The Maze Pathway of Coevolution: A Critical Review over the Leishmania and Its Endosymbiotic History
The description of the genus as the causative agent of leishmaniasis occurred in the modern age. However, evolutionary studies suggest that the origin of can be traced back to the Mesozoic era. Subsequently, during its evolutionary process, it achieved worldwide dispersion predating the breakup of t...
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Veröffentlicht in: | Genes 2021-04, Vol.12 (5), p.657 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The description of the genus
as the causative agent of leishmaniasis occurred in the modern age. However, evolutionary studies suggest that the origin of
can be traced back to the Mesozoic era. Subsequently, during its evolutionary process, it achieved worldwide dispersion predating the breakup of the Gondwana supercontinent. It is assumed that this parasite evolved from monoxenic Trypanosomatidae. Phylogenetic studies locate dixenous
in a well-supported clade, in the recently named subfamily Leishmaniinae, which also includes monoxenous trypanosomatids. Virus-like particles have been reported in many species of this family. To date, several
species have been reported to be infected by
RNA virus (LRV) and
(LBV). Since the first descriptions of LRVs decades ago, differences in their genomic structures have been highlighted, leading to the designation of LRV1 in
. (
) species and LRV2 in
. (
) species. There are strong indications that viruses that infect
spp. have the ability to enhance parasitic survival in humans as well as in experimental infections, through highly complex and specialized mechanisms. Phylogenetic analyses of these viruses have shown that their genomic differences correlate with the parasite species infected, suggesting a coevolutionary process. Herein, we will explore what has been described in the literature regarding the relationship between
and endosymbiotic
viruses and what is known about this association that could contribute to discussions about the worldwide dispersion of |
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ISSN: | 2073-4425 2073-4425 |
DOI: | 10.3390/genes12050657 |