Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
1.
Rev. Soc. Bras. Med. Trop ; 50(2): 239-242, Mar.-Apr. 2017. tab, graf
Article in English | LILACS | ID: biblio-1041406

ABSTRACT

Abstract INTRODUCTION: This study aimed to develop a duplex endpoint PCR assay for rapid detection and differentiation of Leptospira strains. METHODS: Primers were designed to target the rrs (LG1/LG2) and ligB (LP1/LP2) genes to confirm the presence of the Leptospira genus and the pathogenic species, respectively. RESULTS: The assay showed 100% specificity against 17 Leptospira strains with a limit of detection of 23.1pg/µl of leptospiral DNA and sensitivity of 103 leptospires/ml in both spiked urine and water. CONCLUSIONS: Our duplex endpoint PCR assay is suitable for rapid early detection of Leptospira with high sensitivity and specificity.


Subject(s)
DNA, Bacterial/isolation & purification , Polymerase Chain Reaction/methods , DNA Primers , Leptospira/classification , Species Specificity , Sensitivity and Specificity , Leptospira/isolation & purification , Leptospira/genetics
2.
Southeast Asian J Trop Med Public Health ; 2004 Mar; 35(1): 92-6
Article in English | IMSEAR | ID: sea-35698

ABSTRACT

Pulsed field gel electrophoresis (PFGE) and antimicrobial susceptibility analysis were undertaken on twenty-three strains of Salmonella enterica serovar Tshiongwe, an unusual serovar, which recently emerged in Malaysia. Antimicrobial susceptibility analysis showed that all the strains were sensitive to ampicilin, chloramphenicol, cotrimoxazole, and kanamycin. Twenty (87%) and 8 (3.5%) strains had resistance to tetracycline and streptomycin respectively. PFGE analysis subtyped 23 strains into 10 profiles (Dice coefficient of similarity, F = 0.7-1.0). The predominant profile, X1 was found in both clinical and environmental isolates and was widely distributed in different parts of Malaysia during the study period. In addition, isolates recovered from food, a hand-towel, apron and the surface of a table-top in one particular location had unique, indistinguishable profiles (X4/4a) and identical antibiograms. Similarly, isolates from cooked meat and a chopping board had PFGE profiles similar to some human isolates. These probably indicated cross-contamination and poor hygiene in food practices, hence contributing to Salmonellosis. Factors causing the emergence of this rare Salmonella serovar being responsible for food poisoning episodes during the study period remained unclear. The study reiterated the usefulness and versatility of PFGE in the molecular subtyping of this rare Salmonella serovar in Malaysia.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacterial Typing Techniques , DNA, Bacterial/analysis , Electrophoresis, Gel, Pulsed-Field , Humans , Incidence , Malaysia/epidemiology , Microbial Sensitivity Tests , Salmonella Infections/diagnosis , Salmonella enterica/classification , Sensitivity and Specificity
SELECTION OF CITATIONS
SEARCH DETAIL