Distribution and Polymorphisms of Group I Introns in Mitochondrial Genes from Cryptococcus neoformans and Cryptococcus gattii

被引:1
作者
Gomes, Ronald Muryellison Oliveira da Silva [1 ]
da Silva, Kassia Jessica Galdino [1 ]
Ferreira, Leonardo Capistrano [1 ,2 ]
Arantes, Thales Domingos [3 ]
Theodoro, Raquel Cordeiro [1 ,4 ]
机构
[1] Univ Fed Rio Grande do Norte, Inst Trop Med, BR-59064741 Natal, RN, Brazil
[2] Univ Fed Rio Grande do Norte, Ctr Biosci, Dept Biochem, BR-59064741 Natal, RN, Brazil
[3] Univ Fed Goias, Inst Trop Pathol & Publ Hlth, BR-74605050 Goiania, GO, Brazil
[4] Univ Fed Rio Grande do Norte, Ctr Biosci, Dept Cell Biol & Genet, BR-59064741 Natal, RN, Brazil
关键词
cryptococcosis; autocatalytic introns; cryptic species; cob; cox1; CANDIDA-ALBICANS; PATHOGEN CRYPTOCOCCUS; RAPID IDENTIFICATION; VAR; NEOFORMANS; SUSCEPTIBILITY; INHERITANCE; INHIBITION; SYMBIONTS; VARIETIES; SEQUENCE;
D O I
10.3390/jof9060629
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The species complexes Cryptococcus neoformans and Cryptococcus gattii are the causative agents of cryptococcosis. Virulence and susceptibility to antifungals may vary within each species according to the fungal genotype. Therefore, specific and easily accessible molecular markers are required to distinguish cryptic species and/or genotypes. Group I introns are potential markers for this purpose because they are polymorphic concerning their presence and sequence. Therefore, in this study, we evaluated the presence of group I introns in the mitochondrial genes cob and cox1 in different Cryptococcus isolates. Additionally, the origin, distribution, and evolution of these introns were investigated by phylogenetic analyses, including previously sequenced introns for the mtLSU gene. Approximately 80.5% of the 36 sequenced introns presented homing endonucleases, and phylogenetic analyses revealed that introns occupying the same insertion site form monophyletic clades. This suggests that they likely share a common ancestor that invaded the site prior to species divergence. There was only one case of heterologous invasion, probably through horizontal transfer to C. decagattii (VGIV genotype) from another fungal species. Our results showed that the C. neoformans complex has fewer introns compared to C. gattii. Additionally, there is significant polymorphism in the presence and size of these elements, both among and within genotypes. As a result, it is impossible to differentiate the cryptic species using a single intron. However, it was possible to differentiate among genotypes within each species complex, by combining PCRs of mtLSU and cox1 introns, for C. neoformans species, and mtLSU and cob introns for C. gattii species.
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