Efficiency of rLb6H recombinant protein from Leishmania (Viannia) braziliensis for the detection of canine visceral leishmaniasis

Efficacy of rLb6H in CVL diagnosis

Autores

  • Ingrid Estevam Pereira Departamento de Parasitologia, Microbiologia e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Juiz de Fora https://orcid.org/0009-0007-5484-198X
  • Erick Esteves Oliveira Departamento de Parasitologia, Microbiologia e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Juiz de Fora
  • Carolina Martins Moreira Elias Departamento de Parasitologia, Microbiologia e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Juiz de Fora https://orcid.org/0000-0002-7010-8514
  • Alexandre Barbosa Reis Escola de Farmácia, Universidade Federal de Ouro Preto https://orcid.org/0000-0001-8123-4164
  • Malcolm Scott Duthie HDT Biocorp https://orcid.org/0000-0002-8515-5516
  • Henrique Couto Teixeira Departamento de Parasitologia, Microbiologia e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Juiz de Fora

DOI:

https://doi.org/10.34019/1982-8047.2023.v49.41177

Palavras-chave:

Leishmaniose Canina, Diagnóstico, Proteínas Recombinantes, ELISA, rLb6H

Resumo

Introduction: Visceral leishmaniasis (VL) is a serious endemic disease in many tropical and subtropical countries, with a strong incidence in Brazil. The disease is transmitted by the bite of infected female phlebotomine sandflies, with dogs being the main urban reservoirs of the parasite. The diverse clinical profile and the long incubation period are challenges for the diagnosis of canine visceral leishmaniasis (CVL). Recombinant proteins from Leishmania spp. have been studied as antigens that can increase the accuracy of serological tests. Objective: To evaluate the diagnostic performance of the recombinant protein rLb6H, from Leishmania braziliensis, in comparison to the reference antigens rK39 and rK28, from L. donovani, prioritizing the identification of subclinical infected dogs. Material and Methods: Serum IgG reactivity to rLb6H, rK28, and rK39 recombinant proteins was assessed in dogs with previously parasitological confirmation of CVL, subdivided according to their clinical status, using immunoenzymatic assay (ELISA). Diagnostic accuracy of each ELISA was evaluated by receiver operating characteristic (ROC) curve analysis. Results: While all antigens showed a better performance in detecting CVL in symptomatic dogs (SD), detection of CVL in the oligosymptomatic (OD) and asymptomatic (AD) groups was lower, but rLb6H achieved high sensitivity for asymptomatic CVL. Interestingly, the most reactive CVL samples to rK28 were barely detected by rLb6H, while the less reactive to rK28, mostly from the AD group, presented higher reactivity to rLb6H. Conclusion: The recombinant protein rLb6H showed utility in the detection of asymptomatic CVL, displaying a complementary reactivity to rK39 and rK28. Thus, these results suggest that rLb6H could be incorporated into multi-antigen strategies, to increase diagnostic accuracy of CVL.

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Biografia do Autor

Henrique Couto Teixeira, Departamento de Parasitologia, Microbiologia e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Juiz de Fora

Laboratório de Imunologia
Departamento de Parasitologia, Microbiologia e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Juiz de Fora
Tel/Fax: 32-2102-3214

Referências

Piyasiri SB, Samaranayake TN, Silva H, Manamperi NH, Karunaweera ND. ELISA-based evaluation of antibody response to Leishmania in a region endemic for cutaneous leishmaniasis. Parasite Immunol. 2022; 44(9):e12940. doi: 10.1111/pim.12940.

Peixoto HM, de Oliveira MRF, Romero GAS. Serological diagnosis of canine visceral leishmaniasis in Brazil: systematic review and meta-analysis. Trop Med Int Health. 2015; 20:334-52. doi: 10.1111/tmi.12429.

Bates PA. Transmission of Leishmania metacyclic promastigotes by phlebotomine sand flies. Int J Parasitol. 2007; 37(10):1097-106. doi: 10.1016/j.ijpara.2007.04.003.

Ministério da Saúde (BR). Situação epidemiólogica da leishmaniose visceral [Internet]. 2022 [accessed on 2022 sep 4]. Available at: https://www.gov.br/saude/pt-br/assuntos/saude-de-a-a-z/l/leishmaniose-visceral/situacao-epidemiologica-da-leishmaniose-visceral.

Rodrigues MR, Santos LMO, Miyazaki CK, Martins VT, Ludolf FR, Kursancew AC et al. Immunodiagnosis of human and canine visceral leishmaniasis using recombinant Leishmania infantum prohibitin protein and a synthetic peptide containing its conformational B-cell epitope. J Immunol Methods. 2019; 474:112641. doi: doi.org/10.1016/j.jim.2019.112641.

