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Candidatus Mycoplasma haemoalbiventris’ and tick-borne pathogens screening in white-eared opossums (Didelphis albiventris) from Curitiba and Foz do Iguaçu Cities, Paraná State, southern Brazil

Candidatus Mycoplasma haemoalbiventris’ e triagem para patógenos transmitidos por carrapatos em gambás de orelha branca (Didelphis albiventris) das cidades de Curitiba e Foz do Iguaçu, Estado do Paraná, sul do Brasil

Abstract

Hemoplasmas are epierythrocytic bacteria that infect mammals. ‘Candidatus Mycoplasma haemoalbiventris’ was detected in white-eared opossums (Didelphis albiventris) from southern and central-western Brazil. The present study aimed at: i) screening opossums for tick-borne (TBP) pathogens (Piroplasmida and Anaplasmataceae) and ii) detecting and characterizing hemoplasma species infecting opossums from Curitiba and Foz do Iguaçu cities in the Paraná State, southern Brazil. Thirty blood samples from white-eared opossums were evaluated by PCR assays. Animals were not infested by ectoparasites. The mammalian endogenous gapdh gene was consistently amplified in all samples. All opossums tested negative for Theileria/Babesia spp. and Ehrlichia/Anaplasma spp. by PCR based on 18S rRNA and 16S rRNA genes, respectively. A genus-specific PCR assay based on the 16S rRNA gene of hemoplasmas showed that three/13 (23.08%; CI 95%: 8.18-50.26%) opossums from Foz do Iguaçu were positive for hemotropic Mycoplasma sp. All opossums from Curitiba tested negative for hemoplasmas. Sequencing of both the 16S and 23S rRNA genes revealed that the animals were infected by ‘Ca. M. haemoalbiventris’. Although ‘Ca. M. haemoalbiventris’ is prevalent in opossums in Brazil, clinical signs associated with its infection and its putative vectors remain unknown.

Keywords:
Marsupials; hemotropic mycoplasmas; hemoplasmas

Resumo

Hemoplasmas são bactérias epieritrocíticas que infectam mamíferos. ‘Candidatus Mycoplasma haemoalbiventris’ foi detectado previamente em gambás-de-orelha-branca (Didelphis albiventris) das regiões sul e centro-oeste do Brasil. O presente estudo objetivou: i) triar os gambás para as doenças transmitidas por carrapatos (Piroplasmida e Anaplasmataceae); e ii) detectar e caracterizar as espécies de hemoplasma que infectam gambás nas cidades de Curitiba e Foz do Iguaçu, no Estado do Paraná, sul do Brasil. Trinta amostras de sangue de gambás-de-orelha-branca foram analisadas por PCR. Os animais não estavam infestados por ectoparasitos. O gene endógeno de mamífero gapdh foi amplificado em todas as amostras. Todos os gambás testaram negativos para Theileria/Babesia spp. e Ehrlichia/Anaplasma spp. por PCR, respectivamente, para os genes 18S rRNA e 16S rRNA. Uma PCR gene-específica, baseada no gene 16S rRNA de hemoplasmas, mostrou que três/13 (23,08%; CI 95%: 8,18-50,26%) gambás de Foz do Iguaçu foram positivos para Mycoplasma sp. hemotrópico. Todos os gambás de Curitiba testaram negativos para hemoplasmas. O sequenciamento de fragmentos dos genes 16S e 23S rRNA revelou que os animais estavam infectados pelo ‘Ca. M. haemoalbiventris’. Embora ‘Ca. M. haemoalbiventris’ seja prevalente em gambás no Brasil, os sinais clínicos associados à infecção e os prováveis vetores permanecem desconhecidos.

