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1.
Am J Trop Med Hyg ; 81(1): 5-12, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19556558

RESUMEN

This study examined the larval breeding habitat of a major South American malaria vector, Anopheles darlingi, in areas with varying degrees of ecologic alteration in the Peruvian Amazon. Water bodies were repeatedly sampled across 112 km of transects along the Iquitos-Nauta road in ecologically varied areas. Field data and satellite imagery were used to determine the landscape composition surrounding each site. Seventeen species of Anopheles larvae were collected. Anopheles darlingi larvae were present in 87 of 844 sites (10.3%). Sites with A. darlingi larvae had an average of 24.1% forest cover, compared with 41.0% for sites without A. darlingi (P < 0.0001). Multivariate analysis identified seasonality, algae, water body size, presence of human populations, and the amount of forest and secondary growth as significant determinants of A. darlingi presence. We conclude that deforestation and associated ecologic alterations are conducive to A. darlingi larval presence, and thereby increase malaria risk.


Asunto(s)
Anopheles/fisiología , Ecosistema , Insectos Vectores/fisiología , Malaria/transmisión , Árboles , Animales , Cruzamiento , Ecología , Eucariontes/fisiología , Humanos , Perú
2.
Clin Infect Dis ; 46(12): 1822-8, 2008 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-18462104

RESUMEN

BACKGROUND: Chagas disease, caused by Trypanosoma cruzi infection, is an urban problem in Arequipa, Peru, and the epidemiology of Chagas disease is likely to be quite different in this area, compared with in rural zones. METHODS: We conducted a serosurvey of 1615 children <18 years old in periurban districts that included hillside shantytowns and slightly more affluent low-lying communities. In addition, 639 adult residents of 1 shantytown were surveyed to provide data across the age spectrum for this community. RESULTS: Of 1615 children, 75 (4.7%) were infected with Trypanosoma cruzi. Infection risk increased by 12% per year of age, and children living in hillside shantytowns were 2.5 times as likely to be infected as were those living in lower-lying communities. However, age-prevalence data from 1 shantytown demonstrated that adults were no more likely to be seropositive than were teenagers; the results of maximum likelihood modeling suggest that T. cruzi transmission began in this community <20 years ago. CONCLUSIONS: The problem of Chagas disease in periurban settings, such as those around Arequipa, must be addressed to achieve elimination of vector-borne T. cruzi transmission. Identification of infected children, vector-control efforts, and education to avoid modifiable risk factors are necessary to decrease the burden of Chagas disease.


Asunto(s)
Enfermedad de Chagas/epidemiología , Enfermedad de Chagas/transmisión , Trypanosoma cruzi/aislamiento & purificación , Adolescente , Adulto , Factores de Edad , Animales , Niño , Preescolar , Femenino , Humanos , Lactante , Recién Nacido , Funciones de Verosimilitud , Masculino , Perú/epidemiología , Estudios Seroepidemiológicos , Factores de Tiempo , Trypanosoma cruzi/inmunología , Población Urbana
3.
Am J Trop Med Hyg ; 74(4): 546-53, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16606982

RESUMEN

Over the past decade, anti-malarial drug resistance has rapidly become a major public health problem in the Peruvian Amazon. This study compared polymerase chain reaction (PCR) to light microscopy for diagnosing and monitoring the parasitological response of malaria patients to anti-malarial chemotherapy in the Peruvian Amazon region of Iquitos. Typing of P. falciparum using MSP1, MSP2, and glutamine-rich protein distinguished among infecting parasites. Most (73%) P. falciparum patients were parasitologically resistant to sulfadoxine-pyrimethamine (RI = 10, RII = 1). Sensitivity of microscopy was lower than PCR (69% for P. vivax and 78% for P. falciparum), but parasite clearance times were comparable between microscopy and PCR. PCR sensitively and specifically detected mixed infections and low-level parasitemia indicative of drug resistance, making this approach of practical use for the control of malaria at the public health level. Genotyping malaria parasites will be useful to distinguish drug failure from new infections in clinical trials of anti-malarial drugs in the Peruvian Amazon region.


Asunto(s)
Antimaláricos/uso terapéutico , Resistencia a Múltiples Medicamentos/genética , Malaria Falciparum/tratamiento farmacológico , Adolescente , Adulto , Animales , Anopheles/parasitología , Antimaláricos/administración & dosificación , Niño , Estudios de Cohortes , ADN Protozoario/análisis , Combinación de Medicamentos , Femenino , Genotipo , Humanos , Insectos Vectores/parasitología , Malaria Falciparum/epidemiología , Malaria Falciparum/transmisión , Masculino , Persona de Mediana Edad , Perú/epidemiología , Plasmodium falciparum/genética , Reacción en Cadena de la Polimerasa , Pirimetamina/administración & dosificación , Pirimetamina/uso terapéutico , Sensibilidad y Especificidad , Sulfadoxina/administración & dosificación , Sulfadoxina/uso terapéutico , Insuficiencia del Tratamiento
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