SciELO - Scientific Electronic Library Online

 
vol.106 issue8Investigation into in vitro anti-leishmanial combinations of calcium channel blockers and current anti-leishmanial drugsCotrimoxazole enhances the in vitro susceptibility of Coccidioides posadasii to antifungals author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

Share


Memórias do Instituto Oswaldo Cruz

Print version ISSN 0074-0276

Mem. Inst. Oswaldo Cruz vol.106 no.8 Rio de Janeiro Dec. 2011

http://dx.doi.org/10.1590/S0074-02762011000800023 

ARTICLES

 

Distribution of phlebotomine fauna (Diptera: Psychodidae) across an urban-rural gradient in an area of endemic visceral leishmaniasis in northern Brazil

 

 

Davi Marcos Souza de OliveiraI; Elvira Maria SaraivaII; Edna Aoba Yassui IshikawaIII; Adelson Alcimar Almeida de SousaIV; Edilene Oliveira da SilvaI, +; Ivoneide Maria da SilvaI

ILaboratório de Parasitologia, Instituto de Ciências Biológicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil 4Setor de Leishmaniose, Instituto Evandro Chagas, Belém, PA, Brasil
IIDepartamento de Imunologia, Instituto de Microbiologia Paulo Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brasil
IIINúcleo de Medicina Tropical, Universidade Federal do Pará, Av. Augusto Correa 1, 66075-900 Belém, PA, Brasil
IVSetor de Leishmaniose, Instituto Evandro Chagas, Belém, PA, Brasil

 

 


ABSTRACT

The number of visceral leishmaniasis (VL) cases has increased over the past 10 years in Brazil, especially in the North and Northeast regions of the country. The aim of this study was to evaluate the urbanisation of VL vectors in Barcarena, Pará, an area in northern Brazil where VL is endemic. Sandflies were captured using Centers for Disease Control (CDC) light traps along an urban-rural gradient. The CDC traps were installed inside hen houses at a height of 150 cm. A total of 5,089 sandflies were collected and 11 species were identified. The predominant species was Lutzomyia longipalpis (rate of 95.15%), which suggests its participation in the transmission of VL. A total of 1,451 Lu. longipalpis females were dissected and no Leishmania infections were detected. Most of the sandflies were captured at the border of a forest (88.25%) and no flies were captured in the urban area, which suggests that transmission is still restricted to rural sites. However, the fact that a specimen was collected in an intermediate area indicates that urbanisation is a real possibility and that vector monitoring is important.

Key words: Phlebotominae - vectors - visceral leishmaniasis - endemic area


 

 

Visceral leishmaniasis (VL) is a chronic disease that primarily affects children. The etiological agent in South America is the flagellate protozoan Leishmania (Leishmania) infantum chagasi (Lainson & Rangel 2005). The majority of human VL cases in Brazil occur in the northeast regions (MS 2010). In the northern regions, the increase in VL has been most extensive in the states of Pará (PA) and Tocantins (TO) (MS 2010). Although VL is considered to be a rural disease, it has become urbanised in several large and small Brazilian municipalities, including Santarém (PA), Belo Horizonte [Minas Gerais (MG)], Araçatuba (São Paulo), Palmas (TO), Campo Grande [Mato Grosso do Sul (MS)] and Cuiabá [Mato Grosso (MT)] (Oliveira et al. 2003, 2006, Rangel & Lainson 2003, Dujardim 2006, De Paula et al. 2008). The VL urbanisation process is associated with deforestation and disordered urbanisation (Ximenes et al. 2007).

