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Post mortem protozoan hemoparasites detection in wild mammals from Mato Grosso state, Midwestern Brazil

Detecção post mortem de hemoparasitas protozoários em mamíferos selvagens do estado de Mato Grosso, Centro-Oeste do Brasil

Abstract

To a better insight into the epidemiology and genetic diversity of protozoan hemoparasites infections in wild mammals, this study aimed to the post mortem detection of DNA from species of the order Piroplasmida (Babesia sp., Cytauxzoon sp., and Theileria sp.) and suborder Adelorina (Hepatozoon sp.) using polymerase chain reaction based on the 18S rRNA gene followed by genetic sequencing of blood and spleen samples collected from carcasses of 164 free-ranging and captive wild mammals from Mato Grosso state. Among them, one Leopardus pardalis, three Panthera onca, two Puma concolor were positive for Cytauxzoon sp., and six Tapirus terrestris tested positive for Piroplasmida, while one L. pardalis was positive for Hepatozoon sp. Furthermore, an uncharacterized piroplasmid genetically related to Theileria sp. previously detected in cats from Brazil was described in lowland tapirs. Despite the controversy regarding the epidemiological threat of these protozoa, the detection of these tick-borne agents in wild free-living and captive mammals, even when asymptomatic, demonstrates the importance of monitoring, particularly in hotspots such as the state of Mato Grosso, to verify the circulation and genetic diversity, to anticipate the possible emergence of diseases, and even their consequences to other animals as well as humans.

Keywords:
Cytauxzoon sp.; Hepatozoon sp.; Theileria sp.; PCR

Resumo

Para uma melhor compreensão da epidemiologia e diversidade genética das infecções por hemoprotozoários em mamíferos selvagens, este estudo teve como objetivo a detecção post mortem de DNA de espécies da ordem Piroplasmida (Babesia sp., Cytauxzoon sp. e Theileria sp.) e subordem Adelorina (Hepatozoon sp.), utilizando-se a reação em cadeia pela polimerase, baseada no gene 18S rRNA, seguido de sequenciamento genético de amostras de sangue e baço, coletadas de 164 carcaças de mamíferos selvagens de vida livre e cativos do estado de Mato Grosso. Entre eles, um Leopardus pardalis, três Panthera onca, dois Puma concolor foram positivos para Cytauxzoon sp., e seis Tapirus terrestris testaram positivos para Piroplasmida, enquanto um L. pardalis foi positivo para Hepatozoon sp. Além disso, foi descrito em antas, um piroplasmídeo não caracterizado geneticamente, relacionado à Theileria sp., previamente detectado em gatos do Brasil. Apesar da controvérsia quanto à ameaça epidemiológica desses protozoários, a detecção desses agentes em mamíferos silvestres e cativos, mesmo quando assintomáticos, demonstra a importância do monitoramento, principalmente em hotspots, como no estado de Mato Grosso, para verificar a circulação e a diversidade genética, a fim de antecipar o possível surgimento de doenças e, até mesmo, suas consequências para outros animais, bem como os humanos.

Palavras-chave:
Cytauxzoon sp.; Hepatozoon sp.; Theileria sp.; PCR

Living beings interact, and these interactions are the result of natural selection and the activities of evolution. Among these relationships, parasitism is one of the most successful, and one of the main factors responsible for modulating communities (Timi & Poulin, 2020Timi JT, Poulin R. Why ignoring parasites in fish ecology is a mistake. Int J Parasitol 2020; 50(10-11): 755-761. http://dx.doi.org/10.1016/j.ijpara.2020.04.007. PMid:32592807.
http://dx.doi.org/10.1016/j.ijpara.2020....
) and reducing host fitness in various ways. Significant environmental changes and consequent increases in the interaction between domestic and wild animals (André et al., 2015André MR, Herrera HM, Fernandes SJ, deSousa KCM, Gonçalves LR, Domingos IH, et al. Tick-borne agents in domesticated and stray cats from the city of Campo Grande, state of Mato Grosso do Sul, Midwestern Brazil. Ticks Tick Borne Dis 2015; 6(6): 779-786. http://dx.doi.org/10.1016/j.ttbdis.2015.07.004. PMid:26187416.
http://dx.doi.org/10.1016/j.ttbdis.2015....
) can increase the emergence of new diseases in new hosts. Molecular studies of hemoparasite genera belonging to the Apicomplexa have demonstrated the wide distribution and variety of hosts and vectors (Wang et al., 2017Wang JL, Li TT, Liu GH, Zhu XQ, Yao C. Two tales of Cytauxzoon felis infections in domestic cats. Clin Microbiol Rev 2017; 30(4): 861-885. http://dx.doi.org/10.1128/CMR.00010-17. PMid:28637681.
http://dx.doi.org/10.1128/CMR.00010-17...
; van As et al., 2020van As M, Netherlands EC, Smit NJ. Molecular characterization and morphological description of two new species of Hepatozoon Miller, 1908 (Apicomplexa: Adeleorina: Hepatozoidae) infecting leukocytes of African leopards Panthera pardus pardus (L.). Parasit Vectors 2020; 13(1): 222. http://dx.doi.org/10.1186/s13071-020-3933-6. PMid:32357916.
http://dx.doi.org/10.1186/s13071-020-393...
), however, much remains to be elucidated.