Palavras-chave:
Marsupiais; micoplasma hemotrópico; hemoplasmas

Opossums are synanthropic marsupials belonging to the genus Didelphis. In South America, four species have been reported: D. albiventris, D. aurita, D. imperfecta, and D. marsupialis (Nascimento & Horta, 2014Nascimento CC, Horta MC. Didelphimorphia (Gambá, Cuíca). In: Cubas ZS, Silva JCR., Catão-Dias JL, editors. Tratado de animais selvagens: medicina veterinária. 2. ed. São Paulo: Roca; 2014. (vol. 1).). Due to their circulation in urban and rural environments, opossums are potential hosts, suggested reservoirs and/or potential amplifiers of infectious agents (e.g., Trypanossoma cruzi, Leishmania infantum, Rickettsia rickettsii) (Horta et al., 2009Horta MC, Moraes-Filho J, Casagrande RA, Saito TB, Rosa SC, Ogrzewalska M, et al. Experimental infection of opossums Didelphis aurita by Rickettsia rickettsii and evaluation of the transmission of the infection to ticks Amblyomma cajennense. Vector Borne Zoonotic Dis 2009; 9(1): 109-118. http://dx.doi.org/10.1089/vbz.2008.0114. PMid:18945194.
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; Carreira et al., 2012Carreira JCA, Silva AVM, Pita Pereira D, Brazil RP. Natural infection of Didelphis aurita (Mammalia: Marsupialia) with Leishmania infantum in Brazil. Parasit Vectors 2012; 5(1): 111. http://dx.doi.org/10.1186/1756-3305-5-111. PMid:22676324.
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; Zecca et al., 2020Zecca IB, Hodo CL, Slack S, Auckland L, Hamer SA. Trypanosoma cruzi infections and associated pathology in urban-dwelling Virginia opossums (Didelphis virginiana). Int J Parasitol Parasites Wildl 2020; 11: 287-293. http://dx.doi.org/10.1016/j.ijppaw.2020.03.004. PMid:32215248.
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).

In Brazil, tick-borne pathogens (TBP) have been reported in Didelphis spp. from different regions (Melo et al., 2016Melo ALT, Aguiar DM, Spolidorio MG, Yoshinari NH, Matushima ER, Labruna MB, et al. Serological evidence of exposure to tick-borne agents in opossums (Didelphis spp.) in the state of São Paulo, Brazil. Rev Bras Parasitol Vet 2016; 25(3): 348-352. http://dx.doi.org/10.1590/S1984-29612016028. PMid:27276663.
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; Soares et al., 2017Soares HS, Marcili A, Barbieri ARM, Minervino AHH, Moreira TR, Gennari SM, et al. Novel piroplasmid and Hepatozoon organisms infecting the wildlife of two regions of the Brazilian Amazon. Int J Parasitol Parasites Wildl 2017; 6(2): 115-121. http://dx.doi.org/10.1016/j.ijppaw.2017.05.002. PMid:28603688.
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; Guimarães et al., 2019Guimarães A, Raimundo JM, Silva AT, Carpintero FM, Pires JR, Benevenute JL, et al. Detection of a putative novel genotype of Ehrlichia sp. from opossums (Didelphis aurita) from Brazil. Rev Bras Parasitol Vet 2019; 28(1): 140-144. http://dx.doi.org/10.1590/s1984-296120180068. PMid:30427523.
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). This includes a novel ehrlichial agent, Ehrlichia sp. strain Natal, detected in white-eared opossum (D. albiventris) from the northeastern region of the country (Lopes et al., 2018Lopes MG, Muñoz-Leal S, de Lima JTR, Fournier GFSR, Acosta ICL, Martins TF, et al. Ticks, rickettsial and erlichial infection in small mammals from Atlantic forest remnants in northeastern Brazil. Int J Parasitol Parasites Wildl 2018; 7(3): 380-385. http://dx.doi.org/10.1016/j.ijppaw.2018.10.001. PMid:30370217.
http://dx.doi.org/10.1016/j.ijppaw.2018....
).

Hemotropic mycoplasmas (hemoplasmas) are Gram-negative bacteria that attach to the surface of red blood cells from mammals and may cause hemolytic anemia. Two hemotropic Mycoplasma species have been described in Didelphis, namely ‘Candidatus Mycoplasma haemodidelphis’ (Messick et al., 2002Messick JB, Walker PG, Raphael W, Berent L, Shi X. ‘Candidatus Mycoplasma haemodidelphidis’ sp. nov., ‘Candidatus Mycoplasma haemolamae’ sp. nov. and Mycoplasma haemocanis comb. nov., haemotrophic parasites from a naturally infected opossum (Didelphis virginiana), alpaca (Lama pacos) and dog (Canis familiaris): phylogenetic and secondary structural relatedness of their 16S rRNA genes to other mycoplasmas. Int J Syst Evol Microbiol 2002; 52(3): 693-698. http://dx.doi.org/10.1099/00207713-52-3-693. PMid:12054227.
http://dx.doi.org/10.1099/00207713-52-3-...
) and ‘Candidatus Mycoplasma haemoalbiventris’ (Pontarolo et al., 2021Pontarolo GH, Kühl LF, Pedrassani D, Campos M, Figueiredo FB, Valente JDM, et al. ‘Candidatus Mycoplasma haemoalbiventris’, a novel hemoplasma species in white-eared opossums (Didelphis albiventris) from Brazil. Transbound Emerg Dis 2021; 68(2): 565-572. http://dx.doi.org/10.1111/tbed.13716. PMid:32644252.
http://dx.doi.org/10.1111/tbed.13716...
). Due to the proximity of human dwellings and human-animal interactions, monitoring ticks and the health status of opossums is a public health concern. Therefore, this study aimed at investigating the occurrence of TBP and hemotropic mycoplasmas in free-ranging opossums from the Curitiba and Foz do Iguaçu cities of the Paraná State, southern Brazil.

