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Canine visceral leishmaniasis: risk factors and spatial analysis in an endemic area of Northeastern Brazil

Leishmaniose visceral canina: fatores de risco e análise espacial em uma área endêmica do Nordeste do Brasil

Abstract

Canine visceral leishmaniasis is a disease caused by the protozoon Leishmania infantum, an important agent of zoonotic concern. In this study we determined the seroprevalence, risk factors and spatial distribution of infection by L. infantum among dogs in the Pajeú microregion of the Sertão region of Pernambuco, Brazil. Canine serum samples (n = 247) were tested using the Dual Path Platform (DPP®) rapid screening test and ELISA/S7® confirmatory test; and risk factors were assessed through univariate analysis and logistical regression. The spatial distribution of reactive dogs was analyzed by drawing a map using QGIS. Seroprevalence of 13.7% (34/247) was detected, with cases predominating in the municipality of Tabira (26.4%; 9/34). Age above 10 years was considered to be a risk factor associated with the presence of anti-L. infantum antibodies. The high overall prevalence and spatial distribution of positive cases showed wide dispersion of reagents dogs in the study area. Therefore, preventive measures are needed in order to reduce the risk of infection for animals and humans.

Keywords:
Leishmania; epidemiology; serology; domestic dog

Resumo

Leishmaniose Visceral Canina é uma doença causada pelo protozoário Leishmania infantum, importante agente zoonótico. O objetivo deste estudo foi determinar a soroprevalência, avaliar os fatores de risco e a distribuição espacial da infecção por L. infantum em cães da microrregião do Pajeú, Sertão de Pernambuco, Brasil. Amostras de soro canino (n=247) foram testadas (“Dual Path Platform Rapid Test” - TR DPP® (triagem); ELISA/S7 (confirmatório)), e os fatores de risco avaliados por meio de análise univariada e regressão logística. A distribuição espacial dos cães reagentes foi analisada por meio de mapas confeccionados no programa QGIS. Detectou-se soroprevalência de 13,7% (34/247), com predominância dos casos no município de Tabira (26,4%; 9/34). A idade acima de 10 anos foi considerada fator de risco associado à presença de anticorpos anti-L. infantum. A alta prevalência e distribuição espacial dos casos positivos revelou ampla dispersão de cães reagentes na área de estudo. Portanto, medidas preventivas são necessárias a fim de reduzir o risco de infecção para os animais e humanos.

Palavras-chave:
Leishmania; epidemiologia; sorologia; cão doméstico

Introduction

Visceral leishmaniasis (VL) is a disease with cosmopolitan distribution caused by the protozoon Leishmania infantum (Akhoundi et al., 2016Akhoundi M, Kuhls K, Cannet A, Votýpka J, Marty P, Delaunay P, et al. A historical overview of the classification, evolution, and dispersion of Leishmania parasites and sandflies. PLoS Negl Trop Dis 2016; 10(3): e0004349. http://dx.doi.org/10.1371/journal.pntd.0004349. PMid:26937644.
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). It is a matter of zoonotic concern, given that it is responsible for approximately 50,000 to 90,000 cases annually worldwide, with high occurrence rates are in Brazil, East Africa and India (WHO, 2022World Health Organization - WHO. Leishmaniasis [online]. Geneva: WHO; 2022 [cited 2022 Dec 20]. Available from: https://www.who.int/news-room/fact-sheets/detail/leishmaniasis
https://www.who.int/news-room/fact-sheet...
). The parasite is predominantly transmitted by vectors, and sandflies of the genus Lutzomyia are the most important vectors in the Americas (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...
). For a long time, cases of VL were predominantly found in rural areas, but over recent years it has also been occurring in urban areas with high population density (Almeida & Werneck, 2014Almeida AS, Werneck GL. Prediction of high-risk areas for visceral leishmaniasis using socioeconomic indicators and remote sensing data. Int J Health Geogr 2014; 13(1): 13. http://dx.doi.org/10.1186/1476-072X-13-13. PMid:24885128.
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).

