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Detection of anti-Leishmania spp. antibodies in poultry from central region of Rio Grande do Sul, Brazil

Detecção de anticorpos anti-Leishmania spp. em aves domésticas da região central do Rio Grande do Sul, Brasil

Abstract

Domestic birds such as Gallus gallus, Meleagris gallopavo, Anser anser and Numida meleagris are widely distributed throughout the world and maintain contact with humans and other animal species considered reservoirs of both Visceral Leishmaniasis (VL) and American Tegumentary Leishmaniasis (ATL), including dogs and cats; wild canids, marsupials; and synanthropic animals such as rodents and chiroptera. Therefore, this study aimed to detect the presence of anti-Leishmania spp. antibodies in birds from a rural area of the municipality of Santa Maria, southern Brazil. From May to December 2022, 262 blood samples were collected from 244 chickens, 8 turkeys, 7 guinea fowl and 3 geese, distributed in 27 rural properties in 6 districts. All the sites visited presented positive birds for the presence of Leishmania spp. Thus, it is inferred that, contact with this protozoan can induce the production of antibodies, suggesting that these animals can be used as sentinels for the circulation of this agent. In addition, the blood of these animals is a preferred food source for insects of the subfamily Phlebotominae, which can be used them as bioindicators of the presence of these phlebotomes.

Keywords:
Domestic birds; antibodies; indirect immunofluorescence reaction; leishmaniasis

Resumo

Aves domésticas, como Gallus gallus, Meleagris gallopavo, Anser anser e Numida meleagris, são amplamente distribuídas pelo mundo e mantêm contato com humanos e outras espécies animais consideradas reservatórios tanto da Leishmaniose Visceral (LV) quanto da Leishmaniose Tegumentar Americana (LTA), incluindo-se cães e gatos, canídeos silvestres, marsupiais; e animais sinantrópicos, como roedores e quirópteros. Portanto, este estudo teve como objetivo detectar a presença de anticorpos anti-Leishmania spp. em aves de uma área rural do município de Santa Maria, sul do Brasil. De maio a dezembro de 2022, foram coletadas 262 amostras de sangue de 244 galinhas, 8 perus, 7 pintadas e 3 gansos, distribuídas em 27 propriedades rurais de 6 distritos. Todos os locais visitados apresentaram aves positivas para a presença de Leishmania spp. Assim, infere-se que o contato com esse protozoário pode induzir a produção de anticorpos, sugerindo que esses animais possam ser utilizados como sentinelas para a circulação desse agente. Além disso, o sangue desses animais é uma fonte de alimento preferencial para insetos da subfamília Phlebotominae, que podem ser utilizados como bioindicadores da presença desses flebotomíneos.

Palavras-chave:
Aves domésticas; anticorpos; reação de imunofluorescência indireta; leishmaniose

