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Application of pulsed-field gel electrophoresis for molecular identification of pathogenic Leptospira species in Iran: a rapid and reliable method.
Khaki, Pejvak; Bagherpour, Mohsen; Gharakhani, Mehdi; Sadat Soltani, Maryam; Shahcheraghi, Fereshteh; Sadat Nikbin, Vajihe.
Affiliation
  • Khaki P; Department of Microbiology, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.
  • Bagherpour M; Department of Microbiology, Saveh Branch, Islamic Azad University, Saveh, Iran.
  • Gharakhani M; Department of Microbiology, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.
  • Sadat Soltani M; Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran.
  • Shahcheraghi F; Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran.
  • Sadat Nikbin V; Department of Bacteriology, Pasteur Institute of Iran, Tehran, Iran.
Iran J Microbiol ; 16(3): 323-328, 2024 Jun.
Article in En | MEDLINE | ID: mdl-39005606
ABSTRACT
Background and

Objectives:

Leptospirosis is a zoonotic disease caused by pathogenic Leptospira serovars. The genus Leptospira cannot differentiated by conventional techniques. However, identity determination of pathogenic serovar is precious of public health problems and epidemiological studies. Pulsed-field gel electrophoresis facilitates rapid identification of Leptospires to the serovar levels. Materials and

Methods:

In this study, we employed PFGE to evaluate 28 Leptospira isolates, with animal, human and environmental origin, obtained from Razi Vaccine and Serum Research Institute of Karaj, Iran. PFGE patterns of 28 Leptospira serovars were generated using the Not I restriction enzyme in comparison with the lambda ladder.

Results:

Out of 28 serovars evaluated, we identified 22 different pulsed types, designated P1-P22. Out of 22 pulse groups, 3 were found to be a common type, but others were a single Type. Groups consisting of the common type were P3, P9, P14, and P16. The results showed that the discriminatory index of PFGE by Not I enzyme was 0.99, demonstrating heterogeneous differentiation among serovar members.

Conclusion:

The PFGE methodology used in this study showed excellent interlaboratory report usability, rapid, reliable, enabling standardization and data sharing between laboratories.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Iran J Microbiol Year: 2024 Document type: Article Affiliation country: Iran

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Iran J Microbiol Year: 2024 Document type: Article Affiliation country: Iran