Considering the expanse of Brazil and the great biodiversity of mammals in the state of Mato Grosso, there are currently few studies on apicomplexan protozoans and their relationship with large wild mammals in this region (André et al., 2010André MR, Adania CH, Teixeira RHF, Vargas GH, Falcade M, Sousa L, et al. Molecular detection of Hepatozoon spp. in Brazilian and exotic wild carnivores. Vet Parasitol 2010; 173(1-2): 134-138. http://dx.doi.org/10.1016/j.vetpar.2010.06.014. PMid:20630658.
http://dx.doi.org/10.1016/j.vetpar.2010....
; Furtado et al., 2017bFurtado MM, Taniwaki SA, Metzger B, dos Santos Paduan K, O’Dwyer LH, Jácomo ATA, et al. Is the free-ranging jaguar (Panthera onca) a reservoir for Cytauxzoon felis in Brazil? Ticks Tick Borne Dis 2017b; 8(4): 470-476. http://dx.doi.org/10.1016/j.ttbdis.2017.02.005. PMid:28196774.
http://dx.doi.org/10.1016/j.ttbdis.2017....
). Therefore, polymerase chain reaction (PCR)-based methods were used to investigate the diversity and occurrence of the apicomplexan parasites Babesia, Cytauxzoon, Hepatozoon, and Theileria in blood and spleen samples collected from carcasses of wild mammals in the state of Mato Grosso, Brazil.

From December 2019 to July 2021, tissue samples (blood and spleen) were collected from carcasses of road-killed free-roaming and captive wild animals from six municipalities in the State of Mato Grosso, Brazil, attended at Veterinary Hospital and sent for routine necropsy at the Veterinary Pathology sector of the Federal University of Mato Grosso, located in the Cuiabá municipality, as depicted in Table 1 and shown in Figure 1.

Table 1
Molecular detection by polymerase chain reaction (PCR) of Piroplasmida (genera Babesia, Cytauxzoon, and Theileria) and Hepatozoon spp. in blood (B) and spleen (S) samples of free living (FL) and captive (C) wild mammals from Mato Grosso state, Brazil, during 2019-2021.
Figure 1
Map of the municipalities within the State of Mato Grosso, Brazil, where blood and tissue samples (spleen) of wild mammals were collected for molecular detection by polymerase chain reaction (PCR) of Piroplasmida (genera Babesia, Cytauxzoon, and Theileria) and Hepatozoon spp., during 2019–2021. 1. Barão de Melgaço; 2. Cáceres; 3. Chapada dos Guimarães; 4. Cuiabá; 5. Nova Xavantina; 6. Poconé.

Procedures in this study were previously approved by the Ethics Committee on Animal Research of the Federal University of Mato Grosso (CEUA protocol no. 23108.015878/2019-65) and “Instituto Chico Mendes de Conservação da Biodiversidade” (ICMBio permit no. 55104-1).

DNA extraction from blood and tissue samples (spleen) was performed using the DNA extraction PureLink™ Genomic DNA Mini Kit (Thermo Fisher Scientific, Waltham, MA, USA), according to the manufacturer’s instructions. To verify the success of extraction, an initial PCR targeting a fragment of the mammalian glyceraldehyde-3-phosphate dehydrogenase (gapdh) gene was performed as previously described (Birkenheuer et al., 2003Birkenheuer AJ, Levy MG, Breitschwerdt EB. Development and evaluation of a seminested PCR for detection and differentiation of Babesia gibsoni (Asian genotype) and B. canis DNA in canine blood samples. J Clin Microbiol 2003; 41(9): 4172-4177. http://dx.doi.org/10.1128/JCM.41.9.4172-4177.2003. PMid:12958243.
http://dx.doi.org/10.1128/JCM.41.9.4172-...
). Extracted DNA samples were then subjected to further PCR assays to amplify fragments of the small ribosomal DNA subunit 18S of Piroplasmida members (Babesia sp., Cytauxzoon sp., and Theileria sp.) and Hepatozoon spp. Negative controls (nuclease-free water) and appropriate positive controls for each PCR assay were included, as follows: Babesia caballi (GenBank accession number MG906574) and Hepatozoon canis (GenBank accession number MG496257) from blood of naturally infected horse and dog, respectively. DNA samples were subjected to nested PCR (nPCR) to amplify a fragment (~800 base pairs - bp) gene for Piroplasmida (Babesia sp., Cytauxzoon sp., and Theileria sp.), as previously described (Jefferies et al., 2007Jefferies R, Ryan UM, Irwin PJ. PCR–RFLP for the detection and differentiation of the canine piroplasm species and its use with filter paper-based technologies. Vet Parasitol 2007; 144(1-2): 20-7. https://doi.org/10.1016/j.vetpar.2006.09.022.
https://doi.org/10.1016/j.vetpar.2006.09...
). Furthermore, biological samples were screened using a previously described conventional PCR (cPCR) protocol (Ujvari et al., 2004Ujvari B, Madsen T, Olsson M. High prevalence of Hepatozoon spp. (Apicomplexa, Hepatozoidae) infection in water pythons (Liasis fuscus) from tropical Australia. J Parasitol 2004; 90(3): 670-672. http://dx.doi.org/10.1645/GE-204R. PMid:15270125.
http://dx.doi.org/10.1645/GE-204R...
) by targeting a fragment (~600 bp) of the 18S rDNA region of the Hepatozoon spp. The PCR products were resolved on 1.5% agarose gels stained with GelRed™ Nucleic Acid Gel Stain (Biotium Inc, Fremont, CA, USA) and visualized using a ChemiDoc XRS system (Bio-Rad, Hercules, CA, USA). Amplicons of the expected sizes were purified using the Illustra GFX PCR DNA and Gel Band Purification Kit (GE Healthcare Life Sciences, Pittsburgh, PA, USA) and prepared for sequencing according to the instructions provided in the BigDye™ kit (Applied Biosystems, Foster, CA, USA). An ABI PRISM 3500 Genetic Analyzer (ABI DNA Model 3500 Series Genetic Analyzer, Applied Biosystems, Inc., Foster City, CA, USA) was employed to conduct the sequencing procedures using the same primers used for the PCR. The obtained sequences were then subjected to BLAST analyses to determine the closest identities by comparison to organisms available in GenBank.

