Acessibilidade / Reportar erro

Ecological aspects of Pintomyia fischeri and Migonemyia migonei in municipalities with Canine Visceral Leishmaniasis, State of São Paulo, Brazil

Aspectos ecológicos de Pintomyia fischeri e Migonemyia migonei em municípios com Leishmaniose Visceral Canina, estado de São Paulo, Brasil

Abstract

The objective was to study the composition of sand fly species, the seasonal activity of the dominant species and correlation with average rainfall, sex association of the dominant species with domicile habitats and analyze different landscape scenarios for the two study sites in the municipalities of Itapevi and Mogi of the Crosses. Sandflies were captured with CDC(s) traps installed in three households at each study site for a period of 24 hours, biweekly for two years. A total of 2970 specimens were collected. The dominant species were P.fischeri and M.migonei. A statistically significant difference was registered between males and females of the two species in relation to the intra and peridomicile. The seasonal activity of both species showed a weak significant positive correlation with rainfall. The species P.fischeri and M.migonei may be potential vectors of CVL in the studied sites.

Keywords:
Sandfly; composition of species; seasonal activity; landscap scenarios; CVL

Resumo

O objetivo foi estudar a composição das espécies de flebotomíneos, a atividade sazonal das espécies dominantes e a correlação com médias pluviométricas, associação de sexo das espécies dominantes com habitats domiciliares. Também analisar diferentes cenários da paisagem para os dois sítios de estudo nos municípios de Itapevi e Mogi das Cruzes. Os flebotomíneos foram capturados com armadilhas CDC(s) instaladas em três domicílios de cada sítio de estudo por um período de 24 horas, quinzenalmente por dois anos. Um total de 2.970 espécimes foram coletados. As espécies dominantes foram P.fischeri e M.migonei. Foi registrada diferença estatística significante entre machos e fêmeas das duas espécies em relação ao intra e peridomicílio. A atividade sazonal das duas espécies apresentou fraca correlação positiva significante com a chuva. As espécies P.fischeri e M.migonei podem ser potenciais vetores de LVC nos locais de estudo.

Palavras-chave:
Flebotomíneos; composição de espécies; atividade sazonal; cenários da paisagem; CVL

Visceral leishmaniasis is a zoonosis caused by the protozoan Leishmania (Leishmania) infantum chagasi, in the Americas, and is transmitted by the bite of infected sandflies (Diptera: Psychodidae: Phlebotominae). In studies carried out with strains of Leishmania chagasi from South America and Leishmania infantum from the Mediterranean, it was verified that both present the same DNA sequence, and it was proposed that L (L.) chagasi should not be considered a valid species; however, Laison and Shaw, based on its ecological characteristics, defended the maintenance of the parasitological entity at the subspecific level as Leishmania (L.) infantum chagasi. In Brazil, the disease initially had a rural character, but it has changed its epidemiological pattern in recent decades, with its introduction and expansion in urban environments. The main vector species is Lutzomyia longipalpis, but Lutzomyia cruzi has also been implicated in transmission, with the domestic dog (Canis lupus familiaris) being the main reservoir of this protozoan in urban settings (Lainson & Shaw, 2005Lainson R, Shaw JJ. New World Leishmaniasis. In: Cox FEG, Wakelin D, Gillespie SH, Despommier DD, editors. Topley & Wilson’s Microbiology and Microbial Infections: parasitology. 10th ed. London: Hodder Arnold ASM Press; 2005. p. 313-349.; Lainson, 2010Lainson R. The Neotropical Leishmania species: a brief historical review of their discovery, ecology and taxonomy. Pan-Amaz Saude 2010; 1(2): 13-32. http://dx.doi.org/10.5123/S2176-62232010000200002.
http://dx.doi.org/10.5123/S2176-62232010...
; Salomón et al., 2015Salomón OD, Feliciangeli MD, Quintana MG, Afonso MMS, Rangel EF. Lutzomyia longipalpis urbanization and control. Mem Inst Oswaldo Cruz 2015; 110(7): 831-846. http://dx.doi.org/10.1590/0074-02760150207. PMid:26517497.
http://dx.doi.org/10.1590/0074-027601502...
).

In the state of São Paulo, the vector L. longipalpis was identified for the first time in 1997, in an urban area of the city of Araçatuba; the first case of canine visceral Leishmaniasis (CVL) was recorded in 1998 and, in 1999, the first autochthonous cases of human visceral Leishmaniasis (HVL) were diagnosed in this municipality (Camargo-Neves et al., 2001Camargo-Neves VLF, Katz G, Rodas LAC, Poletto DW, Lage LC, Spínola RMF, et al. Utilização de ferramentas de análise espacial na vigilância epidemiológica de leishmaniose visceral americana – Araçatuba, São Paulo, Brasil, 1998-1999. Cad Saude Publica 2001; 17(5): 1263-1267. http://dx.doi.org/10.1590/S0102-311X2001000500026. PMid:11679900.
http://dx.doi.org/10.1590/S0102-311X2001...
). Thereafter, the dispersal of the vector, of CVL and of HVL was reported from the northwest to southeast direction, in this state (Oliveira et al., 2016Oliveira AM, Vieira CP, Dibo MR, Guirado MM, Rodas LAC, Chiaravalloti-Neto F. Dispersal of Lutzomyia longipalpis and expansion of canine and human visceral leishmaniasis in São Paulo State, Brazil. Acta Trop 2016; 164: 233-242. http://dx.doi.org/10.1016/j.actatropica.2016.09.014. PMid:27640322.
http://dx.doi.org/10.1016/j.actatropica....
).

