Abstract: This study sought to investigate the presence of anti- spp. antibodies in georeferenced serum samples from equids across all regions of the state of Goiás, while also presenting variables that indicate risk factors for the circulation of rickettsiae, and evaluating the presence of rickettsial DNA in ticks collected from equids and the surrounding environment in the municipalities of Uruaçu and Porangatu, located in the northern region of the state. A total of 1156 equid serum samples provided by the Goiás Agricultural Defense Agency (Agrodefesa) were analyzed for antibodies against 4 antigens. Additionally, 39 blood samples were collected from equids during a 3-day field expedition in January 2024, alongside 938 ticks collected from both animals and the environment. In total, 297 adult ticks were randomly selected for molecular analysis and tested by qPCR targeting the rickettsial A gene. Positive samples were further analyzed using cPCR to target the A and A genes. Results revealed that 9.6% (111/1156) of the serum samples were seroreactive to at least one antigen. Among these, 36% had antibodies against , 18.9% against , 69.4% against , and 14.4% against . Furthermore, the possible antigen responsible for a homologous reaction was found in 3.6% of equids for , and in the same proportion for , while 23.4% of animals showed antibodies for , and none exhibited a homologous reaction to . Meanwhile, 28.2% of the serum samples collected during the field expedition had antibodies against , with 72.7% identifying as the antigen involved in the homologous reaction. In the logistic regression analysis, the variables of education level, altitude below 500 m, and presence of female mules demonstrated a positive effect on seropositivity. Ticks from animals were identified as sensu lato, , , and , while environmental ticks were identified as s.l., , and . In the qPCR assays, two specimens of s.l., one of , and one of amplified a fragment of the A gene. Of these, one s.l. specimen amplified a fragment of both the A and A genes, and one specimen amplified a fragment of the A gene through conventional PCR. Sequencing confirmed the detection of . These findings highlight the presence of anti- spp. antibodies in equid serum samples from all regions of the state of Goiás, emphasizing the important role of equids as sentinels for spp. To our knowledge, this study represents the largest effort to detect anti- spp. antibodies in equid serum samples in Brazil. Additionally, it is the first nationwide investigation of its kind conducted in collaboration with the Agricultural Defense Agency (Agrodefesa), serving as a significant example of the One Health approach.
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The research article outlines a study conducted to examine the presence and spread of anti-Rickettsia bacteria antibodies in equids across all regions of Goiás, Brazil. It also investigates risk factors for the bacteria’s circulation and evaluates the presence of Rickettsia DNA in ticks gathered from equids and their surrounding environment.
Research Methodology
The analysis involved 1156 equid serum samples provided by the Goiás Agricultural Defense Agency (Agrodefesa). They were analysed for antibodies against 4 Rickettsia antigens.
Over a 3-day field trip in January 2024, 39 blood samples were collected from equids and 938 ticks were taken from both the animals and the environment.
Out of the total ticks, 297 adult ticks were chosen at random for molecular analysis.
The ticks were then tested by qPCR that targeted the rickettsial A gene. Positive samples found were further analysed using cPCR to target the A and A genes.
Research Findings
Results showed that 9.6% of the serum samples were seroreactive to at least one Rickettsia antigen. The antigens presented varied reactions: 36% had antibodies against one antigen, 18.9% against another, 69.4% challenged one more and 14.4% reacted against the final antigen.
A homologous reaction was found in 3.6% of equids for the first two antigens, while 23.4% of animals showed antibodies for another antigen, and no samples exhibited a homologous reaction to the last antigen.
28.2% of the serum samples collected during the field trip had antibodies against one antigen, with 72.7% identifying it as the antigen involved in the homologous reaction.
The variables of education level, altitude below 500 m, and presence of female mules were identified as having a positive impact on seropositivity.
Different types of ticks were identified from animals as well as from the environment, some of which amplified a fragment of the A gene in the qPCR assays. Sequencing confirmed the detection of Rickettsia.
Significance of the Study
This study demonstrated the presence of anti-Rickettsia bacteria antibodies in equid serum samples from all regions of the state of Goiás, highlighting the vital role of equids as sentinels for Rickettsia spp.
