Functional annotation and comparative genomics analysis of Balamuthia mandrillaris reveals potential virulence-related genes

Balamuthia mandrillaris is a pathogenic protozoan that causes a rare but almost always fatal infection of the central nervous system and, in some cases, cutaneous lesions. Currently, the genomic data for this free-living amoeba include the description of several complete mitochondrial genomes. In co...

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Veröffentlicht in:Scientific reports 2023-08, Vol.13 (1), p.14318-14318, Article 14318
Hauptverfasser: Otero-Ruiz, Alejandro, Rodriguez-Anaya, Libia Zulema, Lares-Villa, Fernando, Lozano Aguirre Beltrán, Luis Fernando, Lares-Jiménez, Luis Fernando, Gonzalez-Galaviz, Jose Reyes, Cruz-Mendívil, Abraham
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Sprache:eng
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Zusammenfassung:Balamuthia mandrillaris is a pathogenic protozoan that causes a rare but almost always fatal infection of the central nervous system and, in some cases, cutaneous lesions. Currently, the genomic data for this free-living amoeba include the description of several complete mitochondrial genomes. In contrast, two complete genomes with draft quality are available in GenBank, but none of these have a functional annotation. In the present study, the complete genome of B. mandrillaris isolated from a freshwater artificial lagoon was sequenced and assembled, obtaining an assembled genome with better assembly quality parameter values than the currently available genomes. Afterward, the genome mentioned earlier, along with strains V039 and 2046, were subjected to functional annotation. Finally, comparative genomics analysis was performed, and it was found that homologous genes in the core genome potentially involved in the virulence of Acanthamoeba spp. and Trypanosoma cruzi . Moreover, eleven of fifteen genes were identified in the three strains described as potential target genes to develop new treatment approaches for B. mandrillaris infections. These results describe proteins in this protozoan's complete genome and help prioritize which target genes could be used to develop new treatments.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-023-41657-6