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An atypical case of Babesia bigemina parasitising a dog from a rural area of eastern Mexico

Um caso atípico de Babesia bigemina parasitando um cão de uma área rural do leste do México

Abstract

A dog that shared habitat with domestic animals in a cattle farm and that was exposed to wildlife was taken to a private practitioner for clinical examination. The analyses conducted on the patient revealed the presence of Babesia bigemina by a molecular test. Clinical signs such as lethargy, anorexia and hyperthermia > 39 °C, pale mucous membranes and blood urine were observed in the patient. The animal was treated with imidocarb dipropionate (two doses each 0.5 ml/10 kg b.w. at an interval of 14 days). On treatment day 7, the clinical signs were mostly reduced. On day 30, PCR was carried out to assess the efficacy of the treatment, with a negative result. This case represents the first report of babesiosis due to B. bigemina in a dog living on a cattle farm in Mexico. It indicates the lower host specify of these pathogens and that dogs can play a role as sentinels of vector-borne parasites in livestock animals.

Keywords:
Piroplasms; tick-borne disease; phylogenetic analysis; canine babesiosis

Resumo

Um cão que compartilhava hábitat com animais domésticos em uma fazenda de gado e que foi exposto à vida selvagem foi levado a um clínico particular para que fosse examinado. As análises realizadas no paciente revelaram a presença de Babesia bigemina por um teste molecular. Sinais clínicos, como letargia, anorexia e hipertermia > 39°C, mucosas pálidas e sangue na urina foram observados no paciente. O animal foi tratado com dipropionato de imidocarb (duas doses cada 0,5 ml/10 kg de peso corporal em um intervalo de 14 dias). No dia de tratamento 7, os sinais clínicos foram reduzidos. No dia 30, foi realizada PCR para avaliar a eficácia do tratamento, com resultado negativo. Esse caso representa o primeiro relato de babesiose por B. bigemina em um cão que vive em uma fazenda de gado no México. Isso indica que o hospedeiro inferior especifica esses patógenos, e que os cães podem desempenhar um papel como sentinelas de parasitas transmitidos por vetores em animais de criação.

Palavras-chave:
Piroplasmas; doença transmitida por carrapatos; análise filogenética; babesiose canina