Sequences of the 18S rRNA gene generated in this study and homologue sequences retrieved from GenBank were used to construct alignments for Theileria spp. representatives. The selected sequences were aligned using Clustal X (Thompson et al., 1997Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997; 25(24): 4876-4882. http://dx.doi.org/10.1093/nar/25.24.4876. PMid:9396791.
http://dx.doi.org/10.1093/nar/25.24.4876...
), and manually adjusted with GeneDoc (Nicholas et al., 1997Nicholas KB, Nicholas HB, Deerfield DW. GeneDoc: analysis and visualization of genetic variation. Embnew News 1997; 4: 14.). Two phylogenetic inferences were performed for alignment. Inferences by maximum parsimony were constructed according to their implementation in PAUP version 4.0b10 (Swofford, 2002Swofford DL. PAUP: Phylogenetic analysis using parsimony. Beta Version 4.0b10. Sunderland: Sinauer and Associates; 2002.), using a heuristic search with 1000 replicates, 500 bootstrap replicates, random stepwise addition starting trees (with random addition sequences), and tree bisection and reconnection (TBR) branch swapping. MrBayes v3.1.2 was used to perform Bayesian analyses (Huelsenbeck & Ronquist, 2001Huelsenbeck JP, Ronquist F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 2001; 17(8): 754-755. https://doi.org/10.1093/bioinformatics/17.8.754.
https://doi.org/10.1093/bioinformatics/1...
) with four independent Markov chain runs for 1,000,000 metropolis-coupled MCMC generations, sampling a tree every 100th generations. The first 25% of trees represented burn-in, and the remaining trees were used to calculate the Bayesian posterior probability. GTR+I+G was the standard model used in MrBayes software. The tree was rooted in Toxoplasma gondii as an out-group. GenBank accession numbers for all sequences used for the phylogenetic analyses were embedded in each tree.

A total of 159 blood and 160 spleen samples from 164 specimens of wild mammals belonging to at least 31 different species were subjected to DNA extraction. DNA from all samples tested for gapdh internal control amplified the predicted product. Table 1 provides a list of all tested animals and the results of their molecular analyses grouped according to species, origin, and locality.

Amplicons for Piroplasmida were detected in four species of wild mammals (Leopardus pardalis, Panthera onca, Puma concolor, and Tapirus terrestris). Among the animals that exhibited positive results for this protozoa, one L. pardalis showed a positive spleen sample, and three P. onca and two P. concolor individuals had positive results in the spleen and blood, respectively. Among the six specimens of T. terrestris, Piroplasmida DNA was present in the blood and spleen samples from one animal, two specimens were positive for Piroplasmida in the blood, and three specimens had positive results in the spleen, as determined by the nPCR assay.

Partial sequences of the 18S rRNA gene from L. pardalis, P. onca, and P. concolor were identical to each other and 100% (721/721 bp) identical with sequences of Cytauxzoon felis (MT904037, AF399930, and AY679105). Since the present study relied on a small fragment of the 18S rRNA gene, herein we referred to as Cytauxzoon sp. isolate MT (MZ489665). Furthermore, partial sequences of the 18S rRNA gene obtained from six specimens of T. terrestris yielded two different haplotypes with 99% (743/747 bp) similarity with sequences of the Theileria genera (KP410271, KP410272, and KP410273) detected in free-roaming domestic cats in Midwestern Brazil. The GenBank accession numbers for the partial sequences generated for the Theileria isolates in the present study, herein designated Theileria sp. isolate tapir MT1 and Theileria sp. isolate tapir MT2 are MZ490586 and MZ491096, respectively. The phylogenetic analyses of a partial 18S rDNA obtained from wild felids (L. pardalis, P. onca, and P. concolor) show Cytauxzoon sp. isolate MT clustered in a clade with other C. felis sequences. Furthermore, the phylogenetic analyses of partial 18S rDNA sequences obtained from T. terrestris indicate that Theileria sp. isolate tapir MT1 and Theileria sp. isolate tapir MT2 formed a clade with other Theileria spp. recently detected in domesticated and stray cats in the states of Mato Grosso Sul and São Paulo, Brazil (Figure 2), and genetically related to Theileria equi (6.38% of divergence).

Figure 2
Maximum parsimony and Bayesian tree constructed for an alignment of sequences of Cytauxzoon spp. and Theileria spp. species using 18S rRNA gene sequences. Numbers at nodes are the support values for the major branches (bootstrap over 500 replicates). The sequence obtained in this study is highlighted in bold. Numbers in brackets correspond to GenBank accession numbers.

Among the mammal samples molecularly tested for Hepatozoon spp., only one L. pardalis yielded amplicons in blood samples after the 18S rRNA-based cPCR that revealed 100% (554/554 pb) identity with Hepatozoon felis (AB771570, AB771562). However, considering the small size of the fragment sequenced from 18S rRNA gene, as described above, herein we referred to as Hepatozoon sp. isolate ocelot MT (MZ490540). Co-infection with Hepatozoon and piroplasmid agents was not detected among the samples tested.