Reis AB, Teixeira-Carvalho A, Vale AM, Marques MJ, Giunchetti RC, Mayrink W et al. Isotype patterns of immunoglobulins: Hallmarks for clinical status and tissue parasite density in Brazilian dogs naturally infected by Leishmania (Leishmania) chagasi. Vet Immunol Immunopathol. 2006; 112:102116. doi: doi.org/10.1016/j.rvsc.2017.10.011.

Pereira IE, Silva KP, Menegati LM, Pinheiro AC, Assunção EAO, Araújo MLP et al. Performance of recombinant proteins in diagnosis and differentiation of canine visceral leishmaniasis infected and vaccinated dogs. Eur J Microbiol Immunol. 2020; 10(3):165-71. doi: 10.1556/1886.2020.00018.

Vaish M, Bhatia A, Reed SG, Chakravarty J, Sundar S. Evaluation of rK28 antigen for serodiagnosis of visceral Leishmaniasis in India. Clin Microbiol Infect. 2012; 18(1). doi: 10.1111/j.1469-0691.2011.03540.x.

Paz GF, Rugani JMN, Marcelino AP, Gontijo CMF. Implications of the use of serological and molecular methods to detect infection by Leishmania spp. in urban pet dogs. Acta Trop. 2018; 182:198-201. doi: 10.1016/j.actatropica.2018.03.018.

Nogueira FS, Avino VC, Galvis-Ovallos F, Pereira-Chioccola VL, Moreira MAB, Romariz APPL et al. Use of miltefosine to treat canine visceral leishmaniasis caused by Leishmania infantum in Brazil. Parasit Vectors. 2019; 12. doi: doi.org/10.1186/s13071-019-3323-0.

Rosário EY, Genaro O, França-Silva JC, da Costa RT, Mayrink W, Reis AB et al. Evaluation of enzyme-linked immunosorbent assay using crude Leishmania and recombinant antigens as a diagnostic marker for canine visceral leishmaniasis. Mem Inst Oswaldo Cruz. 2005; 100(2):197203. doi: doi.org/10.1590/S0074-02762005000200015.

Alves AS, Mouta-Confort E, Figueiredo FB, Oliveira RVC, Schubach AO, Madeira MF. Evaluation of serological cross-reactivity between canine visceral leishmaniasis and natural infection by Trypanosoma caninum. Res Vet Sci. 2012; 93:1329-33. doi: dx.doi.org/10.1016/j.rvsc.2012.07.006.

Travi BL, Cordeiro-da-Silva A, Dantas-Torres F, Miró G. Canine visceral leishmaniasis: diagnosis and management of the reservoir living among us. PloS Negl Trop Dis. 2018. doi: doi.org/10.1371/journal.pntd.0006082.

Venturin GL, Bragato JP, Silva KLO, Lima VMF. Recombinant K28 antigen in ELISA in the diagnosis of canine visceral leishmaniosis. Parasite Immunol. 2015; 37(12):670-3. doi: 10.1111/pim.12281.

Schwanke K, Silva AMM, Pacheco AP, Bahia M, Silveira FT, Scofield A et al. Diagnóstico molecular e frequência de anticorpos anti-Leishmania infantum chagasi em cães do município de Belém, Pará. Pesqui Vet Bras. 2014; 34(3):255-60. doi: doi.org/10.1590/S0100-736X2014000300010.

Vale AM, Fujiwara RT, Neto AFS, Miret JA, Alvarez DCC, da Silva JCF et al. Identification of highly specific and cross-reactive antigens of leishmania species by antibodies from leishmania (Leishmania) chagasi naturally infected dogs. Zoonoses Public Health. 2009; 56(1):41-8. doi: 10.1111/j.1863-2378.2008.01183.x.

Sato CM, Sanches MCA, Celeste BJ, Duthie MS, Guderian J, Reed SG et al. Use of recombinant antigens for sensitive serodiagnosis of American tegumentary leishmaniasis caused by different Leishmania species. J Clin Microbiol. 2017; 55(2):495-503. doi: 10.1128/JCM.01904-16.

Porrozzi R, Santos da Costa MV, Teva A, Falqueto A, Ferreira AL, Santos CD et al. Comparative evaluation of enzyme-linked immunosorbent assays based on crude and recombinant leishmanial antigens for serodiagnosis of symptomatic and asymptomatic Leishmania infantum visceral infections in dogs. Clin. Vaccine Immunol. 2007; 14(5):544-8. doi: doi.org/10.1128/CVI.00420-06.