Introduction

Domestic birds, such as chickens (Gallus gallus domesticus), turkeys (Meleagris gallopavo), geese (Anser anser) and guinea fowl (Numida meleagris) are globally distributed animals that are raised and kept in peridomestic spaces, such as backyards, both in urban and rural areas. These birds keep close contact with humans and various domestic animals, such as dogs (Canis familiaris) and cats (Felis catus), wild predators like foxes (Dusicyon vetulus and Cerdocyon thous) and marsupials (Didelphis albiventris and Didelphis marsupialis), and synanthropic animals such as murines (Rattus rattus) (Sherlock, 1996Sherlock IA. Ecological interactions of visceral leishmaniasis in the state of Bahia, Brazil. Mem Inst Oswaldo Cruz 1996; 91(6): 671-683. http://dx.doi.org/10.1590/S0074-02761996000600003. PMid:9283643.
http://dx.doi.org/10.1590/S0074-02761996...
; Alexander et al., 2002Alexander B, Carvalho RL, McCallum H, Pereira MH. Role of the domestic chicken (Gallus gallus) in the epidemiology of urban visceral leishmaniasis in Brazil. Emerg Infect Dis 2002; 8(12): 1480-1485. http://dx.doi.org/10.3201/eid0812.010485. PMid:12498667.
http://dx.doi.org/10.3201/eid0812.010485...
; Ratzlaff et al., 2023Ratzlaff FR, Osmari V, Silva D, Vasconcellos JSP, Pötter L, Fernandes FD, et al. Identification of infection by Leishmania spp. In wild and domestic animals in Brazil: a systematic review with meta-analysis (2001–2021). Parasitol Res 2023; 122(7): 1605-1619. http://dx.doi.org/10.1007/s00436-023-07862-y. PMid:37154922.
http://dx.doi.org/10.1007/s00436-023-078...
) and chiropterans, which some studies found infected by some Leishmania species, indicating that bats may participate in the biological cycle of Leishmania spp. and act as a host, reservoir, and/or source of infection (Savani et al., 2010Savani ESMM, Almeida MF, Camargo MCGO, D’Auria SRN, Silva MMS, Oliveira ML, et al. Detection of Leishmania (Leishmania) amazonensis and Leishmania (Leishmania) infantum chagasi in Brazilian bats. Vet Parasitol 2010; 168(1-2): 5-10. http://dx.doi.org/10.1016/j.vetpar.2009.10.019. PMid:19939568.
http://dx.doi.org/10.1016/j.vetpar.2009....
; Shapiro et al., 2013Shapiro JT, Lima MSC Jr, Dorval MEC, França AO, Matos MFC, Bordignon MO. First record of Leishmania braziliensis presence detected in bats, Mato Grosso do Sul, southwest Brazil. Acta Trop 2013; 128(1): 171-174. http://dx.doi.org/10.1016/j.actatropica.2013.07.004. PMid:23886850.
http://dx.doi.org/10.1016/j.actatropica....
; Ratzlaff et al., 2022Ratzlaff FR, Fernandes FD, Osmari V, Silva D, Vasconcellos JSP, Braunig P, et al. Prevalence and molecular detection of Leishmania spp. in bats from Rio Grande do Sul state, Brazil. Parasitol Res 2022; 121(11): 3193-3202. http://dx.doi.org/10.1007/s00436-022-07639-9. PMid:36048268.
http://dx.doi.org/10.1007/s00436-022-076...
).

These birds are in contact with several blood-sucking insects that are vectors of these protozoa, such as Phlebotominae (Diptera: Psychodidae: Phlebotominae), and transmitters of leishmaniasis in both humans and animals. According to the literature review conducted by Sousa et al. (2021)Sousa RLT, Vasconcelos SA, Santos-Mallet JR, Nascimento EF, Teixeira CR, Silva CLM, et al. Padrões de fonte alimentar dos Flebotomíneos (Diptera: Psychodidae) vetores das Leishmanioses: uma revisão bibliográfica. Rev Eletrônica Acervo Saúde 2021; 13(8): e8567. http://dx.doi.org/10.25248/reas.e8567.2021.
http://dx.doi.org/10.25248/reas.e8567.20...
, chickens were among the seven animals that most participated in the feeding pattern of sandflies in Brazil.

Consequently, chickens may favor a link between wild and domestic disease transmission cycles (Dantas-Torres & Brandão-Filho, 2006Dantas-Torres F, Brandão-Filho SP. Visceral leishmaniasis in Brazil: revisiting paradigms of epidemiology and control. Rev Inst Med Trop São Paulo 2006; 48(3): 151-156. http://dx.doi.org/10.1590/S0036-46652006000300007. PMid:16847505.
http://dx.doi.org/10.1590/S0036-46652006...
).

