Valiria Duarte Cerqueira

Prof. Valiria Duarte Cerqueira

Universidade Federal do Pará, Castanhal, Pará, Brazil

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 July 2020 in Transboundary and Emerging Diseases
Verified
Journal Article
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JSJosileide Araújo Silva
Josileide Araújo Silva
ASAlessandra Scofield
Alessandra Scofield
FBFlavia de Nazaré Barros
Flavia de Nazaré Barros
DFDiana Maria Farias
Diana Maria Farias
GRGabriela Riet‐Correa
Gabriela Riet‐Correa
VCValiria Duarte Cerqueira
Valiria Duarte Cerqueira

1 May 2021 in Acta Tropica
Verified
Journal Article
Closed access
HPHelyanne de Sousa Pereira
Helyanne de Sousa Pereira
ASAlessandra Scofield
Alessandra Scofield
PJPedro Soares Bezerra Júnior
Pedro Soares Bezerra Júnior
DSDaniele Lira dos Santos
Daniele Lira dos Santos
JSJulyanne de Sousa Siqueira
Julyanne de Sousa Siqueira
VCValiria Duarte Cerqueira
Valiria Duarte Cerqueira

18 August 2017 in Journal of Veterinary Diagnostic Investigation
Verified
Journal Article
Closed access
GSGisele C. C. Seade
Gisele C. C. Seade
VCValiria Duarte Cerqueira
Valiria Duarte Cerqueira
ESEva Sierra
Eva Sierra
JCJaese F. Chaves
Jaese F. Chaves
MMMárcio A. O. Moura
Márcio A. O. Moura
PJPedro S. Bezerra Júnior
Pedro S. Bezerra Júnior
We describe herein herpesvirus-associated genital lesions in a Guiana dolphin (Sotalia guianensis) from the northern Brazilian coast. Papillary lesions on the vulva, with epithelial hyperplasia, swollen keratinocytes, and intranuclear inclusions, were positive for a herpesvirus (Gammaherpesvirinae subfamily).

15 September 2016 in Ciência Rural
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Journal Article
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JSJosileide Araújo da Silva
Josileide Araújo da Silva
TDTarcísio Oliveira Domiciano
Tarcísio Oliveira Domiciano
DMDaniele Pina Montão
Daniele Pina Montão
PSPaulo Geovani Silva Sousa
Paulo Geovani Silva Sousa
LRLeandro Lopes Ramos
Leandro Lopes Ramos
VCValiria Duarte Cerqueira
Valiria Duarte Cerqueira
Two outbreaks of trypanosomiasis by Trypanosoma evansi in horses in the municipality of Chaves, Marajó Island, Pará State, Brazil are reported. The first outbreak occurred in April 2011 in a farm with 147 horses; of these, 47 (31.97%) got sick, and 40 (27.21%) died. The second outbreak occurred in May 2012 and involved nine properties. Of a total of 679 horses, 209 (30.07%) got sick, and 183 (26.97%) died. The main clinical signs observed in these horses were weight loss, abdominal edema, toe dragging, and pelvic muscle atrophy. Necropsy was performed in two horses, one from each outbreak. Macroscopic alterations were not seen in the horse from the first outbreak; however, the horse from the second outbreak exhibited emaciation, pallor and icterus, as well as enlarged spleen with prominent white pulp at cut surface. Histopathology of the central nervous system of both animals revealed mild to severe, diffuse lymphoplasmacytic encephalitis, with presence of Mott cells. Immunohistochemistry for T. evansi revealed structures similar to intralesional trypomastigote forms. Between November and December of 2013, an epidemiological survey was carried out in the municipalities of Cachoeira do Arari, Santa Cruz do Arari, Salvaterra, Soure, and Chaves. Only Santa Cruz do Arari and Chaves had reported cases of the disease. Blood samples were collected from 243 horses for detection of T. evansi DNA by polymerase chain reaction (PCR) and 20 were positive.

1 November 2009 in Journal of Veterinary Diagnostic Investigation
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Journal Article
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VCValiria Duarte Cerqueira
Valiria Duarte Cerqueira
GRGabriela Riet-Correa
Gabriela Riet-Correa
JBJosé D. Barbosa
José D. Barbosa
MDMarcos D. Duarte
Marcos D. Duarte
COCarlos M. C. Oliveira
Carlos M. C. Oliveira
FRFranklin Riet-Correa
Franklin Riet-Correa
In the Amazon region of northern Brazil, Panicum maximum cultivars Mombaça, Tanzânia, and Massai cause severe colic and death in horses and mules. The disease occurs in the rainy season, when sprouting pastures are grazed by equidae. In the 8 separate disease outbreaks studied, a total of 52 out of 153 equidae were affected, including 19 that died (10 mules and 9 horses). Clinical signs were colic and abdominal dilatation, with a clinical manifestation period of 12 hr to 4 days. Serum activities of gamma-glutamyl transferase and aspartate aminotransferase were within reference intervals; however, serum urea nitrogen and creatinine concentrations were occasionally elevated. The primary gross and histologic lesions were observed in the digestive system. The stomach, small intestine, and large intestine had severe hemorrhages and occasional mucosal erosions and ulcerations. Ulceration and hemorrhage of the urinary bladder were rarely observed. Histologic examination revealed diffuse lymphoplasmacytic gastritis and enteritis with severe congestion, hemorrhage, and occasional epithelial necrosis and ulceration. Lymphocellular necrosis was occasionally observed within gut-associated lymphoid tissue. Tubular nephrosis occurred in some animals. Degeneration and occasional necrosis of bile duct epithelial cells and degeneration of hepatocytes were observed in the liver. Toxic pastures were negative for diosgenin- and yamogenin-based saponins, and oxalate concentrations were within reference intervals for the species. The toxin or toxins causing disease and the reason for the toxicity of the plant in the northern region are unknown.

26 September 2023 in Transboundary and Emerging Diseases
Verified
Journal Article
Open access
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DFDiana Maria de Farias
Diana Maria de Farias
FBFlávia de Nazaré Leite Barros
Flávia de Nazaré Leite Barros
FSFrancisco Dantas Sampaio-Júnior
Francisco Dantas Sampaio-Júnior
JVJuliana dos Santos Cruz Vieira
Juliana dos Santos Cruz Vieira
TGThamirys de Sousa Gonçalves
Thamirys de Sousa Gonçalves
ASAlessandra Scofield
Alessandra Scofield
Histoplasma capsulatum is the etiological agent of histoplasmosis, which can infect birds and different mammal species, including humans. In Brazil, the disease is not notifiable, and little is known about its infection in domestic and wild mammals. This study aimed to perform the molecular detection of H. capsulatum in small wild mammals from peri-urban forest remnants and in dogs and cats peri-domiciled in rural communities adjacent to these fragments in the Pará State, Brazilian Amazon. Samples of lung, liver, and skin were collected from free-living rats and marsupials captured in three peri-urban forest patches, as well as blood and skin from dogs and cats. H. capsulatum DNA was detected by nested PCR amplification, with products sequenced and subjected to phylogenetic analysis. H. capsulatum DNA was detected in 9.5% (12/126) of small wild mammals, with rats having a higher frequency of positive animals (25.6%; 10/39) when compared to marsupials (2.3%; 2/87) ( ). The frequencies of positive dogs and cats were 1.6% (2/121) and 5.5% (1/18), respectively. A higher frequency of infection by H. capsulatum was observed among small wild mammals when compared to dogs and cats ( ). In conclusion, H. capsulatum infection occurs in rats, marsupials, dogs, and cats in the Brazilian Amazon, with rats being important sentinels of the presence of this fungus in areas of remaining forest.