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Development and evaluation of one-step real-time RT-PCR assay for improved detection of foot-and-mouth disease virus serotypes circulating in Egypt.
El Bagoury, Gabr F; Elhabashy, Rawan; Mahmoud, Ayman H; Hagag, Naglaa M; El Zowalaty, Mohamed E.
Afiliação
  • El Bagoury GF; Department of Virology, Faculty of Veterinary Medicine, Benha University, Toukh 13736, Egypt.
  • Elhabashy R; Biotechnology Research Unit, Animal Health Research Institute, Agricultural Research Center, Dokki 12618, Giza, Egypt. Electronic address: Dr.rawan1990@hotmail.com.
  • Mahmoud AH; Biotechnology Research Unit, Animal Health Research Institute, Agricultural Research Center, Dokki 12618, Giza, Egypt.
  • Hagag NM; Genome Research Unit, Animal Health Research Institute, Agricultural Research Center, Dokki 12618, Giza, Egypt. Electronic address: naglaahagagahri@gmail.com.
  • El Zowalaty ME; Department of Microbiology and Immunology, Faculty of Pharmacy, El Saleheya El Gadida University, El Saleheya El Gadida, 44813, Ash Sharqia, Egypt; Zoonosis Science Center, Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden. Electronic address: Elzow005@gmail.co
J Virol Methods ; 306: 114525, 2022 08.
Article em En | MEDLINE | ID: mdl-35337855
ABSTRACT
Foot-and-mouth disease (FMD) is an extremely contagious and economically important viral disease affecting livestock. Rapid and precise diagnosis of FMD is of critical importance for efficient control and surveillance strategies of the disease. In this study, one-step real-time reverse transcription-polymerase chain reaction (RT-qPCR) assays were developed using newly designed primers/probe sets in the conserved regions within the VP1 coding sequence for specific detection of FMDV serotypes SAT 2 and O with their different lineage circulating in Egypt. The assays were validated for efficacy to detect different lineages of these endemic FMDV serotypes in Egypt; the detection limit was 10 genomic copies for serotype SAT 2 and one genomic copy for serotype O, with no cross-reactivity observed. These findings were confirmed by the specific and sensitive detection of FMDV in clinical samples obtained from different regions in Egypt and representing a range of subtypes within the SAT 2 and O serotypes. The results illustrated the potential of tailored RT-qPCR methods for the rapid detection and serotyping of FMDV belonging to different lineages of serotypes SAT 2 and O circulating in Egypt with high sensitivity and specificity. The developed assays could be easily deployed for routine surveillance and hence improving the disease control measures.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vírus da Febre Aftosa / Febre Aftosa Tipo de estudo: Diagnostic_studies Limite: Animals País/Região como assunto: Africa Idioma: En Revista: J Virol Methods Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vírus da Febre Aftosa / Febre Aftosa Tipo de estudo: Diagnostic_studies Limite: Animals País/Região como assunto: Africa Idioma: En Revista: J Virol Methods Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Egito