To the researchers’ knowledge, this study represents the largest effort to detect anti-Rickettsia spp. antibodies in equid serum samples in Brazil. Furthermore, it is the first nationwide investigation of this kind conducted in partnership with the Agricultural Defense Agency (Agrodefesa), setting a significant precedent for the One Health approach.
Cite This Article
APA
Pádua GT, Tavares MA, de Lima NJ, Paula WVF, Dos Santos GC, Neves LC, Bittencourt RBM, Paludo RLDR, Cardoso ERN, da Silva BBF, Pádua BR, Borsanelli AC, Dantas-Torres F, Polo GP, Krawczak FDS.
(2025).
Spatial Distribution of Equid Exposure to Rickettsia spp. in Goiás State, Midwestern Brazil.
Pathogens, 14(5), 449.
https://doi.org/10.3390/pathogens14050449
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Tavares, Mariana Avelar
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
de Lima, Nicolas Jalowitzki
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Paula, Warley Vieira de Freitas
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Dos Santos, Gabriel Cândido
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Neves, Lucianne Cardoso
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Bittencourt, Raphaela Bueno Mendes
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Paludo, Raquel Loren Dos Reis
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Cardoso, Ennya Rafaella Neves
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
da Silva, Bianca Barbara Fonseca
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Pádua, Bruno Rodrigues de
Agência Goiana de Defesa Agropecuária, Goiânia 74620-030, Brazil.
Borsanelli, Ana Carolina
Laboratório de Doenças Infecciosas e Bacteriologia-LADIB, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
Dantas-Torres, Filipe
Departamento de Imunologia, Centro de Pesquisa Aggeu Magalhães, Fundação Oswaldo Cruz, Recife 50670-420, Brazil.
Polo, Gina Paola
Instituto de Salud Pública, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Krawczak, Felipe da Silva
Laboratório de Doenças Parasitárias-LADOPAR, Setor de Medicina Veterinária Preventiva, Escola de Veterinária e Zootecnica, Universidade Federal de Goiás-UFG, Goiânia 74690-900, Brazil.
MeSH Terms
Animals
Rickettsia / immunology
Rickettsia / genetics
Rickettsia / isolation & purification
Rickettsia Infections / veterinary
Rickettsia Infections / epidemiology
Rickettsia Infections / microbiology
Brazil / epidemiology
Antibodies, Bacterial / blood
Horses
Horse Diseases / epidemiology
Horse Diseases / microbiology
Antigens, Bacterial / immunology
DNA, Bacterial / genetics
Seroepidemiologic Studies
Equidae / microbiology
Female
Ticks / microbiology
Male
Grant Funding
Process Number: 317557/2021-1. / CNPq:
001 / Coordenau00e7u00e3o de Aperfeiu00e7oamento de Pessoal de Nu00edvel Superior, Brazil (CAPES)
Conflict of Interest Statement
The authors declare no conflicts of interest.
References
This article includes 52 references
El Karkouri K, Ghigo E, Raoult D, Fournier P-E. Genomic evolution and adaptation of arthropod-associated Rickettsia. Sci. Rep. 2022;12:3807.
Merhej V, Angelakis E, Socolovschi C, Raoult D. Genotyping, evolution and epidemiological findings of Rickettsia species. Infect. Genet. Evol. 2014;25:122–137.
Souza ZÊS, Moraes BV, Krawczak FS, Zulzke L, Carvalho TV, Sousa AO, Agopian RG, Marcili A, Labruna MB, Moraes-Filho J. Detection of anti-Rickettsia rickettsii antibodies in dogs living in a neglected área in São Paulo, SP, Brazil. Arq. Bras. Med. Vet. Zootec. 2020;72:2141–2147.
Richardson EA, Roe RM, Apperson CS, Ponnusamy L. Rickettsia amblyommatis in ticks: A review of distribution, pathogenicity, and diversity. Microorganisms 2023;11:493.
Halliday JEB, Meredith AL, Knobel DL, Shaw DJ, Bronsvoort BMC, Cleaveland S. A framework for evaluating animals as sentinels for infectious disease surveillance. J. R. Soc. Interface. 2007;4:973–984.
