Services on Demand
Print version ISSN 0034-8910
Rev. Saúde Pública vol.37 n.5 São Paulo Oct. 2003
Ueslei TeodoroI; Dayane AlbertonII; João Balduíno KühlI; Elcio Silvestre dos SantosIII; Demilson Rodrigues dos SantosIII; Ademar Rodrigues dos SantosIII; Otílio de OliveiraIII; Thaís Gomes Verzignassi SilveiraI; Maria Valdrinez Campana LonardoniI
de Análises Clínicas da Universidade Estadual de Maringá, Maringá, PR, Brazil
IIFaculdade de Farmácia e Bioquímica da Universidade Estadual de Maringá, Maringá, PR, Brazil
IIINúcleo de Entomologia da Secretaria de Saúde do Paraná, Maringá, PR, Brazil
To study the fauna, hours of activity and seasonality of phlebotomines in
forest animal habitats in the Ingá Park, on the urban perimeter of the municipality
of Maringá, Paraná State, Brazil.
METHODS: Phlebotomines were collected on the urban perimeter using Shannon traps from 6:00 p.m. to 6:00 a.m. and Falcão traps from 8:00 p.m. to 12:00 midnight, on two nights per month from October 1998 to September 2000. The Shannon traps were installed on the banks of the Moscados stream; the Falcão traps were placed in shelters for captive birds, forest mammals and reptiles.
RESULTS: The Shannon traps yielded 13,656 phlebotomines, with predominance of Lutzomyia whitmani (98.7%). The Falcão traps yielded 4,040 phlebotomines, with L. whitmani again predominating (96.3%). L. whitmani was most frequently found between 12:00 midnight and 2:00 a.m. in the Shannon traps. This species was most frequently collected in the months of August (55.1%) in the Shannon traps, and in March 1999 (19.2%), November 1999 (15.9%) and August 2000 (20.6%) in the Falcão traps. More phlebotomines were collected in Falcão traps installed in shelters for captive mammals (84.0%).
CONCLUSION: There was a clear predominance of L. whitmani in the Ingá Park. The greatest frequency of L. whitmani was in August from Shannon traps, and in March, August and November from Falcão traps. The peak activity of L. whitmani took place between 12:00 midnight and 2:00 a.m.
Keywords: Psychodidae. Leishmaniasis, cutaneous. Ecology, vectors. Insect vectors. Seasonal variations. Urban zones. American tegumentary leishmaniasis. Phlebotominae sandflies. Lutzomyia whitmani.
Up to the middle of the 20th century, approximately 40,000 cases of leishmaniasis had occurred at various localities within Brazilian territory.5 Subsequently, there was a brief period of respite, but over the last two decades the number of cases has noticeably increased and cases are being notified from all Brazilian states.5,7
In the State of Paraná, American tegumentary leishmaniasis had also been recorded since the beginning of the 20th century, with reports of cases up to 1958.5 It started to be officially notified again from 1980, with the occurrence of cases in 276 of the states 399 municipalities and concentration in its northern and western regions, despite the deforestation of more than 90% of the states territory.5
The occurrence of tegumentary leishmaniasis in the urban zones of large and medium-sized cities has been noted in Brazil since the beginning of the 20th century. In the State of Paraná, there has been notification of cases of this disease in the urban areas of small cities (Cianorte) and medium-sized cities (Maringá).5 Thus, there is an interest in studying the ecology of phlebotomines in the urban area of the municipality of Maringá, since these insects transmit the protozoa of the Leishmania genus that act as etiological agents for tegumentary leishmaniasis.1,2,6,8,10 In the Ingá Park, the remaining native forest provides shelter for a variety of forest mammal species, which form a potential reservoir for Leishmania, in addition to species kept in captivity, thereby making possible the existence of a complete enzootic cycle for Leishmania Ross, 1903.
In an earlier study in the Ingá Park and another two preserved areas within the urban perimeter of Maringá that are covered with native forest, phlebotomines were found to be present within the forest, especially within habitats for wild animals.16 In the present investigation, the aim was to expand the knowledge of phlebotomine fauna composition, the inclination of these insects to feed on blood from certain hosts, and the hours of the night and the months in which they are most frequent, in the Ingá Park.
The Ingá Park, where the research was carried out, is a preserved area covered with native forest, located on the urban perimeter of the municipality of Maringá, in the State of Paraná, with an area of 47.43 hectares. The forest is of dense tropical to subtropical transition type, with partial leaf fall from some tree species in the less favorable winter season, when a slight drought takes place. The municipality of Maringá is located in the northwest of the state at the latitude of 23°25 south and longitude of 51°25 west of Greenwich. It has average annual precipitation of between 1500 and 1600 mm and an average annual temperature of 20 to 21°C, with average maximums of 27 to 28°C and minimums of 16 to 17°C. In the least rainy three months (June, July and August), the precipitation measured is 200 to 250 mm and in the rainiest three months (December, January and February) it is 500 to 550 mm.
