6533b862fe1ef96bd12c6da7

RESEARCH PRODUCT

Comparison of two PCR methods for detection of Leptospira interrogans in formalin-fixed and paraffin-embedded tissues

Maria VitaleYarelys Zamora MartínezCarmen Fernandez MolinaAleco D'andreaRosa AlduinaV. Monteverde

subject

DNA BacterialMicrobiology (medical)Serotypelcsh:Arctic medicine. Tropical medicineTissue Fixationlcsh:RC955-962lcsh:QR1-502KidneySettore BIO/19 - Microbiologia GeneralePolymerase Chain Reactionlcsh:Microbiologylaw.invention23S ribosomal RNAlawLeptospiraFormaldehydeRNA Ribosomal 16SmedicinediagnosticsAnimalsFFPE tissueLungPolymerase chain reactionLeptospiraParaffin EmbeddingbiologymicrobiologyRibosomal RNAbiology.organism_classification16S ribosomal RNAmedicine.diseaseLeptospirosisMolecular biologyRNA Ribosomal 23SPCRCattleLeptospira interrogansLeptospira interrogans

description

In this study we compared two polymerase chain reaction (PCR) methods using either 16S ribosomal RNA (rRNA) or 23S rRNA gene primers for the detection of different Leptospira interrogans serovars. The performance of these two methods was assessed using DNA extracted from bovine tissues previously inoculated with several bacterial suspensions. PCR was performed on the same tissues before and after the formalin-fixed, paraffin-embedding procedure (FFPE tissues). The 23S rDNA PCR detected all fresh and FFPE positive tissues while the 16S rDNA-based protocol detected primarily the positive fresh tissues. Both methods are specific for pathogenic L. interrogans. The 23S-based PCR method successfully detected Leptospira in four dubious cases of human leptospirosis from archival tissue specimens and one leptospirosis-positive canine specimen. A sensitive method for leptospirosis identification in FFPE tissues would be a useful tool to screen histological specimen archives and gain a better assessment of human leptospirosis prevalence, especially in tropical countries, where large outbreaks can occur following the rainy season.

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