However, in addition to sandflies, there are records of other ornithophilic hematophagous dipterans naturally infected by protozoa of the family Trypanosomatidae, mainly avian trypanosomes (Svobodová et al., 2015Svobodová M, Weidinger K, Peške L, Volf P, Votýpka J, Voříšek P. Trypanosomes and haemosporidia in the buzzard (Buteo buteo) and sparrowhawk (Accipiter nisus): factors affecting the prevalence of parasites. Parasitol Res 2015; 114(2): 551-560. http://dx.doi.org/10.1007/s00436-014-4217-x. PMid:25403377.
http://dx.doi.org/10.1007/s00436-014-421...
). Srisuton et al. (2019)Srisuton P, Phumee A, Sunantaraporn S, Boonserm R, Sor-Suwan S, Brownell N, et al. Detection of Leishmania and Trypanosoma DNA in field-caught sand flies from endemic and non-endemic areas of leishmaniasis in Southern Thailand. Insects 2019; 10(8): 238. http://dx.doi.org/10.3390/insects10080238. PMid:31382501.
http://dx.doi.org/10.3390/insects1008023...
found that sandflies may be potential vectors of Leishmania spp. and Trypanosoma spp. in southern Thailand, including concomitantly. In Brazil, infections by protozoa of the genus Trypanosoma have been recorded in several species of sandflies, but few parasites have been isolated and characterized (Shaw et al., 2003Shaw J, Rosa AT, Souza A, Cruz AC. Transmissão de outros agentes: os flebotomíneos brasileiros como hospedeiros e vetores de determinadas espécies. In: Rangel EF, Lainson R, organizers. Flebotomíneos do Brasil. Rio de Janeiro: Fiocruz; 2003. p. 337-351.). In addition, there are several reports of birds infected with trypanosomatids of the genera Herpetomonas, Crithidia and Leptomonas (Lukeš et al., 2014Lukeš J, Skalický T, Týč J, Votýpka J, Yurchenko V. Evolution of parasitism in kinetoplastid flagellates. Mol Biochem Parasitol 2014; 195(2): 115-122. http://dx.doi.org/10.1016/j.molbiopara.2014.05.007. PMid:24893339.
http://dx.doi.org/10.1016/j.molbiopara.2...
).

Chickens have physiological characteristics, such as high body temperature (41 ºC), which prevents the multiplication of protozoa in these hosts, protecting them from disease. However, their shelter is considered a place of rest and reproduction for Phlebotominae, which is relevant for maintaining and multiplying vector populations (Nieves et al., 2011Nieves E, Oliveros JL, Rondon M. Impacto de Leishmania amazonensis y la sangre de ave en el potencial biológico y fecundidad de Lutzomyia migonei y Lutzomyia ovallesi (Diptera: Psychodidae). EntomoBrasilis 2011; 4(1): 20-25. http://dx.doi.org/10.12741/ebrasilis.v4i1.93.
http://dx.doi.org/10.12741/ebrasilis.v4i...
). In addition, poultry farms can increase the risk of contracting leishmaniasis by up to four times compared to households without chicken coops (Rodrigues et al., 1999Rodrigues AC, Santos AB, Feitosa LF, Santana CS, Nascimento EG, Moreira ED Jr. Criação peridomiciliar de galináceos aumenta o risco de leishmaniose visceral humana. Rev Soc Bras Med Trop [online] 1999 [cited 2023 Oct 30] (Suppl S1): 12-13. Available from: https://www.arca.fiocruz.br/handle/icict/42802
https://www.arca.fiocruz.br/handle/icict...
).

In this sense, Borges et al. (2009)Borges BKA, Silva JA, Haddad JPA, Moreira EC, Magalhães DF, Ribeiro LML, et al. Presença de animais associada ao risco de transmissão da leishmaniose visceral em humanos em Belo Horizonte, Minas Gerais. Arq Bras Med Vet Zootec 2009; 61(5): 1035-1043. http://dx.doi.org/10.1590/S0102-09352009000500004.
http://dx.doi.org/10.1590/S0102-09352009...
highlight the epidemiological importance of domestic chickens in the leishmaniasis transmission cycle, owing to their potential to generate a favorable environment for the development of Phlebotominae.