This study was approved by the Ethics Committee for Animal Experimentation and Animal Welfare at the Universidade Federal do Paraná, Brazil (protocol number 053/2018). Animal and laboratory procedures were approved and performed under the regulations of the Chico Mendes Institute for Biodiversity Conservation (ICMBio, protocol number 63433-3).

The study was carried out in the Curitiba (25° 26' 27″ S 49° 16' 36″ W) and Foz do Iguaçu cities (25° 32' 45′′ S 54° 35' 07′′ W). Curitiba, the capital of Paraná State, is located in the south-central region and has a humid subtropical highland climate (Köppen: Cfb) with an average temperature of 17.4 °C. Foz do Iguaçu lies in the extreme west of the Paraná State, on the border of Brazil, Argentina, and Paraguay, in the Atlantic rainforest biome. Foz do Iguaçu is internationally recognized as a protected area with diverse fauna (Valente et al., 2019Valente JDM, Mongruel ACB, Machado CAL, Chiyo L, Leandro AS, Britto AS, et al. Tick-borne pathogens in carthorses from Foz do Iguaçu City, Paraná State, southern Brazil: A tri-border area of Brazil, Paraguay and Argentina. Vet Parasitol 2019; 273: 71-79. http://dx.doi.org/10.1016/j.vetpar.2019.08.008. PMid:31446256.
http://dx.doi.org/10.1016/j.vetpar.2019....
) and has a humid subtropical climate (Köppen: Cfa) with rainfall throughout the year and an average temperature of 22.1 °C.

A total of 30 white-eared opossums (D. albiventris) were evaluated. In Foz do Iguaçu, 13 white-eared opossums were captured using Tomahawk wire mesh traps baited with fruit. Sampling was performed between April and December 2019 per the spontaneous demand of the Zoonoses Surveillance Center, based on the report of the occurrence of opossums in human dwellings. In Curitiba City, 17 white-eared opossums were referred to the Veterinary Teaching Hospital, Universidade Federal do Paraná, Parana State, southern Brazil, between June 2018 and December 2020. Samples from Curitiba were also collected per the spontaneous demand based on the report of the occurrence of opossums in human dwellings.

After using chemical restraints (xylazine (4.0 mg/kg) and ketamine (20 mg/kg), the animals were individually identified and visually inspected for ectoparasites (ticks and fleas). Subsequently, EDTA-blood samples were collected by caudal venipuncture and stored at −20 °C until molecular analysis. Post sample collection, the animals were monitored until complete recovery from the chemical restraints and later released (Massini et al., 2019Massini PF, Drozino RN, Otomura FH, Mongruel ACB, Valente JDM, Toledo MJO, et al. Detection of Hemotropic Mycoplasma sp. in white-eared opossums (Didelphis albiventris) from Southern Brazil. Rev Bras Parasitol Vet 2019; 28(4): 797-801. http://dx.doi.org/10.1590/s1984-29612019058. PMid:31390439.
http://dx.doi.org/10.1590/s1984-29612019...
).

DNA was extracted from 200 μL of blood using a commercially available kit (IllustraTM Blood Genomic Prep Mini Spin Kit, GE Healthcare Life Sciences, Little Chalfont, UK), according to the manufacturer's instructions. Ultra-pure water was used as a negative control in parallel to monitor cross-contamination.

