Mem Inst Oswaldo Cruz, Rio de Janeiro, 99(8) December 2004
Original Article

Study on Phlebotomine Sand Fly (Diptera: Psychodidae) Fauna in Belo Horizonte, State of Minas Gerais, Brazil

Carina Margonari de Souza, Jose Eduardo Pessanha*, Ricardo Andrade Barata, Érika Michalsky Monteiro, Daniela Carmargos Costa, Edelberto Santos Dias

Centro de Pesquisas René Rachou-Fiocruz, Av. Augusto de Lima 1715, 30190-002 Belo Horizonte, MG, Brasil
*Secretaria Municipal de Saúde de Belo Horizonte, Departamento de Zoonoses, Belo Horizonte, MG, Brasil

Page: 795-803
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A study on the phlebotomine sand fly fauna in Belo Horizonte city, state of Minas Gerais, Brazil, was carried out. From April 2001 to March 2003, monthly systematic collections were performed in three houses from each of the nine regions of the city, using CDC light traps for four consecutive days. The traps were set into the houses and in peridomestic areas totaling 54 traps. A number of 3871 sand fly specimens of the generau00a0Lutzomyiau00a0andBrumptomyiau00a0were collected. Sixty eight percent of the specimens wereu00a0L. longipalpisu00a0and 16%u00a0L. whitmani, insect vectors of visceral and American cutaneous leishmaniasis, respectively. Environmental factors such as temperature, humidity, and frequency of precipitation suggest that the number of insects increases after rainy periods. During the same period mentioned above, seasonal captures were carried out in parks and green areas of Belo Horizonte, using Shannon trap. A total of 579 phlebotomine sand flies were collected from which 398 (68.7%) were females with the predominance ofu00a0L. whitmaniu00a0andu00a0L. monticola. Those specimens were used for natural infection examination, by polymerase chain reaction. Nou00a0Leishmaniau00a0DNA was present in any of the specimens tested.

Nowadays, leishmaniasis has been observed in large urban centers, showing a wide diversity and adaptation of parasites (Leishmania) and vectors to the environmental changes caused by man (Marzorchi & Marzorchi 1994, Ashford 2000, Travi et al. 2002, Azevedo et al. 2002). Such factors enable the existence of several clinic-epidemiological manifestations of the disease and make control measures difficult in those areas.

The first records of leishmaniasis cases in Belo Horizonte (BH) date from 1940 with the detection of 13 human cases of American cutaneous leishmaniasis (ACL) (Orsini 1940). Afterwards, several investigators have studied human and canine cases in the city (Passos et al. 1998, Silva et al. 2001).

Passos et al. (1998) performed an entomological survey in the Boa Vista quarter, a suburban area of BH, and 
in the district of Venda Nova, where the presence of Lutzomyia whitmani and L. longipalpis, the insect vectors of ACL and visceral leishmaniasis (VL), respectively, had been reported. Such studies associated with recent publications have confirmed VL (Silva et al. 2001) and ACL (Passos et al. 1993, 2001) urbanization in BH.

The present work intends to provide data for optimization of control measures, upon knowing seasonal fluctuations, habitat and the behavior of phlebotomine sand flies.



Study area - The city of Belo Horizonte (BH), in the state of Minas Gerais, Brazil, has a population of 3,420,000 inhabitants (IBGE 2000) and great part of the population live in substandard accommodations, without basic sanitation and hygiene conditions. Lack of infra-structure associated with environmental factors enables the dissemination of several diseases, including leishmaniasis.

