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Volume 27, Number 1—January 2021
Research Letter

Relapsing Fever Group Borreliae in Human-Biting Soft Ticks, Brazil

Sebastián Muñoz-Leal1Comments to Author , Álvaro A. Faccini-Martínez, Bruno M. Teixeira, Maria Marlene Martins, Maria Carolina A. Serpa, Glauber M.B. Oliveira, Felipe R. Jorge, Richard C. Pacheco, Francisco B. Costa, Hermes R. Luz, and Marcelo B. Labruna
Author affiliations: Universidade de São Paulo, São Paulo, Brazil (S. Muñoz-Leal, M.C.A. Serpa, G.M.B. Oliveira, M.B. Labruna); Asociación Colombiana de Infectología, Bogotá, Colombia (Á.A. Faccini-Martínez); Centro Universitario INTA–UNINTA, Sobral, Brazil (B.M. Teixeira, F.R. Jorge); Universidade Federal de Uberlândia, Uberlândia, Brazil (M.M. Martins); Universidade Federal de Mato Grosso, Cuiabá, Brazil (R.C. Pacheco); Universidade Estadual do Maranhão, São Luís, Brazil (F.B. Costa); Universidade Federal do Maranhão, São Luís (H.R. Luz)

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Abstract

We conducted a molecular survey for Borrelia spp. in Ornithodoros ticks previously reported as biting humans. We collected specimens in natural ecosystems and inside human dwellings in 6 states in Brazil. Phylogenetic analyses unveiled the occurrence of 4 putatively new species of relapsing fever group borreliae.

Tick-borne relapsing fever (TBRF) is a vectorborne disease caused by spirochetes of the genus Borrelia that thrive in enzootic cycles and are transmitted mainly by soft ticks of the genus Ornithodoros (1). Humans bitten by infected ticks can become ill and present a typical recurrent febrile syndrome (1). In the New World, research on TBRF persists mainly in North America, where Borrelia turicatae, B. parkeri, and B. hermsii infect humans (1). Meanwhile, the knowledge on relapsing fever spirochetes in South America has remained comparatively incomplete. In Brazil, Ornithodoros brasiliensis, O. fonsecai, O. mimon, O. rietcorreai, and O. rostratus ticks have been reported to parasitize humans (2,3), yet their role as vectors of Borrelia spp. is unknown. Recently, in Brazil, B. venezuelensis, the agent of South American TBRF during the first half of the 20th century, was isolated from the anthropophilic tick O. rudis (4). This finding highlighted the occurrence of pathogenic relapsing fever group borreliae (RFGB) and called attention to study human-biting Ornithodoros ticks as possible vectors of these microorganisms.

During December 2018–October 2019, we conducted collections of soft ticks in the Brazilian states of Ceará (CE), Goiás (GO), Mato Grosso (MT), Mato Grosso do Sul (MS), Maranhão (MA), and Rondônia (RO) (Appendix Figure). Collections in MS were implemented using dry ice as an attractor; in CE, GO, MA, and RO, we collected soft ticks inside caves, abandoned nests or between rocks in rural areas. In MT, specimens were collected on the walls of an inhabited house in an urban area. Collections of ticks were authorized by Instituto Chico Mendes de Conservação da Biodiversidade (ICMBio permits 65137-1 and 36413-1).

A total of 665 specimens (236 males, 145 females, 284 nymphs) belonging to 8 species of the genus Ornithodoros were submitted to individual or pooled DNA extractions (Appendix Table 1). We screened extractions with a Borrelia-specific real-time PCR with primers Bor16S3F and Bor16S3R and probe Bor16S3P, using 2 μL of genomic DNA, to amplify a fragment of the 16S rRNA gene (5). Samples with cycle threshold values <32 were tested with a battery of PCRs targeting the 16S rRNA and the flab and glpQ borrelial genes.

Figure

Bayesian phylogenetic trees inferred for the Borrelia spp. characterized in study of relapsing fever group borreliae in human-biting soft ticks, Brazil. A) Ambiguous alignments of single 16S rRNA gene (1,274 bp); B) concatenated 16S rRNA-flaB-glpQ genes (2,435 bp). Bold indicates borreliae from this study. Trees are drawn to scale. Four independent Markov chain runs for 1,000,000 metropolis-coupled MCMC generations were implemented for the analyses, sampling a tree every 100th generation. The first 25% of the trees represented burn-in, and the remaining trees were used to calculate Bayesian posterior probability values. Both trees were inferred using the Hasegawa-Kishino-Yano model with gamma distribution. Numbers above or below tree branches represent Bayesian posterior probabilities. Light yellow and gray backgrounds denote Old World and New World relapsing fever group Borrelia spp., respectively. Scale bar indicates nucleotide substitutions per site.

