Gp63 gene polymorphism and population structure of Leishmania donovani complex: influence of the host selection

S Guerbouj1, K Victoir, I Guizani

  • 1Institut Pasteur de Tunis, Laboratoire d'Epidémiologie et Ecologie Parasitaire, Tunis Belvédère, Tunisia.

Parasitology
|February 24, 2001
PubMed

Insights

Host immune pressure shapes Leishmania gp63 surface proteins, influencing parasite population structure. This study reveals host selection impacts gp63 gene evolution differently than neutral markers.

Area of Science:

  • Parasitology
  • Molecular Biology
  • Population Genetics

Background:

  • The surface metalloproteinase gp63 is a key virulence factor in Leishmania parasites.
  • Understanding gp63 evolution is crucial for deciphering Leishmania population dynamics and host-parasite interactions.

Purpose of the Study:

  • To investigate the influence of host selective pressure on the genetic structuring of Leishmania populations, focusing on the gp63 gene.
  • To compare the population structure derived from gp63-encoding genes with neutral markers (isoenzymes) and non-coding regions (gp63 intergenic regions).

Main Methods:

  • Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used to analyze gp63 encoding genes and intergenic regions in 35 Leishmania isolates.
  • Comparative analysis with existing isoenzyme data was performed.

Main Results:

  • The gp63 encoding region exhibited higher polymorphism than gp63 intergenic regions.
  • The four species within the Leishmania donovani complex were clearly discriminated by gp63 intra-genic analysis.
  • Geographical structuring was observed within Leishmania infantum based on gp63 data, distinct from isoenzyme and intergenic analyses.

Conclusions:

  • Strong host selection, particularly at the vertebrate immunological level, significantly influences gp63 evolution.
  • The choice of genetic markers (e.g., coding vs. non-coding regions) impacts the perceived population structure of Leishmania.

Related Concept Videos

Leishmaniasis01:30

Leishmaniasis

Leishmaniasis is a protozoal disease caused by species of the genus Leishmania and transmitted through the bite of infected female sandflies. The parasite exists in two principal morphological forms during its life cycle. A sandfly acquires intracellular amastigotes from an infected reservoir host, such as a dog. Within the sandfly, these forms differentiate into motile, flagellated promastigotes. During a subsequent blood meal, promastigotes are injected into the human host, where they...
Antiprotozoal Agents01:21

Antiprotozoal Agents

Leishmaniasis is a widespread parasitic disease caused by several Leishmania species. It affects millions of people each year and remains a major public health problem in endemic regions. First-line treatment relies on pentavalent antimonials, including meglumine antimoniate and sodium stibogluconate. Even so, how these drugs work has not been fully clear, especially their interaction with parasite-specific biochemical pathways. One key target is trypanothione reductase (TR), an enzyme that...
Malaria01:29

Malaria

Malaria pathogenesis in humans reflects a delicate interplay between parasite biology and host response. Clinical illness reflects a host’s immune response to the parasite’s asexual replication cycle, which is often asymptomatic in individuals with partial immunity. From the parasite's perspective, transmission between mosquito and human with minimal host pathology is evolutionarily advantageous. Among the six Plasmodium species infecting humans, P. falciparum and P. vivax dominate in global...
Principles of Pharmacogenetics: Types of Genetic Variants01:27

Principles of Pharmacogenetics: Types of Genetic Variants

The human genome is over 99.9% identical between individuals, yet genetic differences exist at millions of bases. The human genome contains approximately 3 million variant positions per individual, many of which are heterozygous, contributing to genetic diversity and individual traits. Genetic variations include single-nucleotide polymorphisms (SNPs), insertions, deletions, and copy number variations (CNVs).SNPs, the most common variation, involve single-base changes in DNA. These can be...