It should be noted that Visceral Leishmaniasis (VL) and American Tegumentary Leishmaniasis (ATL) affect the most vulnerable human populations with restricted access to health services. In Brazil, VL is caused by protozoa of Leishmania (Leishmania) infantum species and is transmitted by Phlebotominae of the species Lutzomyia longipalpis and Lutzomyia cruzi (Queiroz et al., 2012Queiroz MFM, Varjão JR, Moraes SC, Salcedo GE. Analysis of sandflies (Diptera: Psychodidae) in Barra do Garças, State of Mato Grosso, Brazil, and the influence of environmental variables on the vector density of Lutzomyia longipalpis (Lutz & Neiva, 1912). Rev Soc Bras Med Trop 2012; 45(3): 313-317. http://dx.doi.org/10.1590/S0037-86822012000300007. PMid:22760128.
http://dx.doi.org/10.1590/S0037-86822012...
; Brasil, 2014Brasil. Ministério da Saúde, Secretaria de Vigilância em Saúde, Departamento de Vigilância Epidemiológica. Manual de vigilância da leishmaniose tegumentar americana [online]. Brasília: Ministério da Saúde; 2014 [cited 2023 Oct 30]. Available from: https://bvsms.saude.gov.br/bvs/publicacoes/manual_vigilancia_controle_leishmaniose_visceral_1edicao.pdf
https://bvsms.saude.gov.br/bvs/publicaco...
). Other species, such as Nyssomyia neivai, Pintomyia fischeri, and Migonemyia migonei, are also implicated in the infection (Salomón et al., 2010Salomón OD, Quintana MG, Bezzi G, Morán ML, Betbeder E, Valdéz DV. Lutzomyia migonei as putative vector of visceral leishmaniasis in La Banda, Argentina. Acta Trop 2010; 113(1): 84-87. http://dx.doi.org/10.1016/j.actatropica.2009.08.024. PMid:19716797.
http://dx.doi.org/10.1016/j.actatropica....
; Carvalho et al., 2010Carvalho GML, Gontijo CMF, Falcão AL, Andrade JD Fo. Study of phlebotomine sand flies (Diptera: Psychodidae) collected in a Leishmania-endemic area of the Metropolitan Region of Belo Horizonte, Brazil. J Med Entomol 2010; 47(6): 972-976. http://dx.doi.org/10.1603/ME09127. PMid:21175043.
http://dx.doi.org/10.1603/ME09127...
; Dias et al., 2013Dias ES, Michalsky ÉM, Nascimento JC, Ferreira EC, Lopes JV, Fortes-Dias CL. Detection of Leishmania infantum, the etiological agent of visceral leishmaniasis, in Lutzomyia neivai, a putative vector of cutaneous leishmaniasis. J Vector Ecol 2013; 38(1): 193-196. http://dx.doi.org/10.1111/j.1948-7134.2013.12028.x. PMid:23701627.
http://dx.doi.org/10.1111/j.1948-7134.20...
; Guimarães et al., 2016Guimarães VCFV, Pruzinova K, Sadlova J, Volfova V, Myskova J, Brandão SP Fo. 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...
).

The first autochthonous cases of the disease in Rio Grande do Sul occurred in dogs in 2008 and humans in 2009, in the municipality of São Borja, on the western border of the state (Souza et al., 2009Souza GD, Santos E, Andrade JD Fo. The first report of the main vector of visceral leishmaniasis in America, Lutzomyia longipalpis (Lutz & Neiva) (Diptera: Psychodidae: Phlebotominae), in the state of Rio Grande do Sul, Brazil. Mem Inst Oswaldo Cruz 2009; 104(8): 1181-1182. http://dx.doi.org/10.1590/S0074-02762009000800017. PMid:20140381.
http://dx.doi.org/10.1590/S0074-02762009...
; CEVS, 2011Centro Estadual de Vigilância em Saúde – CEVS. Leishmaniose visceral no Rio Grande do Sul. Bol Epidemiol [online] 2011 [cited 2023 Oct 30]; 13(1): 1-8. Available from: https://www.cevs.rs.gov.br/upload/arquivos/202001/20174707-v13-n1-marco.pdf
https://www.cevs.rs.gov.br/upload/arquiv...
).

In Santa Maria, suspected cases disease has been reported in dogs since 1985 (Pocai et al., 1998Pocai EA, Frozza L, Headley SA, Graça DL. Leishmaniose visceral (Calazar): cinco casos em cães de Santa Maria, Rio Grande do Sul, Brasil. Ciênc Rural 1998; 28(3): 501-505. http://dx.doi.org/10.1590/S0103-84781998000300025.
http://dx.doi.org/10.1590/S0103-84781998...
). However, from 2017 onwards, there was an increase in the cases of canine visceral leishmaniasis (116 cases), and in 2021, two autochthonous human cases were recorded, one of which contributed to the patient's death (Diário de Santa Maria, 2021aDiário de Santa Maria. Desde 2017 foram pelo menos 116 casos de leishmaniose em animais em Santa Maria [online]. Santa Maria: Diário de Santa Maria; 2021a [cited 2023 Oct 30]. Available from: https://diariosm.com.br/noticias/saude/desde_2017_foram_pelo_menos_116_casos_de_leishmaniose_em_animais_em_santa_maria.438567
https://diariosm.com.br/noticias/saude/d...
, bDiário de Santa Maria. Pela primeira vez, Santa Maria registra casos e óbito de humanos com leishmaniose [online]. Santa Maria: Diário de Santa Maria; 2021b [cited 2023 Oct 30]. Available from: https://diariosm.com.br/noticias/saude/video_pela_primeira_vez_santa_maria_registra_casos_e_obito_de_humanos_com_leishmaniose.438568
https://diariosm.com.br/noticias/saude/v...
).

