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Identification of pathogenic Leptospira strains in tissues of a premature foal by use of polymerase chain reaction analysis.

Abstract: Studies were carried out to determine the cause of death in a prematurely born Thoroughbred foal that died 24 hours after birth. Necropsy revealed gross lesions suggestive of septicemia. A commercial Leptospira polymerase chain reaction (PCR) assay designed to specifically amplify the hemolysis-associated protein 1 (hap1) gene present only in pathogenic Leptospira strains detected the presence of Leptospira DNA in various tissues of the foal. Histologic examination of lung, liver, kidney, and myocardium revealed numerous spirochetes in Warthin-Starry-stained tissue sections. Results of PCR analysis and histologic examination suggested a leptospiral infection in the newborn foal. At the moment of death, the infection coexisted with a streptococcal-associated aspiration bronchopneumonia and postpartum septicemia. These findings indicate that the PCR assay based on the amplification of the hap1 gene represents a useful tool for specific detection of pathogenic leptospira in field samples taken from horses.
Publication Date: 2006-04-19 PubMed ID: 16617708DOI: 10.1177/104063870601800216Google Scholar: Lookup
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Summary

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The research article delves into a study aiming at discerning the cause of death in a premature Thoroughbred foal who died 24 hours post-birth. It was established that the foal died due to a Leptospira infection, confirmed through various polymerase chain reaction (PCR) assays and histologic examinations.

About the Research

  • The research was driven by an endeavor to identify the reason behind the sudden death of a prematurely born Thoroughbred foal. The foal had died merely 24 hours after birth, spurring the researchers to explore the causes.
  • The investigation was conducted post-mortem, and a necropsy was conducted on the foal. The necropsy signaled indications of septicemia, a severe infection of the bloodstream.

Findings from PCR Assay

  • The researchers utilized Polymerase Chain Reaction (PCR), a prevalent molecular biology method, for the examination. A commercial Leptospira PCR assay was employed particularly for this study, aiming at amplifying the hemolysis-associated protein 1 (hap1) gene exclusively present in pathogenic Leptospira strains.
  • The test unveiled the presence of Leptospira DNA in various tissues of the foal, suggesting the likelihood of a Leptospira infection.

Revelations from Histologic Examination

  • On examining tissue sections of lung, liver, kidney, and myocardium (heart muscle), the researchers observed numerous spirochetes (a type of bacteria causing diseases like syphilis and Lyme disease).
  • These spirochetes were detected clearly in Warthin-Starry-stained tissue sections, finalizing the presence of a bacterial infection.

Final Inference

  • The researchers concluded through the PCR analysis and histologic examination results that a leptospiral infection was present in the newborn foal. This infection coexisted with aspiration bronchopneumonia associated with Streptococcal bacteria, as well as postpartum septicemia, when the foal passed away.
  • The research underscored the effectiveness of the PCR assay. It was found beneficial for the amplification of the hap1 gene, proving vital for detecting specific pathogenic leptospira in samples collected from horses in the field.

Cite This Article

APA
Léon A, Pronost S, Tapprest J, Foucher N, Blanchard B, André-Fontaine G, Laugier C, Fortier G, Leclercq R. (2006). Identification of pathogenic Leptospira strains in tissues of a premature foal by use of polymerase chain reaction analysis. J Vet Diagn Invest, 18(2), 218-221. https://doi.org/10.1177/104063870601800216

Publication

ISSN: 1040-6387
NlmUniqueID: 9011490
Country: United States
Language: English
Volume: 18
Issue: 2
Pages: 218-221

Researcher Affiliations

Léon, Albertine
  • Laboratoire Départemental Frank Duncombe, Caen, France.
Pronost, Stéphane
    Tapprest, Jackie
      Foucher, Nathalie
        Blanchard, Béatrice
          André-Fontaine, Geneviève
            Laugier, Claire
              Fortier, Guillaume
                Leclercq, Roland

                  MeSH Terms

                  • Animals
                  • Animals, Newborn
                  • Antigens, Bacterial / chemistry
                  • Antigens, Bacterial / genetics
                  • DNA, Bacterial / chemistry
                  • DNA, Bacterial / genetics
                  • Fatal Outcome
                  • Hemolysin Proteins
                  • Horse Diseases / diagnosis
                  • Horse Diseases / microbiology
                  • Horses
                  • Leptospira / genetics
                  • Leptospira / isolation & purification
                  • Leptospirosis / diagnosis
                  • Leptospirosis / microbiology
                  • Leptospirosis / veterinary
                  • Polymerase Chain Reaction / veterinary
                  • RNA, Ribosomal, 16S / chemistry
                  • RNA, Ribosomal, 16S / genetics
                  • RNA, Ribosomal, 23S / chemistry
                  • RNA, Ribosomal, 23S / genetics

                  Citations

                  This article has been cited 6 times.
                  1. Khaki P, Rahimi Zarchi F, Moradi Bidhendi S, Gharakhani M. Application of a Multiplex PCR Assay for Molecular Identification of Pathogenic and Non-Pathogenic Leptospires based on lipL32 and 16S rRNA Genes.. Arch Razi Inst 2023 Feb;78(1):413-418.
                    doi: 10.22092/ARI.2022.359211.2388pubmed: 37312705google scholar: lookup
                  2. Pui CF, Bilung LM, Apun K, Su'ut L. Diversity of Leptospira spp. in Rats and Environment from Urban Areas of Sarawak, Malaysia.. J Trop Med 2017;2017:3760674.
                    doi: 10.1155/2017/3760674pubmed: 28348601google scholar: lookup
                  3. Hamond C, Pinna A, Martins G, Lilenbaum W. The role of leptospirosis in reproductive disorders in horses.. Trop Anim Health Prod 2014 Jan;46(1):1-10.
                    doi: 10.1007/s11250-013-0459-3pubmed: 23990441google scholar: lookup
                  4. Widiyanti D, Koizumi N, Fukui T, Muslich LT, Segawa T, Villanueva SY, Saito M, Masuzawa T, Gloriani NG, Yoshida S. Development of immunochromatography-based methods for detection of leptospiral lipopolysaccharide antigen in urine.. Clin Vaccine Immunol 2013 May;20(5):683-90.
                    doi: 10.1128/CVI.00756-12pubmed: 23467776google scholar: lookup
                  5. Zakeri S, Sepahian N, Afsharpad M, Esfandiari B, Ziapour P, Djadid ND. Molecular epidemiology of leptospirosis in northern Iran by nested polymerase chain reaction/restriction fragment length polymorphism and sequencing methods.. Am J Trop Med Hyg 2010 May;82(5):899-903.
                    doi: 10.4269/ajtmh.2010.09-0721pubmed: 20439973google scholar: lookup
                  6. Båverud V, Gunnarsson A, Engvall EO, Franzén P, Egenvall A. Leptospira seroprevalence and associations between seropositivity, clinical disease and host factors in horses.. Acta Vet Scand 2009 Mar 30;51(1):15.
                    doi: 10.1186/1751-0147-51-15pubmed: 19331656google scholar: lookup