However, in the Metropolitan Region of São Paulo (RMSP), state of São Paulo, CVL occurs in rural areas close to forest fragments, which provides access for dogs to these fragments, in addition to socializing with other animals around the house, such as cats, swine, equine and chickens. In the state of Santa Catarina, Pinto et al. (2022)Pinto AO, Carvalho D, Frizzo C, Lopes K, Tessari GB, Catecati T, et al. First case of canine visceral leishmaniasis in the midwestern of Santa Catarina State, Brazil. Braz J Biol 2022; 82: e241162. http://dx.doi.org/10.1590/1519-6984.241162. PMid:34133561.
http://dx.doi.org/10.1590/1519-6984.2411...
found the same situation in relation to dogs with CVL, that is, the presence and possible and possible entry into forest areas, in addition to the occurrence of poultry and swine farms in the vicinity of the houses. In the RMSP, sand fly collections were carried out in places where cases of CVL occurred, however, the L. longipalpis vector was only detected in the municipality of Caieiras (Pimont et al., 2015Pimont MP, Araújo VC, Duarte AN, Araújo AC, Silva JA Fo, Silva MA, et al. Lutzomyia longipalpis record associated with a canine case of visceral leishmaniasis in the municipality of Caieiras, São Paulo State, Brazil. BEPA 2015; 12(143): 33-37.).

In this study, we aimed to know the composition and diversity of the sandfly species, the activity of dominant species during months of collection, the correlation of rainfall with the numerical abundance of dominant species, the association of the sex of these species with the surveyed households, and to compare landscape analyzes and potential influence on the sandfly species composition, of areas of two municipalities in the RMSP, with local transmission of CVL.

The study area comprises two locations in two municipalities of the RMSP, Itapevi, located west of the city of São Paulo, and Mogi das Cruzes, located east of the same city. In the municipality of Mogi das Cruzes, the first positive dog was identified in 2006, but other cases occurred in 2007 and 2008. In 2017, new cases of canine visceral leishmaniasis were detected in the rural area of Mogi das Cruzes in the neighborhoods Itapeti Residential Park. In that same year, cases of CVL began in dogs residing in the municipality of Itapevi in the neighborhoods Della Vitória Park, in some houses in the rural area that communicated with the same forest fragment.

Collections were carried out fortnightly in households in the two locations of the municipalities of Mogi das Cruzes and Itapevi. Two CDC(s) traps were installed for a period of 24 hours, every two weeks from September of 2017 to July of 2019, in intradomicile and peridomicile habitats, in three households, in each of the at each of the study sites. In the peridomicile, preferably, they were installed close to the place where a food source (dog, chicken) spent the night (Figure 1).

Figure 1
Map of the studied area, with landscape data analysis of the collect sites in Itapevi (left side) and Mogi das Cruzes (right side), MRSP, SP, Brazil.

The Sandflys specimens collected with CDC(s) traps were transported from the field to the laboratory in trap cups packed in transport boxes. In the laboratory, the process of clarification, assembly and identification down to the species category was in accordance with Shimabukuro et al. (2011)Shimabukuro PHF, Tolezano JE, Galati EAB. Chave de identificação ilustrada dos Phlebotominae (Diptera, Psychodidae) do Estado de São Paulo, Brasil. Pap Avulsos Zool 2011; 51(27): 399-441. http://dx.doi.org/10.1590/S0031-10492011002700001.
http://dx.doi.org/10.1590/S0031-10492011...
. The abbreviations for the genus and species were made in accordance with Marcondes (2007)Marcondes CB. A proposal of generic and subgeneric abbreviations for phlebotomine sandflies (Diptera: Psychodidae: Phlebotominae) of the word. Entomol News 2007; 118(4): 351-356. http://dx.doi.org/10.3157/0013-872X(2007)118[351:APOGAS]2.0.CO;2.
http://dx.doi.org/10.3157/0013-872X(2007...
. The identified specimens were confirmed and deposited in the collection of the Department of Epidemiology of the FSP/USP. Data were recorded in an appropriate bulletin and entered into Microsoft Excel spreadsheets.

Diversity analysis was undertaken for composition of the phlebotomine species collected study sites, Margalef’s index (Mg), Simpson’s dominance index (Ds) and Shannon’s diversity index (H) were used for the measurements. Student's t test was used to calculate the variance and degrees of freedom, the latter always tending to infinity when dealing with Shannon's diversity (Magurran, 1988Magurran E. Ecological diversity and its measurement. Princeton: Springer Dordrecht; 1988. http://dx.doi.org/10.1007/978-94-015-7358-0.
http://dx.doi.org/10.1007/978-94-015-735...
).

