Abstract
BackgroundThe transmission of malaria in the extra-Amazonian regions of Brazil, although interrupted in the 1960s, has persisted to the present time in some areas of dense Atlantic Forest, with reports of cases characterized by particular transmission cycles and clinical presentations. Bromeliad-malaria, as it is named, is particularly frequent in the state of Espírito Santo, with Plasmodium vivax being the parasite commonly recognized as the aetiologic agent of human infections. With regard to the spatial and temporal distances between cases reported in this region, the transmission cycle does not fit the traditional malaria cycle. The existence of a zoonosis, with infected simians participating in the epidemiology, is therefore hypothesized. In the present study, transmission of bromeliad-malaria in Espírito Santo is investigated, based on the complete mitochondrial genome of DNA extracted from isolates of Plasmodium species, which had infected humans, a simian from the genus Allouata, and Anopheles mosquitoes. Plasmodium vivax/simium was identified in the samples by both nested PCR and real-time PCR. After amplification, the mitochondrial genome was completely sequenced and compared with a haplotype network which included all sequences of P. vivax/simium mitochondrial genomes sampled from humans and simians from all regions in Brazil.ResultsThe haplotype network indicates that humans and simians from the Atlantic Forest become infected by the same haplotype, but some isolates from humans are not identical to the simian isolate. In addition, the plasmodial DNA extracted from mosquitoes revealed sequences different from those obtained from simians, but similar to two isolates from humans.ConclusionsThese findings strengthen support for the hypothesis that in the Atlantic Forest, and especially in the state with the highest frequency of bromeliad-malaria in Brazil, parasites with similar molecular backgrounds are shared by humans and simians. The recognized identity between P. vivax and P. simium at the species level, the sharing of haplotypes, and the participation of the same vector in transmitting the infection to both host species indicate interspecies transference of the parasites. However, the intensity, frequency and direction of this transfer remain to be clarified.
Highlights
The transmission of malaria in the extra-Amazonian regions of Brazil, interrupted in the 1960s, has persisted to the present time in some areas of dense Atlantic Forest, with reports of cases characterized by particular transmission cycles and clinical presentations
The recent evidence presented by Brasil et al [11] of some single nucleotide polymorphisms differentiating P. simium from P. vivax do not imply their separation in two different species
In order to better ascertain the distinctive genetic characteristics of these variants, this study presents the molecular characterization of P. vivax/simium based on the sequencing of the mitochondrial genomes of parasites isolated from both human and simian hosts, and, unprecedentedly, from Anopheles mosquitoes in an endemic area of the Brazilian Atlantic Forest
Summary
The transmission of malaria in the extra-Amazonian regions of Brazil, interrupted in the 1960s, has persisted to the present time in some areas of dense Atlantic Forest, with reports of cases characterized by particular transmission cycles and clinical presentations. Following the first report of a natural infection of P. simium in a human being [5], the identity between P. simium and P. vivax has been established many times: (1) by studies regarding the CSP protein in the early 1990s [6], (2) by phylogenetic analyses based on sequencing of the cytochrome b gene of the mitochondrial genome [7], (3) by microsatellite polymorphisms [8], (4) again by CSP variations [9], and (5) by Msp-1 gene sequencing [10] In this context, the recent evidence presented by Brasil et al [11] of some single nucleotide polymorphisms differentiating P. simium from P. vivax do not imply their separation in two different species. This hypothesis is supported by Rodrigues et al [25] based on limited genetic variability between P. simium and P. vivax
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