Infection by L. infantum can occur in several wild animal species (e.g. foxes, rodents and marsupials), as well as in domestic animals such as dogs and, less frequently, cats (Roque & Jansen, 2014Roque ALR, Jansen AM. Wild and synanthropic reservoirs of Leishmania species in the Americas. Int J Parasitol Parasites Wildl 2014; 3(3): 251-262. http://dx.doi.org/10.1016/j.ijppaw.2014.08.004. PMid:25426421.
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; Bezerra-Santos et al., 2021Bezerra-Santos MA, Ramos RAN, Campos AK, Dantas-Torres F, Otranto D. Didelphis spp. opossums and their parasites in the Americas: a one health perspective. Parasitol Res 2021; 120(12): 4091-4111. http://dx.doi.org/10.1007/s00436-021-07072-4. PMid:33788021.
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; Berenguer et al., 2021Berenguer LKAR, Gomes CFCA, Nascimento JO, Bernardi JCM, Lima VFS, Oliveira JB, et al. Leishmania infantum infection in a domestic cat: a real threat or an occasional finding? Acta Parasitol 2021; 66(2): 673-676. http://dx.doi.org/10.1007/s11686-020-00294-z. PMid:33044603.
http://dx.doi.org/10.1007/s11686-020-002...
). Dogs are threatened more by the disease and present a wide range of clinical signs (e.g. skin lesions, onychogryphosis, ophthalmopathies and weight loss). However, it is important to note that most infected animals remain asymptomatic, while serving as important reservoirs (Akhtardanesh et al., 2021Akhtardanesh B, Mostafavi M, Khedri J, Fakhri A, Sharifi I, Shahraki MK. Seroepidemiology of visceral leishmaniasis among free-roaming dogs and children in Zahedan city, southeast of Iran, 2018-2020. Microb Pathog 2021; 161(Pt A): 105234. http://dx.doi.org/10.1016/j.micpath.2021.105234. PMid:34653543.
http://dx.doi.org/10.1016/j.micpath.2021...
; Peris et al., 2021Peris MP, Esteban-Gil A, Ortega-Hernández P, Morales M, Halaihel N, Castillo JA. Comparative study of real-time PCR (TaqMan Probe and Sybr Green), Serological techniques (ELISA, IFA and DAT) and clinical signs evaluation, for the diagnosis of canine leishmaniasis in experimentally infected dogs. Microorganisms 2021; 9(12): 2627. http://dx.doi.org/10.3390/microorganisms9122627. PMid:34946227.
http://dx.doi.org/10.3390/microorganisms...
). Because of the presence of asymptomatic animals in endemic regions, serological surveys are pivotal for understanding the distribution of potential reservoirs in these areas (Rondon et al., 2008Rondon FCM, Bevilaqua CML, Franke CR, Barros RS, Oliveira FR, Alcântara AC, et al. Cross-sectional serological study of canine Leishmania infection in Fortaleza, Ceará state, Brazil. Vet Parasitol 2008; 155(1-2): 24-31. http://dx.doi.org/10.1016/j.vetpar.2008.04.014. PMid:18565676.
http://dx.doi.org/10.1016/j.vetpar.2008....
; Bermudi et al., 2020Bermudi PMM, Costa DNCC, Nunes CM, Tolezano JE, Hiramoto RM, Rodas LAC, et al. Canine serological survey and dog culling and its relationship with human visceral leishmaniasis in an endemic urban area. BMC Infect Dis 2020; 20(1): 401. http://dx.doi.org/10.1186/s12879-020-05125-0. PMid:32503461.
http://dx.doi.org/10.1186/s12879-020-051...
).

The seroprevalence of canine visceral leishmaniasis (CVL) varies widely depending on the geographic region, level of exposure to the vectors and type of test used (Carvalho et al., 2020Carvalho MR, Dias AFLR, Almeida ABPF, Alves MR, Paes AS, Sousa VRF. Canine visceral leishmaniasis: perception, prevalence, and spatial distribution in municipality of Nossa Senhora do Livramento, Mato Grosso, Brazil. Rev Bras Parasitol Vet 2020; 29(2): e021019. http://dx.doi.org/10.1590/s1984-29612020017. PMid:32428187.
http://dx.doi.org/10.1590/s1984-29612020...
). For instance, in the state of Pernambuco, Brazil, prevalence rates from 2.4% (Lins et al., 2018Lins TNB, Souza IB, Barros GMMR, Santos CVB, Silva RP, Alves LC, et al. Seroprevalence and spatial distribution of canine leishmaniasis in an endemic region in Brazil: how has the situation changed after 10 years? Rev Soc Bras Med Trop 2018; 51(5): 680-682. http://dx.doi.org/10.1590/0037-8682-0087-2018. PMid:30304278.
http://dx.doi.org/10.1590/0037-8682-0087...
) to 42.8% (Evaristo et al., 2020Evaristo AMCF, Sevá AP, Oliveira GMB, Silva IWG, Ferreira MS, Souza EAR, et al. Canine leishmaniasis in the semi-arid region of Pernambuco, northeastern Brazil: epidemiology, factors associated with seropositivity and spatial analysis. Rev Bras Parasitol Vet 2020; 29(2): e001120. http://dx.doi.org/10.1590/s1984-29612020027. PMid:32490894.
http://dx.doi.org/10.1590/s1984-29612020...
) have been detected. This serological information on dogs is useful from an epidemiological perspective, since canine cases precede human ones. In addition, early diagnosis in these animals may drive measures that should be implemented for maintaining good health status of dogs. With the aim of improving the prevention of canine infection, several risk factors have been assessed over time, and features such as living in rural areas or close to green areas, male sex and crossbreeding have been considered to be potential risk factors (Araujo et al., 2016Araujo AC, Costa AP, Silva IWG, Matos NNVG, Dantas ACS, Ferreira F, et al. Epidemiological aspects and risk factors for infection by Leishmania infantum chagasi in dogs from municipality of Petrolina, Northeastern Brazil. Vet Parasitol Reg Stud Reports 2016; 3-4: 41-48. http://dx.doi.org/10.1016/j.vprsr.2016.07.001. PMid:31014498.
http://dx.doi.org/10.1016/j.vprsr.2016.0...
; Evaristo et al., 2020Evaristo AMCF, Sevá AP, Oliveira GMB, Silva IWG, Ferreira MS, Souza EAR, et al. Canine leishmaniasis in the semi-arid region of Pernambuco, northeastern Brazil: epidemiology, factors associated with seropositivity and spatial analysis. Rev Bras Parasitol Vet 2020; 29(2): e001120. http://dx.doi.org/10.1590/s1984-29612020027. PMid:32490894.
http://dx.doi.org/10.1590/s1984-29612020...
).