Figure. Bayesian phylogenetic trees inferred for the Borreliaspp. characterized in study of relapsing fever group borreliae in human-biting soft ticks, Brazil. A) Ambiguous alignments of single 16S rRNA gene...

Four species of ticks were positive by Borrelia- specific real-time PCR. We generated sequences of Borrelia 16S rRNA, flaB, and glpQ genes for these specimens (Appendix Table 1). Two haplotypes of 16S rRNA gene were sequenced from each of the 2 positive O. mimon ticks, and the obtained sequences of flaB and glpQ were identical for both specimens. One haplotype for each gene was obtained for O. hasei and the Ornithodoros sp. ticks from CE, and only a 16S rDNA sequence was obtained from O. rietcorreai ticks (Appendix Table 2). With high support values, Bayesian phylogenetic analyses showed that the Borrelia spp. characterized from O. mimon, O. rietcorreai, and the Ornithodoros sp. ticks from CE form a monophyletic clade related to RFGB occurring in the Old World. In turn, the Borrelia sp. harbored by O. hasei ticks clustered within New World RFGB (Figure). These results add further evidence that Old and New World RFGB do not necessarily have defined geographic distributions but rather correspond to arbitrary groups.

Five species of Ornithodoros ticks have been reported to parasitize humans in Brazil (2,3). We have added 2 more species to this list, as O. hasei and the Ornithodoros sp. ticks from CE avidly bit us during collections in the field (data not shown). Although with low prevalence, these 2 species, together with O. mimon and O. rietocorreai, harbored DNA of putatively new Borrelia spp. phylogenetically related to the relapsing fever group. The implications of these new spirochetes as human pathogens are still unknown. O. mimon and O. rietcorreai ticks are associated with human parasitism in urban and rural dwellings in Brazil (2,3), so vector roles of both species should not be overlooked.

TBRF courses with febrile episodes and should be considered as a differential diagnosis within the spectrum of diseases that cause an undifferentiated febrile syndrome (UFS) (6). Although specific data are vague for the states where tick collections were performed in this study, UFS is common in Brazil; mosquitoborne viruses and malaria are the main etiologic agents (7,8). Nevertheless, febrile illnesses still remain underdiagnosed in a substantial proportion of the cases in the country (7,8). The results of this study are a contribution to the knowledge of RFGB in human-biting Ornithodoros ticks, and stress the investigation of TBRF as a possible cause of UFS in Brazil. It is known that antibodies of patients exposed to RFGB infection cross-react in serologic tests for the diagnosis of Lyme borreliosis (9). This cross-reactivity is particularly relevant in Brazil because serologic evidence for an alleged Lyme-like disease in humans has been reiteratively published, yet refuted (10), and TBRF has not yet been considered as a possible cause of such disease.

Dr. Muñoz-Leal is a veterinarian affiliated with Universidad de Concepción, Chillán, Chile, who specializes in tickborne diseases. His research is focused on soft ticks and tickborne relapsing fever in South America.

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Acknowledgments

We thank Gilson Miranda from Serra das Almas Natural Reserve for his assistance during our visit to this location; Jerônimo Carvalho Martins from Jericoacoara National Park for gently allowing us the use of their facilities at Jericoacoara village; and Adriane Suzin, Ana Carolina Souza, Flavio A. Terassini, Ivaneide N. Costa, Luís Marcelo A. Camargo, Romilson S. Lopes Jr., Simone D. Tojal, and Vinicius S. Rodrigues for their valuable assistance in field work.

Laboratory work was funded by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq, grant no. 09262/2018-8). S.M.L. was funded by FAPESP (grant nos. 2018/02521-1 and 2019/17960-3).

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References

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Cite This Article

DOI: 10.3201/eid2701.200349

Original Publication Date: December 17, 2020

1Current affiliation: Universidad de Concepción, Chillán, Ñuble, Chile.

Table of Contents – Volume 27, Number 1—January 2021

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Sebastián Muñoz-Leal, Departamento de Patología y Medicina Preventiva, Facultad de Ciencias Veterinarias, Universidad de Concepción, Av. Vicente Méndez 595–Casilla 537, Chillán–Región de Ñuble, Chile

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