The present study demonstrated the presence of apicomplexan parasites in blood and/or spleen samples from wild mammals from the state of Mato Grosso, Midwestern Brazil. Infections found in L. pardalis, P. onca, and P. concolor by Cytauxzoon sp. corroborate previous studies that demonstrated a high occurrence of this agent in wild felids in Brazil (de Sousa et al., 2018de Sousa KCM, Fernandes MP, Herrera HM, Freschi CR, Machado RZ, André MR. Diversity of piroplasmids among wild and domestic mammals and ectoparasites in Pantanal wetland, Brazil. Ticks Tick Borne Dis 2018; 9(2): 245-253. http://dx.doi.org/10.1016/j.ttbdis.2017.09.010. PMid:28941935.
http://dx.doi.org/10.1016/j.ttbdis.2017....
; Furtado et al., 2017bFurtado MM, Taniwaki SA, Metzger B, dos Santos Paduan K, O’Dwyer LH, Jácomo ATA, et al. Is the free-ranging jaguar (Panthera onca) a reservoir for Cytauxzoon felis in Brazil? Ticks Tick Borne Dis 2017b; 8(4): 470-476. http://dx.doi.org/10.1016/j.ttbdis.2017.02.005. PMid:28196774.
http://dx.doi.org/10.1016/j.ttbdis.2017....
; Santos et al., 2021Santos FM, de Sousa KCM, Sano NY, Nantes WAG, Liberal SC, Machado RZ, et al. Relationships between vector-borne parasites and free-living mammals at the Brazilian Pantanal. Parasitol Res 2021; 120(3): 1003-1010. http://dx.doi.org/10.1007/s00436-020-07028-0. PMid:33420620.
http://dx.doi.org/10.1007/s00436-020-070...
).

In North America, bobcat (Lynx rufus) is the most common natural host for C. felis, with both Amblyomma americanum and Dermacentor variabilis ticks as suitable vectors (Wang et al., 2017Wang JL, Li TT, Liu GH, Zhu XQ, Yao C. Two tales of Cytauxzoon felis infections in domestic cats. Clin Microbiol Rev 2017; 30(4): 861-885. http://dx.doi.org/10.1128/CMR.00010-17. PMid:28637681.
http://dx.doi.org/10.1128/CMR.00010-17...
). Despite the pathogenicity of the genotypes that circulate in domestic cats and wild felids in the country is still unknown (André et al., 2015André MR, Herrera HM, Fernandes SJ, deSousa KCM, Gonçalves LR, Domingos IH, et al. Tick-borne agents in domesticated and stray cats from the city of Campo Grande, state of Mato Grosso do Sul, Midwestern Brazil. Ticks Tick Borne Dis 2015; 6(6): 779-786. http://dx.doi.org/10.1016/j.ttbdis.2015.07.004. PMid:26187416.
http://dx.doi.org/10.1016/j.ttbdis.2015....
), one case of death of cytauxzoonosis has been described in Brazil in lions from Rio de Janeiro State (Peixoto et al., 2007Peixoto PV, Soares CO, Scofield A, Santiago CD, França TN, Barros SS. Fatal cytauxzoonosis in captive-reared lions in Brazil. Vet Parasitol 2007; 145(3-4): 383-387. http://dx.doi.org/10.1016/j.vetpar.2006.12.023. PMid:17306459.
http://dx.doi.org/10.1016/j.vetpar.2006....
). In Brazil, high infection rates in P. onca incriminate this felid as a possible reservoir host for Cytauxzoon (Furtado et al., 2017bFurtado MM, Taniwaki SA, Metzger B, dos Santos Paduan K, O’Dwyer LH, Jácomo ATA, et al. Is the free-ranging jaguar (Panthera onca) a reservoir for Cytauxzoon felis in Brazil? Ticks Tick Borne Dis 2017b; 8(4): 470-476. http://dx.doi.org/10.1016/j.ttbdis.2017.02.005. PMid:28196774.
http://dx.doi.org/10.1016/j.ttbdis.2017....
), although this assumption should be verified, along with the role of other neotropical felid species serving as natural reservoirs (André et al., 2009André MR, Adania CH, Machado RZ, Allegretti SM, Felippe PAN, Silva KF, et al. Molecular detection of Cytauxzoon spp. in Asymptomatic Brazilian wild captive felids. J Wildl Dis 2009; 45(1): 234-237. http://dx.doi.org/10.7589/0090-3558-45.1.234. PMid:19204356.
http://dx.doi.org/10.7589/0090-3558-45.1...
), as well as possible clinical signs of infection in wild Brazilian felines. Finally, little is known about the natural vectors of Brazilian isolates of Cytauxzoon sp.. It is possible that ticks of the genus Amblyomma are responsible for maintaining and transmitting this pathogen (Furtado et al., 2017bFurtado MM, Taniwaki SA, Metzger B, dos Santos Paduan K, O’Dwyer LH, Jácomo ATA, et al. Is the free-ranging jaguar (Panthera onca) a reservoir for Cytauxzoon felis in Brazil? Ticks Tick Borne Dis 2017b; 8(4): 470-476. http://dx.doi.org/10.1016/j.ttbdis.2017.02.005. PMid:28196774.
http://dx.doi.org/10.1016/j.ttbdis.2017....
).