The principal vector of Lu. chagasi in Brazil is the phlebotomine sandfly Lutzomyia longipalpis s.l. (Lainson & Rangel 2003), which is considered a species complex due to strong evidence involving morphological and physiological differences (Lainson & Rangel 2005, Bauzer et al. 2007). Lu. longipalpis is distributed among all neotropical regions from Mexico-Argentina and occurs in all Brazilian regions (Souza et al. 2009). In addition to Lu. longipalpis, there are other species related to VL transmission in Brazil, including Lutzomyia cruzi Mangabeira, 1938, which has been associated with transmission in MT and MS (Santos et al. 1998). Lutzomyia forattinii, an anthropophilic species, has been determined to be naturally infected with Lu. chagasi (Pita-Pereira et al. 2008) and Lutzomyia evansi naturally infected with Lu. chagasi has been detected in endemic areas of Colombia (Rangel & Lainson 2003).

No study has been published regarding the relationship between anthroponotic transmission and the increasing cases of VL in PA. In addition, no study monitoring the possible urbanisation process of Lu. longipalpis has been performed. Deforestation, which is a consequence of increasing agriculture, cattle and urbanisation, plays an important role in the ecologic niche changes to thousands of phlebotomine species (Lainson & Rangel 2005). Therefore, a study to investigate the presence of Lu. longipalpis in environments altered by man is a requirement for the better control of VL in endemic areas. Thus, the present study investigated phlebotomine fauna across an urban-rural gradient and the probable urbanisation of sandflies, mainly Lu. longipalpis, which is the putative vector of L. (L.) infantum chagasi in Barcarena (PA).

 

MATERIALS AND METHODS

Study area - Barcarena (01º30'24"S 48º37'12"W) is located northeast of PA and belongs to the metropolitan mesoregion of Belém (Figure). The municipality occupies an area of 1,310 km2 and has 94,641 inhabitants.

 

 

Until 2002, the diverse vegetation of Barcarena was mostly flood forest, upland forest (mature and secondary) and swamp forest (Amaral et al. 2002). However, as a result of deforestation, the forests have given way to secondary forests in different stages of development (Pacheco et al. 2007). This region was selected because VL is endemic and the occurrence of VL has increased from 2000-2008 in this region. A total of 301 cases were reported between 2001-2008 according to the Health Department of the municipality of Barcarena.

Phlebotomine capture - Captures were performed in five excursions of 10 days each. The captures occurred in October, November and December of 2007, February of 2008 and January of 2009, totalling 50 days. From November-February, the phlebotomine population density is higher than in other months, most likely because it is the end of the summer period in PA. To evaluate phlebotomine movement from the forest to the urban areas, the captures were performed along two transects. Each transect crossed four areas: (i) forest, an area with dense vegetation and without the presence of human habitation, (ii) edge of forest, an area adjacent to the woods with sparse human habitation and scarce street lighting, (iii) intermediate areas, corresponding to the city periphery with blocks of houses and street lighting, but with less vegetation cover than the edge of forest area, and (iv) urban areas, areas with high population density, night lighting, little vegetation and where most of the buildings in the city are located. Three similar sampling points were selected in each area and totalled 12 sampling points per transect.

The first transect covered an area that has been colonised by humans for over 12 years and the four collection areas were represented by the neighbourhoods of Araticu (forest and edge of forest), Bairro Novo (intermediate area) and City Centre (urban area). The second transect covered an area that has been recently colonised (4 years ago) and the captures were made in the neighbourhoods of Barbolândia (forest and edge of forest), Betânia (intermediate area) and City Centre (urban area), as shown in Figure. The two transects are similar; however, the edge of forest area in the second transect contained human habitation, low vegetation density and intense wind exposure.

Phlebotomines were captured using Centers for Disease Control (CDC) light traps (HP model) installed 1.5 m above ground level at 6:00 pm and removed the next day at 6:00 am. In all areas, except for the forest, the CDC light traps were installed in peridomicile areas or next to or inside hen houses. Phlebotomine species were identified according to Young and Duncan (1994) using a Zeiss optical microscope.

Detection of natural infection - To evaluate the rate of natural infection with Leishmania parasites, phlebotomine females captured at the sampling points were taken to the laboratory where they were positioned on a glass slide with a drop of saline solution to remove the digestive tube, and the flies were examined to identify the presence of promastigotes.