In a study performed by Osmari (2023)Osmari V. Fauna e sazonalidade de flebotomíneos (Diptera: Psychodidae: Phlebotominae) em área de transmissão de leishmaniose na região central do estado do Rio Grande do Sul, Brasil [thesis]. Santa Maria: Universidade Federal de Santa Maria; 2023., the author confirmed the presence of three species of vectors of importance for public and animal health, being the first report of the presence of L. longipalpis (Osmari et al., 2022Osmari V, Tatto M, Andrade AJ, Ratzlaff FR, Vasconcellos JSP, Botton SA, et al. First identification of Lutzomyia longipalpis in an area of visceral leishmaniasis transmission in central Rio Grande do Sul State, southern Brazil. Parasitol Res 2022; 121(11): 3327-3330. http://dx.doi.org/10.1007/s00436-022-07647-9. PMid:36109382.
http://dx.doi.org/10.1007/s00436-022-076...
), which is considered the primary vector of VL in Brazil by the Ministry of Health. In addition, P. fischeri and M. migonei are also implicated as transmitters of the visceral and mucocutaneous form of the disease (Rêgo et al., 2020Rêgo FD, Souza GD, Miranda JB, Peixoto LV, Andrade-Filho JD. Potential vectors of Leishmania parasites in a recent focus of visceral leishmaniasis in neighborhoods of Porto Alegre, State of Rio Grande do Sul, Brazil. J Med Entomol 2020; 57(4): 1286-1292. http://dx.doi.org/10.1093/jme/tjaa036. PMid:32112089.
http://dx.doi.org/10.1093/jme/tjaa036...
).

Considering the epidemiological importance of leishmaniasis and the scarcity of research on Leishmania spp. infection in birds, this study aimed to detect the presence of anti-Leishmania spp. antibodies in poultry in a rural area of the municipality of Santa Maria, southern Brazil.

Materials and Methods

The municipality of Santa Maria is in the central region of the state of Rio Grande do Sul (RS) in southern Brazil, where the Atlantic Forest and Pampa biomes predominate. The city has an area of 1,780.194 km2, an estimated population of 296,081 inhabitants, a humid subtropical climate, and an average annual temperature of 19.4 °C (IBGE, 2021Instituto Brasileiro de Geografia e Estatística – IBGE. Cidades e estados [online]. Rio de Janeiro: IBGE; 2021 [cited 2023 Oct 30]. Available from: https://www.ibge.gov.br/cidades-e-estados/rs/santa-maria.html
https://www.ibge.gov.br/cidades-e-estado...
) (Figure 1).

Figure 1
Study site map [adapted from Schiavo et al. (2016)Schiavo B, Gaiad N, Anater MJ, Corte AP, Sanquetta CR. Uso de imagens orbitais de alta resolução espacial para amostragem da arborização urbana no município de Santa Maria – RS. Encicl Biosf 2016; 13(23): 1336-1346. http://dx.doi.org/10.18677/Enciclopedia_Biosfera_2016_118.
http://dx.doi.org/10.18677/Enciclopedia_...
].

According to data provided by the Epidemiology and Statistics Section of the Department of Agriculture, Livestock, and Rural Development of Rio Grande do Sul, Santa Maria has 5021 chickens, 42 guinea fowl, 27 geese, and nine turkeys. Rural producers in the region provided this information during the 2021 annual herd declaration.

In this study, samples were collected according to the availability of those responsible for the animals. Between May and December 2022, 262 blood samples were collected from 244 chickens, eight turkeys, seven guinea fowl, and three geese distributed across 27 rural properties in six districts of the municipality of Santa Maria, Rio Grande do Sul, Brazil.