Williams’ average (x¯w) (Forattini, 2002Forattini OP. Culicidologia médica. Vol. 2. São Paulo: Edusp; 2002.) was calculated for each month, for those species which occurred in greater abundance, taking into consideration the number of collections undertaken during each month for both study sites.

Pearson’s correlation (r) was used to verify the association between the monthly averages (x¯w) of P.fischeri and M.migonei, with the accumulated rainfall of the month prior to the collections.

Chi-squared analysis, at the 5% significance level (α=0.05), was used to establish the existence or not of any association between the variable categories sex (male and female) and habitats (peridomicile and intradomicile) for dominant sandflies species.

The data were analyzed on Excel spread sheets. Statistical inferences were performed in softwares BioEstat (version 5.3).

In both two selected sites, the forested patches landscape parameters were identified by visual analysis of high-resolution satellite images (CNES/Astrium, DigitalGlobe and Terrametrics compositions, with passage date until October 2021), provided in Google Earth Pro 7.1.5.1557 (Google, Inc. Mountain View, CA, USA), polygons of the forest areas were scanned on screen, and the edge linear and total area calculations were performed in the same software. It was included in the metrics, the total area, in hectares, of all connected forest surrounding the studied site within a radius of 2 km, and the sum in kilometers of the total forest edge perimeters. All forest patches with no structural connection in between, but within a maximum distance of 100 meters from each other were included in the metrics.

During the study period, a total of 2,970 specimens were collected. In relation to the general totals, 1,928 (64.9%) were P.fischeri and 607 (20.4%) M.migonei. The third numerically dominant species is P.lloydi, with 259 (8.7%) specimens (Table 1) (Marcondes, 2007Marcondes CB. A proposal of generic and subgeneric abbreviations for phlebotomine sandflies (Diptera: Psychodidae: Phlebotominae) of the word. Entomol News 2007; 118(4): 351-356. http://dx.doi.org/10.3157/0013-872X(2007)118[351:APOGAS]2.0.CO;2.
http://dx.doi.org/10.3157/0013-872X(2007...
).

Table 1
Composition of sandfly species, by sex and habitat, collected in the in two locations, what are the neighborhoods Della Vitória Park and Itapeti Residential Park, respectively located in the municipalities of Itapevi and Mogi das Cruzes from 2017 to 2019.

The greatest species richness (S=15) and diversity were registered respectively by Margalef’s index (Mg=1.86) and Shannon’s index (H=1.23) for Della Vitoria Park in Itapevi. The highest Simpson's dominance (Ds=0.62) was estimated for the species collected in Itapeti Residential Park. (Table 1). Student's t-test indicated that the values of Shannon's diversity index (H) estimated for the species composition of sandflies, when comparing the localities of Della Vitoria Park (H=1.23) and Itapeti Residential Park (H=0.69), it was found to differ greatly and highly significant (t=8.2; p<0.001).

The highest peaks of activity recorded by Williams’ average (X ̅w) measured over the months compared to rainfall in the month previous to each collection were found for the species P.fischeri, both in Della Vitoria Park and in Itapeti Residential Park. Spring and summer months were those of the most intense activity for both species (Figure 2).

Figure 2
Variation of Williams mean of P.fischeri and M.migonei collected in different months, in two locations, what are the neighborhoods Della Vitória Park and Itapeti Residential Park, respectively located in the municipalities of Itapevi and Mogi das Cruzes from august 2017 to july 2019.

Pearson's coefficient of correlation (r) presented a weak positive, though significant, correlation (p<0.05) for Williams' monthly average of P.fischeri, with the accumulated rainfall for the previous month on the occasion of each collection in Della Vitória Park (r = 0.45; p=0.03). Also, weak but significant was the correlation between the same variables for the specimens of M. migonei collected in Itapeti Residential Park (r = 0.43; p=0.04).

According to the categorical variable’s habitat and sex, it was observed that the species P. fischeri had a greater number of females than males, both in the intradomicile of Della Vitória Park and in the peridomicile of Itapeti Residential Park. For the M.migonei species, the number of females was greater and the males in the intradomicile of Della Vitória Park. The same is true for Ps.lloydi species (Table 1).

The chi-square distribution showed that there is a highly significant statistical difference between the female and male variables of the dominant species P.fischeri and M.migonei, in relation to the intra and peridomiciliary variables in Della Vitória Park and Itapeti Residential Park (χ2 = 285.8 , gl = 9, p <0.001).

The landscape metrics analysis yielded different scenarios for each site, the total remain forest area within 2 km radius and the total border forest perimeter were 595.64 ha and 95.00 km for Itapevi and 494.31 ha and 67.32 km for Mogi das Cruzes (Figure 1). In Itapevi, 47.4% of the area (within 2 km radium) is composed by remain forest patches whereas this value was 39.3% for Mogi das Cruzes, but in proportion, in Itapevi the total forest perimeter over total forest area was 0.16, in Mogi das Cruzes was 0.13. Therefore, Itapevi was characterized by occurrence of larger forest area and larger proportion of forest edge when compared to Mogi das Cruzes (Figure 1).