Systematic collections - BH is formed by nine regional areas: Barreiro, Centro Sul (Center-South), Leste (East), Nordeste (Northeast), Noroeste (Northwest), Norte (North), Oeste (West), Pampulha, and Venda Nova. Three residences were chosen for each region totaling 27 houses for insect collection (Fig. 1). Selected residents signed a consent term in order to assure their participation and collaboration during the period of the study. Systematic collections began in April 2001 after a detailed evaluation of the nine regions comprising BH. Several ecological and environmental factors were observed for a posterior selection of the houses to be part of the present study. The presence of a favorable environment for reproduction and development of sand flies was one of the pre-requisites required for the selection of the target-houses. The houses under study had the following features: large back yards, orchard with plants and domestic animals (dogs, chickens, birds, and others). Orientation about the selection of the collection sites of each region was provided by the Municipal Health Secretary of BH (MHSBH), through which data on leishmaniasis prevalence in dogs and man was assessed. Regions with higher leishmaniasis prevalence rates were determined as being searching areas of residences that fit the demands of the present investigation.

Two CDC light traps (Sudia & Chamberlain 1962) were placed for each house: one into the house and another in the peridomiciliary area, totaling 54 traps. Collections were performed on the last four days of each month, from April 2001 to March 2003. The traps were put at 5:00 pm and removed at 7:00 am of the following day. The insects collected each night were killed in chambers with 70% ether P./a solution and then they were placed in hemolysis tubes with 70% alcohol solution, labeled and taken to the laboratory. All specimens collected were identified based on their morphological characteristics, according to the identification-key proposed by Young and Duncan (1994).

Non-systematic collections - Four seasonal collections were carried out in different parks and green areas of each region, totaling 36 collections in two consecutive years. All collection sites were georeferred by GPS (global positioning system) and located in the map of BH city (Fig. 1). Luminous Shannon traps (Shannon 1939) were used between 5:30 pm and 10:00 pm, totaling 162 h of collection. The insects were collected alive with the help of a manual suction tube and then transferred to chambers with humidified plaster bottoms and covered with a cloth. Afterwards, they were taken to the laboratory, killed in the freezer, identified and then submitted to DNA extraction according to Margonari et al. (2004). DNA samples were used for Leishmania spp. search by polymerase chain reaction (PCR).

PCR - A volume of 2 µl DNA (10ng/ ml) was added to the amplification mix with 10 µl buffer solution (100 mM TRIS-HCl, 500 mM KCl, 15 mM MgCl2, pH 9.0), 5 µl dNTPs (2 mM each), 2 µl of each primer (200 ng/µl), 0.5 ml Taq polymerase (2.5 U/µl), and 26.5 µl mili-Q water in a final volume of 60 ml. Specific primers for the genusLeishmania were used: 5'GGG GAG GGG CGT TCT GCG AA3', 5'CCG CCC CTA TTT TAC ACC AAC CCC3', 5'GGC CCA CTA TAT TAC ACC AAC CCC3'. Amplification cycles were: at 94oC for 4 min, followed by 35 cycles at 94oC for 30 s; 60oC for 30 s; and finally at 72oC for 30 s in the thermocycler GeneAmp PCR System 2400 (Perkin Elmer) (Michalsky et al. 2002).

PCR products were visualized on 2% ethidium bromide stained agarose gels.

Statistical analysis - It was performed with the software SigmaStat (Jandel 1995) by which likely environmental interferences were determined for the phlebotomine sand fly fauna in BH.



A number of 3871 specimens of phlebotomine sand flies were collected in of BH from April 2001 to March 2003. The phlebotomine fauna collected comprised 15 different species and the most frequent were: L. longipalpis(68.23%) and L. whitmani, (16.04%). The least frequent species were: L. sallesi (6.77%), L. intermedia (1.42%),L. firmatoi (0.75%), L. pessoai (0.46%), L. monticola (0.34%), L. quinquefer (0.34%), L. termitophila (0.15%), L. lenti (0.09%), Brumptomyia sp. (0.08%), L. longipennis (0.05%), L. misionensis (0.05%), L. aragaoi (0.03%), andL. migonei (0.03%). Four percent out of the total amount of collected insects could not be identified due to mutilation caused by the traps or technical problems (Table I).