Tapirus terrestris (lowland tapir) is a wide-ranging herbivore ungulate of the order Perissodactyla, that is found in all biomes in Brazil and is highly susceptible to anthropogenic threats, including cohabitation and increased exposure to domestic and wild animal pathogens (Medici, 2011Medici EP. Family tapiridae (TAPIRS). In: Wilson DE, Mittermeier RA, editors. Handbook of the mammals of the world. Vol. 2. Spain: Hoofed Mammals, Lynx Edicions; 2011. p. 182-204.). In this study, a natural infection is described with Theileria genus positioned by phylogenetic analysis with Theileria sp. detected in cats (André et al., 2014André MR, Denardi NCB, de Sousa KCM, Gonçalves LR, Henrique PC, Ontivero CRGR, et al. Arthropod-borne pathogens circulating in free-roaming domestic cats in a zoo environment in Brazil. Ticks Tick Borne Dis 2014; 5(5): 545-551. http://dx.doi.org/10.1016/j.ttbdis.2014.03.011. PMid:24889035.
http://dx.doi.org/10.1016/j.ttbdis.2014....
, 2015André MR, Herrera HM, Fernandes SJ, deSousa KCM, Gonçalves LR, Domingos IH, et al. Tick-borne agents in domesticated and stray cats from the city of Campo Grande, state of Mato Grosso do Sul, Midwestern Brazil. Ticks Tick Borne Dis 2015; 6(6): 779-786. http://dx.doi.org/10.1016/j.ttbdis.2015.07.004. PMid:26187416.
http://dx.doi.org/10.1016/j.ttbdis.2015....
). Piroplasms have been described infecting domestic cats worldwide, being a major veterinary concern mainly in South Africa, with animals presenting severe clinical abnormalities (Penzhorn & Oosthuizen, 2020Penzhorn BL, Oosthuizen MC. Babesia species of domestic cats: molecular characterization has opened Pandora’s Box. Front Vet Sci 2020; 7: 134. http://dx.doi.org/10.3389/fvets.2020.00134. PMid:32292793.
http://dx.doi.org/10.3389/fvets.2020.001...
). In Brazil, molecular occurrences (11.9-19%) of Babesia/Theileria spp., genetically related to Theileria molecularly detected in the present study, were described in clinically health domesticated and stray cats (André et al., 2014André MR, Denardi NCB, de Sousa KCM, Gonçalves LR, Henrique PC, Ontivero CRGR, et al. Arthropod-borne pathogens circulating in free-roaming domestic cats in a zoo environment in Brazil. Ticks Tick Borne Dis 2014; 5(5): 545-551. http://dx.doi.org/10.1016/j.ttbdis.2014.03.011. PMid:24889035.
http://dx.doi.org/10.1016/j.ttbdis.2014....
, 2015André MR, Herrera HM, Fernandes SJ, deSousa KCM, Gonçalves LR, Domingos IH, et al. Tick-borne agents in domesticated and stray cats from the city of Campo Grande, state of Mato Grosso do Sul, Midwestern Brazil. Ticks Tick Borne Dis 2015; 6(6): 779-786. http://dx.doi.org/10.1016/j.ttbdis.2015.07.004. PMid:26187416.
http://dx.doi.org/10.1016/j.ttbdis.2015....
), suggesting that cats are able to maintain the infection with no discernible untoward effects (Penzhorn & Oosthuizen, 2020Penzhorn BL, Oosthuizen MC. Babesia species of domestic cats: molecular characterization has opened Pandora’s Box. Front Vet Sci 2020; 7: 134. http://dx.doi.org/10.3389/fvets.2020.00134. PMid:32292793.
http://dx.doi.org/10.3389/fvets.2020.001...
).

Regardless the natural infections with Theileria (molecularly identified as Theileria equi) have previously been reported in lowland tapirs (Gonçalves et al., 2020Gonçalves TS, Barros FNL, Inoue LS, de Farias DM, Lima JS, Nobre AV, et al. Natural Theileria equi infection in captive Tapirus terrestris (Perissodactyla: Tapiridae) in the Brazilian Amazon. Ticks Tick Borne Dis 2020; 11(4): 101452. http://dx.doi.org/10.1016/j.ttbdis.2020.101452. PMid:32360027.
http://dx.doi.org/10.1016/j.ttbdis.2020....
), neither clinical manifestation nor the impact were described of these infections in tapirids with this protozoan. Furthermore, there was no evidence of lowland tapirs as possible natural reservoirs or even potential vectors for Theileria sp., since these mammals have the greatest richness of tick species in South America (Labruna et al., 2021Labruna MB, Martins TF, Acosta ICL, Serpa MCA, Soares HS, Teixeira RHF, et al. Ticks and rickettsial exposure in lowland tapirs (Tapirus terrestris) of three Brazilian biomes. Ticks Tick Borne Dis 2021; 12(3): 101648. http://dx.doi.org/10.1016/j.ttbdis.2021.101648. PMid:33508536.
http://dx.doi.org/10.1016/j.ttbdis.2021....
).