The most abundant species in Della Vitória Park and Itapeti Residential Park were also predominant in collections undertaken by other authors in in the MRSP. In Embu das Artes, a place with transmission of VLC, the majority of the specimens colleted corresponded to the species P.fischeri, however M.migonei was also present (Galvis-Ovallos et al., 2017Galvis-Ovallos F, Silva MD, Bispo GBS, Oliveira AG, Gonçalves JR No, Malafronte RS, et al. Canine visceral leishmaniasis in the metropolitan area of São Paulo: Pintomyia fischeri as potential vector of Leishmania infantum. Parasite 2017; 24: 2. http://dx.doi.org/10.1051/parasite/2017002. PMid:28134092.
http://dx.doi.org/10.1051/parasite/20170...
). In São Paulo, P.fischeri was collected in the parks of the Cantareira, Alfredo Volpi and the Zoological Park, and M.migonei in the Zoological Park and of Anhanguera and Cantareira (Oliveira Castelo et al., 2015Oliveira Castelo NOC, Nascimento AC, Oliveira RC, Marques S, Gonçalves EFB, Galati EAB. Fauna flebotomínea (Diptera, Psychodidae) em parques do Município de São Paulo, estado de São Paulo, Brasil. BEPA [online]. 2015 [cited 2022 Apr 4]; 12(141): 1-9. Available from: https://periodicos.saude.sp.gov.br/BEPA182/article/view/38142
https://periodicos.saude.sp.gov.br/BEPA1...
). The species M. migonei is permissive to several species of Leishmania spp. and Guimarães et al. (2016)Guimarães VCFV, Pruzinova K, Sadlova J, Volfova V, Myskova J, Filho SP, et al. Lutzomyia migonei is a permissive vector competent for Leishmania infantum. Parasit Vectors 2016; 9(1): 159. http://dx.doi.org/10.1186/s13071-016-1444-2. PMid:26988559.
http://dx.doi.org/10.1186/s13071-016-144...
have demonstrated in the laboratory that M. migonei is susceptible to the development of Leishmania infantum. In a study carried out in Fortaleza (CE), M.migonei was considered a potential vector of VL, along with L. longipalpis (Silva et al., 2014Silva RA, Santos FKM, Souza LC, Rangel EF, Bevilaqua CML. Ecology of Lutzomyia longipalpis and Lutzomyia migonei in an endemic area for visceral leishmaniasis. Rev Bras Parasitol Vet 2014; 23(3): 320-327. http://dx.doi.org/10.1590/S1984-29612014068. PMid:25271451.
http://dx.doi.org/10.1590/S1984-29612014...
).

The greatest richness and diversity for the sandfly species registered for the Della Vitória Park may be due to the increase in breeding sites caused by the loss of leaves of tree species during the dry period, which are characteristic of the forest fragments at the study site (Barreto & Catharino, 2015Barreto EHP, Catharino ELM. Florestas maduras da região metropolitana de São Paulo: diversidade, composição arbórea e variação florística ao longo de um gradiente litoral-interior, Estado de São Paulo, Brasil. Hoehnea 2015; 42(3): 445-469. http://dx.doi.org/10.1590/2236-8906-72/2014.
http://dx.doi.org/10.1590/2236-8906-72/2...
), besides the landscape metrics showed that Della Vitória Park site had 47.4% of area composed by remain forest and larger proportion of forest edges, larger forest areas may increase the diversity of the sandflies and the larger proportion of forest edge may increase the contact of between households and forest patches (Figure 1).

In Itapeti Residential Park, which presents greater diversification of agricultural activities, expansion pasture areas and the proximity of households to urbanized areas reflect into smaller remain forest patches area, when compared to Della Vitória Park, which may explain there is less richness and diversity and the greatest dominance of species (São Paulo, 2013São Paulo. Governo do Estado. Secretaria de Estado do Meio Ambiente – SEMA. Fundação Florestal do Estado de São Paulo. Proposta para Criação das Unidades de Conservação na Serra do Itapeti e do Masaico Itapeti – Tiete. Relatório Final [online]. São Paulo: SEMA; 2013 [cited 2022 Apr 4]. Available from: https://smastr16.blob.core.windows.net/fundacaoflorestal/2013/10/Relat%C3%B3rio-Cria%C3%A7%C3%A3o-UCs-Serra-Itapeti.pdf
https://smastr16.blob.core.windows.net/f...
).

The significant value of the test of hypotheses (t=8.2; p<0.001) for Shannon’s diversity index, showed that in fact the diversity value for the phlebotomine species in Della Vitoria Park was greater than that estimated for Itapeti Residential Park. It is believed that this difference may be related to the different stages of the conservation of the forest fragments around the residences researched and a greater availability or variety of trophic niches in the peridomiciliary areas.

The recorded of the occurrence of a weak though significant correlation between the Williams’ averages of P. fischeri and M. migonei collected respectively in Della Vitória Park and Itapeti Residential Park, and the rainfall of the month prior to the collection, may be related to the humidity in the soil caused by the rains, an occurrence which probably aided the decomposition of the organic material there present thus creating appropriate places for the oviposition and favoring the development of immature forms, and the increase in the abundance of adult forms collected in the months subsequent to the rainiest ones, a condition which has already been observed by Almeida et al. (2010)Almeida PS, Minzão ER, Minzão LD, Silva SR, Ferreira AD, Faccenda O, et al. Ecological aspects of Phlebotomines (Diptera: Psychodidae) in the urban area of Ponta Porã municipality, State of Mato Grosso do Sul, Brazil. Rev Soc Bras Med Trop 2010; 43(6): 723-727. http://dx.doi.org/10.1590/S0037-86822010000600025. PMid:21181032.
http://dx.doi.org/10.1590/S0037-86822010...
, for other species of sandflies.

