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. 2020 Aug 10;14(8):e0008411.
doi: 10.1371/journal.pntd.0008411. eCollection 2020 Aug.

Modelling geospatial distributions of the triatomine vectors of Trypanosoma cruzi in Latin America

Affiliations

Modelling geospatial distributions of the triatomine vectors of Trypanosoma cruzi in Latin America

Andreas Bender et al. PLoS Negl Trop Dis. .

Abstract

Approximately 150 triatomine species are suspected to be infected with the Chagas parasite, Trypanosoma cruzi, but they differ in the risk they pose to human populations. The largest risk comes from species that have a domestic life cycle and these species have been targeted by indoor residual spraying campaigns, which have been successful in many locations. It is now important to consider residual transmission that may be linked to persistent populations of dominant vectors, or to secondary or minor vectors. The aim of this project was to define the geographical distributions of the community of triatomine species across the Chagas endemic region. Presence-only data with over 12, 000 observations of triatomine vectors were extracted from a public database and target-group background data were generated to account for sampling bias in the presence data. Geostatistical regression was then applied to estimate species distributions and fine-scale distribution maps were generated for thirty triatomine vector species including those found within one or two countries and species that are more widely distributed from northern Argentina to Guatemala, Bolivia to southern Mexico, and Mexico to the southern United States of America. The results for Rhodnius pictipes, Panstrongylus geniculatus, Triatoma dimidiata, Triatoma gerstaeckeri, and Triatoma infestans are presented in detail, including model predictions and uncertainty in these predictions, and the model validation results for each of the 30 species are presented in full. The predictive maps for all species are made publicly available so that they can be used to assess the communities of vectors present within different regions of the endemic zone. The maps are presented alongside key indicators for the capacity of each species to transmit T. cruzi to humans. These indicators include infection prevalence, evidence for human blood meals, and colonisation or invasion of homes. A summary of the published evidence for these indicators shows that the majority of the 30 species mapped by this study have the potential to transmit T. cruzi to humans.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Construction of background points.
Illustration of the construction of background points using the TGB approach for species Panstrongylus megistus. Panel (A): A convex hull is constructed around the presence locations of the species. Panel (B): The hull is extended by a fixed width of 5 degrees (extended hull). Panel (C): Background points are added using presence locations of all other species within the extended hull. Panel (D): Blocks of width wk are allocated randomly across the extended hull. The observations in blocks numbered 1-4 are used as training data, and the observations in blocks numbered 5 are assigned to the test data. One fold consists of all blocks sharing the same number. Figure created by the authors using R package tmap [41].
Fig 2
Fig 2. Predicted relative probability of occurrence.
Predictions for 4 selected species at a resolution of 5 × 5 km within the respective extended hull of species occurrence (left panel) and bivariate map (right panel), where darker colours indicate higher predicted probabilities while the transition from white/pink to turquoise/blue indicates increased uncertainty. Row 1 (A, B): Triatoma gerstaeckeri; row 2 (C, D): Triatoma dimidiata; row 3 (E, F): Rhodnius pictipes; row 4 (G, H): Panstrongylus geniculatus. Figure created by the authors using R package tmap [41].
Fig 3
Fig 3
Left panel: Final predicted map for T.infestans. Right panel: A bivariate map of the predictions that indicates areas of high vs. low probabilities together with the model uncertainty. Darker colours indicate higher predicted probability. Transitions from white/pink to turquoise/blue indicate higher uncertainty.

References

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