Statistical analysis - Statistical analysis of the differences between male and female phlebotomine numbers were performed using the chi-square test. All p values < 0.05 were considered to be statistically significant.

 

RESULTS

During the experiment, 5,089 phlebotomines, which were comprised of 3,440 males and 1,649 females and belonged to 11 species, were captured (Table I). The predominant species was Lu. longipalpis (95.15%), followed by Lutzomyia (Sciopemyia) sordellii (2.06%) and Lutzomyia (Nissomyia) flaviscutellata (1.76%), and the latter is a proven vector of Lutzomyia amazonensis. The number of Lu. longipalpis males was significantly higher than the number of Lu. longipalpis females (p < 0.0001) (Table I). In contrast, among the other species captured, the number of females was equal to or greater than the number of males. Other epidemiologically important species captured in the study areas include Lutzomyia (Nissomyia) antunesi and Lutzomyia (Psychodopigus) paraensis, which represented less than 1% of the phlebotomine sandflies captured. These species are associated with the transmission of Leishmania sp. in PA.

 

 

All specimens were collected in the forest area or at the edge of the forest (Table II) except for one specimen of Lu. sordellii, which was collected in the intermediate area of the first transect. No sandflies were captured in the urban area during this study. Most of the specimens (90%) were captured in the first transect and only 10% were captured in the second transect. The species richness and abundance patterns differed between the first and second transects. In the first transect (longer human colonisation), Lu. longipalpis was the most abundant species at the forest edge and Lu. flaviscutellata was the predominant species in the forest area. In the second transect, phlebotomines were only captured in the forest edge area and Lu. longipalpis was the most abundant species.

The greatest species richness was observed in the forest edge area of the first transect (10 species) and the species richness was reduced by half (5 species) in the forest edge area of the second transect. The forest area of the first transect presented the second highest species richness (7) and no sandflies were captured in the forest area of the second transect.

A total of 1,451 Lu. longipalpis females were dissected to evaluate the natural infection rate; however, none of the flies were infected with Leishmania promastigotes. Among the other species, one Lu. sordellii female captured at the edge of the forest in the first transect was infected with unidentified flagellates.

 

DISCUSSION

This phlebotomine capture study revealed that Barcarena presents phlebotomine species of high richness and abundance in areas under anthropic impact. Similar results showing phlebotomine fauna richness have been obtained in other Brazilian cities (Andrade-Filho et al. 2001, Silva et al. 2007, 2008). Oliveira et al. (2003) captured 1,245 phlebotomines belonging to 28 species in Campo Grande (MS) and Lu. longipalpis was captured in an urban area.

In Barcarena, 98% of the specimens were collected at the edge of the forest. This finding is similar to results reported by Andrade-Filho et al. (2001), where 2,677 phlebotomines were captured in TO and 89.17% were captured at the edge of the forest with high species richness. Feliciangeli et al. (2006) captured Lutzomyia pseudolongipalpis in high abundance (98.16%) in four houses at the forest edge in El Brasilar, a rural community of Venezuela. The authors also observed that the abundance of sandflies decreased with distance from the forest edge. Quintana et al. (2010) also observed a higher abundance of phlebotomines in modified areas compared to primary vegetation areas.

Lu. longipalpis represented more than 93% of all specimens and it was the most abundant species captured at the edge of the forest in both transects. The adaptation of Lu. longipalpis to an anthroponotic environment has been observed in several studies (Oliveira et al. 2003, Ribeiro et al. 2007, Missawa et al. 2008, Rangel & Vilela 2008). This species has been found in shelters for domestic animals, such as birds, dogs and pigs, and it has also been found indoors, which demonstrates its attraction to humans (Rangel & Vilela 2008, Michalsky et al. 2009).