To monitor DNA extraction, PCR for the mammalian endogenous gene glyceraldehyde-3-phosphate dehydrogenase (gapdh) was performed in all samples (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-...
). Conventional PCR was used to screen samples for hemotropic Mycoplasma spp. genus-specific primers targeting a portion (900 bp) of the 16S rRNA gene of hemotropic Mycoplasma spp. (Hoelzle et al., 2011Hoelzle K, Winkler M, Kramer MM, Wittenbrink MM, Dieckmann SM, Hoelzle LE. Detection of Candidatus Mycoplasma haemobos in cattle with anaemia. Vet J 2011; 187(3): 408-410. http://dx.doi.org/10.1016/j.tvjl.2010.01.016. PMid:20188610.
http://dx.doi.org/10.1016/j.tvjl.2010.01...
; Machado et al., 2017Machado CAL, Vidotto O, Conrado FO, Santos NJR, Valente JDM, Barbosa IC, et al. Mycoplasma ovis infection in goat farms from northeastern Brazil. Comp Immunol Microbiol Infect Dis 2017; 55: 1-5. http://dx.doi.org/10.1016/j.cimid.2017.08.004. PMid:29127988.
http://dx.doi.org/10.1016/j.cimid.2017.0...
). Opossum DNA samples that tested positive in the PCR assay based on the 16S rRNA gene were subjected to a genus-specific PCR assay targeting a fragment (800 bp) of the 23S rRNA gene of hemoplasmas (Mongruel et al., 2020Mongruel ACB, Spanhol VC, Valente JDM, Porto PP, Ogawa L, Otomura FH, et al. Survey of vector-borne and nematode parasites involved in the etiology of anemic syndrome in sheep from Southern Brazil. Rev Bras Parasitol Vet 2020; 29(3): e007320. http://dx.doi.org/10.1590/s1984-29612020062. PMid:32935770.
http://dx.doi.org/10.1590/s1984-29612020...
). Nuclease-free water and Mycoplasma ovis DNA from a naturally infected goat blood sample were used as the negative and positive controls, respectively, in both PCR assays. Additionally, DNA samples were also tested by PCR assays targeting a fragment (551 bp) of the 18S rRNA gene of Theileria/Babesia spp. (Almeida et al., 2012Almeida AP, Marcili A, Leite RC, Nieri-Bastos FA, Domingues LN, Martins JR, et al. Coxiella symbiont in the tick Ornithodoros rostratus (Acari: argasidae). Ticks Tick Borne Dis 2012; 3(4): 203-206. http://dx.doi.org/10.1016/j.ttbdis.2012.02.003. PMid:22480930.
http://dx.doi.org/10.1016/j.ttbdis.2012....
) and a fragment (349 bp) of the 16S rRNA gene of Ehrlichia/Anaplasma spp. (Parola et al., 2000Parola P, Roux V, Camicas JL, Baradji I, Brouqui P, Raoult D. Detection of ehrlichiae in African ticks by polymerase chain reaction. Trans R Soc Trop Med Hyg 2000; 94(6): 707-708. http://dx.doi.org/10.1016/S0035-9203(00)90243-8. PMid:11198664.
http://dx.doi.org/10.1016/S0035-9203(00)...
). Babesia vogeli and Ehrlichia canis DNA obtained from naturally infected dogs were used as positive controls, and nuclease-free water was used as a negative control (Vieira et al., 2013Vieira TSWJ, Vieira RFC, Nascimento DAG, Tamekuni K, Toledo RS, Chandrashekar R, et al. Serosurvey of tick-borne pathogens in dogs from urban and rural areas from Parana State, Brazil. Rev Bras Parasitol Vet 2013; 22(1): 104-109. http://dx.doi.org/10.1590/S1984-29612013000100019. PMid:24252955.
http://dx.doi.org/10.1590/S1984-29612013...
). The amplified PCR products were subjected to gel electrophoresis in 1.5% agarose gels for 1 hour at 100 V, followed by SYBR safe staining (6 μg/mL; SYBR® Safe DNA Gel Stain, Invitrogen, CA, USA), and viewed under a UV light transilluminator at a wavelength of 312 nm.

The amplicons of the 16S rRNA (900 bp) and 23S rRNA (800 bp) obtained from three and two Mycoplasma spp.-positive samples were from Foz do Iguaçu. They were sequenced in both directions using the Sanger method. Three nucleotide sequences of the 16S rRNA gene and two sequences of 23S rRNA gene of hemotropic Mycoplasma sp. amplified herein were submitted to the GenBank® database (accession numbers: MW703800, MW703801, MW703802, and MW694786 and MW694787, respectively).