The highest peaks of activity as measured by Williams’ averages registered for P. fischeri during the rainy periods, were preceded by accumulated rainfall values for the month which did not exceed 300 mm in Della Vitória Park - Itapevi or 200 mm in Itapeti Residential Park - Mogi das Cruzes (Figure 2). Very probably, the low average values for the activity of the dominant species observed in Itapeti Residential Park, may be related to the high rainfall peaks which preceded the collection. Some authors also point out that sandflies are benefited by moderate rainfall and that very intense rainfall delays development, consequently there will be a low abundance of adult specimens (Dias et al., 2007Dias ES, França-Silva JC, Silva JC, Monteiro EM, Paula KM, Gonçalves CM, et al. Flebotomíneos (Diptera: Psychodidae) de um foco de leishmaniose tegumentar no Estado de Minas Gerais. Rev Soc Bras Med Trop 2007; 40(1): 49-52. http://dx.doi.org/10.1590/S0037-86822007000100009. PMid:17486253.
http://dx.doi.org/10.1590/S0037-86822007...
; Macedo et al., 2008Macedo ITF, Bevilaqua CML, Morais NB, Souza LC, Linhares FE, Amóra SSA, et al. Sazonalidade de flebotomíneos em área endêmica de leishmaniose Visceral no município de Sobral, Ceará, Brasil. Ciênc Anim 2008; 18(2): 67-74.).

The numerical dominance of P. fischeri and M. migonei (Table 1) for the intradomestic and peridomestic habitats in the two study sites may be related to the existence of favorable habitat for oviposition, present in the domiciles or in the forest fragments close to the domiciles. It is also easy for females to obtain blood and thus develop their gonotrophic cycle, due to the presence of humans and the canine reservoirs that are very present in both study sites. Pasanisi (2020)Pasanisi C. Inquérito epidemiológico sobre a leishmaniose visceral canina no Município de Itapevi: relato do primeiro inquérito sorológico. Pubvet 2020; 14(3): 1-7. http://dx.doi.org/10.31533/pubvet.v14n3a539.1-7.
http://dx.doi.org/10.31533/pubvet.v14n3a...
carried out the first serological canine survey for the municipality of Itapevi and found that among 104 dogs from the peridomestic environment, 16 of them were diagnosed seropositive, totaling 15.3% of the samples. The seropositive animals were submitted to parasitological tests to confirm Leishmania infection. The author mentions that in the entomological investigation carried out, no specimen of L. longipalpis was found, however the two species recorded here by us as numerically dominant were found.

Although P. fischeri and M. migonei use the blood of dogs and birds, they present a high degree of anthropophily (Gomes & Galati, 1989Gomes AC, Galati EAB. Aspectos Ecológicos da leishmaniose Tegumentar Americana. 7 - Capacidade Vetorial Flebotomínea em Ambiente Florestal Primário do Sistema da Serra do Mar, Região do Vale do Ribeira, Estado de São Paulo, Brasil. Rev Saude Publica 1989; 23(2): 136-142. http://dx.doi.org/10.1590/S0034-89101989000200007. PMid:2617105.
http://dx.doi.org/10.1590/S0034-89101989...
). In Parque Della Vitória in Itapevi, the abundance of the species P. fischeri, later associated with studies of competence and vectorial capacity, could explain the occurrence of the first autochthonous human case of visceral leishmaniasis in 2018, without the occurrence of the L. longipalpis (São Paulo, 2023São Paulo. Governo do Estado. Secretaria de Estado da Saúde – SES. Centro de Vigilância Epidemiológica “Prof. Alexandre Vranjac”. Casos confirmados de Leishmaniose Visceral segundo LPI e ano de notificação, Estado de São Paulo, 2017 a 2023 [online]. São Paulo: SES; 2023 [cited 2023 June 14]. Available from: https://www.saude.sp.gov.br/resources/cve-centro-de-vigilancia-epidemiologica/areas-de-vigilancia/doencas-de-transmissão-por-vetores-e-zoonoses/dados/leish/Iv1723_IP.pdf?attach=true
https://www.saude.sp.gov.br/resources/cv...
).

Also in the case of Mogi das Cruzes, the great abundance of P. fischeri females in the peridomicile of Parque Residencial Itapeti (Table 1) may be related to the great attractiveness that these species have for performing the blood meal in dogs, since this domestic animal also was very frequent in the peridomicile habitats of this locality.