Blood was collected from the birds by restraining, cleaning the skin, using hydrophilic cotton and alcohol, followed by puncture of the medial ulnar vein or through the most viable vessel during handling, using sterile 3 mL syringes with disposable hypodermic needles of 26 G (0.45 x 13 mm), with a maximum volume of 2.5 mL collected per animal, proportional to live weight. The blood was stored in collection tubes without anticoagulant at a temperature between 3º and 8 ºC, stored in isothermal boxes, and sent to the Laboratório de Doenças Parasitárias the Universidade Federal de Santa Maria (LADOPAR-UFSM). Subsequently, the samples of blood were centrifuged at 1600 x g for 10 min to obtain the serum. The serum samples stored at -20 ºC until the Indirect Immunofluorescence Reaction (IFA) was performed.

For the detection of anti-Leishmania spp. antibodies, IFA was performed using 12-well slides sensitized with L. infantum promastigotes, which were used as antigens to detect immunoglobulin Y (IgY). As a secondary antibody, IgY (Affinity Purified Antibody Fluorescein. Sigma, St Louis, MO, USA) was used as an anti-chicken antibody conjugated with fluorescein, at dilution 1:100, according to the technique described by Otranto et al. (2010)Otranto D, Testini G, Buonavoglia C, Parisi A, Brandonisio O, Circella E, et al. Experimental and field investigations on the role of birds as hosts of Leishmania infantum, with emphasis on the domestic chicken. Acta Trop 2010; 113(1): 80-83. http://dx.doi.org/10.1016/j.actatropica.2009.09.014. PMid:19818726.
http://dx.doi.org/10.1016/j.actatropica....
. Positive and negative samples were obtained from the serum bank of LADOPAR-UFSM and used as controls. All positive serum samples in the 1:30 dilution was considered reactive according to the same author, and were subsequently diluted to determine the maximum antibody titer. After conducting the tests, the results were tabulated on a spreadsheet, and descriptive analyses were performed using Microsoft Excel.

To minimize the influence of cross-reactivity between trypanosomatids, IFA was performed according to Camargo & Rebonato (1969)Camargo ME, Rebonato C. Cross-reactivity in fluorescence tests for Trypanosoma and Leishmania antibodies. A simple inhibition procedure to ensure specific results. Am J Trop Med Hyg 1969; 18(4): 500-505. http://dx.doi.org/10.4269/ajtmh.1969.18.500. PMid:4978596.
http://dx.doi.org/10.4269/ajtmh.1969.18....
, for detection of anti-Trypanosoma spp. antibodies in those reagent samples for Leishmania sp., using IgY (Affinity Purified Antibody Fluorescein. Sigma, St Louis, MO, USA) as a secondary antibody at dilution 1:100.). Positive and negative samples were obtained from the serum bank of LADOPAR-UFSM and used as controls. All positive serum samples in the 1:30 dilution was considered reactive according to the same author, and were subsequently diluted to determine the maximum antibody titer.

Results

All locations visited had reactive birds with IgY anti-Leishmania spp. antibody titers. Of the 244 blood samples collected from the chickens, 181 (74.2%) were reactive presenting titles ranging from 30 to 960 (Table 1). On the other hand, no reactive sample for Leishmania spp. was positive for Trypanosoma spp.

Table 1
Frequency of anti-Leishmania spp. antibodies detected through the indirect immunofluorescence reaction in chickens reared extensively in six rural districts of Santa Maria/RS, from May to December 2022.

Among the locations where the study was performed, the district of Arroio do Só had the highest number of reactive samples, although the results remained proportional to the number of samples collected in each location.

Three Geese and six turkeys showed reactive tests for 30 and 60 antibody titers, respectively; three turkey samples were still reactive for 120 anti-Leishmania spp. antibody titers. Both species were bred in the Palma District (Table 2).

Table 2
Frequency of anti-Leishmania spp. antibodies detected by indirect immunofluorescence reaction in turkeys and geese reared extensively in six rural districts of Santa Maria/RS, from May to December 2022.

Discussion

Several studies have attempted to elucidate the role of domestic birds in leishmaniasis infection. These animals are raised worldwide as protein sources, either for the production of meat or eggs, mainly on rural properties, and are raised by the most vulnerable populations with restricted access to health services.