Although the target-houses showed very similar ecological characteristics, a heterogeneous entomological collection was observed both in the number of insects (Table II) and in the species diversity: Barreiro 146 phlebotomine sand flies (3.8%), Centro Sul 34 (0.9%), Leste 282 (7.3%), Nordeste 1114 (28.8%), Noroeste 60 (1.5%), Norte 565 (14.6%), Oeste 991 (25.6%), Pampulha - 475 (12.3%), and Venda Nova _ 204 (5.3%) (Table II).

Concerning diversity, L. longipalpis was the predominant species in the following regions: Leste, Nordeste, Noroeste, Oeste, Pampulha, and Venda Nova. The species L. lenti was the most collected one in Barreiro whereasL. sallesi and L. monticola showed to be numerous in Centro Sul. L. whitmani was the most frequent in (the North region) Norte (Table III).

In general terms, the number of collected phlebotomine sand flies showed to be higher in the peridomiciliary areas than into the houses. The species L. whitmani had similar concentrations in both environments (Tables III,IV).

Analysis on the phlebotomine sand fly populations according to the variables, monthly average temperature, relative humidity and frequency of precipitation, showed no significant statistical differences (Fig. 2).

Analysis on the insects which were proven to be ACL vectors (L. intermedia, L. pessoai, L. whitmani) versus the number of ACL human cases, during the period of our investigation, suggests that there is an increasing trend of ACL cases just after the highest population densities of the vectors (Fig. 3). The same was observed when the number of L. longipalpis specimens and VL human cases were assessed (Fig. 4).

Collections performed with the Shannon traps in the parks and green areas of BH comprised 579 phlebotomine sand flies of the following species: L. whitmani (60.6%), L. monticola (22.3%), L. pessoai (5.2%), L. longipalpis(2.6%), L. misionensis (2.1%), L. intermedia (1.7%), L. sallesi (1.4%), L. fischeri (0.5%), L. shannoni (0.5%), L. termitophila (0.3%), L. bianchigalatiae (0.2%), and L. sordellii (0.2%). Out of the, insects collected, a rate of 2.4% could not be identified (TableV).

Females collected _ 398 specimens (69.3%) _ and submitted to an evaluation regarding natural infection byLeishmania had their results negative through the PCR technique.



A favorable environment to phlebotomine reproduction associated with the presence of domestic animals in peridomiciliary areas may explain the high number of insects found compared to inner houses under study. The presence of domestic animals in the houses was recorded as follows: 66.7% with dogs; 48.2% with poultry; 18.5% with rodents; 7.4% with cats; 3.7% with skunk, goats and horses, and equine.

The highest population density was represented by the species L. longipalpis in BH during the period studied.Such species has been described in several endemic areas of VL in Brazil and in several Latin American countries. Its high vectorial capacity (Deane 1956, Killick-Kendrick 1990) associated with its high anthropophilia and the presence of the insect in peridomiciliary areas turn the species L. longipalpis as the greatest medical importance phlebotomine sand fly (Lainson & Shaw 1998, Soares & Turco 2003). This species has been collected through several punctual studies carried out in BH. In 1997, aimed at knowing habits and behaviour of phlebotomine sand flies, entomological collections were undertaken by the Municipal Department of Health in some sites of the city. The results showed a predominance of L. longipalpis (Resende et al. 2004). Afterwards, Passos et al. (1998) also demonstrated the presence of L. longipalpis and L. whitmani in other locations of Belo Horizonte.

Probably due to the adaptability to urban micro environments, the species L. longipalpis was the most frequently found in six of the nine regions under study.

