Tatiane Marques Porangaba de Oliveira, Peter Gordon Foster, Ivy Luizi Rodrigues de Sá, Maria Anice Mureb Sallum
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引用次数: 0
Abstract
Background: Culex (Melanoconion) species are known to act as vectors for different arboviruses, and little is known about the mitochondrial genome of these species.
Objectives: Aiming to expand the genetic knowledge of this subgenus, a 12Kb fragment of the mitochondrial genome was sequenced from 23 specimens belonging to the Atratus and Educator Groups of the subgenus Melanoconion of Culex.
Methods: The sequenced specimens were morphologically identified as Culex dunni, Culex ensiformis, Culex theobaldi, Culex trigeminatus, Culex eknomios, Culex zeteki, Culex near commevynenis, Culex angularis, Culex longistriatus, and Culex near vaxus. The reads were assembled with the reference genome of Culex quinquefasciatus and MITOS2 was used for gene annotation. Values of guanine-cytosine (GC) and adenine-thymine (AT) skews, nucleotide diversity, ratio between non-synonymous (Ka) and synonymous (Ks) substitution, and nucleotide composition were calculated, and phylogenetic analysis was performed.
Findings: As in other Culex mitogenomes, the partial mitochondrial genomes include 12 protein coding genes (PCGs), 15 tRNA, and 1 rRNA (rrnL). The PCGs showed no length variation between the species studied. ND5 gene presented one less base in the new sequences, which generated a stop codon and, consequently, a shorter length in relation to the Cx. quinquefasciatus sequence reference. All specimens showed a positive value for AT-skew and negative for GC-skew. Nucleotide diversity varied between 0.00407 and 0.12085. Ka/Ks values ranged from 0.0 to 2.775.
Main conclusions: Leucine and Serine were the most abundant amino acids. Phylogenetic analysis suggested three putative species.
期刊介绍:
Memórias do Instituto Oswaldo Cruz is a journal specialized in microbes & their vectors causing human infections. This means that we accept manuscripts covering multidisciplinary approaches and findings in the basic aspects of infectious diseases, e.g. basic in research in prokariotes, eukaryotes, and/or virus. Articles must clearly show what is the main question to be answered, the hypothesis raised, and the contribution given by the study.
Priority is given to manuscripts reporting novel mechanisms and general findings concerning the biology of human infectious prokariotes, eukariotes or virus. Papers reporting innovative methods for diagnostics or that advance the basic research with these infectious agents are also welcome.
It is important to mention what we do not publish: veterinary infectious agents research, taxonomic analysis and re-description of species, epidemiological studies or surveys or case reports and data re-analysis. Manuscripts that fall in these cases or that are considered of low priority by the journal editorial board, will be returned to the author(s) for submission to another journal.