Galvis-Ovallos et al. (2017)Galvis-Ovallos F, Silva MD, Bispo GBS, Oliveira AG, Gonçalves JR No, Malafronte RS, et al. Canine visceral leishmaniasis in the metropolitan area of São Paulo: Pintomyia fischeri as potential vector of Leishmania infantum. Parasite 2017; 24: 2. http://dx.doi.org/10.1051/parasite/2017002. PMid:28134092.
http://dx.doi.org/10.1051/parasite/20170...
carried out a vectorial capacity study in specimens of P. fischeri and M. migonei collected in Embu das Artes; concluded that the great attractiveness of dogs for P. fischeri, their susceptibility to infection by Leishmania infantum, life expectancy and predominance in the RMSP, made it clear that P. fischeri is a potential vector of this parasite in the region. In the same municipality, they sequentially collected sandflies and found infection by L. infantum PCR positive in P. fischeri (Galvis-Ovallos et al., 2021Galvis-Ovallos F, Ueta AE, Marques GO, Sarmento AMC, Araujo G, Sandoval C, et al. Detection of Pintomyia fischeri (Diptera: Psychodidae) With Leishmania infantum (Trypanosomatida: Trypanosomatidae) Promastigotes in a Focus of Visceral Leishmaniasis in Brazil. J Med Entomol 2021; 58(2): 830-836. http://dx.doi.org/10.1093/jme/tjaa199. PMid:33047129.
http://dx.doi.org/10.1093/jme/tjaa199...
).

However, in an area of transmission of visceral leishmaniasis, in São Vicente Férrer, State of Pernambuco, females of the species M. migonei were found naturally infected by L. infantum, indicating that this species of sand fly can be the vector of visceral leishmaniasis in areas where the presence of Lutzomyia longipalpis was not detected (Carvalho et al., 2010Carvalho MR, Valença HF, Silva FJ, Pita-Pereira D, Pereira TA, Britto C, et al. Natural Leishmania infantum infection in Migonemyia migonei (França, 1920) (Diptera: Psychodidae: Phlebotominae) the putative vector of visceral leishmaniasis in Pernambuco state, Brazil. Acta Trop 2010; 116(1): 108-110. http://dx.doi.org/10.1016/j.actatropica.2010.03.009. PMid:20457120.
http://dx.doi.org/10.1016/j.actatropica....
). The three studies demonstrated the possibility of infection of P. fischeri and M. migonei by L. infantum, in addition to the attractiveness of P. fischeri for dogs, which is an indication of the importance of the numerical dominance of these two species of sandflies in an area of transmission of canine visceral leishmaniasis, as has already been recorded for the capture sites here in this study.

What we focus on in this study is limited, for future studies it should be increased the samples in relation to the number of households and also other habitats should be accessed, therefore it could validate the results for the municipalities of Mogi das Cruzes and Itapevi, here represented by neighborhood localities.

Certainly, a canine survey and an entomological survey in a larger number of households, with the collection of sandflies in other sites, in addition to those surveyed here, in which there was a confirmed of dogs infected with visceral Leishmaniasis; would give us a greater epidemiological view of the situation of disease in the studied cities.

Besides the numerical dominance, for P. fischeri and M. migonei and their respective seasonal activities, and frequencies in the home environment, we emphasize that for these species or others recorded here, in the studied sites, to be considered potential vectors of Leishmania infantum chagasi, in the reported conditions, it is necessary to isolate the parasite from collected sandflies specimens. Future studies must still be developed with the aim of verifying whether the aforementioned sandfly species are vectors based on parameters of competence and vectorial capacity.

Acknowledgments

The authors thank the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) for financial support; Process no.: 2017/03805-0. We also thank José Arcanjo da Silva Filho, Maria Alice da Silva, Ana Cláudia de Araújo for their collaboration in field activities and in the screening and identification of sandflies.

  • How to cite: Dibo MR, Menezes RMT, Souza FF, Gil HB, Pinter A. Ecological aspects of Pintomyia fischeri and Migonemyia migonei in municipalities with Canine Visceral Leishmaniasis, State of São Paulo, Brazil. Braz J Vet Parasitol 2023; 32(3): e002123. https://doi.org/10.1590/S1984-29612023040