It is widely known that the CVL has passed through an urbanization process in Brazil, such that the full epidemiological chain now also occurs in urban areas (Arruda et al., 2019Arruda RMF, Cardoso DT, Teixeira-Neto RG, Barbosa DS, Ferraz RK, Morais MHF, et al. Space-time analysis of the incidence of human visceral leishmaniasis (VL) and prevalence of canine VL in a municipality of southeastern Brazil: identification of priority areas for surveillance and control. Acta Trop 2019; 197: 105052. http://dx.doi.org/10.1016/j.actatropica.2019.105052. PMid:31233726.
http://dx.doi.org/10.1016/j.actatropica....
; Batista-Santos et al., 2021Batista-Santos F, Dória DAN, Sincurá YR, Rosário SS, Fujiwara RT, Barata RA. Eco-epidemiological aspects of visceral leishmaniasis in the municipality of Diamantina, Jequitinhonha Valley (Minas Gerais State, Brazil). Yale J Biol Med 2021; 94(2): 209-215. PMid:34211342.). Anthropic actions (e.g. deforestation and unplanned urban growth), along with absence of basic sanitation in many regions, have certainly contributed towards worsening of this panorama (Batista-Santos et al., 2021Batista-Santos F, Dória DAN, Sincurá YR, Rosário SS, Fujiwara RT, Barata RA. Eco-epidemiological aspects of visceral leishmaniasis in the municipality of Diamantina, Jequitinhonha Valley (Minas Gerais State, Brazil). Yale J Biol Med 2021; 94(2): 209-215. PMid:34211342.). In this context, understanding the spatial distribution of cases and how they spread in an endemic region is pivotal to establishing barriers and avoiding dispersion of cases (Arruda et al., 2019Arruda RMF, Cardoso DT, Teixeira-Neto RG, Barbosa DS, Ferraz RK, Morais MHF, et al. Space-time analysis of the incidence of human visceral leishmaniasis (VL) and prevalence of canine VL in a municipality of southeastern Brazil: identification of priority areas for surveillance and control. Acta Trop 2019; 197: 105052. http://dx.doi.org/10.1016/j.actatropica.2019.105052. PMid:31233726.
http://dx.doi.org/10.1016/j.actatropica....
; Evaristo et al., 2020Evaristo AMCF, Sevá AP, Oliveira GMB, Silva IWG, Ferreira MS, Souza EAR, et al. Canine leishmaniasis in the semi-arid region of Pernambuco, northeastern Brazil: epidemiology, factors associated with seropositivity and spatial analysis. Rev Bras Parasitol Vet 2020; 29(2): e001120. http://dx.doi.org/10.1590/s1984-29612020027. PMid:32490894.
http://dx.doi.org/10.1590/s1984-29612020...
).

Therefore, the aim of this study was to determine the seroprevalence, risk factors and spatial distribution of infection by L. infantum among dogs in the Pajeú microregion of the Sertão region of Pernambuco.

Material and Methods

Study area

This study was conducted in the Pajeú microregion of the Sertão, in the state of Pernambuco, northeastern Brazil. Eight municipalities from which human VL cases were notified from 2009 to 2019 were included in the study: Afogados da Ingazeira (07°45'03” S and 37°38'21” W), Brejinho (07°20'58” S and 37°17'10” W), Carnaíba (07°48'19” S and 37°47'38” W), Iguaracy (07°50'07” S and 37°30'55” W), Quixaba (07°43'13” S and 37°50'54” W), São José do Egito (07°28'44” S and 37°16'28” W), Tabira (07°35'27” S and 37°32'22” W) and Tuparetama (07°36'08” S and 37°18'41” W) (Figure 1). The study area is characterized by a hot and dry tropical climate. It forms part of the caatinga biome, has stretches of hyper-xerophilous forest and has an average temperature ranging from 17 to 36 °C. The rainy season runs from November to July, with an average annual precipitation that varies from 5 to 118 millimeters (IBGE, 2022Instituto Brasileiro de Geografia e Estatística - IBGE. IBGE cidades [online]. Rio de Janeiro: IBGE; 2022 [cited 2022 June 13]. Available from: https://cidades.ibge.gov.br/
https://cidades.ibge.gov.br/...
).

Figure 1
Map of Brazil indicating the state of Pernambuco and municipalities where animals were sampled.

