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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Molecular identification of Salmonella enterica subsp enterica serovar Gallinarum biovars Gallinarum and Pullorum by a duplex PCR assay

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Autor(es):
Alves Batista, Diego Felipe [1] ; de Freitas Neto, Oliveiro Caetano [2] ; de Almeida, Adriana Maria [1] ; Barrow, Paul Andrew [3] ; Barbosa, Fernanda de Oliveira [1] ; Berchieri Junior, Angelo [1]
Número total de Autores: 6
Afiliação do(s) autor(es):
[1] Sao Paulo State Univ, Fac Agr & Vet Sci, Sao Paulo - Brazil
[2] Univ Fed Paraiba, Agron Sci Ctr, Campus 2, BR-58397000 Areia, Paraiba - Brazil
[3] Univ Nottingham, Sch Vet Med & Sci, Loughborough, Leics - England
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION; v. 28, n. 4, p. 419-422, JUL 2016.
Citações Web of Science: 4
Resumo

Salmonella enterica subsp. enterica serovar Gallinarum biovar Gallinarum (S. Gallinarum) and biovar Pullorum (S. Pullorum) are 2 poultry pathogens that cause major economic losses to the poultry industry worldwide. Control of both diseases mainly relies on the adoption of biosecurity programs, and success is dependent on accurate and fast detection. Based on this concept, we developed a duplex PCR assay, targeting 2 chromosomal sequences, which allowed us to precisely identify and differentiate S. Gallinarum and S. Pullorum field strains. This assay was validated by testing genomic DNA from 40 S. Gallinarum and 29 S. Pullorum field strains, 87 other Salmonella serovars, and 7 non-Salmonella strains. The serovar identifier region (SIR) primers produced a fragment only in S. Gallinarum and S. Pullorum strains, whereas the fragment from the ratA coding sequence, which was previously demonstrated to differentiate the 2 biovars, was also amplified from other Salmonella serovars. Our results showed that the combination of both SIR and ratA amplifications could be used to identify as well as to differentiate colonies of S. Gallinarum and S. Pullorum reliably. Thus, we believe this methodology can be a useful ancillary tool for routine veterinary diagnostic laboratories by providing rapid, accurate results. (AU)

Processo FAPESP: 11/23483-1 - Salmonella Gallinarum (SG): 1. Comparação do genoma de Sg e S. Pullorum. 2. Sequenciamento de mutante atenuado (Sg "cobS" cbiA) e análise do transcriptoma em macrófagos de aves. 3. Patogenia de estirpes com e sem flagelos
Beneficiário:Angelo Berchieri Junior
Linha de fomento: Auxílio à Pesquisa - Regular