The consensus sequences were subjected to multiple alignment with the sequences selected from GenBank® using MAFFT available on the GUIDANCE2 server for each gene. The best-fit model of nucleotide substitution was determined using jModeltest v.2.1.10 and was set as GTR+I+G for 16S rRNA and TrN+G for 23S rRNA genes, based on the Akaike Information Criterion (AIC), respectively. Each Bayesian reconstruction was performed in Beast 1.10.4 with three independent runs of 100 million MCMC steps sampled at every 10,000 trees, 10% of the burn-in. The phylogenetic tree was visualized with FigTree software version 1.4.4 and the final layout was done with Inkscape version 0.92.2.

Opossums from both cities were not infested by ectoparasites (ticks and fleas) at the time of sampling. The mammalian endogenous gapdh gene was consistently amplified in all samples. All opossums tested negative for Theileria/Babesia spp. and Ehrlichia/Anaplasma spp. by PCR. While all opossums from Curitiba tested negative for hemoplasmas, three out of 13 (23.08%; CI 95%: 8.18-50.26%) animals from Foz do Iguaçu were positive for hemotropic Mycoplasma spp., as observed via PCR.

Sequencing of the 16S rRNA fragment showed 100% identity to ‘Ca. M. haemoalbiventris’ (MH158514, MH158515, MN423256, MN423258-MN423260, and MT170012-MT170016) detected in white-eared opossums from Brazil; on the other hand, sequencing of the 23S rRNA fragment showed 99.74-100% identity ‘Ca. M. haemoalbiventris’ (MN442081-MN442085) detected in white-eared opossums from Brazil. Phylogenetic analysis of the 16S and 23S rRNA gene fragments confirmed the white-eared opossum were infected by ‘Ca. M. haemoalbiventris’ (Figures 1 and 2).

Figure 1
Phylogenetic tree based on partial sequences of the 16S rRNA gene, showing the relationship between the ‘Candidatus Mycoplasma haemoalbiventris’ detected in the white-eared opossums (Didelphis albiventris) from this study and other hemoplasmas. Mycoplasma pneumoniae (CP039761) was used as outgroup. The GenBank accession number is in parentheses after the species name and origin of each agent. Bayesian inferences were carried out applying the GTR+I+G model and 1,000 bootstrap replicates for all analyses.
Figure 2
Phylogenetic tree based on partial sequences of the 23S rRNA gene, showing the relationship between the ‘Candidatus Mycoplasma haemoalbiventris’ detected in the white-eared opossums (Didelphis albiventris) from this study and other hemoplasmas. Mycoplasma pneumoniae (CP039761) was used as outgroup. The GenBank accession number is in parentheses after the species name and origin of each agent. Bayesian inferences were carried out applying the TrN+G model and 1,000 bootstrap replicates for all analyses.