It is important to highlight the abundance of Lu. longipalpis at the edge of the forest in the second transect, which is where 500 Lu. longipalpis specimens were captured and only 13 phlebotomines from other species were captured. The natural vegetation in the area of the second transect was recently removed for the construction of human dwellings; therefore, the human impact is greater in this area than along the first transect. This finding suggests that Lu. longipalpis is more adaptable to disturbed areas than the other phlebotomine species captured in this area. These results are similar to those observed by Oliveira et al. (2003) in Campo Grande (MS), where a total of five species were detected in the urban area and Lu. longipalpis was the most abundant (49%). Ribeiro et al. (2007) observed that Lu. longipalpis presented higher capture rates in occupied areas of land than other captured species.

The number of Lu. longipalpis males captured in Barcarena was significantly higher than the number of Lu. longipalpis females. This pattern was also observed by Michalsky et al. (2009), who captured 78.72% Lu. longipalpis males in Janaúba (MG) and by Silva et al. (2007), who captured 79% males in Campo Grande (MS). One hypothesis to explain this pattern is that Lu. longipalpis males form groups at blood meal sites for mating purposes (Kelly & Dye 1997). According to previous studies, chemical mediators produced by hosts and vectors for finding a sexual partner may be related to the larger number of males observed compared to females for some species of sandflies (Kelly & Dye 1997).

During this study, evidence of Lu. longipalpis urbanisation in the Barcarena was not observed. However, the urbanisation of this species has been reported in many Brazilian municipalities, including Campo Grande (MS) (Oliveira et al. 2003, 2006), Uberlândia (MG) (De Paula et al. 2008), Teresina (Piauí) and São Borja (Rio Grande do Sul) (Costa et al. 2007, Souza et al. 2009). In Natal (Rio Grande do Norte), the presence of Lu. longipalpis was detected in urban and peri-urban areas (Ximenes et al. 2007). In addition, in Belo Horizonte (MG), the VL urbanisation process was found to be rapid and 29 out of the 30 reports of VL in the metropolitan area of MG in 1994 were from Belo Horizonte (Da Luz et al. 2001). More recently, 1,550 Lu. longipalpis females, six of which were infected with Lu. chagasi, were captured in the Janaúba, which is an area of intense transmission of VL. Janaúba is similar to Barcarena with respect to environmental alterations, which can be described by rapid and intense rural population migration to an urban periphery that lacks adequate housing and sanitation infrastructure (Michalsky et al. 2011).

Another phlebotomine species of epidemiological importance captured in the study area was Lu. flaviscutellata, a species that has been incriminated as a vector of L. (Leishmania) amazonensis, the etiological agent of cutaneous leishmaniasis (Lainson et al. 1994). Lu. flaviscutellata was the most abundant species in forest areas (73.33%) and the second most abundant at the edge of the forest (26.67%). Similar results were observed by Rebêlo et al. (1999), where 69.8% were captured in the forest area in São Luiz (Maranhão) and by Oliveira et al. (2003), who verified a higher abundance of Lu. flaviscutellata in the forest area (5) compared to the peridomicile area (1) in Campo Grande (MS).

Other species of epidemiological importance captured during this study in Barcarena include Lu. antunesi and Lu. paraensis. These species are involved in transmitting Leishmania sp. in PA (Rangel & Lainson 2003). Lu. paraensis naturally infected with Leishmania (Viannia) naiff was captured in Benevides (PA) (Rangel & Lainson 2003). Although Barcarena has had no reports of autochthonous cutaneous leishmaniasis, the presence of the vector species in the forest and forest edge areas suggest the possibility of the establishment of a cutaneous leishmaniasis transmission cycle. It is important to note that even though Lu. sordellii has not been incriminated in Leishmania sp. transmission, it was the only species captured in the intermediate area, which suggests the possibility of its urbanisation. These data emphasise the need for entomological monitoring in Barcarena.