The genus Hepatozoon can infect a wide range of domestic and wild animals, including avians, mammals, and reptiles worldwide, and despite its frequent presence in wild and domestic felids (van As et al., 2020van As M, Netherlands EC, Smit NJ. Molecular characterization and morphological description of two new species of Hepatozoon Miller, 1908 (Apicomplexa: Adeleorina: Hepatozoidae) infecting leukocytes of African leopards Panthera pardus pardus (L.). Parasit Vectors 2020; 13(1): 222. http://dx.doi.org/10.1186/s13071-020-3933-6. PMid:32357916.
http://dx.doi.org/10.1186/s13071-020-393...
), few studies on Hepatozoon infection have been conducted with neotropical felines (Metzger et al., 2008Metzger B, Paduan KS, Rubini AS, Oliveira TG, Pereira C, O’Dwyer LH. The first report of Hepatozoon sp. (Apicomplexa: Hepatozoidae) in neotropical felids from Brazil. Vet Parasitol 2008; 152(1-2): 28-33. http://dx.doi.org/10.1016/j.vetpar.2007.12.006. PMid:18243562.
http://dx.doi.org/10.1016/j.vetpar.2007....
; André et al., 2010André MR, Adania CH, Teixeira RHF, Vargas GH, Falcade M, Sousa L, et al. Molecular detection of Hepatozoon spp. in Brazilian and exotic wild carnivores. Vet Parasitol 2010; 173(1-2): 134-138. http://dx.doi.org/10.1016/j.vetpar.2010.06.014. PMid:20630658.
http://dx.doi.org/10.1016/j.vetpar.2010....
; Furtado et al., 2017aFurtado MM, Metzger B, de Almeida Jácomo AT, Labruna MB, Martins TF, O’Dwyer LH, et al. Hepatozoon spp. infect free-ranging Jaguars (Panthera onca) in Brazil. J Parasitol 2017a; 103(3): 243-250. http://dx.doi.org/10.1645/16-99. PMid:28207298.
http://dx.doi.org/10.1645/16-99...
; de Sousa et al., 2018de Sousa KCM, Fernandes MP, Herrera HM, Freschi CR, Machado RZ, André MR. Diversity of piroplasmids among wild and domestic mammals and ectoparasites in Pantanal wetland, Brazil. Ticks Tick Borne Dis 2018; 9(2): 245-253. http://dx.doi.org/10.1016/j.ttbdis.2017.09.010. PMid:28941935.
http://dx.doi.org/10.1016/j.ttbdis.2017....
). At least four species of Hepatozoon are capable of infecting domestic and wild felines worldwide, as follows: H. felis was described in Spain (Felis catus), India (Panthera tigris tigris, Panthera leo persica, and Panthera pardus fusca), Brazil (Felis catus), and Thailand (Panthera leo persica); Hepatozoon silvestris was detected in Felis silvestris silvestris from Bosnia and Herzegovin; Hepatozoon ingwe and Hepatozoon luiperdjie were detected in Panthera pardus pardus in South Africa (van As et al., 2020van As M, Netherlands EC, Smit NJ. Molecular characterization and morphological description of two new species of Hepatozoon Miller, 1908 (Apicomplexa: Adeleorina: Hepatozoidae) infecting leukocytes of African leopards Panthera pardus pardus (L.). Parasit Vectors 2020; 13(1): 222. http://dx.doi.org/10.1186/s13071-020-3933-6. PMid:32357916.
http://dx.doi.org/10.1186/s13071-020-393...
). A putative new species of Hepatozoon sp. have been detected in wild felids from Brazil (André et al., 2010André MR, Adania CH, Teixeira RHF, Vargas GH, Falcade M, Sousa L, et al. Molecular detection of Hepatozoon spp. in Brazilian and exotic wild carnivores. Vet Parasitol 2010; 173(1-2): 134-138. http://dx.doi.org/10.1016/j.vetpar.2010.06.014. PMid:20630658.
http://dx.doi.org/10.1016/j.vetpar.2010....
). Despite several tick genera, including Amblyomma, Dermacentor, Haemaphysalis, Ixodes, and Rhipicephalus have been reported to harbor H. felis, the vectors of this protozoan species remain unknown (Bhusri et al., 2017Bhusri B, Sariya L, Mongkolphan C, Suksai P, Kaewchot S, Changbunjong T. Molecular characterization of Hepatozoon felis in Rhipicephalus sanguineus ticks infested on captive lions (Panthera leo). J Parasit Dis 2017; 41(3): 903-907. http://dx.doi.org/10.1007/s12639-017-0902-x. PMid:28848300.
http://dx.doi.org/10.1007/s12639-017-090...
). The infection with H. felis has previously been described in L. pardalis from Brazil (Metzger et al., 2008Metzger B, Paduan KS, Rubini AS, Oliveira TG, Pereira C, O’Dwyer LH. The first report of Hepatozoon sp. (Apicomplexa: Hepatozoidae) in neotropical felids from Brazil. Vet Parasitol 2008; 152(1-2): 28-33. http://dx.doi.org/10.1016/j.vetpar.2007.12.006. PMid:18243562.
http://dx.doi.org/10.1016/j.vetpar.2007....
; Santos et al., 2021Santos FM, de Sousa KCM, Sano NY, Nantes WAG, Liberal SC, Machado RZ, et al. Relationships between vector-borne parasites and free-living mammals at the Brazilian Pantanal. Parasitol Res 2021; 120(3): 1003-1010. http://dx.doi.org/10.1007/s00436-020-07028-0. PMid:33420620.
http://dx.doi.org/10.1007/s00436-020-070...
). Although Hepatozoon infections are often subclinical in wild felids (Metzger et al., 2008Metzger B, Paduan KS, Rubini AS, Oliveira TG, Pereira C, O’Dwyer LH. The first report of Hepatozoon sp. (Apicomplexa: Hepatozoidae) in neotropical felids from Brazil. Vet Parasitol 2008; 152(1-2): 28-33. http://dx.doi.org/10.1016/j.vetpar.2007.12.006. PMid:18243562.
http://dx.doi.org/10.1016/j.vetpar.2007....
; van As et al., 2020van As M, Netherlands EC, Smit NJ. Molecular characterization and morphological description of two new species of Hepatozoon Miller, 1908 (Apicomplexa: Adeleorina: Hepatozoidae) infecting leukocytes of African leopards Panthera pardus pardus (L.). Parasit Vectors 2020; 13(1): 222. http://dx.doi.org/10.1186/s13071-020-3933-6. PMid:32357916.
http://dx.doi.org/10.1186/s13071-020-393...
), studies have demonstrated that it can be fatal in domestic cats, particularly immunocompromised animals or those with concomitant infections (Wang et al., 2017Wang JL, Li TT, Liu GH, Zhu XQ, Yao C. Two tales of Cytauxzoon felis infections in domestic cats. Clin Microbiol Rev 2017; 30(4): 861-885. http://dx.doi.org/10.1128/CMR.00010-17. PMid:28637681.
http://dx.doi.org/10.1128/CMR.00010-17...
). Considering that some Brazilian felids are threatened, especially keystone species such as P. onca, studies are recommended, especially based on postmortem investigations, due to the inherent difficulties to obtain samples from wild animals, to clarify whether Hepatozoon or other pathogens infections represent a risk to these animals.