In the present study, 23.08% opossums from Foz do Iguaçu (Paraná, southern Brazil) were positive for ‘Ca. M. haemoalbiventris’, while all the animals from Curitiba City tested negative. Previous studies have found higher hemoplasma prevalence rates (ranging from 32.5-87.5%) in white-eared opossums from different geographic regions and biomes (Atlantic Forest and Cerrado) of Brazil (Massini et al., 2019Massini PF, Drozino RN, Otomura FH, Mongruel ACB, Valente JDM, Toledo MJO, et al. Detection of Hemotropic Mycoplasma sp. in white-eared opossums (Didelphis albiventris) from Southern Brazil. Rev Bras Parasitol Vet 2019; 28(4): 797-801. http://dx.doi.org/10.1590/s1984-29612019058. PMid:31390439.
http://dx.doi.org/10.1590/s1984-29612019...
; Gonçalves et al., 2020Gonçalves LR, Herrera HM, Nantes WAG, Santos FM, Porfírio GEO, Barreto WTG, et al. Genetic diversity and lack of molecular evidence for hemoplasma cross-species transmission between wild and synanthropic mammals from Central-Western Brazil. Acta Trop 2020; 203: 105303. http://dx.doi.org/10.1016/j.actatropica.2019.105303. PMid:31857081.
http://dx.doi.org/10.1016/j.actatropica....
; Pontarolo et al., 2021Pontarolo GH, Kühl LF, Pedrassani D, Campos M, Figueiredo FB, Valente JDM, et al. ‘Candidatus Mycoplasma haemoalbiventris’, a novel hemoplasma species in white-eared opossums (Didelphis albiventris) from Brazil. Transbound Emerg Dis 2021; 68(2): 565-572. http://dx.doi.org/10.1111/tbed.13716. PMid:32644252.
http://dx.doi.org/10.1111/tbed.13716...
). Although Curitiba City is also located in the Atlantic rainforest biome, we hypothesize that its altitude (940 m a.s.l.) and annual average temperature (17.4 °C) may influence habits and behavior of the opossums, and thus, their exposure to hemoplasmas, which may explain the negative results found herein. Additionally, differences in the prevalence of hemoplasma between studies may have not be due to the diagnostic test used, since to date, all studies on the detection of hemoplasmas in Brazilian opossums have used conventional PCR assays as diagnostic method (Massini et al., 2019Massini PF, Drozino RN, Otomura FH, Mongruel ACB, Valente JDM, Toledo MJO, et al. Detection of Hemotropic Mycoplasma sp. in white-eared opossums (Didelphis albiventris) from Southern Brazil. Rev Bras Parasitol Vet 2019; 28(4): 797-801. http://dx.doi.org/10.1590/s1984-29612019058. PMid:31390439.
http://dx.doi.org/10.1590/s1984-29612019...
; Gonçalves et al., 2020Gonçalves LR, Herrera HM, Nantes WAG, Santos FM, Porfírio GEO, Barreto WTG, et al. Genetic diversity and lack of molecular evidence for hemoplasma cross-species transmission between wild and synanthropic mammals from Central-Western Brazil. Acta Trop 2020; 203: 105303. http://dx.doi.org/10.1016/j.actatropica.2019.105303. PMid:31857081.
http://dx.doi.org/10.1016/j.actatropica....
; Pontarolo et al., 2021Pontarolo GH, Kühl LF, Pedrassani D, Campos M, Figueiredo FB, Valente JDM, et al. ‘Candidatus Mycoplasma haemoalbiventris’, a novel hemoplasma species in white-eared opossums (Didelphis albiventris) from Brazil. Transbound Emerg Dis 2021; 68(2): 565-572. http://dx.doi.org/10.1111/tbed.13716. PMid:32644252.
http://dx.doi.org/10.1111/tbed.13716...
).

