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1.
Infect Genet Evol ; 123: 105633, 2024 Jul 03.
Article in English | MEDLINE | ID: mdl-38969193

ABSTRACT

Canine parvovirus (CPV) is a significant pathogen in domestic dogs worldwide, causing a severe and often fatal disease. CPV comprises three antigenic variants (2a, 2b, and 2c) distributed unevenly among several phylogenetic groups. The present study compared genetic variability and evolutionary patterns in South American CPV populations. We collected samples from puppies suspected of CPV infection in the neighboring Argentina and Uruguay. Antigenic variants were preliminarily characterized using PCR-RFLP and partial vp2 sequencing. Samples collected in Argentina during 2008-2018 were mainly of the 2c variant. In the Uruguayan strains (2012-2019), the 2a variant wholly replaced the 2c from 2014. Full-length coding genome and vp2 sequences were compared with global strains. The 2c and 2a strains fell by phylogenetic analysis into two phylogroups (Europe I and Asia I). The 2c strains from Argentina and Uruguay clustered in the Europe I group, with strains from America, Europe, Asia, and Oceania. Europe I is widely distributed in South America in the dog population and is also being detected in the wildlife population. The 2a strains from Uruguay formed the distinct Asia I group with strains from Asia, Africa, America, and Oceania. This Asia I group is increasing its distribution in South America and worldwide. Our research reveals high genetic variability in adjacent synchronic samples and different evolutionary patterns in South American CPV. We also highlight the importance of ancestral migrations and local diversification in the evolution of global CPV strains.

3.
PLoS One ; 14(6): e0218735, 2019.
Article in English | MEDLINE | ID: mdl-31237902

ABSTRACT

Canine circovirus (CanineCV) was detected, together with canine parvovirus (CPV), in samples from an outbreak of fatal gastroenteritis in dogs in Argentina. We obtained the full-length genome of this recently discovered virus by overlapping PCR, designated strain UBA-Baires. Sequence analysis revealed a highly conserved genome but also showed several unique mutations in amino acids from the capsid protein that have not been previously reported. Phylogenetic analysis shows that this strain is more closely related to European strains than to viruses detected in North America or Asia. Although the pathogenic role of CanineCV in dogs is still unclear, this study highlights the importance of CanineCV as a coinfecting virus in disease development. To our knowledge, this is the first report of the involvement of CanineCV in severe clinical disease in dogs in South America. Our results expand our information on the geographical extent of this virus and contribute to the understanding of its role in disease.


Subject(s)
Circoviridae Infections/veterinary , Circovirus/genetics , Dog Diseases/virology , Amino Acid Substitution , Animals , Argentina/epidemiology , Capsid Proteins/genetics , Circoviridae Infections/epidemiology , Circoviridae Infections/virology , Circovirus/classification , Circovirus/pathogenicity , DNA, Viral/genetics , Disease Outbreaks/veterinary , Dog Diseases/epidemiology , Dogs , Gastroenteritis/veterinary , Gastroenteritis/virology , Genome, Viral , Parvoviridae Infections/epidemiology , Parvoviridae Infections/veterinary , Parvoviridae Infections/virology , Parvovirus, Canine/genetics , Phylogeny , South America/epidemiology
4.
J Zoo Wildl Med ; 49(4): 1054-1060, 2018 12 13.
Article in English | MEDLINE | ID: mdl-30592932

ABSTRACT

Since its emergence in the 1970s, canine parvovirus (CPV) has spread worldwide and infects a wide variety of mammalian hosts, including domestic and nondomestic carnivores. Today it is one of the most important pathogenic viruses associated with high morbidity and mortality in domestic dogs ( Canis familiaris). In South America, the range of wild hosts has been scarcely studied and the epidemiology of CPV in wildlife is still unclear. In 2011, feces from five wild carnivores (bush dog [ Speothos venaticus] , jaguar [ Panthera onca], puma [ Puma concolor], oncilla [ Leopardus guttulus], and ocelot [ Leopardus pardalis]) were collected in Misiones, Argentina, using a detection dog. Of the 289 feces collected, 209 (72.3%) had sufficient sample remaining to be used in this study and the majority of these were genetically confirmed to individual (81.3%) and sex (78.4%) level. In fact, these samples represent a minimum of 115 individuals (10 jaguars, 13 pumas, 33 ocelots, 38 oncillas, and 21 bush dogs). Through polymerase chain reaction, a 583-bp fragment in the VP2 gene of CPV was amplified in these samples. While no samples showed evidence of infection, this does not exclude the occurrence of CPV in wild carnivores in the area, as intermittent viral shedding could condition the diagnosis of CPV in feces of infected wild mammals. Locally, it is recommended that long-term monitoring of parvovirus be continued in wildlife and expanded to domestic carnivores. Internationally, this study provides a useful contribution to the approach to the sylvatic cycle of parvovirus in wild carnivores.


