Abstract
Abstract
Background
In South America, cutaneous leishmaniasis (CL) and visceral leishmaniasis (VL) are emerging diseases, expanding in the border area of Argentina, Brazil and Paraguay. Outbreaks of CL were reported since the 1990s, with Nyssomyia whitmani as the main vector in this region. Regarding VL, urban reports started in 2010 with Lutzomyia longipalpis as the main vector. The aim of this study was to evaluate environmental determinants related to the main vectors of leishmaniasis, to contribute to the prevention and control response to the emergence of VL and CL in the Argentina-Brazil-Paraguay border region.
Methods
The cross-sectional survey includes two cities and two close rural areas in the Argentinean Northeast Region, between November 2014 and January 2015, with a total of 95 sampling sites. REDILA-BL traps were set for three consecutive nights, and a total of 68 meso- and microscale environmental and landscape characteristics were surveyed. The association between vector abundance with different variables was evaluated using a generalized linear model with zero-inflated negative binomial distribution. We analyzed females for detection of Leishmania DNA.
Results
The analysis for Lu. longipalpis indicates an excess of absences when the mean NDWI around the sites were higher. The abundance of Lu. longipalpis at mesoscale level was higher when more urban services were present, and when blood sources such as chickens or dogs at the microscale level were present. For Ny. whitmani, no variable was found to be associated with the absences, while its abundance increased in association with the following variables: percentage of tree cover, presence of garbage collection service, hosted people and, at microscale, the presence of poultry. Leshmania infantum DNA was detected in 2/49 (4%) Lu. longipalpis.
Conclusions
The abundance of both species is influenced by variables at different scales, their influence probably has a hierarchy and they are acting on different aspects of the biology of these vectors. The urban spatial segregation of Lu. longipalpis and the peri-urban and rural segregation of N. whitmani increase the risk of VL and CL. The selection of the better variables for each scale will allow the design of appropriate control strategies depending on species.
Funder
International Development Research Centre
Publisher
Springer Science and Business Media LLC
Subject
Infectious Diseases,Parasitology
Reference82 articles.
1. WHO. Control of leishmaniasis: report of the meeting of the WHO Expert Commitee on the control of leishmaniases. Geneva: World Health Organization; 2010. https://apps.who.int/iris/handle/10665/44412.
2. PAHO. Plan of action for the elimination of neglected infectious diseases and post-elimination actions 2016–2022. Resolution CD55/15. 2016. Washington: Pan American Health Organization; 2016. http://iris.paho.org/xmlui/handle/123456789/31434.
3. Salomón O, Sinagra A, Nevot M, Barberian G, Paulin P, Estévez JO, et al. First visceral leishmaniasis focus in Argentina. Mem Inst Oswaldo Cruz. 2008;103:109–11.
4. Quintana MG, Fernández MS, Salomón OD. Distribution and abundance of Phebotominae, vectors of leishmaniasis, in Argentina: spatial and temporal analysis at different scales. J Trop Med. 2012;2012:652803.
5. Salomon OD. Instructions on how to make an outbreak of American cutaneous leishmaniasis. J Trop Med Health. 2019;3:146.
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