Animals, sampling and serological examination

The minimum sample size required (n = 246) was calculated considering the estimated canine population of the region (n = 35,129). This requirement followed the proportion established in a previous study (Canatto et al., 2012Canatto BD, Silva EA, Bernardi F, Mendes MCNC, Paranhos NT, Dias RA. Caracterização demográfica das populações de cães e gatos supervisionados do município de São Paulo. Arq Bras Med Vet Zootec 2012; 64(6): 1515-1523. http://dx.doi.org/10.1590/S0102-09352012000600017.
http://dx.doi.org/10.1590/S0102-09352012...
). A margin of error of 5% and a confidence interval of 95% were taken into account (Thrusfield, 2004Thrusfield MV. Epidemiologia veterinária. São Paulo: Roca; 2004.). The collection points in each municipality were randomly determined (Reis, 2003Reis JC. Estatística aplicada à pesquisa em ciência veterinária. Olinda: Luci Artes Gráficas Ltda; 2003.).

Blood samples were obtained from animals of both sexes, different breeds and aged between 6 months and 13 years-old. A physical examination was performed on each animal and clinical signs suggestive of infection by L. infantum were recorded in individual clinical charts. Additionally, an epidemiological questionnaire was applied to each owner to obtain data for analysis of risk factors.

All samples were screened using the Dual Path Platform (DPP®) rapid test (Bio-Manguinhos/FIOCRUZ, Rio de Janeiro, Brazil), which is a qualitative test that detects antibodies anti-Leishmania IgG. Afterwards, reactive samples were analyzed through a quantitative ELISA/S7® test (Biogene, Recife, Brazil) and antibody concentrations were measured in a spectrophotometer at absorbance of 450 nm. All tests were performed in accordance with the manufacturers' recommendations, and animals were considered reactive when they were found to be positive in both techniques.

Data analysis

The data were analyzed using descriptive statistics to obtain absolute and relative frequencies. Subsequently, the G test was used to assess the seropositivity of dogs in each municipality, as well as in both rural and urban areas of these municipalities. Risk factors were calculated using univariate analysis for the variable of interest and by means of logistic regression in which the serology result was taken to be the dependent variable. The significance level was taken to be 5% in both analyses. The G test and risk factor analyses were conducted using the BioEstat software, version 5.3 (Instituto Mamirauá, Brazil), and the Epi-InfoTM 7.2.2.6 software, respectively.

Spatial analysis

The geographic coordinates of each collection point (each animal’s home) were obtained through the global positioning system (GPS). Maps were created using the QGIS 3.22.10 software, in which georeferenced data were inserted in continuous cartographic base maps (Shapefiles, version 2017), which are available from the database of the Brazilian Institute for Geography and Statistics (IBGE, 2022Instituto Brasileiro de Geografia e Estatística - IBGE. IBGE cidades [online]. Rio de Janeiro: IBGE; 2022 [cited 2022 June 13]. Available from: https://cidades.ibge.gov.br/
https://cidades.ibge.gov.br/...
).

A thematic map and a Kernel density map were created to indicate the distribution of cases and clusters of positive cases, respectively. An influence radius of 3 km with pixels size 100 were used to generate a good visualization of plotted points in the raster layer. In addition, considering the mean dispersion of vectors (250 m), a buffer zone was established surrounding positive and negative cases, to demonstrate risk areas of potential transmission.

Results

The overall seroprevalence obtained was 13.7% (34/247). The highest number of positive animals (26.4%; 9/34) was in the municipality of Tabira. Non-reactive animals were observed in Afogados da Ingazeira, Brejinho, Iguaracy and Tuparetama. The detailed results from the serological analysis, according to the municipality and collection area (urban or rural), are presented in Table 1.

Table 1
Detection of anti-Leishmania (Leishmania) infantum antibodies among dogs in rural and urban areas of the Pajeú microregion.

A total of 13.9% (26/187) of the animals living in rural areas were reactive, while among those living in urban areas the seroprevalence was 13.3% (8/60). It is important to note that in the municipalities of Tabira and Quixaba, the reactive animals were predominantly found in rural areas, rather than urban areas (G test = 10.2792; p = 0.0059).

Among all the animals evaluated, 53% (131/247) presented at least one clinical sign. Among the seroreactive animals, 61.8% (21/34) presented clinical signs suggestive of infection by L. infantum. Lymphadenomegaly (38.2%; 13/34) and alopecia (23.5%; 8/34) were the signs most commonly observed (Table 2).

Table 2
Clinical signs observed among all sampled/seropositive dogs, and the frequency of signs among seropositive animals.

From the univariate analysis, the only risk factor identified was the animals’ age. In particular, those older than 10 years of age were more prone to become infected (OR = 4.94; p = 0.029). Table 3 shows the analysis on risk factors associated with the presence of anti-L-infantum antibodies.

Table 3
Univariate analysis on risk factors associated with the presence of anti-Leishmania (Leishmania) infantum antibodies in dogs in the Pajeú microregion.

The spatial analysis revealed that reactive dogs were widely distributed in the study area (Figure 2).