Herein, the animals were not infested with ticks and fleas at the time of sampling. However, hemoplasma-positive white-eared opossums from the Maringá municipality (state of Paraná) (Massini et al., 2019Massini PF, Drozino RN, Otomura FH, Mongruel ACB, Valente JDM, Toledo MJO, et al. Detection of Hemotropic Mycoplasma sp. in white-eared opossums (Didelphis albiventris) from Southern Brazil. Rev Bras Parasitol Vet 2019; 28(4): 797-801. http://dx.doi.org/10.1590/s1984-29612019058. PMid:31390439.
http://dx.doi.org/10.1590/s1984-29612019...
) and Campo Grande municipality (state of Mato Grosso do Sul) (Gonçalves et al., 2020Gonçalves LR, Herrera HM, Nantes WAG, Santos FM, Porfírio GEO, Barreto WTG, et al. Genetic diversity and lack of molecular evidence for hemoplasma cross-species transmission between wild and synanthropic mammals from Central-Western Brazil. Acta Trop 2020; 203: 105303. http://dx.doi.org/10.1016/j.actatropica.2019.105303. PMid:31857081.
http://dx.doi.org/10.1016/j.actatropica....
) were infested by Amblyomma dubitatum ticks. On the other hand, opossums from the Canoinhas municipality (state of Santa Catarina) were infested with Ctenocephalides felis fleas (Pontarolo et al., 2021Pontarolo GH, Kühl LF, Pedrassani D, Campos M, Figueiredo FB, Valente JDM, et al. ‘Candidatus Mycoplasma haemoalbiventris’, a novel hemoplasma species in white-eared opossums (Didelphis albiventris) from Brazil. Transbound Emerg Dis 2021; 68(2): 565-572. http://dx.doi.org/10.1111/tbed.13716. PMid:32644252.
http://dx.doi.org/10.1111/tbed.13716...
). Previous studies have failed to detect hemotropic Mycoplasma spp. in A. dubitatum ticks infesting ‘Ca. M. haemoalbiventris’-positive opossums from Brazil (Gonçalves et al., 2020Gonçalves LR, Herrera HM, Nantes WAG, Santos FM, Porfírio GEO, Barreto WTG, et al. Genetic diversity and lack of molecular evidence for hemoplasma cross-species transmission between wild and synanthropic mammals from Central-Western Brazil. Acta Trop 2020; 203: 105303. http://dx.doi.org/10.1016/j.actatropica.2019.105303. PMid:31857081.
http://dx.doi.org/10.1016/j.actatropica....
), and canine hemoplasmas in Rhipicephalus sanguineus sensu lato ticks in dogs from an animal shelter in Turkey (Aktas & Ozubek, 2017Aktas M, Ozubek S. Molecular survey of haemoplasmas in shelter dogs and associations with Rhipicephalus sanguineus sensu lato. Med Vet Entomol 2017; 31(4): 457-461. http://dx.doi.org/10.1111/mve.12244. PMid:28685834.
http://dx.doi.org/10.1111/mve.12244...
). High hemoplasma prevalence rates have been found in tropical regions, favoring the establishment of arthropod vectors for these bacteria. Additionally, hemotropic Mycoplasma spp. have been detected in Amblyomma sculptum ticks infesting hemoplasma-positive capybaras (Hydrochoerus hydrochaeris) from central-western Brazil (Gonçalves et al., 2020Gonçalves LR, Herrera HM, Nantes WAG, Santos FM, Porfírio GEO, Barreto WTG, et al. Genetic diversity and lack of molecular evidence for hemoplasma cross-species transmission between wild and synanthropic mammals from Central-Western Brazil. Acta Trop 2020; 203: 105303. http://dx.doi.org/10.1016/j.actatropica.2019.105303. PMid:31857081.
http://dx.doi.org/10.1016/j.actatropica....
). However, the lack of experimental studies on hemoplasma transmission, due to its uncultivable status in vitro, precludes robust evidence to implicate the involvement of ticks in the epidemiological cycle of this group of bacteria. Finally, A. dubitatum ticks are widespread and have already been found to infest opossums from Curitiba and Foz do Iguaçu cities (Valente et al., 2020Valente JDM, Silva PW, Arzua M, Barros-Battesti DM, Martins TF, Silva AM, et al. Records of ticks (Acari: Ixodidae) on humans and distribution of spotted-fever cases and its tick vectors in Paraná State, southern Brazil. Ticks Tick Borne Dis 2020; 11(6): 101510. http://dx.doi.org/10.1016/j.ttbdis.2020.101510. PMid:32993930.
http://dx.doi.org/10.1016/j.ttbdis.2020....
). Based on the above evidence, we hypothesize that ticks from this group may have previously bitten animals evaluated in the present study, although we cannot associate the low hemoplasma infection rate found to the absence of ticks.