L. whitmani, however, has been regarded to be a species "under adaptation" to the urban environment by several investigators due to the fact that it is collected in high concentrations in thickly forested areas and in peridomi-ciliary areas of large centers (Camargo-Neves et al. 2002, Dos Santos et al. 2003, Salomón et al. 2003, Oliveira et al. 2003) and it has been associated with peridomiciliary transmissions in Brazilian Northeastern and Southeastern areas (Cuba-Cuba et al. 1985, Azevedo & Rangel 1991, Rangel et al. 1996). Due to this fact, several studies have been undertaken in order to better understand the biology of L. whitmani. Particular features regarding genetics and adaptation of the species allow it to have different feeding and behavioral habits, depending on the habitat they live in (Rangel et al. 1996, Ready et al. 1997, 1998, Campbell-Ledrum et al. 2000, Azevedo et al. 2002, Margonari et al. 2004). Upon collecting L. whitmani in BH, it could be observed that the species is present in peridomiciliary areas as well as inside the houses (Tables IVV), besides being predominant in thickly forested areas (Table V). Such observation has revealed that L. whitmani may be considered totally adapted to large urban areas being able to live and reproduce in this environment. These results also suggest that ACL has been transmitted not only in peridomiciliary areas but also into the houses.

Therefore, although L. intermedia is considered to be the most important ACL vector in the Southeast of Brazil (Marcondes et al. 1997, Laison & Shaw 1998), L. whitmani is probably the responsible insect vector for ACL transmission in BH.

In literature data, climatic factors have been reported to influence phlebotomine sand fly populations, depending on the region under study. Usually, phlebotomines are found in high densities during rainy summer months (Gomes & Galati 1987, Salomón et al. 2003). On the other hand, Condino et al. (1998) have reported no relationship between such factors and the phlebotomine sand fly density. In Porterinha (north of the state of Minas Gerais), frequency of precipitation showed to affect directly the amount of phlebotomine collected in the region (Barata et al. 2004).

Rebêlo (2001a) have showed that there was a high frequency of L. longipalpis during the whole year in São Luis Island, with an increasing trend in rainy periods when compared to the dry periods. Temperature, humidity, and precipitation showed no influence in monthly insect density. However, precipitation affected seasonal distribution of L. longipalpis.

In the states of Ceará, Bahia, and Mato Grosso do Sul, a higher population density of phlebotomine sand flies has been observed during the rainy periods (Deane 1956, Sherlok & Guilton 1969, Galati et al. 1997), while in Costa Rica, higher densities occur in the dry periods (Zeledón et al. 1984) In Amazônia Maranhense, there have been abundant phlebotomine species during the rainy periods, others in dry periods and several species irregularly distributed throughout the year, L. longipalpis and L. whitmani (Rebêlo et al. 2001b).

Analysis on climate influences in phlebotomine sand fly populations in BH showed no statistically significant results. However, there is an increasing trend in the number of phlebotomine insects just after rainny periods (Fig. 2).

The higher population densities of phlebotomine sand flies may be associated with leishmaniasis cases in the city under study. This association was reported by Rebêlo (2001a) for the municipality of Buriticupu (state of Maranhão) where high densities of L. whitmani were coincident with increasing ACL human cases. In the present work, a similar analysis provided information on the same trend, i.e, increasing numbers of ACL human cases just after higher population densities of insect vectors (Figs 34).

The CDC traps have been systematically used in studies on phlebotomine populations. Previous investigations have proven that the single use of CDC traps does not allow the identification of phlebotomine fauna concerning its quantitative and qualitative features (Azevedo et al. 2002, Oliveira et al. 2003). Based on the results of the current work, the use of Shannon traps allowed us to evaluate the presence of some species that were not collected by CDC traps such as L. bianchigalatiaeL. fischeri, L. shannoni,and L. sordellii, corroborating previous reports.

Females collected by Shannon traps and submitted to examination of possible Leishmania sp. natural infection, showed negative results through PCR. This technique has been widely used for diagnosis purposes (Passos et al. 1993) and it has been shown to be highly sensitive in detecting protozoa parasites into phlebotomine sand flies (Rodriguez et al. 1999, Miranda et al. 2002, Michalsky et al. 2002). Nevertheless, previous reports have shown that phlebotomine infectivity rates in nature are low, 0.2 to 2%, making the parasite finding difficult (Rodriguez et al. 1999, Miranda et al. 2002).