In Brazil, Alexander et al. (2002)Alexander B, Carvalho RL, McCallum H, Pereira MH. Role of the domestic chicken (Gallus gallus) in the epidemiology of urban visceral leishmaniasis in Brazil. Emerg Infect Dis 2002; 8(12): 1480-1485. http://dx.doi.org/10.3201/eid0812.010485. PMid:12498667.
http://dx.doi.org/10.3201/eid0812.010485...
summarized that the role of domestic birds in the epidemiology of VL involves a balance between zooprophylaxis, maintenance of Phlebotominae populations, and attraction of predators that are reservoirs and hosts of L. infantum. However, until now, Leishmania sp. infection has not developed in birds (Dantas-Torres & Brandão-Filho, 2006Dantas-Torres F, Brandão-Filho SP. Visceral leishmaniasis in Brazil: revisiting paradigms of epidemiology and control. Rev Inst Med Trop São Paulo 2006; 48(3): 151-156. http://dx.doi.org/10.1590/S0036-46652006000300007. PMid:16847505.
http://dx.doi.org/10.1590/S0036-46652006...
).

This occurs owing to factors that have been suggested by Alexander et al. (2002)Alexander B, Carvalho RL, McCallum H, Pereira MH. Role of the domestic chicken (Gallus gallus) in the epidemiology of urban visceral leishmaniasis in Brazil. Emerg Infect Dis 2002; 8(12): 1480-1485. http://dx.doi.org/10.3201/eid0812.010485. PMid:12498667.
http://dx.doi.org/10.3201/eid0812.010485...
, such as a body temperature higher than that of mammals (41 and 37 ºC) and nucleated erythrocytes that stimulate DNAase activity, which can be fatal for Leishmania spp. in the gut of sandflies, among others.

The IFA technique is based on the use of the intact parasite as an antigen and is very useful in epidemiological studies, as its sensitivity varies from 83 to 100% and its specificity is approximately 80% for serum samples (Bresciani et al., 2008Bresciani KDS, Costa AJ, Navarro IT, Toniollo GH, Sakamoto CAM, Arantes TP, et al. Toxoplasmose canina: aspectos clínicos e patológicos. Semina: Ciênc Agrár 2008; 29(1): 189-202. http://dx.doi.org/10.5433/1679-0359.2008v29n1p189.
http://dx.doi.org/10.5433/1679-0359.2008...
). This test has been used to demonstrate contact between host and parasite with very high sensitivity (Desquesnes et al., 2022Desquesnes M, Gonzatti M, Sazmand A, Thévenon S, Bossard G, Boulangé A, et al. A review on the diagnosis of animal trypanosomoses. Parasit Vectors 2022; 15(1): 64. http://dx.doi.org/10.1186/s13071-022-05190-1. PMid:35183235.
http://dx.doi.org/10.1186/s13071-022-051...
).

However, the overlapping of areas where closely related etiological groups are present, such as parasite species belonging to the Trypanosomatidae family, is a limiting aspect of the interpretation of serological data due to possible cross-serological reactions caused by phylogenetic proximity, which can give false results. positive (Caballero et al., 2007Caballero ZC, Sousa OE, Marques WP, Saez-Alquezar A, Umezawa ES. Evaluation of serological tests to identify Trypanosoma cruzi infection in humans and determine cross-reactivity with Trypanosoma rangeli and Leishmania spp. Clin Vaccine Immunol 2007; 14(8): 1045-1049. http://dx.doi.org/10.1128/CVI.00127-07. PMid:17522327.
http://dx.doi.org/10.1128/CVI.00127-07...
).

The family Trypanosomatidae (phylum Protozoa, class Kinetoplastida) comprises: 14 monoxenic genera that infect insects (e.g. Leptomonas spp., Herpetomonas spp.) and five dixenic genera, with invertebrates as vectors (genus that infects Phytomonas plants), and another four that infect animals and humans (Desquesnes et al., 2022Desquesnes M, Gonzatti M, Sazmand A, Thévenon S, Bossard G, Boulangé A, et al. A review on the diagnosis of animal trypanosomoses. Parasit Vectors 2022; 15(1): 64. http://dx.doi.org/10.1186/s13071-022-05190-1. PMid:35183235.
http://dx.doi.org/10.1186/s13071-022-051...
). Although most representatives of this family are not pathogenic for their hosts, some are important etiological agents of human and domestic animal diseases, such as African and American trypanosomiasis (Chagas disease) and leishmaniasis (Simpson et al., 2006Simpson AGB, Stevens JR, Lukeš J. The evolution and diversity of kinetoplastid flagellates. Trends Parasitol 2006; 22(4): 168-174. http://dx.doi.org/10.1016/j.pt.2006.02.006. PMid:16504583.
http://dx.doi.org/10.1016/j.pt.2006.02.0...
).