TBP are of great concern worldwide. In Brazil, Ehrlichia spp., Anaplasma spp., and Babesia spp. have been reported to infect domestic and wild animals (Soares et al., 2017Soares HS, Marcili A, Barbieri ARM, Minervino AHH, Moreira TR, Gennari SM, et al. Novel piroplasmid and Hepatozoon organisms infecting the wildlife of two regions of the Brazilian Amazon. Int J Parasitol Parasites Wildl 2017; 6(2): 115-121. http://dx.doi.org/10.1016/j.ijppaw.2017.05.002. PMid:28603688.
http://dx.doi.org/10.1016/j.ijppaw.2017....
; André, 2018André MR. Diversity of Anaplasma and Ehrlichia/Neoehrlichia agents in terrestrial wild carnivores worldwide: implications for human and domestic animal health and wildlife conservation. Front Vet Sci 2018; 5: 293. http://dx.doi.org/10.3389/fvets.2018.00293. PMid:30533417.
http://dx.doi.org/10.3389/fvets.2018.002...
). A novel ehrlichial agent, Ehrlichia sp. strain Natal, has been detected in the northeastern region of the country (Lopes et al., 2018Lopes MG, Muñoz-Leal S, de Lima JTR, Fournier GFSR, Acosta ICL, Martins TF, et al. Ticks, rickettsial and erlichial infection in small mammals from Atlantic forest remnants in northeastern Brazil. Int J Parasitol Parasites Wildl 2018; 7(3): 380-385. http://dx.doi.org/10.1016/j.ijppaw.2018.10.001. PMid:30370217.
http://dx.doi.org/10.1016/j.ijppaw.2018....
). A putative novel genotype of Ehrlichia sp. has been detected in big-eared opossums (D. aurita) from southeastern Brazil (Guimarães et al., 2019Guimarães A, Raimundo JM, Silva AT, Carpintero FM, Pires JR, Benevenute JL, et al. Detection of a putative novel genotype of Ehrlichia sp. from opossums (Didelphis aurita) from Brazil. Rev Bras Parasitol Vet 2019; 28(1): 140-144. http://dx.doi.org/10.1590/s1984-296120180068. PMid:30427523.
http://dx.doi.org/10.1590/s1984-29612018...
). Morphological identification of piroplasmids (previously named as Nuttallia brasiliensis/Theileria brasiliensis/Babesia ernestoi, and currently Babesia brasiliensis) in marsupials circulating in Brazil was performed virtually 100 years ago (Regendanz & Kikuth, 1928Regendanz P, Kikuth W. Sur un parasite du sang des “Quica” (Metachirus quica) Nuttallia brasiliensis n. sp., et influence de la rate sur les infections latentes du sang. C R H Seanc Mem Soc Biol 1928; 98: 1567.). Additionally, a novel piroplasmid closely related to a Babesia sp. detected in Monodelphis domestica opossums from the Brazilian Pantanal has been found in D. marsupialis opossums from the Brazilian Amazon (Soares et al., 2017Soares HS, Marcili A, Barbieri ARM, Minervino AHH, Moreira TR, Gennari SM, et al. Novel piroplasmid and Hepatozoon organisms infecting the wildlife of two regions of the Brazilian Amazon. Int J Parasitol Parasites Wildl 2017; 6(2): 115-121. http://dx.doi.org/10.1016/j.ijppaw.2017.05.002. PMid:28603688.
http://dx.doi.org/10.1016/j.ijppaw.2017....
), and another Piroplasmida genotype was reported in two/31 (6.45%) D. marsupialis trapped in Sinop municipality, State of Mato Grosso (Colle et al., 2019Colle AC, Mendonça RFB, Maia MO, Freitas LC, Witter R, Marcili A, et al. Molecular survey of tick-borne pathogens in small mammals from Brazilian Amazonia. Rev Bras Parasitol Vet 2019; 28(4): 592-604. http://dx.doi.org/10.1590/s1984-29612019086. PMid:31800885.
http://dx.doi.org/10.1590/s1984-29612019...
). In the present study, all white-eared opossums tested negative for Theileria/Babesia spp. and Ehrlichia/Anaplasma spp. Although neither clinical signs of infection nor tick vectors have been established for the novel pathogens described in opossums from Brazil, further studies should focus on evaluating this group of marsupials to better understand and characterize the pathogens found.

In conclusion, ‘Candidatus Mycoplasma haemoalbiventris’ has been detected in white-eared opossums from the Foz do Iguaçu city (Paraná state, southern Brazil), while the animals from Curitiba city tested negative. However, the clinical signs associated with the infection caused by this organism and its putative vectors remain unknown. All animals from both cities tested negative for Theileria/Babesia spp. and Ehrlichia/Anaplasma spp.

Acknowledgments

This research was funded by Universidade Federal do Paraná (Grant no. 23075.058259/2020-23). This study is part of a PhD degree for Renata Antonangelo at the Universidade Federal do Paraná. Flávia Collere, Rafaella Martini and André Saldanha were sponsored by a fellowship from the the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) at the time of research. Vanessa Coradi and Nathália Soares were sponsored by a fellowship from the Brazilian National Council of Scientific and Technological Development (CNPq). CNPq also provided a fellowship of research productivity (PQ) to Dr. Rafael F.C. Vieira (CNPq - 313161/2020-8).

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Publication Dates

  • Publication in this collection
    06 Sept 2021
  • Date of issue
    2021

History

  • Received
    26 May 2021
  • Accepted
    13 July 2021
Colégio Brasileiro de Parasitologia Veterinária FCAV/UNESP - Departamento de Patologia Veterinária, Via de acesso Prof. Paulo Donato Castellane s/n, Zona Rural, , 14884-900 Jaboticabal - SP, Brasil, Fone: (16) 3209-7100 RAMAL 7934 - Jaboticabal - SP - Brazil
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