Ministério da Saúde Casos confirmados e óbitos por Febre Maculosa. Brasil, Grandes Regiões e Unidades Federadas (infecção) 2007–2025. Sistema de Informação de Agravos de Notificação, Brazil. [(accessed on 13 February 2025)];2025 Available online: https://www.gov.br/saude/pt-br/assuntos/saude-de-a-a-z/f/febre-maculosa/situacao-epidemiologica.
Paula LGF, Zeringóta V, Sampaio ALN, Bezerra GP, Barreto ALG, Santos AA, Miranda VC, Paula WVF, Neves LCN, Secchis MV. Seasonal dynamics of Amblyomma sculptum in two areas of the Cerrado biome midwestern Brazil, where human cases of rickettsiosis have been reported. Exp. Appl. Acarol. 2021;84:215–225.
Françoso RD, Brandão R, Nogueira CC, Salmona YB, Machado RB, Colli GR. Habitat loss and the effectiveness of protected areas in the Cerrado biodiversity hotspot. Nat. Conserv. 2015;13:35–40.
Horta MC, Labruna MB, Sangioni LA, Vianna MCB, Gennari MS, Galvão MAM. Prevalence of antibodies to spotted fever group rickettsiae in humans and domestic animals in a Brazilian spotted fever endemic area in the state of S.o Paulo, Brazil: Serological evidence for infection by Rickettsia rickettsii and another spotted fever groups Rickettsia. Am. J. Trop. Med. Hyg. 2004;71:93–97.
Labruna MB, Horta MC, Aguiar DM, Cavalcante GT, Pinter A, Gennari SM, Camargo CMA. Prevalence of Rickettsia infection in dogs from the urban and rural areas of Monte Negro municipality, western Amazon, Brazil. Vector Borne Zoonotic Dis. 2007;7:249–255.
Barbieri ARM, Filho JM, Nieri-Bastos FA, Souza JC, Szabó MPJ, Labruna MB. Epidemiology of Rickettsia sp. strain Atlantic rainforest in a spotted fever endemic area of southern Brazil. Ticks Tick-Borne Dis. 2014;5:848–853.
Szabó MPJ, Nieri-Bastos FA, Spolidorio MG, Martins TF, Barbieri AM, Labruna MB. In vitro isolation from Amblyomma ovale (Acari: Ixodidae) and ecologiacal aspects of the Atlantic rainforest Rickettsia, the causative agent of a new spotted fever rickettsiosis in Brazil. Parasitology 2013;140:719–728.
R core team. R: A Language and Environment for Statistical Computing. 2022.
Terassini FA, Barbieri FS, Albuquerque S, Szabó MPJ, Camargo LMA, Labruna MM. Comparison of two methods for collecting free-living ticks in the Amazonian Forest. Ticks Tick-Borne Dis. 2010;1:194–196.
Barros-Battesti DM, Arzua M, Bechara GH. Carrapatos de Importância Médico-Veterinária da Região Neotropical: Um Guia Ilustrado para Identificacão de Espécies. Vox/ICTTD-3,/Butantan; São Paulo, Brazil: 2006. p. 223.
Martins TF, Onofrio VC, Barros-Battesti DM, Labruna MB. Nymphs of the genus Amblyomma (Acari: Ixodidae) of Brazil: Descriptions, redescriptions, and identification Key. Ticks Tick-Borne Dis. 2010;1:75–99.
Martins TF, Barbieri ARM, Costa FB, Terassini FA, Camargo LMA, Peterka CRL, Pacheco RdC, Dias RA, Nunes PH, Marcili A. Geographical distribution of Amblyomma cajennense (sensu lato) ticks (Parasitiformes: Ixodidae) in Brazil, with description of the nymph of A. cajennense (sensu stricto). Parasites Vectors 2016;9:186.
Nava S, Beati L, Labruna MB, Cáceres AG, Mangold AJ, Guglielmone AA. Reassessment of the taxonomic status of Amblyomma cajennense (Fabricius, 1787) with the description of three new species, Amblyomma tonelliae n. sp., Amblyomma interandinum n. sp. and Amblyomma patinoi n. sp., and reinstatement of Amblyomma mixtum Koch, 1. Ticks Tick-Borne Dis. 2014;5:252–276.