Figure 2
Map indicating the distribution of reactive and non-reactive animals regarding the presence of anti-L. infantum antibodies.

The Kernel density map revealed clusters of positive cases in the urban areas of three municipalities (Carnaíba, Quixaba and Tabira). Moreover, the rural area of Quixaba also demonstrated a cluster of reactive cases (Figure 3).

Figure 3
Kernel density map demonstrating clusters of animals that were reactive regarding the presence of anti-L. infantum antibodies.

Confluence of the buffer zone between positive and negative cases was observed. It is also important to note that some overlapping between vegetated areas and the buffer zone of positive cases also occurred (Figure 4).

Figure 4
Map indicating the buffer zones (250 m) surrounding the locations of reactive and non-reactive animals regarding the presence of anti-L. infantum antibodies.

Discussion

In this study, the presence of anti-L. infantum antibodies in dogs was assessed. It was demonstrated that age (> 10 years) was a risk factor for occurrence of reactive cases, which were widely distributed across the study area.

The overall seroprevalence (13.7%) indicates that Leishmania parasites were circulating in the population assessed, thus following a trend that had already been observed in other regions of the state of Pernambuco (Dantas-Torres et al., 2006Dantas-Torres F, Brito MEF, Brandão-Filho SP. Seroepidemiological survey on canine leishmaniasis among dogs from an urban area of Brazil. Vet Parasitol 2006; 140(1-2): 54-60. http://dx.doi.org/10.1016/j.vetpar.2006.03.008. PMid:16621286.
http://dx.doi.org/10.1016/j.vetpar.2006....
; Araujo et al., 2016Araujo AC, Costa AP, Silva IWG, Matos NNVG, Dantas ACS, Ferreira F, et al. Epidemiological aspects and risk factors for infection by Leishmania infantum chagasi in dogs from municipality of Petrolina, Northeastern Brazil. Vet Parasitol Reg Stud Reports 2016; 3-4: 41-48. http://dx.doi.org/10.1016/j.vprsr.2016.07.001. PMid:31014498.
http://dx.doi.org/10.1016/j.vprsr.2016.0...
; Lins et al., 2018Lins TNB, Souza IB, Barros GMMR, Santos CVB, Silva RP, Alves LC, et al. Seroprevalence and spatial distribution of canine leishmaniasis in an endemic region in Brazil: how has the situation changed after 10 years? Rev Soc Bras Med Trop 2018; 51(5): 680-682. http://dx.doi.org/10.1590/0037-8682-0087-2018. PMid:30304278.
http://dx.doi.org/10.1590/0037-8682-0087...
; Macedo et al., 2022Macedo LO, Bezerra-Santos MA, Ubirajara CRC Fo, Sales KGS, Sousa-Paula LC, Silva LG, et al. Vector-borne pathogens of zoonotic concern in dogs from a Quilombola community in northeastern Brazil. Parasitol Res 2022; 121(11): 3305-3311. http://dx.doi.org/10.1007/s00436-022-07661-x. PMid:36102968.
http://dx.doi.org/10.1007/s00436-022-076...
). Recently, in a study carried out in the Sertão region of Pernambuco, a mean prevalence of 13.9% was reported (Evaristo et al., 2021Evaristo AMCF, Silva IWG, Oliveira GMB, Silva RE, Costa JOJ, Veschi JLA, et al. Detection and molecular characterization of Leishmania in dogs from northeastern Brazil. Braz J Glo Health 2021; 1(4): 23-29. http://dx.doi.org/10.56242/globalhealth;2021;1;4;23-29.
http://dx.doi.org/10.56242/globalhealth;...
), similar to what was found in the present study.

It is known that this region presents favorable climatic conditions for vector development (Macedo et al., 2008Macedo ITF, Bevilaqua CML, Morais NB, Sousa 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.). Additionally, a wide variety of wild hosts (rodents, canids and marsupials) that are epidemiologically important in relation to leishmaniasis have been observed in this area. Nonetheless, in four municipalities (Afogados da Ingazeira, Brejinho, Iguaracy and Tuparetama), no reactive animals were observed. However, this result should be interpreted with caution, due to the low number of samples (n = 40), which may have influenced the final outcome. The low number of samples in some municipalities is considered a limitation of this study, which difficult a more reliable analysis. It is known that the study area presents environmental features (e.g. climate, relative humidity, vegetation and wild host population) that are similar to the conditions required for vector development and occurrence of cases.