Although Barcarena is considered to be an area where VL is endemic, no natural infections were detected in the sandflies captured in this study. Several studies have reported that the natural infection rate is low among sandflies and is approximately 1%. Nascimento et al. (2007) dissected 81 females and detected only one infected fly. Neitzke et al. (2008) analysed 2,487 females and found an infection rate of 0.04%. Therefore, the negative results from the microscopic analysis performed in this study are probably attributable to the low rates of natural infection and not to a lack of infection in the studied areas, especially considering that 301 cases of human VL were reported between 2000-2008 in Barcarena.

Intensive and constant monitoring of sandflies on the edge of the forest and in intermediate areas is recommended to detect local patterns and periods of higher vector abundance, which will allow for better preventive anti-vector intervention (Salomón et al. 2009).

In conclusion, Barcarena has a rich sandfly fauna and Lu. longipalpis was the most abundant species in the forest area and at the forest edge. These data suggest that, among the 11 species captured in Barcarena, Lu. longipalpis is the species most adapted to disturbed areas. Thus, this study demonstrates the importance of constant entomological surveillance and monitoring in this area.

 

ACKNOWLEDGEMENTS

To the Health Department of Barcarena, for all collaborations, which were essential for the development of this research, and to the technicians of the Instituto Evandro Chagas, for assisting with our field and laboratory work.

 

REFERENCES

Amaral DD, Bastos MNC, Silva ASL, Oliveira J, Lobato RC, Lobato LCB, Rosário CS, Gomes A, Silva CA, Aguiar J 2002. Inventário da flora da região de Barcarena, PA, Relatório final, Ministério da Ciência e Tecnologia/Museu Paraense Emílio Goeldi, Belém, p. 1-64.         [ Links ]

Andrade-Filho JD, Valente MB, Andrade WA, Brazil RP, Falcão AL 2001. Flebotomíneos do estado de Tocantins, Brasil (Diptera: Psychodidae). Rev Soc Bras Med Trop 34: 323-329.         [ Links ]

Bauzer LGSR, Souza NA, Maingon RDC, Peixoto AA 2007. Lutzomyia longipalpis in Brazil: a complex or a single species? A mini-review. Mem Inst Oswaldo Cruz 102: 1-12.         [ Links ]

Costa CHN, Tapety CMM, Werneck GL 2007. Controle de leishmaniose visceral em meio urbano: estudo de intervenção randomizado fatorial. Rev Soc Bras Med Trop 40: 415-419.         [ Links ]

Da Luz ZM, Pimenta DN, Cabral ALLV, Fiúza VOP, Rebello A 2001. A urbanização das leishmanioses e a baixa resolutividade diagnóstica em municípios da região metropolitana de Belo Horizonte. Rev Soc Bras Med Trop 34: 3249-3254.         [ Links ]

De Paula MBC, Rodrigues EAS, Souza AA, Dos Reis AA, De Paula FP, Neto AAP, Limongi JE 2008. Primeiro encontro de Lutzomyia longipalpis (Lutz & Neiva, 1912) na área urbana de Uberlândia, MG, concomitante com relato de primeiro caso autóctone de leishmaniose visceral humana. Rev Soc Bras Med Trop 41: 304-305.         [ Links ]

Dujardim JC 2006. Risk factors in the spread of leishmaniasis: towards integrated monitoring? Trends in Parasitol 22: 4-6.         [ Links ]

Feliciangeli MD, Delgado O, Suarez B, Bravo A 2006. Leishmania and sand flies: proximity to woodland as a risk factor for infection in a rural focus of visceral leishmaniasis in west central Venezuela. Trop Med Int Health 12: 1785-1791.         [ Links ]

Kelly DW, Dye C 1997. Pheromones, kairomones and the aggregation dynamics of the sandfly Lutzomyia longipalpis. Anim Behav 53: 721-731.         [ Links ]

Lainson R, Rangel EF 2003. Ecologia das leishmanioses: Lutzomyia longipalpis e a eco-epidemiologia da leishmaniose visceral americana (LVA) no Brasil. In EF Rangel, R Lainson, Flebotomíneos do Brasil, Fiocruz, Rio de Janeiro, p. 291-305        [ Links ]