Clifford CM, Anastos G, Elbl A. The Larval Ixodid Ticks of the Eastern United States (Acarina-Ixodidae) Volume 2. Publications of the Entomological Society of America 1961;pp. 213–237.
Labruna MB, Whitworth T, Horta MC, Bouyer DH, Mcbride JW, Pinter A, Popov V, Gennari SM, Walker DH. Rickettsia species infecting Amblyomma cooperi Ticks from an area in the state of São Paulo Brazil, where Brazilian spotted fever is endemic. J. Clin. Microbiol. 2004;42:90–98.
Guedes E, Leite RC, Prata MCA, Pacheco RC, Walker DH, Labruna MB. Detection of Rickettsia rickettsii in the tick Amblyomma cajennense in a new Brazilian spotted fever endemic area in the state of Minas Gerais. Mem. Inst. Oswaldo Cruz 2005;100:841–845.
Regnery RL, Spruil CL, Plikaytis BD. Genotipic identification of rickettsiae and estimation of intraspecific sequences divergence for portion of two Rickettsial gene. J. Bacteriol. 1991;173:1576–1589.
Mangold AJ, Bargues MD, Mas-Coma S. Mitochondrial 16S rDNA sequences and phylogenetic relationships of species of Rhipicephalus and other tick genera among Metastriata (Acari: Ixodidae). Parasitol. Res. 1998;84:478–484.
Neves LC, Paula WVF, de Paula LGF, Silva BBF, Dias SA, Pereira BG, Silva BSA, Sevá AP, Dantas-Torres F, Labruna MB. Detection of Rickettsia spp. in animals and ticks in midwestern Brazil, where human cases of rickettsiosis were reported. Animals 2023;13:1288.
Amorin Filho EF, Costa FB, Moraes-Filho J, Santos ACG, Vale TL, Costa AP, Silva AB, Labruna MB, Nogueira RMS. Exposure of Baixadeiro horses to Rickettsia spp. and to ticks infected by Rickettsia amblyommatis in the Baixada Maranhense micro-region, Maranhão, Brazil. Ciência Rural 2018;48:e20180002.
Neves LC, Barreto ALG, Souza MX, Martins DB, Barbieri ARM, Serpa MCA, Muñoz-Leal S, Labruna MB, Krawczak FS. Serosurvey on rickettsiae of the spotted fever group and Rickettsia bellii among dogs in the state of Goiás, Brazil. Braz. J. Vet. Parasitol. 2020;29:e021419.
Paludo RLdR, Paula WVdF, Neves LC, de Paula LGF, de Lima NJ, da Silva BBF, Pereira BG, Padua GT, Dantas-Torres F, Labruna MB. Rickettsial infection in ticks from a National Park in the Cerrado biome, midwestern Brazil. Pathogens 2024;13:13.
de Lima NJ, Pádua GT, Cardoso ER, Bittencourt RBM, Tavares MA, Paula WVdF, Neves LC, Segovia CD, Santos GC, Serpa MCdA. Serological and molecular survey of rickettsial agents in wild boars (Sus. scrofa) from Midwestern Brazil. Animals 2024;14:2224.
Costa FB, da Costa AP, Moraes-Filho J, Martins TF, Soares HS, Ramirez DG, Dias RA, Labruna MB. Rickettsia amblyommatis infecting ticks and exposure of domestic dogs to Rickettsia spp. in na Amazon-Cerrado transition region of northeastern Brazil. PLoS ONE 2017;12:e0179163.
Karpathy SE, Slater KS, Goldsmith CS, Nicholson WL, Paddock CD. Rickettsia amblyommatis sp. Nov., a spotted fever group Rickettsia associated with multiple species of Amblyomma ticks in North, Central and South America. Int. J. Syst. Evol. Microbiol. 2016;66:5236–5243.
Han H, Guo X, Yu H. Variable selection using mean decrease accuracy and mean decrease gini based on random forest. Proceedings of the 2016 7th IEEE International Conference on Software Engineering and Service Science (ICSESS); Beijing, China. 26–28 August 2016; pp. 219–224.
Nicodemus KK. On the stability and ranking of predictors from random forest variable importance measures. Brief. Bioinform. 2011;12:369–373.