AI Article Synopsis

  • Leishmaniasis is a significant public health issue in Iran, and this study focuses on the genetic diversity and relationships among various parasite isolates using multi-locus sequence typing (MLST).
  • A total of 41 Leishmaniasis isolates from humans, canines, and rodents were analyzed, leading to the identification of 22 unique haplotypes in the parasites, with one species showing the highest genetic diversity.
  • The findings suggest that MLST is an effective method for studying genetic variation in Leishmaniasis parasites, which is valuable for understanding their evolution and impact on epidemiology.

Article Abstract

Background: Leishmaniasis is an important public health parasitic infection, which is endemic in many parts of the world, including Iran. We aimed to investigate genetic diversity and phylogenetic relationship among different isolates using multi-locus sequence typing (MLST).

Methods: Totally, 41 isolates collected either from patients referred to Leishmaniasis Diagnostics and Treatment Center at Tehran University of Medical Sciences, Tehran, Iran or from animals during 2019-2021, were subjected to the study. They included and from human, from canine, and from rodents from different endemic foci of Iran analyzed using MLST including and genes.

Results: A total of 5010 bps was analyzed from each isolate. The three targets, , , and , generated better topology comparing to the other genes. In the 44 isolates, 22 haplotypes (STs) were identified. contained the highest number of haplotypes (n=12) comparing to (n=8), (n=1) and (n=1). All five genomic loci caused separation of Iranian species at the species level, indicating conservation of these genes in the parasite.

Conclusion: The highest number of haplotypes belonged to , indicating that the genetic diversity of this species is higher than that of . It was further confirmed that the MLST is a suitable method to examine genetic variation of parasites with respect to evolutionary and epidemiological studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11246199PMC
http://dx.doi.org/10.18502/ijpa.v19i2.15853DOI Listing

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