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TaqMan real-time PCR for detection of pathogenic Leptospira spp. in canine clinical samples.
Rahman, Mohammad Sabri Abdul; Khor, Kuan Hua; Khairani-Bejo, Siti; Lau, Seng Fong; Mazlan, Mazlina; Roslan, Mohd Azri; Ajat, Mohd Mokrish Md; Noor, Mohd Akmal Mohd.
Afiliación
  • Rahman MSA; Department of Veterinary Clinical Studies, Guelph, Selangor, Malaysia.
  • Khor KH; Department of Veterinary Diagnostics, Faculty of Veterinary Medicine, Universiti Malaysia Kelantan, Pengkalan Chepa, 16100, Kota Bharu, Kelantan, Malaysia.
  • Khairani-Bejo S; Department of Veterinary Clinical Studies, Guelph, Selangor, Malaysia.
  • Lau SF; University Veterinary Hospital, Faculty of Veterinary Medicine, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
  • Mazlan M; Department of Veterinary Pathology and Microbiology, Selangor, Malaysia.
  • Roslan MA; Department of Veterinary Clinical Studies, Guelph, Selangor, Malaysia.
  • Ajat MMM; University Veterinary Hospital, Faculty of Veterinary Medicine, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
  • Noor MAM; Department of Veterinary Pathology and Microbiology, Selangor, Malaysia.
J Vet Res ; 67(2): 187-195, 2023 Jun.
Article en En | MEDLINE | ID: mdl-38143826
ABSTRACT

Introduction:

Canine leptospirosis has always been a differential diagnosis in dogs presenting with clinical signs and blood profiles associated with kidney and/or liver disease. The conventional polymerase chain reaction (PCR) provides diagnoses, but real-time PCR-based tests provide earlier confirmation and determine the severity of infection, especially in the acute stage, allowing early detection for immediate treatment decisions. To our knowledge, real-time PCR has not been routinely adopted for clinical investigation in Malaysia. This study evaluated TaqMan real-time PCR (qPCR) assays diagnosing leptospirosis and compared their applicability to clinical samples from dogs with kidney and/or liver disease against a conventional PCR reference. Material and

Methods:

The qPCR assays were validated using existing leptospiral isolates. Whole blood and urine samples were analysed using a conventional PCR, LipL32(1) and LipL32(2) qPCRs and a microscopic agglutination test. The sensitivity and specificity of the qPCRs were determined.

Results:

The LipL32(1) qPCR assay had more diagnostic value than the LipL32(2) qPCR assay. Further evaluation of this assay revealed that it could detect as low as five DNA copies per reaction with high specificity for the tested leptospiral strains. No cross-amplification was observed with other organisms. Analysing the clinical samples, the LipL32(1) qPCR assay had 100.0% sensitivity and >75.0% specificity.

Conclusion:

The LipL32(1) qPCR assay is sensitive, specific and has the potential to be applied in future studies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Vet Res Año: 2023 Tipo del documento: Article País de afiliación: Malasia Pais de publicación: Polonia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Vet Res Año: 2023 Tipo del documento: Article País de afiliación: Malasia Pais de publicación: Polonia