The present study showed that Cytauxzoon sp. and Hepatozoon sp. circulate among wild felids, while an uncharacterized piroplasmid genetically related to T. equi was detected in lowland tapirs in the state of Mato Grosso. Despite controversy regarding the epidemiological threat of these protozoan infections, the detection in free-living and captive wild mammals demonstrates the importance of monitoring, especially in regions of conservation interest, such as the state of Mato Grosso, to verify the circulation and genetic diversity of these agents in order to anticipate the possible emergence of diseases, and even their consequences. Furthermore, although clinical disease does not always develop in wildlife, mammals can be important reservoirs by contributing to the spread of the disease to other wild and domestic animals, as well as humans.

Acknowledgements

A. Marcili, L. Nakazato, R. C. Pacheco, and V. Dutra are in receipt of productivity scholarships from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). This research was financially supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) – financial code 001.

References

  • André MR, Adania CH, Machado RZ, Allegretti SM, Felippe PAN, Silva KF, et al. Molecular detection of Cytauxzoon spp. in Asymptomatic Brazilian wild captive felids. J Wildl Dis 2009; 45(1): 234-237. http://dx.doi.org/10.7589/0090-3558-45.1.234 PMid:19204356.
    » http://dx.doi.org/10.7589/0090-3558-45.1.234
  • André MR, Adania CH, Teixeira RHF, Vargas GH, Falcade M, Sousa L, et al. Molecular detection of Hepatozoon spp. in Brazilian and exotic wild carnivores. Vet Parasitol 2010; 173(1-2): 134-138. http://dx.doi.org/10.1016/j.vetpar.2010.06.014 PMid:20630658.
    » http://dx.doi.org/10.1016/j.vetpar.2010.06.014
  • André MR, Denardi NCB, de Sousa KCM, Gonçalves LR, Henrique PC, Ontivero CRGR, et al. Arthropod-borne pathogens circulating in free-roaming domestic cats in a zoo environment in Brazil. Ticks Tick Borne Dis 2014; 5(5): 545-551. http://dx.doi.org/10.1016/j.ttbdis.2014.03.011 PMid:24889035.
    » http://dx.doi.org/10.1016/j.ttbdis.2014.03.011
  • André MR, Herrera HM, Fernandes SJ, deSousa KCM, Gonçalves LR, Domingos IH, et al. Tick-borne agents in domesticated and stray cats from the city of Campo Grande, state of Mato Grosso do Sul, Midwestern Brazil. Ticks Tick Borne Dis 2015; 6(6): 779-786. http://dx.doi.org/10.1016/j.ttbdis.2015.07.004 PMid:26187416.
    » http://dx.doi.org/10.1016/j.ttbdis.2015.07.004
  • Bhusri B, Sariya L, Mongkolphan C, Suksai P, Kaewchot S, Changbunjong T. Molecular characterization of Hepatozoon felis in Rhipicephalus sanguineus ticks infested on captive lions (Panthera leo). J Parasit Dis 2017; 41(3): 903-907. http://dx.doi.org/10.1007/s12639-017-0902-x PMid:28848300.
    » http://dx.doi.org/10.1007/s12639-017-0902-x
  • Birkenheuer AJ, Levy MG, Breitschwerdt EB. Development and evaluation of a seminested PCR for detection and differentiation of Babesia gibsoni (Asian genotype) and B. canis DNA in canine blood samples. J Clin Microbiol 2003; 41(9): 4172-4177. http://dx.doi.org/10.1128/JCM.41.9.4172-4177.2003 PMid:12958243.
    » http://dx.doi.org/10.1128/JCM.41.9.4172-4177.2003
  • de Sousa KCM, Fernandes MP, Herrera HM, Freschi CR, Machado RZ, André MR. Diversity of piroplasmids among wild and domestic mammals and ectoparasites in Pantanal wetland, Brazil. Ticks Tick Borne Dis 2018; 9(2): 245-253. http://dx.doi.org/10.1016/j.ttbdis.2017.09.010 PMid:28941935.
    » http://dx.doi.org/10.1016/j.ttbdis.2017.09.010
  • Furtado MM, Metzger B, de Almeida Jácomo AT, Labruna MB, Martins TF, O’Dwyer LH, et al. Hepatozoon spp. infect free-ranging Jaguars (Panthera onca) in Brazil. J Parasitol 2017a; 103(3): 243-250. http://dx.doi.org/10.1645/16-99 PMid:28207298.
    » http://dx.doi.org/10.1645/16-99
  • Furtado MM, Taniwaki SA, Metzger B, dos Santos Paduan K, O’Dwyer LH, Jácomo ATA, et al. Is the free-ranging jaguar (Panthera onca) a reservoir for Cytauxzoon felis in Brazil? Ticks Tick Borne Dis 2017b; 8(4): 470-476. http://dx.doi.org/10.1016/j.ttbdis.2017.02.005 PMid:28196774.
    » http://dx.doi.org/10.1016/j.ttbdis.2017.02.005