To the clerks of the Municipal Secretary of Health for collaborating on the collections of phlebotomine sand flies and to Marcelo Rezende de Freitas, (State Secretariat of Health of Minas Gerais) for providing the traps.



Ashford RW 2000. The leishmaniases as emerging and reemerging zoonoses. Int J Parasitol 30: 1269-1281.

Azevedo ACR, Rangel EF 1991. A study of sandfly species (Diptera: Psychodidae: Phlebotominae) in a focus of cutaneous leishmaniasis in the municipality of Baturité, Ceará State, Brazil. Mem Inst Oswaldo Cruz 88: 509-512.

Azevedo ACR, Souza NA, Meneses CRV, Costa WAC, Costa SM, Lima JB, Rangel EF 2002. Ecology of sand flies (Diptera: Psychodidae: Phlebotominae) in the north of the state of Mato Grosso, Brazil. Mem Inst Oswaldo Cruz 97: 459-464.

Barata RA, França- Silva JC, Fortes-Dias CL, Costa RT, Silva JC, Vieira EP, Prata A, Michalsky EM, Dias ES 2004. Phlebotomines sand flies in Porteirinha, an endemic area of American visceral leishmaniasis in the state of Minas Gerais, Brazil. Mem Inst Oswaldo Cruz 99: 481-487.

Camargo-Neves VL, Gomes AC, Antunes JLF 2002. Correlação da presença de espécies de flebotomíneos (Diptera: Psychodidae) com registros de casos da leishmaniose tegumentar americana no estado de São Paulo, Brasil. Rev Soc Bras Med Trop 35: 299-306.

Campbell-Ledrum DH, Brandão-Filho SP, Pinto M C, Ready PD, Davies CR 2000. Domesticity of Lutzomyia whitmani (Diptera: Psychodidae) populations: fiel experiments indicate behavioural differences. Bull Entomol Res 90: 41-48.

Condino MLF, Sampaio SMP, Henriques LF, Galati EAB, Wanderley DMV, Corrêa FMA 1998. Leishmaniose tegu-mentar americana: flebotomíneos de área de transmissão no município de Teodoro Sampaio, região sudoeste do estado de São Paulo, Brasil. Rev Soc Bras Med Trop 31: 355-360.

Cuba-Cuba CA, Miles MA, Vexenat A, Barker DC, Mc Mahon Pratt D, Butcher J, Barreto AC, Marsden PH 1985. A focus of mucocutaneous leishmaniasis in Três Braços, Bahia, Brazil: Characterization and identification of Leishmania stocks isolated from man and dogs. Trans R Soc Trop Med Hyg 79: 500-507.

Deane LM 1956. Leishmaniose Visceral no Brasil. Estudos sobre Reservatórios e Transmissores no Estado do Ceará, Serviço Nacional de Educação Sanitária, Rio de Janeiro, 162 pp.

Dos Santos TG, de Mello Gaia MC, Brazil RP 2003. Attraction of sand flies (Diptera: Psychodidae) to light traps in rural áreas of Minas Gerais state, Brazil. J Am Mosq Control Assoc 19: 74-78.

Galati EAB, Nunes VLB, Rego Jr EA, Oshiro ET, Chang MR 1997. Estudo de flebotomíneos (Diptera, Psychodidae) em foco de leishmaniose visceral no estado de Mato Grosso do Sul, Brasil. Rev Saúde Pública 31: 378-390.

Gomes A, Galati EAB 1987. Aspectos ecológicos da lei-shmaniose tegumentar americana. 5. Estratificação da atividade espacial e estacional de phlebotominae (Diptera, Psychodidae) em áreas de cultura agrícola da região de Vale do Ribeira, Estado de São Paulo, Brasil. Rev Inst Med Trop São Paulo 82: 467-473.