References

  • Almeida PS, Minzão ER, Minzão LD, Silva SR, Ferreira AD, Faccenda O, et al. Ecological aspects of Phlebotomines (Diptera: Psychodidae) in the urban area of Ponta Porã municipality, State of Mato Grosso do Sul, Brazil. Rev Soc Bras Med Trop 2010; 43(6): 723-727. http://dx.doi.org/10.1590/S0037-86822010000600025 PMid:21181032.
    » http://dx.doi.org/10.1590/S0037-86822010000600025
  • Barreto EHP, Catharino ELM. Florestas maduras da região metropolitana de São Paulo: diversidade, composição arbórea e variação florística ao longo de um gradiente litoral-interior, Estado de São Paulo, Brasil. Hoehnea 2015; 42(3): 445-469. http://dx.doi.org/10.1590/2236-8906-72/2014
    » http://dx.doi.org/10.1590/2236-8906-72/2014
  • Camargo-Neves VLF, Katz G, Rodas LAC, Poletto DW, Lage LC, Spínola RMF, et al. Utilização de ferramentas de análise espacial na vigilância epidemiológica de leishmaniose visceral americana – Araçatuba, São Paulo, Brasil, 1998-1999. Cad Saude Publica 2001; 17(5): 1263-1267. http://dx.doi.org/10.1590/S0102-311X2001000500026 PMid:11679900.
    » http://dx.doi.org/10.1590/S0102-311X2001000500026
  • Carvalho MR, Valença HF, Silva FJ, Pita-Pereira D, Pereira TA, Britto C, et al. Natural Leishmania infantum infection in Migonemyia migonei (França, 1920) (Diptera: Psychodidae: Phlebotominae) the putative vector of visceral leishmaniasis in Pernambuco state, Brazil. Acta Trop 2010; 116(1): 108-110. http://dx.doi.org/10.1016/j.actatropica.2010.03.009 PMid:20457120.
    » http://dx.doi.org/10.1016/j.actatropica.2010.03.009
  • Dias ES, França-Silva JC, Silva JC, Monteiro EM, Paula KM, Gonçalves CM, et al. Flebotomíneos (Diptera: Psychodidae) de um foco de leishmaniose tegumentar no Estado de Minas Gerais. Rev Soc Bras Med Trop 2007; 40(1): 49-52. http://dx.doi.org/10.1590/S0037-86822007000100009 PMid:17486253.
    » http://dx.doi.org/10.1590/S0037-86822007000100009
  • Forattini OP. Culicidologia médica Vol. 2. São Paulo: Edusp; 2002.
  • Galvis-Ovallos F, Silva MD, Bispo GBS, Oliveira AG, Gonçalves JR No, Malafronte RS, et al. Canine visceral leishmaniasis in the metropolitan area of São Paulo: Pintomyia fischeri as potential vector of Leishmania infantum. Parasite 2017; 24: 2. http://dx.doi.org/10.1051/parasite/2017002 PMid:28134092.
    » http://dx.doi.org/10.1051/parasite/2017002
  • Galvis-Ovallos F, Ueta AE, Marques GO, Sarmento AMC, Araujo G, Sandoval C, et al. Detection of Pintomyia fischeri (Diptera: Psychodidae) With Leishmania infantum (Trypanosomatida: Trypanosomatidae) Promastigotes in a Focus of Visceral Leishmaniasis in Brazil. J Med Entomol 2021; 58(2): 830-836. http://dx.doi.org/10.1093/jme/tjaa199 PMid:33047129.
    » http://dx.doi.org/10.1093/jme/tjaa199
  • Gomes AC, Galati EAB. Aspectos Ecológicos da leishmaniose Tegumentar Americana. 7 - Capacidade Vetorial Flebotomínea em Ambiente Florestal Primário do Sistema da Serra do Mar, Região do Vale do Ribeira, Estado de São Paulo, Brasil. Rev Saude Publica 1989; 23(2): 136-142. http://dx.doi.org/10.1590/S0034-89101989000200007 PMid:2617105.
    » http://dx.doi.org/10.1590/S0034-89101989000200007
  • Guimarães VCFV, Pruzinova K, Sadlova J, Volfova V, Myskova J, Filho SP, et al. Lutzomyia migonei is a permissive vector competent for Leishmania infantum. Parasit Vectors 2016; 9(1): 159. http://dx.doi.org/10.1186/s13071-016-1444-2 PMid:26988559.
    » http://dx.doi.org/10.1186/s13071-016-1444-2
  • Lainson R, Shaw JJ. New World Leishmaniasis. In: Cox FEG, Wakelin D, Gillespie SH, Despommier DD, editors. Topley & Wilson’s Microbiology and Microbial Infections: parasitology 10th ed. London: Hodder Arnold ASM Press; 2005. p. 313-349.
  • Lainson R. The Neotropical Leishmania species: a brief historical review of their discovery, ecology and taxonomy. Pan-Amaz Saude 2010; 1(2): 13-32. http://dx.doi.org/10.5123/S2176-62232010000200002
    » http://dx.doi.org/10.5123/S2176-62232010000200002
  • Macedo ITF, Bevilaqua CML, Morais NB, Souza LC, Linhares FE, Amóra SSA, et al. Sazonalidade de flebotomíneos em área endêmica de leishmaniose Visceral no município de Sobral, Ceará, Brasil. Ciênc Anim 2008; 18(2): 67-74.
  • Magurran E. Ecological diversity and its measurement Princeton: Springer Dordrecht; 1988. http://dx.doi.org/10.1007/978-94-015-7358-0
    » http://dx.doi.org/10.1007/978-94-015-7358-0