The phlebotomine collections were carried out using Shannon and Falcão traps. During the period when the research was carried out, infrastructure work was being performed inside the Ingá Park, which made it difficult to access the Shannon trap installation localities. Thus, it was decided to move the Shannon trap locations, such that the Shannon trap collections were divided into two stages. In the first stage, collections were done from October 1998 to September 1999. On two nights per month, from 6:00 p.m. to 6:00 a.m., collections were done using Shannon traps installed on the banks of the Moscados stream (Figure 1). On another two nights, from 8:00 p.m. to 12:00 midnight, collections were done using Falcão traps installed in shelters for captive birds, mammals and reptiles.
In the second stage, from October 1999 to September 2000, the Shannon traps were installed on a kiosk used for recreation, beside the lake formed by the Moscados stream (Figure 1). At this new locality, there was no interference between the collections via the two trap types. Thus, on two nights of each month, collection was done simultaneously for the two collection methods, at the same times as for the first stage.
The Falcão traps (FT) were distributed in the following manner (Figure 1):
FT1 in a cage divided in two, housing a pair of lions (Panthera leo) in one half and a howler monkey (Alouatta fusca) in the other;
FT2 in a shelter containing a large number of capuchin monkeys (Cebus apella);
FT3 in a pair of coupled shelters containing a raccoon (Procyon cancrivorus), two tiger cats (Leopardus tigrinus) and one bird (Penelope obscura);
FT4 in a shelter containing a pair of peccaries (Tayassu pecari), which were substituted by a raccoon (Procyon cancrivorus) in April 1999 that, in its turn, was substituted by a large number of coatis (Nasua nasua) (close to 100), in April 2000;
FT5 in a shelter containing a large number of forest bird species;
FT6 in an area closed off by wire netting, containing several tortoises (Geochelone chilensis), which were substituted by caimans (Caiman spp.) in April 1999.
The light source for the Shannon traps was a 100W incandescent light bulb. The phlebotomines were collected from the internal and external walls of the trap by two persons using glass tubes containing cotton steeped in chloroform. Hour by hour, the insects collected in these traps were packed in small cardboard boxes and subsequently prepared and identified in the laboratory.
The Falcão traps were provided with 3W light bulbs 3W. After collection, the insects were killed using chloroform and also packed into small cardboard boxes, for subsequent preparation and identification in the laboratory.
The changes in animal distribution made during the period that the work was performed were made by the administration of the Ingá Park, with the aim of the animals wellbeing.
To draw up the graph of monthly phlebotomine distribution, the Williams geometrical average (MGW)4 for the collections done was utilized. The numbers of phlebotomines captured in the different traps were compared via variance analysis. The chi-squared test was utilized for comparing the numbers of phlebotomines of each sex. The significance level considered was p=0.05, with the utilization of the Statistica software, version 5.5.
The species collected are reported in the Table.
It was noted that the quantities of phlebotomines collected in the Shannon and Falcão traps were 13,654 (hourly average of 23.7) and 4,039 (hourly average of = 21.0), respectively (Table). It was also observed that L. whitmani accounted for 98.7% of the phlebotomines (13,473 specimens) collected from the Shannon traps and 96.3% (3,888 specimens) from the Falcão traps. The numbers of species collected in the Falcão and Shannon traps were 10 and 8, respectively. More female phlebotomines were collected in the Shannon traps than males (p<0.01), but this was not seen in the Falcão traps.
Figure 2 shows that the annual distribution of L. whitmani (MGW) was similar for the two trap types. In the Shannon traps, L. whitmani was most frequent in November 1998, August 1999 and April and August 2000. In the Falcão traps, L. whitmani was most frequent in March, July and November 1999 and March/April and August 2000.
Figure 3 shows the distribution of L. whitmani (MGW) in each of the Falcão traps. The quantity of phlebotomines collected in FT4 was significantly different from the quantities collected in FT1, FT2, FT5 and FT6 (p£0.05). Although the quantities of this phlebotomine in the traps FT3 and FT4 were not statistically different from each other (p=0.95), the quantity of phlebotomines collected in FT3 was not statistically different from what was collected in the other traps (p£0.18).
In FT3, located in the coupled shelters containing forest animals (raccoon, tiger cats and a bird), an average of 7.8 phlebotomines were collected per hour. During the period when collections were done, there were changes in the animals kept in the shelter where FT4 was installed, thus giving rise to three sub-periods. From October 1998 to March 1999, when the shelter was housing a pair of peccaries, an hourly average of 10.9 phlebotomines was collected. From April 1999 to March 2000, when a raccoon was substituted for the pair of peccaries, the hourly average was 4.6 phlebotomines. From April to September 2000, a large number of coatis was substituted for the raccoon and the hourly average was 19.1 phlebotomines. Analysis of the distribution of L. whitmani during these three sub-periods showed that there was no significant difference between them. Over these same sub-periods, there was also no observed difference in the distribution of phlebotomines among the other Falcão traps.