IBGE 2000. Anuário Estatístico do Brasil, Instituto Brasileiro de Geografia e Estatística, Rio de Janeiro.

Jandel 1995. SigmaStat Statistical User's Mmanual, version 2.0. Jandel, San Rafael, CA.

Killick-Kendrick R 1990. Phlebotomine vectors of the leishmaniases: a review. Med Vet Entomol 4: 1- 24.

Lainson R, Shaw J 1998. New world leishmaniasis The neotropical Leishmania species. In Feg Cox, JP Kreier, D Wakelen (eds), Topley & Wilson's Microbiology and Microbial Infections, Arnold, London, Auckland, Sydney, p. 241-266.

Marcondes CB, Day JC, Ready PD 1997. Introgression between Lutzomyia intermedia and both Lutzomyia neivaiand Lutzomyia whitmani, and their roles as vector of Leishmania braziliensisTrans R Soc Trop Med Hyg 91: 725-726.

Margonari CS, Dias-Fortes CL, Dias ES 2004. Genetic variability of Lutzomyia whitmani (Antunes & Coutinho) (Diptera: Psychodidae: Phlebotominae) in four geographical Brazilian populations by RAPD-PCR. J Med Entomol 41: 187-192.

Marzochi MCA, Marzochi KBF 1994. Tegumentary and visceral leishmaniases in Brazil - Emerging anthropozoonosis and possibilites for their control. Cad Saúde Pública 10: 359-375.

Miranda JC, Reis E, Schriefer A, Gonçalves M, Reis MG, Carvalho L, Fernandes O, Barral-Neto M, Barral A 2002. Frequency of infection of Lutzomyia Phlebotominae with Leishmania braziliensis in a Brazilian endemic area as assessed by pinpoint capture and polymerase chain reaction. Mem Inst Oswaldo Cruz 97: 185-188.

Michalsky EM, Fortes-Dias CL, Pimenta PFEP, Secundino NEC, Dias ES 2002. Assessment of PCR in the detection of Leishmania spp. in experimentally infected individual phlebotomine sandflies (Diptera: Psychodidae: Phlebotominae). Rev Inst Med Trop São Paulo 44: 255-259.

Oliveira AG, Andrade Filho JD, Falcão AL, Brazil RP 2003. Estudo de flebotomíneos (Diptera, Psychodidae, Phle-botominae) na zona urbana da cidade de Campo Grande, Mato Grosso do Sul, Brasil, 1999-2000. Cad Saúde Pública 19: 933-943.

Orsini O 1940. Leishmaniose em Minas Gerais. Brasil Médico 54: 762-766.

Passos VMA, Falcão AL, Marzochi MCA. Gontijo CMF, Dias ES, Barbosa-Santos EGO, Guerra HL, Katz N 1993. Epidemiological aspects of American cutaneous leishnmaniasis in a periurban area of the metropolitan region of Belo Horizonte, Minas Gerais, Brazil. Mem Inst Oswaldo Cruz 88: 103-110.

Passos VMA, Gontijo CMF, Dias ES, Katz N, Falcão AL 1998. Cutaneous leishmaniases in periurbans foci of the metropolitan region of Belo Horizonte, Minas Gerais state, Brazil. Proceedings of Workshop "Research and Control of Leishmaniasis in Brazil" 81: 83-88.

Passos VMA Barreto SM, Romanha AR, Krettli AU, Volpini AC, Gontijo CMF, Falcão AL, Lima-Costa MFF 2001. Leishmaniose tegumentar na região metropolitana de Belo Horizonte: aspectos clínicos, laboratoriais, terapêuticos e evolutivos (1989-1995). Rev Soc Bras Med Trop 34: 5-12.

Rangel EF, Lainson R, Souza AA, Azevedo ACR 1996. Variation between geographical populations ofLutzomyia (Nyssomyia) whitmani (Antunes & Coutinho, 1939) sensu lato (Diptera, Psychodidae, Phlebotominae): in Brazil. Mem Inst Oswaldo Cruz 91: 43-50.