  • Marcondes CB. A proposal of generic and subgeneric abbreviations for phlebotomine sandflies (Diptera: Psychodidae: Phlebotominae) of the word. Entomol News 2007; 118(4): 351-356. http://dx.doi.org/10.3157/0013-872X(2007)118[351:APOGAS]2.0.CO;2
    » http://dx.doi.org/10.3157/0013-872X(2007)118[351:APOGAS]2.0.CO;2
  • Oliveira AM, Vieira CP, Dibo MR, Guirado MM, Rodas LAC, Chiaravalloti-Neto F. Dispersal of Lutzomyia longipalpis and expansion of canine and human visceral leishmaniasis in São Paulo State, Brazil. Acta Trop 2016; 164: 233-242. http://dx.doi.org/10.1016/j.actatropica.2016.09.014 PMid:27640322.
    » http://dx.doi.org/10.1016/j.actatropica.2016.09.014
  • Oliveira Castelo NOC, Nascimento AC, Oliveira RC, Marques S, Gonçalves EFB, Galati EAB. Fauna flebotomínea (Diptera, Psychodidae) em parques do Município de São Paulo, estado de São Paulo, Brasil. BEPA [online]. 2015 [cited 2022 Apr 4]; 12(141): 1-9. Available from: https://periodicos.saude.sp.gov.br/BEPA182/article/view/38142
    » https://periodicos.saude.sp.gov.br/BEPA182/article/view/38142
  • Pasanisi C. Inquérito epidemiológico sobre a leishmaniose visceral canina no Município de Itapevi: relato do primeiro inquérito sorológico. Pubvet 2020; 14(3): 1-7. http://dx.doi.org/10.31533/pubvet.v14n3a539.1-7
    » http://dx.doi.org/10.31533/pubvet.v14n3a539.1-7
  • Pimont MP, Araújo VC, Duarte AN, Araújo AC, Silva JA Fo, Silva MA, et al. Lutzomyia longipalpis record associated with a canine case of visceral leishmaniasis in the municipality of Caieiras, São Paulo State, Brazil. BEPA 2015; 12(143): 33-37.
  • Pinto AO, Carvalho D, Frizzo C, Lopes K, Tessari GB, Catecati T, et al. First case of canine visceral leishmaniasis in the midwestern of Santa Catarina State, Brazil. Braz J Biol 2022; 82: e241162. http://dx.doi.org/10.1590/1519-6984.241162 PMid:34133561.
    » http://dx.doi.org/10.1590/1519-6984.241162
  • Salomón OD, Feliciangeli MD, Quintana MG, Afonso MMS, Rangel EF. Lutzomyia longipalpis urbanization and control. Mem Inst Oswaldo Cruz 2015; 110(7): 831-846. http://dx.doi.org/10.1590/0074-02760150207 PMid:26517497.
    » http://dx.doi.org/10.1590/0074-02760150207
  • São Paulo. Governo do Estado. Secretaria de Estado do Meio Ambiente – SEMA. Fundação Florestal do Estado de São Paulo. Proposta para Criação das Unidades de Conservação na Serra do Itapeti e do Masaico Itapeti – Tiete. Relatório Final [online]. São Paulo: SEMA; 2013 [cited 2022 Apr 4]. Available from: https://smastr16.blob.core.windows.net/fundacaoflorestal/2013/10/Relat%C3%B3rio-Cria%C3%A7%C3%A3o-UCs-Serra-Itapeti.pdf
    » https://smastr16.blob.core.windows.net/fundacaoflorestal/2013/10/Relat%C3%B3rio-Cria%C3%A7%C3%A3o-UCs-Serra-Itapeti.pdf
  • São Paulo. Governo do Estado. Secretaria de Estado da Saúde – SES. Centro de Vigilância Epidemiológica “Prof. Alexandre Vranjac”. Casos confirmados de Leishmaniose Visceral segundo LPI e ano de notificação, Estado de São Paulo, 2017 a 2023 [online]. São Paulo: SES; 2023 [cited 2023 June 14]. Available from: https://www.saude.sp.gov.br/resources/cve-centro-de-vigilancia-epidemiologica/areas-de-vigilancia/doencas-de-transmissão-por-vetores-e-zoonoses/dados/leish/Iv1723_IP.pdf?attach=true
    » https://www.saude.sp.gov.br/resources/cve-centro-de-vigilancia-epidemiologica/areas-de-vigilancia/doencas-de-transmissão-por-vetores-e-zoonoses/dados/leish/Iv1723_IP.pdf?attach=true
  • Shimabukuro PHF, Tolezano JE, Galati EAB. Chave de identificação ilustrada dos Phlebotominae (Diptera, Psychodidae) do Estado de São Paulo, Brasil. Pap Avulsos Zool 2011; 51(27): 399-441. http://dx.doi.org/10.1590/S0031-10492011002700001
    » http://dx.doi.org/10.1590/S0031-10492011002700001
  • Silva RA, Santos FKM, Souza LC, Rangel EF, Bevilaqua CML. Ecology of Lutzomyia longipalpis and Lutzomyia migonei in an endemic area for visceral leishmaniasis. Rev Bras Parasitol Vet 2014; 23(3): 320-327. http://dx.doi.org/10.1590/S1984-29612014068 PMid:25271451.
    » http://dx.doi.org/10.1590/S1984-29612014068

Publication Dates

  • Publication in this collection
    17 July 2023
  • Date of issue
    2023

History

  • Received
    07 Feb 2023
  • Accepted
    31 May 2023
Colégio Brasileiro de Parasitologia Veterinária FCAV/UNESP - Departamento de Patologia Veterinária, Via de acesso Prof. Paulo Donato Castellane s/n, Zona Rural, , 14884-900 Jaboticabal - SP, Brasil, Fone: (16) 3209-7100 RAMAL 7934 - Jaboticabal - SP - Brazil
E-mail: cbpv_rbpv.fcav@unesp.br