Biology subjects

Calzada, J. E.

Publications and source records attributed to Calzada, J. E..

3 recordsLinked to original sources

bioRxiv2026

Forest fragmentation, anthropogenic land use, and climate shape sand fly community composition in central Panama.

Background: American cutaneous leishmaniasis (ACL) is endemic in central Panama, where rapid land use change is transforming tropical landscapes and potentially altering the ecology of sand fly vectors. Although researchers have widely studied environmental determinants of individual vector species, community-level responses of sand fly assemblages to landscape modification remain poorly understood. We evaluated how landscape composition, fragmentation, climate, and topography influence sand fly community structure in a rural landscape of central Panama. Methodology/Principal Findings: We combined metacommunity analyses with joint species distribution models (JSDMs) to quantify species-specific and community-level responses to climatic variables, land-cover composition, and forest configuration. We collected 1,692 individuals representing 30 species, including nine anthropportunist taxa of epidemiological importance. Sand fly assemblages had strong nestedness, low species turnover, and predominantly positive residual associations. Several anthropportunist sand fly species occurred across heterogeneous landscapes, although their responses to environmental conditions differed among taxa. Land-cover composition, forest fragmentation metrics, and elevation together explained about half of the variance in species occurrence and abundance, with the remainder attributed to climate and spatial, temporal, and community-level random effects. Grassland cover contributed most strongly to sand fly occurrence and abundance, whereas artificial surfaces consistently reduced both metrics. Fragmentation effects varied by species: edge density often increased occurrence and abundance, whereas more forest patches generally suppressed populations. Increased precipitation broadly enhanced occurrence and abundance, whereas higher temperatures negatively affected several taxa. Conclusions/significance: Landscape heterogeneity predictably structures sand fly communities, and different forms of anthropogenic disturbance exert non-uniform effects on vector assemblages. The nested organization of these assemblages and the co-occurrence of several anthropophilic species suggest that multiple potential vector species may be present across heterogeneous landscapes. These findings highlight the need for landscape-informed surveillance and control strategies that prioritize grassland-forest interfaces and other disturbed ecotones where sand fly species of epidemiological importance frequently co-occur.

ecology↗

bioRxiv2018

Repeat-driven generation of antigenic diversity in a major human pathogen, Trypanosoma cruzi

Trypanosoma cruzi, a zoonotic kinetoplastid protozoan with a complex genome, is the causative agent of American trypanosomiasis (Chagas disease). The parasite uses a highly diverse repertoire of surface molecules, with roles in cell invasion, immune evasion and pathogenesis. Thus far, the genomic regions containing these genes have been impossible to resolve and it has been impossible to study the structure and function of the several thousand repetitive genes encoding the surface molecules of the parasite. We here present an improved genome assembly of a T. cruzi clade I (TcI) strain using high coverage PacBio single molecule sequencing, together with Illumina sequencing of 34 T. cruzi TcI isolates and clones from different geographic locations, sample sources and clinical outcomes. Resolution of the surface molecule gene structure reveals an unusual duality in the organisation of the parasite genome, a core genomic region syntenous with related protozoa flanked by unique and highly plastic subtelomeric regions encoding surface antigens. The presence of abundant interspersed retrotransposons in the subtelomeres suggests that these elements are involved in a recombination mechanism for the generation of antigenic variation and evasion of the host immune response. The comparative genomic analysis of the cohort of TcI strains revealed multiple cases of such recombination events involving surface molecule genes and has provided new insights into T. cruzi population structure.

genomics↗

bioRxiv2017

Human Migration And The Spread Of Malaria Parasites To The New World

BackgroundThe Americas were the last continent to be settled by modern humans, but how and when human malaria parasites arrived in the New World is uncertain. Here, we apply phylogenetic analysis and coalescent-based gene flow modeling to a global collection of Plasmodium falciparum and P. vivax mitogenomes to infer the demographic history and geographic origins of malaria parasites circulating in the Americas. Importantly, we examine P. vivax mitogenomes from previously unsampled forest-covered sites along the Atlantic Coast of Brazil, including the vivax-like species P. simium that locally infects platyrrhini monkeys.\n\nResultsThe best-supported gene flow models are consistent with migration of both malaria parasites from Africa and South Asia to the New World, with no genetic signature of a population bottleneck upon parasite's arrival in the Americas. We found evidence of additional gene flow from Melanesia in P. vivax (but not P. falciparum) mitogenomes from the Americas and speculate that some P. vivax lineages might have arrived with the Australasian peoples who contributed genes to Native Americans in pre-Columbian times. Mitochondrial haplotypes characterized in P. simium from monkeys from the Atlantic Forest are shared by local humans. These vivax-like lineages have not spread to the Amazon Basin, are much less diverse than P. vivax circulating elsewhere in Brazil, and show no close genetic relatedness with P. vivax populations from other continents.\n\nConclusionsEnslaved peoples brought from a wide variety of African locations were major carriers of P. falciparum mitochondrial lineages into the Americas, but additional human migration waves are likely to have contributed to the extensive genetic diversity of present-day New World populations of P. vivax. The reduced genetic diversity of vivax-like monkey parasites, compared with human P. vivax from across this country, argues for a recent human-to-monkey transfer of these lineages in the Atlantic Forest of Brazil.\n\nAuthor summaryMalaria is currently endemic to the Americas, with over 400,000 laboratory-confirmed infections reported annually, but how and when human malaria parasites entered this continent remains largely unknown. To determine the geographic origins of malaria parasites currently circulating in the Americas, we examined a global collection of Plasmodium falciparum and P. vivax mitochondrial genomes, including those from understudied isolates of P. vivax and P. simium, a vivax-like species that infect platyrrhini monkeys, from the Atlantic Forest of Brazil. We found evidence of significant historical migration to the New World of malaria parasites from Africa and, to a lesser extent, South Asia, with further genetic contribution of Melanesian lineages to South American P. vivax populations. Importantly, mitochondrial haplotypes of P. simium are shared by monkeys and humans from the Atlantic Forest, most likely as a result of a recent human-to-monkey transfer. Interestingly, these potentially zoonotic lineages are not found in the Amazon Basin, the main malaria-endemic area in the Americas. We conclude that enslaved Africans were the main carriers of P. falciparum mitochondrial lineages into the Americas, whereas additional migration waves of Australasian peoples and parasites may have contributed to the genetic makeup of present-day New World populations of P. vivax.

microbiology↗