Lainson R, Rangel EF 2005. Lutzomyia longipalpis and the eco-epidemiology of American visceral leishmaniasis, with particular reference to Brazil - A Review. Mem Inst Oswaldo Cruz 100: 811-827.         [ Links ]

Lainson R, Shaw JJ, Silveira FT, de Souza AAA, Braga RR, Ishikawa EAY 1994. The dermal leishmaniases of Brazil, with special reference to the eco-epidemiology of the disease in Amazonia. Mem Inst Oswaldo Cruz 89: 435-443.         [ Links ]

Michalsky EM, França-Silva JC, Barata RA, Silva FOL, Loureiro AMF, Fortes-Dias CL, Dias ES 2009. Phlebotominae distribution in Janaúba, an area of transmission for visceral leishmaniasis in Brazil. Mem Inst Oswaldo Cruz 104: 56-61.         [ Links ]

Michalsky EM, Guedes KS, Silva FOL, Silva JCF, Dias CLF, Barata RA, Dias ES 2011. Infecção natural de Lutzomyia (Lutzomyia) longipalpis (Diptera: Psychodidae) por Leishmania infantum chagasi em flebotomíneos capturados no município de Janaúba, estado de Minas Gerais, Brasil. Rev Soc Bras Med Trop 44: 58-62.         [ Links ]

Missawa AN, Lorosa ES, Dias ES 2008. Preferência alimentar de Lutzomyia longipalpis (Lutz & Neiva, 1912) em área de transmissão de leishmaniose visceral em Mato Grosso. Rev Soc Bras Med Trop 41: 365-368.         [ Links ]

MS - Ministério da Saúde, Brasil 2010. [database on the internet] Distribuição da leishmaniose no Brasil, Brasília, [cited 2010 Jul 9]. Available from: saude.gov.br.         [ Links ]

Nascimento JC, Paiva BR, Malafronte RS, Fernandes WD, Galti EAB 2007. Natural infection of phlebotomines (Diptera: Psychodidae) in a visceral-leishmaniasis focus in Mato Grosso do Sul, Brazil. Rev Inst Med Trop Sao Paulo 49: 119-122.         [ Links ]

Neitzke HC, Scodro RBL, De Castro KRR, Sversutti ACD, Silveira TGV, Teodoro U 2008. Pesquisa de infecção natural de flebotomíneos por Leishmania no estado do Paraná. Rev Soc Bras Med Trop 41: 17-22.         [ Links ]

Oliveira AG, Filho JDA, Falcão AL, Brasil RP 2003. Estudo de flebotomíneos (Diptera, Psychodidae, Phlebotominae) na zona urbana da cidade de Campo Grande, Mato Grosso do Sul, Brasil, 1999-2000. Cad Saude Publica 19: 933-944.         [ Links ]

Oliveira AG, Galati EA, de Oliveira O, de Oliveira GR, Espindola IA, Dorval ME, Brazil RP 2006. Abundance of Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae) and urban transmission of visceral leishmaniasis in Campo Grande, state of Mato Grosso do Sul, Brazil. Mem Inst Oswaldo Cruz 101: 869-874.         [ Links ]

Pacheco AS, Silva ASL, Medeiros CG, Oliveira CDC, Souza EF, Amarante ES, Lopes JAS, Pacheco JJ, Silva MAM, Moreira MGP, Rocha NA, Couto SJM, Freitas Z 2007. Estatística Municipal de Barcarena-Pará, Governo do Estado do Pará/Secretaria Especial de Gestão/Secretaria Executiva de Estado e Planejamento, Orçamento e Finanças, Belém, p. 1-46.         [ Links ]

Pita-Pereira D, Cardoso MAB, Alves CR, Brazil RP, Britto C 2008. Detection of natural infection in Lutzomyia cruzi and Lutzomyia forattinii (Diptera: Psychodidae: Phlebotominae) by Leishmania infantum chagasi in an endemic area of visceral leishmaniasis in Brazil using a PCR multiplex assay. Acta Trop 107: 66-69.         [ Links ]