Subject(s)
Carnivora , Feces/virology , Parvoviridae Infections/veterinary , Parvovirus, Canine/physiology , Virus Shedding , Animals , Argentina/epidemiology , Endangered Species , Parvoviridae Infections/epidemiology , Parvoviridae Infections/virology
5.
Rev. argent. microbiol ; 48(4): 293-297, dic. 2016. ilus, tab
Article in English | LILACS | ID: biblio-1041764

ABSTRACT

A cross-sectional study was carried out on cats attending the Small Animal Hospital at the Faculty of Veterinary Sciences of the University of Buenos Aires to assess the prevalence and associated risk factors of Feline immunodeficiency virus (FIV) and Feline leukemia virus (FeLV) in the city of Buenos Aires, Argentina. Blood samples from 255 cats with symptoms compatible with FIV or FeLV infection, collected between 2009 and 2013 were analyzed by serology (immunochromatography, IA) and by hemi-nested PCR (n-PCR). The IA and n-PCR assays showed similar percentages of positivity for FIV while the n-PCR test was more sensitive for FeLV. Differences between the diagnostic tests and their choice according to the age of the animal are discussed. The clinical histories of ninety of the 255 cats showed blood profiles similar to others previously reported and revealed a higher risk of infection in male adult cats with outdoor access.


Para determinar la prevalencia en la ciudad de Buenos Aires del virus de la inmunodeficiencia felina (FIV) y del virus de la leucemia felina (FeLV), y analizar los factores de riesgo que pudieran estar asociados a ellos, se realizó un estudio transversal en gatos atendidos en el Hospital de Pequeños Animales de la Facultad de Ciencias Veterinarias de la Universidad de Buenos Aires. Se analizaron por serología (inmunocromatografía --#91;IA--#93;) y por hemi-nested PCR (n-PCR) 255 muestras de sangre de gatos con síntomas compatibles con infección por FIV o FeLV. La IA y la n-PCR revelaron porcentajes similares de animales positivos para FIV, mientras que para FeLV el diagnóstico por n-PCR resultó más sensible. Se discuten las diferencias halladas entre los métodos diagnósticos y su elección según la edad del animal. Las historias clínicas de 90 de los 255 gatos mostraron perfiles sanguíneos similares a otros ya reportados y revelaron el mayor riesgo de infección con ambos virus en machos adultos con acceso al exterior.


Subject(s)
Animals , Cats , Cat Diseases/blood , Immunodeficiency Virus, Feline/growth & development , Leukemia Virus, Feline/growth & development , Polymerase Chain Reaction/methods , Prevalence , Risk Factors , Immunodeficiency Virus, Feline/pathogenicity , Leukemia Virus, Feline/pathogenicity
6.
Rev Argent Microbiol ; 48(4): 293-297, 2016.
Article in English | MEDLINE | ID: mdl-27825735

ABSTRACT

A cross-sectional study was carried out on cats attending the Small Animal Hospital at the Faculty of Veterinary Sciences of the University of Buenos Aires to assess the prevalence and associated risk factors of Feline immunodeficiency virus (FIV) and Feline leukemia virus (FeLV) in the city of Buenos Aires, Argentina. Blood samples from 255 cats with symptoms compatible with FIV or FeLV infection, collected between 2009 and 2013 were analyzed by serology (immunochromatography, IA) and by hemi-nested PCR (n-PCR). The IA and n-PCR assays showed similar percentages of positivity for FIV while the n-PCR test was more sensitive for FeLV. Differences between the diagnostic tests and their choice according to the age of the animal are discussed. The clinical histories of ninety of the 255 cats showed blood profiles similar to others previously reported and revealed a higher risk of infection in male adult cats with outdoor access.


Subject(s)
Chromatography, Affinity/methods , Feline Acquired Immunodeficiency Syndrome/diagnosis , Immunodeficiency Virus, Feline/isolation & purification , Leukemia Virus, Feline/isolation & purification , Leukemia, Feline/diagnosis , Polymerase Chain Reaction/methods , Viremia/diagnosis , Animals , Argentina/epidemiology , Cats/virology , Cross-Sectional Studies , DNA, Viral/analysis , Feline Acquired Immunodeficiency Syndrome/epidemiology , Feline Acquired Immunodeficiency Syndrome/virology , Female , Immunodeficiency Virus, Feline/genetics , Immunodeficiency Virus, Feline/immunology , Leukemia Virus, Feline/genetics , Leukemia Virus, Feline/immunology , Leukemia, Feline/epidemiology , Leukemia, Feline/virology , Male , Prevalence , Proviruses/isolation & purification , Reagent Kits, Diagnostic , Risk Factors , Sensitivity and Specificity , Viremia/epidemiology , Viremia/virology
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