No difference between rural areas (13.9%; 26/187) and urban areas (13.3%; 8/60) was observed (G test = 0.0095; p = 0.9223). Even if CVL cases have occurred predominantly in rural areas, the urbanization of the disease over recent years has been responsible for occurrences of cases in areas with high population density (Araujo et al., 2016Araujo AC, Costa AP, Silva IWG, Matos NNVG, Dantas ACS, Ferreira F, et al. Epidemiological aspects and risk factors for infection by Leishmania infantum chagasi in dogs from municipality of Petrolina, Northeastern Brazil. Vet Parasitol Reg Stud Reports 2016; 3-4: 41-48. http://dx.doi.org/10.1016/j.vprsr.2016.07.001. PMid:31014498.
http://dx.doi.org/10.1016/j.vprsr.2016.0...
). Urbanization of CVL is a negative consequence of anthropic actions (deforestation, disorderly urban growth and lack of basic sanitation), which have favored movement of wild reservoirs closer to urban areas, as well as establishment of vector populations (Barbosa et al., 2010Barbosa DS, Rocha AL, Santana AA, Souza CSF, Dias RA, Costa-Júnior LM, et al. Soroprevalência e variáveis epidemiológicas associadas à leishmaniose visceral canina em área endêmica no município de São Luís, Maranhão, Brasil. Ciênc Anim Bras 2010; 11(3): 653-659. http://dx.doi.org/10.5216/cab.v11i3.5933.
http://dx.doi.org/10.5216/cab.v11i3.5933...
; Pimentel et al., 2015Pimentel DS, Ramos RAN, Santana MA, Maia CS, Carvalho GA, Silva HP, et al. Prevalence of zoonotic visceral leishmaniasis in dogs in an endemic area of Brazil. Rev Soc Bras Med Trop 2015; 48(4): 491-493. http://dx.doi.org/10.1590/0037-8682-0224-2014. PMid:26132498.
http://dx.doi.org/10.1590/0037-8682-0224...
). Furthermore, studies conducted since the urbanization of VL was first recognized have suggested that there is a positive correlation between the presence of infected dogs and VL outbreaks among humans (Mello et al., 2014Mello CX, Figueiredo FB, Mendes AAV Jr, Furtado MC, Miranda LFC, Madeira MF. Outbreak of canine visceral leishmaniasis in Barra Mansa, State of Rio de Janeiro. Rev Soc Bras Med Trop 2014; 47(6): 788-790. http://dx.doi.org/10.1590/0037-8682-0042-2014. PMid:25626661.
http://dx.doi.org/10.1590/0037-8682-0042...
; Sales et al., 2019Sales KGS, Miranda DEO, Costa PL, Silva FJ, Figueredo LA, Brandão-Filho SP, et al. Home sweet home: sand flies find a refuge in remote indigenous villages in north-eastern Brazil, where leishmaniasis is endemic. Parasit Vectors 2019; 12(1): 118. http://dx.doi.org/10.1186/s13071-019-3383-1. PMid:30909958.
http://dx.doi.org/10.1186/s13071-019-338...
).

Clinically, the most common signs found in our study were lymphadenomegaly (38.2%; 13/34) and alopecia (23.5%; 8/34), which are frequently observed in dogs with VL (Akhtardanesh et al., 2021Akhtardanesh B, Mostafavi M, Khedri J, Fakhri A, Sharifi I, Shahraki MK. Seroepidemiology of visceral leishmaniasis among free-roaming dogs and children in Zahedan city, southeast of Iran, 2018-2020. Microb Pathog 2021; 161(Pt A): 105234. http://dx.doi.org/10.1016/j.micpath.2021.105234. PMid:34653543.
http://dx.doi.org/10.1016/j.micpath.2021...
; Peris et al., 2021Peris MP, Esteban-Gil A, Ortega-Hernández P, Morales M, Halaihel N, Castillo JA. Comparative study of real-time PCR (TaqMan Probe and Sybr Green), Serological techniques (ELISA, IFA and DAT) and clinical signs evaluation, for the diagnosis of canine leishmaniasis in experimentally infected dogs. Microorganisms 2021; 9(12): 2627. http://dx.doi.org/10.3390/microorganisms9122627. PMid:34946227.
http://dx.doi.org/10.3390/microorganisms...
). It is important to highlight that 38.2% (9/34) of the seroreactive animals were asymptomatic. From an epidemiological point of view, these animals are very important, since they may act as sources of infection while remaining unperceived because of their clinical status. Therefore, it is necessary to carry out serological surveys for early detection of these cases and for preventive measures to be adopted (Rondon et al., 2008Rondon FCM, Bevilaqua CML, Franke CR, Barros RS, Oliveira FR, Alcântara AC, et al. Cross-sectional serological study of canine Leishmania infection in Fortaleza, Ceará state, Brazil. Vet Parasitol 2008; 155(1-2): 24-31. http://dx.doi.org/10.1016/j.vetpar.2008.04.014. PMid:18565676.
http://dx.doi.org/10.1016/j.vetpar.2008....
; Bermudi et al., 2020Bermudi PMM, Costa DNCC, Nunes CM, Tolezano JE, Hiramoto RM, Rodas LAC, et al. Canine serological survey and dog culling and its relationship with human visceral leishmaniasis in an endemic urban area. BMC Infect Dis 2020; 20(1): 401. http://dx.doi.org/10.1186/s12879-020-05125-0. PMid:32503461.
http://dx.doi.org/10.1186/s12879-020-051...
). The univariate analysis revealed that age (> 10 years) was considered to be the sole risk factor (OR = 0.029). Despite of important, this data should be interpreted with caution since only ten animals with more than 10-year-old were sampled. Even though, it is known that the longer exposure to vectors and the immunological weakness observed among elderly patients may contributed to this outcome (Araujo et al., 2016Araujo AC, Costa AP, Silva IWG, Matos NNVG, Dantas ACS, Ferreira F, et al. Epidemiological aspects and risk factors for infection by Leishmania infantum chagasi in dogs from municipality of Petrolina, Northeastern Brazil. Vet Parasitol Reg Stud Reports 2016; 3-4: 41-48. http://dx.doi.org/10.1016/j.vprsr.2016.07.001. PMid:31014498.
http://dx.doi.org/10.1016/j.vprsr.2016.0...
). In fact, adult dogs remain outside for long periods, which increases the chance of contact with vectors and natural exposition to Leishmania parasites (Selim et al., 2021Selim A, Shoulah S, Abdelhady A, Alouffi A, Alraey Y, Al-Salem WS. Seroprevalence and risk factors associated with canine leishmaniasis in Egypt. Vet Sci 2021; 8(10): 236. http://dx.doi.org/10.3390/vetsci8100236. PMid:34679066.
http://dx.doi.org/10.3390/vetsci8100236...
).

