Epidemiol Health.  2015;37:e2015012. 10.4178/epih/e2015012.

An epidemiological comparative study on diagnosis of rodent leptospirosis in Mazandaran Province, northern Iran

Affiliations
  • 1Department of Epidemiology, Pasteur Institute of Iran, Tehran, Iran.
  • 2Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran.
  • 3Centre for Diseases Control and Prevention, Ministry of Health, Tehran, Iran.
  • 4Microbiology Department, Razi Vaccine and Serum Research Institute, Karaj, Iran.
  • 5Department of Biology, Ferdowsi University of Mashhad, Mashhad, Iran.
  • 6Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran. mobcghn@gmail.com

Abstract


OBJECTIVES
Leptospirosis is a zoonosis caused by leptospires, in which transmission occurs through contact with contaminated biological fluids from infected animals. Rodents can act as a source of infection for humans and animals. The disease has a global distribution, mainly in humid, tropical and sub-tropical regions. The aim of this study was to compare culture assays, the microscopic agglutination test (MAT), polymerase chain reaction (PCR), and nested PCR (n-PCR), for the diagnosis of leptospirosis in rodents in Mazandaran Province, northern Iran.
METHODS
One hundred fifty-one rodents were trapped alive at 10 locations, and their urine and kidney samples were collected and used for the isolation of live Leptospira. The infecting serovars were identified and the antibody titres were measured by MAT, using a panel of 20 strains of live Leptospira species as antigens. The presence of leptospiral DNA was evaluated in urine and kidney samples using PCR and n-PCR.
RESULTS
No live leptospires were isolated from the kidney and urine samples of the rodents. Different detection rates of leptospirosis were observed with MAT (21.2%), PCR (11.3%), and n-PCR (3.3%). The dominant strain was Leptospira serjoehardjo (34.4%, p=0.28), although other serotypes were also found. The prevalence of positive leptospirosis tests in rodents was 15.9, 2.6, and 2.6% among Rattus norvegicus, R. rattus, and Apodemus sylvaticus, respectively.
CONCLUSIONS
Leptospirosis was prevalent in rodents in Mazandaran Province, northern Iran. MAT was able to detect leptospires more frequently than culture or PCR. The kidney was a more suitable site for identifying leptospiral DNA by n-PCR than urine. Culture was not found to be an appropriate technique for clinical diagnosis.

Keyword

Culture; Iran; Leptospira; Microscopic agglutination test; Mazandaran; Nested polymerase chain reaction; Rodent

MeSH Terms

Agglutination Tests
Animals
Diagnosis*
DNA
Humans
Iran*
Kidney
Leptospira
Leptospirosis*
Murinae
Polymerase Chain Reaction
Prevalence
Rats
Rodentia*
DNA
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