In Figure 4, it can be seen that L. whitmani was present in the Shannon traps from 6:00 p.m. to 6:00 a.m.
The species L. shannoni can now be added to the nine species of phlebotomine previously noted in the Ingá Park.16 The almost absolute domination of L. whitmani over the other species corroborates what was previously observed in this park.16 The high prevalence of this species has been observed in endemic areas of tegumentary leishmaniasis in northern Paraná.6,11-16 The infection of L. whitmani by Leishmania (Viannia) braziliensis that has been proven in the States of Paraná6 and Ceará1,8 highlights the importance of this species in the epidemiology of that disease.
The hourly average number of phlebotomines collected in the Shannon traps (23.7 specimens) was similar to what was collected among the Falcão traps (hourly average of 21.1). However, the distribution of the Falcão traps among a greater number of ecotypes favored the collection of a greater number of species.
The concentration of phlebotomines in the shelters for captive forest animals, especially mammals (FT3 and FT4) suggests that these insects are strongly attracted to such animals, except in the cases of primates and felines (lion). This fact has already been noted in the Ingá Park.16 The results suggest that the larger quantities of phlebotomines collected in FT3 and FT4 may have been due to the presence of mammals in the shelters where these traps were placed. However, according to Campbell-Lendrum et al3 (1999) and Quinnel et al9 (1991), the order of preference that these insects show in relation to hosts is a function of the size or density of such hosts.
The small number of phlebotomines collected in the shelter housing the lions and howler monkey (FT1) was different from what was previously collected,16 when this same shelter was housing a jaguar and yielded the greatest number of phlebotomines of all the shelters for captive forest animals. The low attractive power of the pair of lions for phlebotomines may be explained by the fact that this mammal does not form part of the native Brazilian fauna. The presence of a howler monkey in the cage coupled to the cage of the pair of lions suggests that primates attract few phlebotomines. This was also seen in the trap installed in the shelter for the capuchin monkeys (FT2). This was observed previously,16 in the same shelter, thereby giving evidence that these insects are little attracted towards primates.
The time of greatest frequency of L. whitmani was from 12:00 midnight to 2:00 a.m. However, in the Ingá Park there is a risk of infection by Leishmania throughout the night, especially between 8:00 p.m. and 5:00 a.m. In the endemic areas in northern Paraná, times of greatest frequency of phlebotomines similar to those observed in the present investigation have been observed.11,13
In the collections done using Falcão traps, the majority of L. whitmani specimens (52.2%) were collected during months that are normally hotter and rainier (March, April and November), although a considerable proportion (31.1%) were collected in colder and drier months (June, August and September). Thus, seasonality similar to what has previously been observed in rural areas of northern Paraná for L. whitmani using the same trap type can be confirmed.11,14,15 The results from the present work also show that, in the collections performed in the Shannon traps, the greatest number of specimens of L. whitmani (55.1%) was collected in one of the driest and coldest months of the year (August). This therefore differs from the seasonality observed previously,12 which was also in the rural area of this region, and using the same trap type.
The results from the present investigation show that there is clear predominance of L. whitmani in the Ingá Park, since this species had almost absolute prevalence using both collection methods. The results suggest that raccoons, coatis, peccaries and tiger cats attract more phlebotomines that the other mammals, forest birds and reptiles present in the Ingá Park. The frequency of L. whitmani increases up to 12:00 midnight, remains constant until 2:00 a.m. and thereafter gradually decreases. In the collections using Falcão traps, L. whitmani is most frequent in March, April and November, when the temperatures and rainfall in northern Paraná are higher. In the collections using Shannon traps, L. whitmani is more frequent in August, when the temperatures and rainfall are lower. It is recommended that people be prohibited from entering and remaining in the Ingá Park during the night, so as to avoid infection by Leishmania. Further evaluation through studies on the attraction of phlebotomines towards forest animals needs to be undertaken.
