Piacenza M.F.,CONICET |
Piacenza M.F.,National University of Rio Cuarto |
Gomez D.M.,CONICET |
Gomez D.M.,National University of Rio Cuarto |
And 5 more authors.
International Journal of Pest Management | Year: 2011
We evaluate several management options for Calomys musculinus populations through the formulation and validation of a cohort structured model. Initially, a basic model was constructed and validated using field population data. Next, the model was altered to allow us to evaluate different management options. In general, basic model results were in agreement with field data, demonstrating that this model would be useful in describing aspects of corn mouse population dynamics. Restricting control measures to when mouse numbers reach high levels would be inadequate, because population numbers tend to increase in size after some years. In contrast, reducing vegetation cover in spring was more effective in reducing field population abundances. Despite some limitations, the model could be useful for evaluating the relationships between population dynamics and some biotic or physical environmental variables, and thus ensure more efficient use of resources in integrated pest management. © 2011 Taylor & Francis.
Moreno E.S.,Federal University of Para |
Agostini I.,CONICET |
Holzmann I.,CONICET |
Di Bitetti M.S.,CONICET |
And 9 more authors.
Memorias do Instituto Oswaldo Cruz | Year: 2015
In South America, yellow fever (YF) is an established infectious disease that has been identified outside of its traditional endemic areas, affecting human and nonhuman primate (NHP) populations. In the epidemics that occurred in Argentina between 2007-2009, several outbreaks affecting humans and howler monkeys (Alouatta spp) were reported, highlighting the importance of this disease in the context of conservation medicine and public health policies. Considering the lack of information about YF dynamics in New World NHP, our main goal was to apply modelling tools to better understand YF transmission dynamics among endangered brown howler monkey (Alouatta guariba clamitans) populations in northeastern Argentina. Two complementary modelling tools were used to evaluate brown howler population dynamics in the presence of the disease: Vortex, a stochastic demographic simulation model, and Outbreak, a stochastic disease epidemiology simulation. The baseline model of YF disease epidemiology predicted a very high probability of population decline over the next 100 years. We believe the modelling approach discussed here is a reasonable description of the disease and its effects on the howler monkey population and can be useful to support evidence-based decision-making to guide actions at a regional level. © 2015, Fundacao Oswaldo Cruz. All rights reserved.
Bisordi I.,Instituto Adolfo Lutz |
Levis S.,Instituto Nacional Of Enfermedades Virales Humanas Dr Julio I Maiztegui |
Maeda A.Y.,Instituto Adolfo Lutz |
Suzuki A.,Instituto Adolfo Lutz |
And 7 more authors.
Vector-Borne and Zoonotic Diseases | Year: 2015
Arenavirus Sabiá was originally isolated from a fatal human infection in Brazil, and after the occurrence of the second fatal human case in São Paulo state, epidemiologic and virologic studies were performed in the area where the patient lived, aiming at the identification of the Sabiá natural rodent reservoir. A broadly cross-reactive enzyme-linked immunosorbent assay (ELISA) was used to screen for antibody-positive samples. Antibodies to arenavirus were detected in two of the 55 samples of Calomys tener, and from these results, samples of rodents were analyzed by a broad RT-PCR assay. RT-PCR amplification detected arenavirus sequences in five of the 55 C. tener samples, and sequencing showed that this virus is a distinct form of Sabiá virus. Thus, we describe here the evidence for the circulation of a new arenavirus in Brazil (proposed name Pinhal virus) and its genetic characterization compared to other arenaviruses. This study also suggests C. tener as a probable rodent reservoir for this virus and associates this new virus with the lineage C of New World arenaviruses. Although we have defined some characteristics of this virus, so far, there is no evidence of its involvement in human disease. Copyright 2015, Mary Ann Liebert, Inc.
Biscayart C.,Ministerio de Salud de la Nacion |
Carrega M.E.P.,Ministerio de Salud de la Nacion |
Sagradini S.,Ministerio de Salud de la Nacion |
Bentancourt S.,Administracion Nacional de Medicamentos |
And 9 more authors.
Vaccine | Year: 2014
As a consequence of YF outbreaks that hit Brazil, Argentina, and Paraguay in 2008-2009, a significant demand for YF vaccination was subsequently observed in Argentina, a country where the usual vaccine recommendations are restricted to provinces that border Brazil, Paraguay, and Bolivia. The goal of this paper is to describe the adverse events following immunization (AEFI) against YF in Argentina during the outbreak in the northeastern province of Misiones, which occurred from January 2008 to January 2009. During this time, a total of nine cases were reported, almost two million doses of vaccine were administered, and a total of 165 AEFI were reported from different provinces. Case study analyses were performed using two AEFI classifications. Forty-nine events were classified as related to the YF vaccine (24 serious and 1 fatal case), and 12 events were classified as inconclusive. As the use of the YF 17D vaccine can be a challenge to health systems of countries with different endemicity patterns, a careful clinical and epidemiological evaluation should be performed before its prescription to minimize serious adverse events. © 2014 Elsevier Ltd.
Mahmutovic S.,Harvard University |
Clark L.,Harvard University |
Levis S.C.,Instituto Nacional Of Enfermedades Virales Humanas Dr Julio I Maiztegui |
Briggiler A.M.,Instituto Nacional Of Enfermedades Virales Humanas Dr Julio I Maiztegui |
And 5 more authors.
Cell Host and Microbe | Year: 2015
Summary In the Western hemisphere, at least five mammarenaviruses cause human viral hemorrhagic fevers with high case fatality rates. Junín virus (JUNV) is the only hemorrhagic fever virus for which transfusion of survivor immune plasma that contains neutralizing antibodies ("passive immunity") is an established treatment. Here, we report the structure of the JUNV surface glycoprotein receptor-binding subunit (GP1) bound to a neutralizing monoclonal antibody. The antibody engages the GP1 site that binds transferrin receptor 1 (TfR1) - the host cell surface receptor for all New World hemorrhagic fever mammarenaviruses - and mimics an important receptor contact. We show that survivor immune plasma contains antibodies that bind the same epitope. We propose that viral receptor-binding site accessibility explains the success of passive immunity against JUNV and that this functionally conserved epitope is a potential target for therapeutics and vaccines to limit infection by all New World hemorrhagic fever mammarenaviruses. © 2015 Elsevier Inc.