Development and validation of a modified TaqMan based real-time PCR assay targeting the lipl32 gene for detection of pathogenic Leptospira in canine urine samples

Abstract A modified TaqMan real-time polymerase chain reaction targeting a 138 bp fragment within the lipl32 gene was developed to identify exclusively pathogenic Leptospira spp. in dog urine samples. Thirty-five samples from dogs with suspected clinical leptospirosis and 116 samples from apparently...

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Main Authors: Bruno Alonso Miotto, Aline Santana da Hora, Sueli Akemi Taniwaki, Paulo Eduardo Brandão, Marcos Bryan Heinemann, Mitika Kuribayashi Hagiwara
Format: Article
Language:English
Published: Sociedade Brasileira de Microbiologia
Series:Brazilian Journal of Microbiology
Subjects:
Dog
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822018000300584&lng=en&tlng=en
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spelling doaj-2b82bdb762144a489323b8c361263f2b2020-11-25T00:59:50ZengSociedade Brasileira de MicrobiologiaBrazilian Journal of Microbiology1678-440549358459010.1016/j.bjm.2017.09.004S1517-83822018000300584Development and validation of a modified TaqMan based real-time PCR assay targeting the lipl32 gene for detection of pathogenic Leptospira in canine urine samplesBruno Alonso MiottoAline Santana da HoraSueli Akemi TaniwakiPaulo Eduardo BrandãoMarcos Bryan HeinemannMitika Kuribayashi HagiwaraAbstract A modified TaqMan real-time polymerase chain reaction targeting a 138 bp fragment within the lipl32 gene was developed to identify exclusively pathogenic Leptospira spp. in dog urine samples. Thirty-five samples from dogs with suspected clinical leptospirosis and 116 samples from apparently healthy dogs were tested for presence of leptospiral DNA using the TaqMan-based assay. The results were compared with those from a well-established conventional PCR targeting the 16S RNA encoding gene associated with nucleotide sequencing analysis. The overall agreement between the assays was 94.8% (confidence interval [CI] 95% 88-100%). The newly developed assay presented 91.6% (CI 95% 71.5-98.5%) relative sensitivity (22[+] lipl32 PCR/24[+] 16S RNA and sequencing), 100% (CI 95% 96.3-100%) relative specificity and 98.7% accuracy (CI 95% 94.8-100%). The lipl32 assay was able to detect and quantify at least 10 genome equivalents/reaction. DNA extracted from 17 pathogenic Leptospira spp., 8 intermediate/saprophytic strains and 21 different pathogenic microorganisms were also tested using the lipl32 assay, resulting in amplification exclusively for pathogenic leptospiral strains. The results also demonstrated high intra and inter-assay reproducibility (coefficient of variation 1.50 and 1.12, respectively), thereby qualifying the newly developed assay as a highly sensitive, specific and reliable diagnostic tool for leptospiral infection in dogs using urine specimens.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822018000300584&lng=en&tlng=enLeptospirosisDogUrineqPCRlipl32
collection DOAJ
language English
format Article
sources DOAJ
author Bruno Alonso Miotto
Aline Santana da Hora
Sueli Akemi Taniwaki
Paulo Eduardo Brandão
Marcos Bryan Heinemann
Mitika Kuribayashi Hagiwara
spellingShingle Bruno Alonso Miotto
Aline Santana da Hora
Sueli Akemi Taniwaki
Paulo Eduardo Brandão
Marcos Bryan Heinemann
Mitika Kuribayashi Hagiwara
Development and validation of a modified TaqMan based real-time PCR assay targeting the lipl32 gene for detection of pathogenic Leptospira in canine urine samples
Brazilian Journal of Microbiology
Leptospirosis
Dog
Urine
qPCR
lipl32
author_facet Bruno Alonso Miotto
Aline Santana da Hora
Sueli Akemi Taniwaki
Paulo Eduardo Brandão
Marcos Bryan Heinemann
Mitika Kuribayashi Hagiwara
author_sort Bruno Alonso Miotto
title Development and validation of a modified TaqMan based real-time PCR assay targeting the lipl32 gene for detection of pathogenic Leptospira in canine urine samples
title_short Development and validation of a modified TaqMan based real-time PCR assay targeting the lipl32 gene for detection of pathogenic Leptospira in canine urine samples
title_full Development and validation of a modified TaqMan based real-time PCR assay targeting the lipl32 gene for detection of pathogenic Leptospira in canine urine samples
title_fullStr Development and validation of a modified TaqMan based real-time PCR assay targeting the lipl32 gene for detection of pathogenic Leptospira in canine urine samples
title_full_unstemmed Development and validation of a modified TaqMan based real-time PCR assay targeting the lipl32 gene for detection of pathogenic Leptospira in canine urine samples
title_sort development and validation of a modified taqman based real-time pcr assay targeting the lipl32 gene for detection of pathogenic leptospira in canine urine samples
publisher Sociedade Brasileira de Microbiologia
series Brazilian Journal of Microbiology
issn 1678-4405
description Abstract A modified TaqMan real-time polymerase chain reaction targeting a 138 bp fragment within the lipl32 gene was developed to identify exclusively pathogenic Leptospira spp. in dog urine samples. Thirty-five samples from dogs with suspected clinical leptospirosis and 116 samples from apparently healthy dogs were tested for presence of leptospiral DNA using the TaqMan-based assay. The results were compared with those from a well-established conventional PCR targeting the 16S RNA encoding gene associated with nucleotide sequencing analysis. The overall agreement between the assays was 94.8% (confidence interval [CI] 95% 88-100%). The newly developed assay presented 91.6% (CI 95% 71.5-98.5%) relative sensitivity (22[+] lipl32 PCR/24[+] 16S RNA and sequencing), 100% (CI 95% 96.3-100%) relative specificity and 98.7% accuracy (CI 95% 94.8-100%). The lipl32 assay was able to detect and quantify at least 10 genome equivalents/reaction. DNA extracted from 17 pathogenic Leptospira spp., 8 intermediate/saprophytic strains and 21 different pathogenic microorganisms were also tested using the lipl32 assay, resulting in amplification exclusively for pathogenic leptospiral strains. The results also demonstrated high intra and inter-assay reproducibility (coefficient of variation 1.50 and 1.12, respectively), thereby qualifying the newly developed assay as a highly sensitive, specific and reliable diagnostic tool for leptospiral infection in dogs using urine specimens.
topic Leptospirosis
Dog
Urine
qPCR
lipl32
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822018000300584&lng=en&tlng=en
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