Quintana MG, Salomón OD, Lizarralde De Grosso MS 2010. Distribution of Phlebotomine sandflies (Diptera: Psychodidae) in a primary forest-crop interface, Salta, Argentina. J Med Entomol 47: 1004-1010.         [ Links ]

Rangel EF, Lainson R 2003. Ecologia das leishmanioses: transmissores de leishmaniose tegumentar Americana. In EF Rangel, R Lainson, Flebotomíneos do Brasil, Fiocruz, Rio de Janeiro, p. 291-305.         [ Links ]

Rangel EF, Vilela ML 2008. Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae) and urbanization of visceral leishmaniasis in Brazil. Cad Saude Publica 24: 2948-2952.         [ Links ]

Rebêlo JMM, Araújo JAC, Carvalho VLLB, Silva FS, Oliveira ST 1999. Flebótomos (Diptera: Phlebotominae) da Ilha de São Luís, zona do Golfão Maranhense, Brasil. Rev Soc Bras Med Trop 32: 247-253.         [ Links ]

Ribeiro ALM, Missawa NA, Zeilhofer P 2007. Distribution of Phlebotomine sandflies (Díptera: Psychodidae) of medical importance in Mato Grosso state, Brazil. Rev Soc Bras Med Trop 45: 317-321.         [ Links ]

Salomón OD, Quintana MG, Bruno MR, Quiriconi RV, Cabral V 2009. Visceral leishmaniasis in border areas: clustered distribution of phlebotomine sandflies in Clorinda, Argentina. Mem Inst Oswaldo Cruz 104: 801-804.         [ Links ]

Santos SO, Arias J, Ribeiro AA, Hoffmann MP, Freitas RA, Malacco MAF 1998. Incrimination of Lutzomyia cruzi as a vector of american visceral leishmaniasis. Med Vet Entomol 12: 315-317.         [ Links ]

Silva AM, Camargo NJ, Santos DR, Massafera R, Ferreira AC, Postai C, Cristóvão EC, Konolsaisen JF, Júnior AB, Perinazo R, Teodoro U, Galati EA 2008. Diversidade, distribuição e abundância de flebotomíneos (Diptera: Psychodidae) no Paraná. Neotrop Entomol 37: 209-225.         [ Links ]

Silva EA, Andreotti R, Honer MR 2007. Comportamento de Lutzomyia longipalpis, vetor principal da leishmaniose visceral americana, em Campo Grande, estado do Mato Grosso do Sul. Rev Soc Bras Med Trop 40: 420-425.         [ Links ]

Souza GD, Santos E, Andrade-Filho JD 2009. The first report of the main vector of visceral leishmaniasis in America, Lutzomyia longipalpis (Lutz & Neiva) (Diptera: Psychodidae: Phlebotominae), in the state of Rio Grande do Sul, Brazil. Mem Inst Oswaldo Cruz 104: 1181-1182.         [ Links ]

Ximenes MFF, Silva VPM, Queiroz PSV, Rego MM, Cortez AM, Batista LMM, Medeiros AS, Jeronimo SBM 2007. Flebotomíneos (Diptera: Psychodidae) e leishmanioses no Rio Grande do Norte, Nordeste do Brasil - Reflexos do ambiente antrópico. Neotrop Entomol 36: 128-137.         [ Links ]

Young DC, Duncan NA 1994. Guide to the identification and geographic distribution of Lutzomyia sandflies in Mexico, the West Indies, Central and South America (Diptera: Psychodidae). Mem Amer Entomol Inst 54: 1-881.         [ Links ]

 

 

Received 6 July 2011
Accepted 1 December 2011
Financial support: CAPES, CNPq (MCT/CNPq/CT-Saúde/MS/SCTIE/DECIT 34/2008)

 

 

+ Corresponding author: edilene@ufpa.br

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License