Vernal S, Casal Y, Vieira LT, Amato VS, Duarte MIS, Nastri ACSS. Tegumentary leishmaniasis mimicking visceralization in a cirrhotic patient: atypical cutaneous lesions and local immunological features. Rev Soc Bras Med Trop. 2020; 53:e20190380. doi: 10.1590/0037-8682-0380-2019

Reimão JQ, Coser EM, Lee MR, Coelho AC. Laboratory diagnosis of cutaneous and visceral leishmaniasis: current and future methods. Microorganisms. 2020; 8:1632; doi: 10.3390/microorganisms8111632.

Carvalho FLN, Ribold EO, Bello GL, Ramos RR, Barcelos RB, Gehlen M et al. Canine visceral leishmaniasis diagnosis: a comparative performance of serological and molecular tests in symptomatic and asymptomatic dogs. Epidemiol Infect. 2018; 146(05):571-6. doi: doi.org/10.1017/S0950268818000225.

Fujimori M, de Almeida ABPF, Barrouin-Melo SM, Cortez LRPB, Duthie MS, Hiramoto RM et al. Validation of ELISA with recombinant antigens in serological diagnosis of canine Leishmania infantum infection. Mem Inst Oswaldo Cruz. 2021; 116:e200428. doi: 10.1590/0074-02760200428.

Pessoa-e-Silva R, Vaitkevicius-Antão V, de Andrade TAS, Silva ACO, Oliveira GA, Trajano-Silva LAM et al. The diagnosis of canine visceral leishmaniasis in Brazil: Confronting old problems. Exp Parasitol. 2019; 199: 9-16. doi: doi.org/10.1016/j.exppara.2019.02.012.

Steverding D. The history of leishmaniasis. Parasit Vectors. 2017; 10:82. doi: 10.1186/s13071-017-2028-5.

Silva DA, Madeira MF, Teixeira AC, de Souza CM, Figueiredo FB. Laboratory tests performed on Leishmania seroreactive dogs euthanized by the leishmaniasis control program. Vet Parasitol. 2011; 179(2011):257-61. doi: 10.1016/j.vetpar.2011.01.048.

Madeira MF, Schubach AO, Schubach TMP, Serra CMB, Pereira SA, Figueiredo FB et al. Is Leishmania (Viannia) braziliensis preferentially restricted to the cutaneous lesions of naturally infected dogs? Parasitol Res. 2005; 97:73-6. doi: 10.1007/s00436-005-1374-y.

Dantas-Torres F, Miró G, Bowman DD, Gradoni L, Otranto D. Culling dogs for zoonotic visceral leishmaniasis control: the wind of change. Trends Parasitol. 2019; 35(2). doi: doi.org/10.1016/j.pt.2018.11.005.

Marcondem M, Biondo AW, Gomes AAD, Silva ARS, Vieira RFC, Camacho AA et al. Validation of a Leishmania infantum ELISA rapid test for serological diagnosis of Leishmania chagasi in dogs. Vet Parasitol. 2011; 175(2011):15-9. doi: doi.org/10.1016/j.vetpar.2010.09.036.

Abad LPM, Almeida CS, Mattos AAM, Mendonça ACP, Alves MJM, Pinheiro AC et al. Diagnostic accuracy of rKLO8 versus rK26 ELISAs for screening of canine visceral leishmaniasis. Acta Trop. 2016; 166:133-8. doi: doi.org/10.1016/j.actatropica.2016.11.021.

Fonseca THS, Faria AR, Leite HM, Silveira JAG, Carneira AM. Chemiluminescent ELISA with multi-epitope proteins to improve the diagnosis of canine visceral leishmaniasis. Vet J. 2019; 253:105387. doi: dx.doi.org/10.1016/j.tvjl.2019.105387.

Lima CS, Esteves S, Costa I, Brancal H, Lima C, Amorim C et al. Use of antigen combinations to address complex Leishmania-seropositivity patterns in dogs living in canine leishmaniosis endemic regions of Portugal. Microorganisms. 2018; 2022:10. doi: doi.org/10.3390/microorganisms10102018.

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Publicado

2024-01-29

Como Citar

1.
Estevam Pereira I, Esteves Oliveira E, Martins Moreira Elias C, Barbosa Reis A, Scott Duthie M, Teixeira HC. Efficiency of rLb6H recombinant protein from Leishmania (Viannia) braziliensis for the detection of canine visceral leishmaniasis: Efficacy of rLb6H in CVL diagnosis. HU Rev [Internet]. 29º de janeiro de 2024 [citado 29º de abril de 2024];49:1-8. Disponível em: https://periodicos.ufjf.br/index.php/hurevista/article/view/41177

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