  • Gonçalves TS, Barros FNL, Inoue LS, de Farias DM, Lima JS, Nobre AV, et al. Natural Theileria equi infection in captive Tapirus terrestris (Perissodactyla: Tapiridae) in the Brazilian Amazon. Ticks Tick Borne Dis 2020; 11(4): 101452. http://dx.doi.org/10.1016/j.ttbdis.2020.101452 PMid:32360027.
    » http://dx.doi.org/10.1016/j.ttbdis.2020.101452
  • Huelsenbeck JP, Ronquist F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 2001; 17(8): 754-755. https://doi.org/10.1093/bioinformatics/17.8.754
    » https://doi.org/10.1093/bioinformatics/17.8.754
  • Jefferies R, Ryan UM, Irwin PJ. PCR–RFLP for the detection and differentiation of the canine piroplasm species and its use with filter paper-based technologies. Vet Parasitol 2007; 144(1-2): 20-7. https://doi.org/10.1016/j.vetpar.2006.09.022
    » https://doi.org/10.1016/j.vetpar.2006.09.022
  • Labruna MB, Martins TF, Acosta ICL, Serpa MCA, Soares HS, Teixeira RHF, et al. Ticks and rickettsial exposure in lowland tapirs (Tapirus terrestris) of three Brazilian biomes. Ticks Tick Borne Dis 2021; 12(3): 101648. http://dx.doi.org/10.1016/j.ttbdis.2021.101648 PMid:33508536.
    » http://dx.doi.org/10.1016/j.ttbdis.2021.101648
  • Medici EP. Family tapiridae (TAPIRS). In: Wilson DE, Mittermeier RA, editors. Handbook of the mammals of the world Vol. 2. Spain: Hoofed Mammals, Lynx Edicions; 2011. p. 182-204.
  • Metzger B, Paduan KS, Rubini AS, Oliveira TG, Pereira C, O’Dwyer LH. The first report of Hepatozoon sp. (Apicomplexa: Hepatozoidae) in neotropical felids from Brazil. Vet Parasitol 2008; 152(1-2): 28-33. http://dx.doi.org/10.1016/j.vetpar.2007.12.006 PMid:18243562.
    » http://dx.doi.org/10.1016/j.vetpar.2007.12.006
  • Nicholas KB, Nicholas HB, Deerfield DW. GeneDoc: analysis and visualization of genetic variation. Embnew News 1997; 4: 14.
  • Peixoto PV, Soares CO, Scofield A, Santiago CD, França TN, Barros SS. Fatal cytauxzoonosis in captive-reared lions in Brazil. Vet Parasitol 2007; 145(3-4): 383-387. http://dx.doi.org/10.1016/j.vetpar.2006.12.023 PMid:17306459.
    » http://dx.doi.org/10.1016/j.vetpar.2006.12.023
  • Penzhorn BL, Oosthuizen MC. Babesia species of domestic cats: molecular characterization has opened Pandora’s Box. Front Vet Sci 2020; 7: 134. http://dx.doi.org/10.3389/fvets.2020.00134 PMid:32292793.
    » http://dx.doi.org/10.3389/fvets.2020.00134
  • Santos FM, de Sousa KCM, Sano NY, Nantes WAG, Liberal SC, Machado RZ, et al. Relationships between vector-borne parasites and free-living mammals at the Brazilian Pantanal. Parasitol Res 2021; 120(3): 1003-1010. http://dx.doi.org/10.1007/s00436-020-07028-0 PMid:33420620.
    » http://dx.doi.org/10.1007/s00436-020-07028-0
  • Swofford DL. PAUP: Phylogenetic analysis using parsimony Beta Version 4.0b10. Sunderland: Sinauer and Associates; 2002.
  • Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997; 25(24): 4876-4882. http://dx.doi.org/10.1093/nar/25.24.4876 PMid:9396791.
    » http://dx.doi.org/10.1093/nar/25.24.4876
  • Timi JT, Poulin R. Why ignoring parasites in fish ecology is a mistake. Int J Parasitol 2020; 50(10-11): 755-761. http://dx.doi.org/10.1016/j.ijpara.2020.04.007 PMid:32592807.
    » http://dx.doi.org/10.1016/j.ijpara.2020.04.007
  • Ujvari B, Madsen T, Olsson M. High prevalence of Hepatozoon spp. (Apicomplexa, Hepatozoidae) infection in water pythons (Liasis fuscus) from tropical Australia. J Parasitol 2004; 90(3): 670-672. http://dx.doi.org/10.1645/GE-204R PMid:15270125.
    » http://dx.doi.org/10.1645/GE-204R
  • van As M, Netherlands EC, Smit NJ. Molecular characterization and morphological description of two new species of Hepatozoon Miller, 1908 (Apicomplexa: Adeleorina: Hepatozoidae) infecting leukocytes of African leopards Panthera pardus pardus (L.). Parasit Vectors 2020; 13(1): 222. http://dx.doi.org/10.1186/s13071-020-3933-6 PMid:32357916.
    » http://dx.doi.org/10.1186/s13071-020-3933-6
  • Wang JL, Li TT, Liu GH, Zhu XQ, Yao C. Two tales of Cytauxzoon felis infections in domestic cats. Clin Microbiol Rev 2017; 30(4): 861-885. http://dx.doi.org/10.1128/CMR.00010-17 PMid:28637681.
    » http://dx.doi.org/10.1128/CMR.00010-17

Publication Dates

  • Publication in this collection
    29 Oct 2021
  • Date of issue
    2021

History

  • Received
    27 July 2021
  • Accepted
    27 Sept 2021
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