Abstract
Rickettsia rickettsii is the etiological agent of Rocky Mountain spotted fever, which is an important tick-borne zoonosis and, in Brazil, it causes Brazilian spotted fever, which has high lethality rate. This study aimed to evaluate a synthetic peptide corresponding to a segment of the outer membrane protein A (OmpA) as an antigen in a serological test for the diagnosis of rickettsial infections. The amino acid sequence of the peptide was selected by predicting B cell epitopes using B Cell Epitope Prediction (Immune Epitope Database and Analysis Resource) and Epitopia and OmpA sequences of Rickettsia rickettsii strain ‘Brazil’ and Rickettsia parkeri strains ‘Maculatum 20’ and ‘Portsmouth’. A peptide with amino acid sequence common to both Rickettsia species was synthesized and arbitrarily named OmpA-pLMC. To evaluate this peptide in enzyme-linked immunosorbent assay (ELISA), serum samples of capybara (Hydrochoerus hydrochaeris), horse (Equus caballus), and opossum (Didelphis albiventris) that had been previously tested by indirect immunofluorescence assay (IFA) for rickettsial infection were separated into IFA-positive and IFA-negative groups and used in the assay. There were no significant differences in ELISA optical density (OD) values between IFA-positive and IFA-negative groups with horse samples. The mean OD values were significantly higher in the IFA-positive capybara serum samples (IFA-pos vs. IFA-neg = 2.389 ± 0.761 vs. 1.760 ± 0.840). However, receiver operating characteristic (ROC) curve analysis did not show significant diagnostic parameters. On the other hand, 12 out of 14 (85.7%) opossum samples of the IFA-positive group showed reactivity in ELISA, and this was significantly higher than of the IFA-negative group (0.7196 ± 0.440 vs. 0.2318 ± 0.098, respectively; 85.7% sensitivity, 100% specificity). Therefore, our results show that OmpA-pLMC has a potential to be used in immunodiagnostic assays to detect spotted fever group rickettsial infections.
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Acknowledgements
We would like to thank Prof. Dr. Luis Ricardo Goulart Filho, Universidade Federal de Uberlândia, for allowing the use of the Peptide Synthesizer.
Funding
This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nívedl Superior—Brasil (CAPES)—Finance Code 001, by Conselho Nacional de Desenvolvimento Científico e Tecnológico—CNPq (Grant 445490/ 2014-4 and Academic Career Research Fellowship to M.P.J. Szabó) and Fundação de Amparo à Pesquisa do Estado de Minas Gerais—FAPEMIG (Grant PPM 0191-16).
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APMM: Methodology, investigation, methodology, validation, formal analysis, writing—original draft, visualization. GT-P: Resources, investigation. RBKV: Resources, investigation. MGP: Methodology, investigation. VSR: Resources, investigation. HTG: Methodology, statistical analysis, writing. CCNM: Methodology, resources, investigation. NCC: Resources. MJPS: Resources. JY: Conceptualization, methodology, validation, writing—review and editing, visualization, supervision, project administration, funding acquisition.
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Muniz, A.P.M., Tolesano-Pascoli, G., Vieira, R.B.K. et al. Evaluation of a mimotope of the Rickettsia outer membrane protein A (OmpA) as an antigen in enzyme-linked immunosorbent assay to detect rickettsiosis in capybaras (Hydrochoerus hydrochaeris), horses (Equus caballus), and opossums (Didelphis sp.). Exp Appl Acarol 89, 317–327 (2023). https://doi.org/10.1007/s10493-023-00776-5
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DOI: https://doi.org/10.1007/s10493-023-00776-5