Ready DP, Day JC, Souza AA, Rangel EF, Davies CR 1997. Mitochondrial DNA characterization of populations of Lutzomyia whitmani (Diptera, Psychodidae) incriminated in the peri-domestic and silvatic transmission in the of Leishmania species in Brazil. Bull Entomol Res 87: 187-195.

Ready DP, Souza AA, Macario Rabelo JM, Day JC, Silveira FT, Campell-Ledrum D, Davies CR, Costa JML 1998. Phylogenetic species and domesticity of Lutzomyia whitmani at the south-east boundary of Amazonian Brazil. Trans R Soc Trop Med Hyg 92: 159-160.

Rebêlo JMM 2001a. Frequência horária e sazonalidade de Lutzomyia longipalpis (Diptera: Psychodidae: Phle-botominae) na Ilha de São Luis, Maranhão, Brasil. Cad Saúde Pública 17: 221-227.

Rebêlo JMM, Oliveira ST, de Silva FS, Barros VLL, Costa JML 2001b. Sandflies (Diptera: Psychodidae) of the Amazônia of Maranhão.V. Seasonal occurrence in ancient colonization area and endemic for cutaneous leishmaniasis. Rev Bras Biol 61: 107-115.

Resende MC 2004. Seasonal variation of Lutzomyia longipalpis in Belo Horizonte, Minas Gerais. Rev Saúde Públicain press.

Rodriguez N, Aguilar CM, Barrios MA, Barker DC 1999. Detection of Leishmania braziliensis in naturally infected individual sandflies by the polymerase chain reaction. Trans R Soc Trop Med Hyg 93: 47-49.

Salomón OD, Rossi GC, Cousiño B, Spinelli GR, Arias AR, Puerto DGL, Ortiz AJ 2003. Phlebotominae sand flies in Paraguay. Abundance distribution in the Southeastern region. Mem Inst Oswaldo Cruz 98: 185-190.

Shannon RC 1939. Methods for collecting and seeding mosquitoes in jungle yellow fever studies. J Med Entomol19: 131-140.

Sherlock IA, Guitton N 1969. Observações sobre calazar em Jacobina, Bahia. IV. Variação horária e estacional dePhlebotomus longipalpisRev Bras Malac 21: 715-727.

Silva SS, Gontijo CMF, Pacheco RS, Fiuza VOP, Brazil RP 2001. Visceral leishmaniasis in the metropolitan region of Belo Horizonte, state of Minas Gerais, Brazil. Mem Inst Oswaldo Cruz 96: 285-291.

Soares RPP, Turco SJ 2003. Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae): a review. An Acad Bras Ciênc 75: 301-330.

Sudia WA, Chamberlain RW 1962. Battery-operated light trap: an improved model. Mosq News 22: 126-129.

Travi BL, Adler GH, Lozano M, Cadena H, Montoya-Lerma J 2002. Impact of habitat degradation on phlebotominae (Diptera: Psychodidae) of tropical dry forests in Northem Colombia. J Med Entomol 39: 451-456.

Young DG, Duncan MA 1994. Guide to the identification and geographic distribution of Lutzomyia sand flies in Mexico, the West Indies, Central and South America (Diptera, Psychodidae). Mem Am Entomol Inst 54: 1-881.

Zeledón R, Murillo J, Gutierrez H 1984. Observaciones sobre la ecologia de Lutzomyia longipalpis (Lutz & Neiva, 1912) y possibilidades de existencia de leishmaniasis visceral en Costa Rica. Mem Inst Oswaldo Cruz 79: 455-459.

+Corresponding author. Fax: +55-31-3295.3115.
Received 11 May 2004
Accepted 6 October 2004
Financial support: Centro de Pesquisas René Rachou-Fiocruz, Fapemig (CBB-2761/98)

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