and airsacculitis with syncytial cells associated with intranuclear inclusion bodies were found. Herpesvirus was detected in lungs and liver by PCR, and a nearly complete genome sequence of a Psittacid alphaherpesvirus 5 was obtained from the lung of a bird. Metagenomic analysis also identified beak and feather disease virus in the same samples. The study also highlights the importance of quarantine for avoiding the introduction of new diseases in captive aviaries.


Subject(s)
Alphaherpesvirinae , Bird Diseases , Circoviridae Infections , Circovirus , Coinfection , Psittacula , Alphaherpesvirinae/genetics , Animals , Brazil , Circoviridae Infections/veterinary , Circovirus/genetics , Coinfection/veterinary , Humans , Oncogenic Viruses , Parakeets
4.
Viruses ; 13(12)2021 12 06.
Article in English | MEDLINE | ID: mdl-34960715

ABSTRACT

Newcastle disease virus (NDV) can infect over 250 bird species with variable pathogenicity; it can also infect humans in rare cases. The present study investigated an outbreak in feral pigeons in São Paulo city, Brazil, in 2019. Affected birds displayed neurological signs, and hemorrhages were observed in different tissues. Histopathology changes with infiltration of mononuclear inflammatory cells were also found in the brain, kidney, proventriculus, heart, and spleen. NDV staining was detected by immunohistochemistry. Twenty-seven out of thirty-four tested samples (swabs and tissues) were positive for Newcastle disease virus by RT-qPCR test, targeting the M gene. One isolate, obtained from a pool of positive swab samples, was characterized by the intracerebral pathogenicity index (ICPI) and the hemagglutination inhibition (HI) tests. This isolate had an ICPI of 0.99, confirming a virulent NDV strain. The monoclonal antibody 617/161, which recognizes a distinct epitope in pigeon NDV strains, inhibited the isolate with an HI titer of 512. A complete genome of NDV was obtained using next-generation sequencing. Phylogenetic analysis based on the complete CDS F gene grouped the detected isolate with other viruses from subgenotype VI.2.1.2, class II, including one previously reported in Southern Brazil in 2014. This study reports a comprehensive characterization of the subgenotype VI.2.1.2, which seems to have been circulating in Brazilian urban areas since 2014. Due to the zoonotic risk of NDV, virus surveillance in feral pigeons should also be systematically performed in urban areas.


Subject(s)
Columbidae , Disease Outbreaks/veterinary , Newcastle Disease/epidemiology , Newcastle disease virus/genetics , Animals , Brazil/epidemiology , Genome, Viral , Genotype , High-Throughput Nucleotide Sequencing , Newcastle Disease/pathology , Newcastle Disease/virology , Newcastle disease virus/classification , Newcastle disease virus/isolation & purification , Newcastle disease virus/pathogenicity , Phylogeny , Virulence , Whole Genome Sequencing
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