1. Azevedo ACR, Rangel EF, Costa EM, David JR, Vasconcelos AW, Lopes UG. Natural infection of L. (Nyssomyia) whitmani (Antunes & Coutinho,1939) by Leishmania of the braziliensis complex in Baturité, Ceará State, Northeastern Brazil. Mem Inst Oswaldo Cruz 1990;85:251. [ Links ]
2. Azevedo ACR, Rangel EF, Queiroz RG. L. migonei (França, 1920) naturally infected with peripylarian flagellates in Baturité, a focus of cutaneous leishmaniasis in Ceará State, Brazil. Mem Inst Oswaldo Cruz 1990;85:479. [ Links ]
3. Campbell-Lendrum DH, Pinto MC, Brandão-Filho SP, Souza AA, Ready PD, Davies CR. Experimental comparison of anthropophily between geographically dispersed populations of Lutzomyia whitmani (Diptera: Psychodidae). Med Vet Entomol 1999;13:299-309. [ Links ]
4. Forattini OP, Gomes AC, Santos JLF, Galati EAB, Rabello EX, Natal D. Observações sobre atividades de mosquitos Culicidae, em mata residual no Vale do Ribeira, São Paulo, Brasil. Rev Saúde Pública 1981;15:557-86. [ Links ]
5. Lima AP. Distribuição da leishmaniose tegumentar e análise da sua ocorrência em ambientes antrópicos, no Estado do Paraná, Brasil [dissertação de mestrado]. Londrina: Universidade Estadual de Londrina; 2000. [ Links ]
6. Luz E, Membrive N, Castro EA, Dereure J, Pratlong J, Dedet A et al. Lutzomyia whitmani Diptera: Psychodidae) as vector of Leishmania (V). braziliensis in Paraná State, southern Brazil. Ann Trop Med Parasitol 2000;94:623-31. [ Links ]
7. Ministério da Saúde. Fundação Nacional de Saúde. Manual de controle da leishmaniose tegumentar americana. Brasília (DF); 2000. [ Links ]
8. Queiroz RG, Vasconcelos IAB, Vasconcelos AW, pessoa FAC, Sousa RN, David JR. Cutaneous leishmaniasis in Ceara in Northeastern Brazil: incrimination of Lutzomyia whitmani (Diptera: Psychodidae) as a vector of Leishmania braziliensis in Baturité municipality. Am J Trop Med Hyg 1994;50:693-8. [ Links ]
9. Quinnel RJ, Dye C, Shaw JJ. Host preference of phlebotomine sandfly Lutzomyia longipalpis in Amazonian Brazil. Med Vet Entomol 1991;6:195-200. [ Links ]
10. Rangel EF, Souza NA, Wermelinger ED, Barbosa F. Infecção natural de L. neivai Lutz & Neiva, 1912, em área endêmica de leishmaniose tegumentar no Estado do Rio de Janeiro. Mem Inst Oswaldo Cruz 1984;79:395-6. [ Links ]
11. Teodoro U. Características ecológicas de Flebotomíneos (Diptera, Psychodidae) em habitats antrópicos, município de Jussara, Paraná, Brasil [tese de doutorado]. Curitiba: Universidade Federal do Paraná; 1995. [ Links ]
12. Teodoro U, La Salvia Filho V, Lima EM, Misuta NM, Verzignassi TG, Ferreira MEMC. Leishmaniose tegumentar: flebotomíneos de área de transmissão na região norte do Paraná, Brasil. Rev Saúde Pública 1991;25:129-33. [ Links ]
13. Teodoro U, La Salvia Filho V, Lima EM, Spinosa RP, Barbosa OC, Ferreira MEMC, Silveira TGV. Flebotomíneos em áreas de trasnmissão de leishmaniose tegumentar na região norte do Estado do Paraná, Brasil: variação sazonal e atividade noturna. Rev Saúde Pública 1993;27:190-4. [ Links ]
14. Teodoro U, La Salvia Filho V, Lima EM, Spinosa RP, Barbosa OC, Ferreira MEMC, Lonardoni MVC. Observações sobre o comportamento de flebotomíneos em ecótopos florestais e extraflorestais, em área endêmica de leishmaniose tegumentar americana no norte do Estado do Paraná, sul do Brasil. Rev Saúde Pública 1993;27:242-9. [ Links ]
15. Teodoro U, Kühl JB, Thomaz-Soccol V, Ferreira MEMC, Lozovei AL, Silveira TGV. Influence of peri-domiciliar environmental conditions in the dispersion and proliferation of phlebotomine sandflies in Paraná State, Southern Brazil. Arq Biol Tecnol 1997;40:747-51. [ Links ]
16. Teodoro U, Kühl JB, Rodrigues M, Santos ES, Santos DR, Maróstica LMF. Flebotomíneos coletados em matas remanescentes e abrigos de animais silvestres de zoológico no perímetro urbano de Maringá, Sul do Brasil: estudo preliminar. Rev Soc Bras Med Trop 1998;31:517-22. [ Links ]
Departamento de Análises Clínicas da Universidade Estadual de Maringá
Av. Colombo, 5790
87020-900 Maringá, PR, Brazil
Received on 20/7/2002.
Reviewed on 15/4/2003.
Approved on 13/5/2003.
Fundação Nacional de Saúde e Universidade Estadual de Maringá