Otranto et al. (2010)Otranto D, Testini G, Buonavoglia C, Parisi A, Brandonisio O, Circella E, et al. Experimental and field investigations on the role of birds as hosts of Leishmania infantum, with emphasis on the domestic chicken. Acta Trop 2010; 113(1): 80-83. http://dx.doi.org/10.1016/j.actatropica.2009.09.014. PMid:19818726.
http://dx.doi.org/10.1016/j.actatropica....
tested 121 serum samples from poultry, including 34 domestic geese seven wild ducks (Cairina moschata), five pheasants (Phasianus colchicus), two guinea fowls and 73 chickens, for the presence of anti-L. infantum antibodies by indirect immunofluorescence testing. At the time, all 73 serum samples from chickens were negative in IFA, while three serum samples of A. anser and one P. colchicus were positive with titers ranging from 30 to 60.

In our study, it was also possible to detect anti-Leishmania sp. antibodies in the three geese, and 6 turkeys, in addition to 181 chickens, totaling 190 (74.5%) reactive animals, with titers ranging from 30 to 960. On the other hand, none of these samples obtained the same result when we aimed to detect anti-Trypanosoma sp. antibodies, which minimized the limitation imposed by the possible cross-reaction between the genus Leishmania and Trypanosoma.

These results indicate a high rate of anti- Leishmania spp. antibodies in these animals. Therefore, this study can be characterized as the first report of Leishmania spp. antibodies in chickens, turkeys and geese raised extensively in the central region of RS and additional more specific diagnostic tests such as polymerase chain reaction (PCR) are necessary to confirm the species to which these animals are exposed and/or infected. These findings provide data regarding monitoring VL in endemic or silent regions for the disease, can become an additional element in epidemiological and environmental surveillance systems. The high prevalence of anti-Leishmania antibodies in these animals may indicate the presence of insect vectors, specifically sandflies, and the circulation of protozoa of the genus Leishmania.

In a similar approach, Hamer et al. (2012)Hamer SA, Lehrer E, Magle SB. Wild birds as sentinels for multiple zoonotic pathogens along an urban to rural gradient in Greater Chicago, Illinois. Zoonoses Public Health 2012; 59(5): 355-364. http://dx.doi.org/10.1111/j.1863-2378.2012.01462.x. PMid:22353581.
http://dx.doi.org/10.1111/j.1863-2378.20...
demonstrate the presence of multiple zoonotic pathogens using migratory birds as sentinels, providing an assessment of potential public health risks to human populations.

Thus, this type of study may result in an additional tool for health surveillance systems with regard to the monitoring of Leishmaniasis in Brazil.

Conclusion

Given the results presented in this study, it can be concluded that, although birds have physiological mechanisms that possibly make them refractory to the development of diseases caused by Leishmania spp., the blood of these animals is a preferred food source for insect vectors of the subfamily Phlebotominae and contact with these protozoa can induce the production of antibodies. This suggests to us that these animals can be used both as bioindicators for to verify the presence of these insects, as sentinels for the circulation of species of the genus Leishmania, becoming an additional tool for health surveillance systems.

However, we consider that further studies using other more specific diagnostic tools, such as PCR, are necessary to deepen the understanding of the relationship between poultry and the epidemiology of leishmaniasis in Brazil.

Acknowledgements

This work was supported by the National Research and Development Council (CNPq) and Coordination for the Improvement of Higher Education Personnel (CAPES).

  • How to cite: Tatto M, Fernandes FD, Costa EP, Shibuya FY, Freitas LI, Osmari V, et al. Detection of anti-Leishmania spp. antibodies in poultry from central region of Rio Grande do Sul, Brazil. Braz J Vet Parasitol 2023; 32(4): e007723. https://doi.org/10.1590/S1984-29612023077

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Publication Dates

  • Publication in this collection
    08 Dec 2023
  • Date of issue
    2023

History

  • Received
    07 May 2023
  • Accepted
    30 Oct 2023
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