Affiliation:
1. N. H. Swellengrebel Laboratory for Tropical Hygiene, Royal Tropical Institute, Amsterdam, The Netherlands.
Abstract
Primers for polymerase chain reaction (PCR) were synthesized from clones derived from a Leptospira hardjo (type hardjobovis) library. One pair of synthetic oligonucleotide primers was selected for further analysis. Under experimental conditions an amplification was obtained with DNA of Leptospira interrogans of some serovars belonging to serogroup sejroe. However, very little or no amplification was observed with DNA from other serovars of this group. No amplification was observed with DNA from other serogroups, other bacteria, or eucaryotic organisms. Cattle urine, seeded with hardjobovis, was processed in several ways and subsequently subjected to PCR. Boiling of the samples or treatment with detergents appeared to be most effective. Urine samples containing fewer than 10 leptospires gave a positive result in the PCR assay. Twenty urine samples obtained from a slaughterhouse or farm cows were investigated using the PCR assay, culture isolation, dot and quick blot hybridization, and serological tests. This comparative study suggests that amplification by PCR may be a valuable method for the detection of leptospires in cattle urine.
Publisher
American Society for Microbiology
Reference21 articles.
1. Detection of cytomegalovirus in urine from newborns by using polymerase chain reaction DNA amplification;Demmler G. J.;J. Infect. Dis.,1988
2. Ellis W. A. 1986. The diagnosis of leptospirosis in farm animals p. 13-31. In W. A. Ellis and T. W. A. Little (ed.) The present state of leptospirosis diagnosis and control. Martinus Nijhoff Publ. Dortrecht The Netherlands.
3. The use of bacterial restriction endonuclease analysis to classify Icterohaemorrhagiae and Autumnalis serovars;Hookey J. V.;Isr. J. Vet. Med.,1987
4. Differentiation of pathogenic and saphrophytic leptospires. I. Growth at low temperatures;Johnson R. C.;J. Bacteriol.,1967
5. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A;Kogan S. C.;N. Engl. J. Med.,1987
Cited by
103 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献