| Literature DB >> 33724149 |
Jovana Sádlová1, Lucie Podešvová2, Tomáš Bečvář1, Claretta Bianchi2, Evgeny S Gerasimov3, Andreu Saura2, Kristýna Glanzová1, Tereza Leštinová1, Nadezhda S Matveeva3,4, Ľubomíra Chmelová2, Denisa Mlacovská2, Tatiana Spitzová1, Barbora Vojtková1, Petr Volf1, Vyacheslav Yurchenko2,4, Natalya Kraeva2.
Abstract
Catalase is one of the most abundant enzymes on Earth. It decomposes hydrogen peroxide, thus protecting cells from dangerous reactive oxygen species. The catalase-encoding gene is conspicuously absent from the genome of most representatives of the family Trypanosomatidae. Here, we expressed this protein from the Leishmania mexicana Β-TUBULIN locus using a novel bicistronic expression system, which relies on the 2A peptide of Teschovirus A. We demonstrated that catalase-expressing parasites are severely compromised in their ability to develop in insects, to be transmitted and to infect mice, and to cause clinical manifestation in their mammalian host. Taken together, our data support the hypothesis that the presence of catalase is not compatible with the dixenous life cycle of Leishmania, resulting in loss of this gene from the genome during the evolution of these parasites.Entities:
Keywords: Leishmania; catalase; dixeny; evolution; virulence
Year: 2021 PMID: 33724149 PMCID: PMC7971327 DOI: 10.1080/21505594.2021.1896830
Source DB: PubMed Journal: Virulence ISSN: 2150-5594 Impact factor: 5.882