The Kernel map showed clusters of CVL cases in five municipalities, thus demonstrating that this type of mapping is an important tool that can identify specific zones where preventive measures are needed. Active surveillance should be implemented in these areas in order to reduce the risk of transmission and occurrence of human and animal cases (Araujo et al., 2016Araujo AC, Costa AP, Silva IWG, Matos NNVG, Dantas ACS, Ferreira F, et al. Epidemiological aspects and risk factors for infection by Leishmania infantum chagasi in dogs from municipality of Petrolina, Northeastern Brazil. Vet Parasitol Reg Stud Reports 2016; 3-4: 41-48. http://dx.doi.org/10.1016/j.vprsr.2016.07.001. PMid:31014498.
http://dx.doi.org/10.1016/j.vprsr.2016.0...
; Evaristo et al., 2020Evaristo AMCF, Sevá AP, Oliveira GMB, Silva IWG, Ferreira MS, Souza EAR, et al. Canine leishmaniasis in the semi-arid region of Pernambuco, northeastern Brazil: epidemiology, factors associated with seropositivity and spatial analysis. Rev Bras Parasitol Vet 2020; 29(2): e001120. http://dx.doi.org/10.1590/s1984-29612020027. PMid:32490894.
http://dx.doi.org/10.1590/s1984-29612020...
). The buffer zone (250 m) around the locations of positive dogs showed overlaps with forested areas, thus indicating a bridge between these areas. From an epidemiological perspective, this is very important because it may indicate close contact between vectors and domestic and wild reservoirs. Additionally, it reflects the indiscriminate growth of cities, which has been an important factor in the urbanization of the disease (Batista-Santos et al., 2021Batista-Santos F, Dória DAN, Sincurá YR, Rosário SS, Fujiwara RT, Barata RA. Eco-epidemiological aspects of visceral leishmaniasis in the municipality of Diamantina, Jequitinhonha Valley (Minas Gerais State, Brazil). Yale J Biol Med 2021; 94(2): 209-215. PMid:34211342.).

The data presented here are very important, especially because the distribution area of CVL has expanded in several regions, with domestic dogs as the main source of infection in these places (Oliveira et al., 2021Oliveira MR, Oliveira MB No, Bezerra TL, Silva WSI, Paz WS, Santos IG, et al. Canine leishmaniasis in an endemic region, Northeastern Brazil: a comparative study with four groups of animals. Parasitol Res 2021; 120(11): 3915-3923. http://dx.doi.org/10.1007/s00436-021-07319-0. PMid:34626235.
http://dx.doi.org/10.1007/s00436-021-073...
; Silva et al., 2021Silva MMS, Silva JMS, Alves DS, Skrapec MVC, Queiroz DB, Silva DFS, et al. Epidemiologia da leishmaniose visceral humana em Petrolina, Pernambuco, no período de 2009 a 2020: uma análise descritiva. Res Soc Dev 2021; 10(14): e202101421848. http://dx.doi.org/10.33448/rsd-v10i14.21848.
http://dx.doi.org/10.33448/rsd-v10i14.21...
; Veloso et al., 2021Veloso ECM, Negreiros AS, Silva JP, Moura LD, Nascimento LFM, Silva TS, et al. Socio-economic and environmental factors associated with the occurrence of canine infection by Leishmania infantum in Teresina, Brazil. Vet Parasitol Reg Stud Reports 2021; 24: 100561. http://dx.doi.org/10.1016/j.vprsr.2021.100561. PMid:34024377.
http://dx.doi.org/10.1016/j.vprsr.2021.1...
). Although the lack of collection of sandflies can be considered a limitation of this study, it is known that the study area presents favorable environmental conditions for their development (Macedo et al., 2008Macedo ITF, Bevilaqua CML, Morais NB, Sousa 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.). Furthermore, during the samplings, a great diversity of livestock (e.g. horses, pigs and ruminants) and some synanthropic animals (rodents and marsupials) were observed in peridomestic areas. This highlights the wide variety of food sources for vectors, as well as the presence of reservoirs of L. infantum, which contribute to occurrence of the disease.

VL continues to cause deaths of humans and dogs in endemic regions of Brazil (Sousa et al., 2018Sousa JMS, Ramalho WM, Melo MA. Demographic and clinical characterization of human visceral leishmaniasis in the State of Pernambuco, Brazil between 2006 and 2015. Rev Soc Bras Med Trop 2018; 51(5): 622-630. http://dx.doi.org/10.1590/0037-8682-0047-2018. PMid:30304268.
http://dx.doi.org/10.1590/0037-8682-0047...
; Oliveira et al., 2021Oliveira MR, Oliveira MB No, Bezerra TL, Silva WSI, Paz WS, Santos IG, et al. Canine leishmaniasis in an endemic region, Northeastern Brazil: a comparative study with four groups of animals. Parasitol Res 2021; 120(11): 3915-3923. http://dx.doi.org/10.1007/s00436-021-07319-0. PMid:34626235.
http://dx.doi.org/10.1007/s00436-021-073...
). The measures that should be taken to control VL are widely known, but the divergent ways in which these preventive actions are applied, along with the poor infrastructure of many municipalities, make controlling this disease a great public health challenge. Awareness about CVL control in Brazil has improved over recent years (Belo et al., 2017Belo VS, Gregório EA, Teixeira-Neto RG, Lima ACVMR, Pereira AAS, Marcelino AP, et al. Reliability of techniques used in the diagnosis of canine visceral leishmaniasis by the national control program in Brazil: a survey in an area of recent transmission. Prev Vet Med 2017; 146: 10-15. http://dx.doi.org/10.1016/j.prevetmed.2017.07.011. PMid:28992913.
http://dx.doi.org/10.1016/j.prevetmed.20...
), but in many regions this control is still based on isolated measures focusing especially on dogs (Alves et al., 2018Alves EB, Figueiredo FB, Rocha MF, Werneck GL. Operational difficulties in the use of insecticidal dog collars for the control of visceral leishmaniasis, municipality of Montes Claros, MG, Brazil, 2012. Epidemiol Serv Saude 2018; 27(4): e2017469. http://dx.doi.org/10.5123/S1679-49742018000400001. PMid:30427397.
http://dx.doi.org/10.5123/S1679-49742018...
). The best way to control neglected diseases is through the One Health approach, in which the conditions of humans, animals and the environment in which these hosts live are considered together (Costa et al., 2020Costa DNCC, Codeço CT, Bermudi PMM, Rodas LAS, Nunes CM, Hiramoto RM, et al. Controle da leishmaniose visceral canina por eutanásia: estimativa de efeito baseado em inquérito e modelagem matemática. Cad Saude Publica 2020; 36(2): e00221418. http://dx.doi.org/10.1590/0102-311x00221418. PMid:32130320.
http://dx.doi.org/10.1590/0102-311x00221...
; Silva et al., 2021Silva MMS, Silva JMS, Alves DS, Skrapec MVC, Queiroz DB, Silva DFS, et al. Epidemiologia da leishmaniose visceral humana em Petrolina, Pernambuco, no período de 2009 a 2020: uma análise descritiva. Res Soc Dev 2021; 10(14): e202101421848. http://dx.doi.org/10.33448/rsd-v10i14.21848.
http://dx.doi.org/10.33448/rsd-v10i14.21...
; Brasil, 2014Brasil. Ministério da Saúde. Secretaria de Vigilância em Saúde. Manual de vigilância e controle da leishmaniose visceral. Brasília: Ministério da Saúde; 2014.).

In summary, the findings from this study demonstrated the presence of anti- L. infantum antibodies in dogs and indicated that age (> 10 years) was a risk factor. Preventive measures (use of repellent products, control of vectors and environmental management) are needed in order to reduce the risk of infection among animals, thus mitigating the potential impact on local public health.

Acknowledgements

Authors would like thank Kelvin da Silva e Siqueira (Veterinarian of Tabira) and all staff of the Health Secretary of Carnaíba for the support on the field work. This article is based on the MSc dissertation (Graduate Program in Animal Bioscience) of the first author, developed at the Federal Rural University of Pernambuco, supported by a grant fellowship from the Fundação de Amaparo a Ciência e Tecnologia do Estado de Pernambuco (FACEPE).

  • How to cite: Silva SS, Macedo LO, Oliveira JCP, Alves LC, Carvalho GA, Ramos RAN. Canine visceral leishmaniasis: risk factors and spatial analysis in an endemic area of Northeastern Brazil. Braz J Vet Parasitol 2023; 32(2): e003223. https://doi.org/10.1590/S1984-29612023029

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Publication Dates

  • Publication in this collection
    22 May 2023
  • Date of issue
    2023

History

  • Received
    22 Feb 2023
  • Accepted
    24 Apr 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