Canine babesiosis is one of the most widespread tick-borne diseases which affects dog populations worldwide. The disease may cause a multi-organ dysfunction syndrome, which can compromise the life of the host. It is caused by several species of the protozoan genus Babesia. Based on the size of the intraerythrocytic stages of the parasite, two main groups have been recognised: the large group (Babesia canis, Babesia rossi and Babesia vogeli) and the small group (Babesia gibsoni, Babesia conradae, Babesia vulpes and Babesia negevi) (Baneth et al., 2015Baneth G, Florin-Christensen M, Cardoso L, Schnittger L. Reclassification of Theileria annae as Babesia vulpes sp. nov. Parasit Vectors 2015; 8(1): 207. http://dx.doi.org/10.1186/s13071-015-0830-5. PMid:25890372.
http://dx.doi.org/10.1186/s13071-015-083...
, 2020Baneth G, Nachum-Biala Y, Birkenheuer AJ, Schreeg ME, Prince H, Florin-Christensen M, et al. A new piroplasmid species infecting dogs: morphological and molecular characterization and pathogeny of Babesia negevi n. sp. Parasit Vectors 2020; 13(1): 130. http://dx.doi.org/10.1186/s13071-020-3995-5. PMid:32312309.
http://dx.doi.org/10.1186/s13071-020-399...
; Bawm et al., 2021Bawm S, Myaing TT, Thu MJ, Akter S, Htun LL, Win MM, et al. PCR detection and genetic characterization of piroplasms from dogs in Myanmar, and a possible role of dogs as reservoirs for Theileria parasites infecting cattle, water buffaloes, and goats. Ticks Tick Borne Dis 2021; 12(4): 101729. http://dx.doi.org/10.1016/j.ttbdis.2021.101729. PMid:33984595.
http://dx.doi.org/10.1016/j.ttbdis.2021....
). Among them, B. vogeli is most widely distributed in canids throughout the tropical and subtropical regions (Penzhorn, 2020Penzhorn BL. Don’t let sleeping dogs lie: unravelling the identity and taxonomy of Babesia canis, Babesia rossi and Babesia vogeli. Parasit Vectors 2020; 13(1): 184. http://dx.doi.org/10.1186/s13071-020-04062-w. PMid:32312292.
http://dx.doi.org/10.1186/s13071-020-040...
). It has been postulated that the species of the genus Babesia has been considered as highly specific for a given host species or group. However, the specificity of these piroplasms is probably lower than expected (Uilenberg, 2006Uilenberg G. Babesia: a historical overview. Vet Parasitol 2006; 138(1-2): 3-10. http://dx.doi.org/10.1016/j.vetpar.2006.01.035. PMid:16513280.
http://dx.doi.org/10.1016/j.vetpar.2006....
). Since the implementation of molecular methods, which has increased the sensitivity for the detection of infectious agents, unusual parasite-host associations have started to be described more frequently in dogs. Such is the case of piroplasms from livestock and wild artiodactyls (Theileria annulata, Theileria equi, Theileria sinensis, Theileria velifera and uncharacterized Theileria), which have been reported in dogs from different countries of the Afrotropical and Oriental regions (Nayyar Ghauri et al., 2019Nayyar Ghauri H, Ijaz M, Farooqi SH, Ali A, Ghaffar A, Saleem S, et al. A comprehensive review on past, present and future aspects of canine theileriosis. Microb Pathog 2019; 126: 116-122. http://dx.doi.org/10.1016/j.micpath.2018.10.033. PMid:30385396.
http://dx.doi.org/10.1016/j.micpath.2018...
). On the other hand, on cattle farms, canids may share ectoparasites (that act as vectors of several pathogens) with livestock and wildlife. However, the role of dogs as sentinels of tick-borne parasites in livestock is not fully understood. Thus, considering the high prevalence of several tick’s species in canine populations throughout Mexico, it is not surprising to find these shared pathogens among species of hosts that are infested by the same tick species (Ojeda‐Chi et al., 2019Ojeda‐Chi MM, Rodriguez‐Vivas RI, Esteve‐Gasent MD, Pérez de León AA, Modarelli JJ, Villegas‐Perez SL. Ticks infesting dogs in rural communities of Yucatan, Mexico and molecular diagnosis of rickettsial infection. Transbound Emerg Dis 2019; 66(1): 102-110. http://dx.doi.org/10.1111/tbed.12990. PMid:30102850.
http://dx.doi.org/10.1111/tbed.12990...
). This report is the first record of the livestock piroplasm Babesia bigemina infecting a dog. All applicable international, national, and/or institutional guidelines for the care and use of animals were followed. No approval was required. Anesthesia, euthanasia, or any other kind of animal sacrifice was not a part of the study. A 4-year-old male mixed-breed dog that shared habitat with livestock and was exposed to wildlife was taken to a private practice in the municipality of Jesus Carranza (southern Veracruz, Mexico) with a 1-week history of anorexia, pigmented faeces, pigmenturia, fever of 40 °C and lethargy. The dog had not travelled outside of the state of Veracruz and had never received a blood transfusion. After the first physical examination, the dog was evaluated via a baseline assessment consisting on automatic hematological (XT-4000i, Sysmex), and serum biochemistry analyses (Cobas Integra 400 Plus analyzer). Then, a screening for vector-borne diseases, using a immunochromatographic test SNAP® 4Dx® Plus followed by a blood smear stained with Giemsa and observed at 100x. Additionally, ticks on the dog´s body were removed using forceps, and each one was kept in a small flask with 70% ethanol. Ticks were identified according to the morphologic characteristics as described elsewhere (Gúzman-Cornejo et al., 2011Guzmán-Cornejo C, Robbins RG, Guglielmone AA, Montiel-Parra G, Pérez TM. The Amblyomma (Acari: Ixodida: Ixodidae) of Mexico: identification keys, distribution and hosts. Zootaxa 2011; 2998(1): 16-38. http://dx.doi.org/10.11646/zootaxa.2998.1.2.
http://dx.doi.org/10.11646/zootaxa.2998....
; Nava et al., 2014Nava 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, 1844, and Amblyomma sculptum Berlese, 1888 (Ixodida: ixodidae). Ticks Tick Borne Dis 2014; 5(3): 252-276. http://dx.doi.org/10.1016/j.ttbdis.2013.11.004. PMid:24556273.
http://dx.doi.org/10.1016/j.ttbdis.2013....
). According to taxonomic keys, we identified the tick species Amblyomma mixtum on the dog (Figure 1a). Blood and serum analyses revealed anaemia; thrombocytopenia, leucocytosis, eosinophilia, blood urea nitrogen and creatinine levels were increased (Table 1). The SNAP 4Dx test was negative. However, light microscopy of the blood smear revealed the presence of pyriform structures inside erythrocytes (Figure 1b). To confirm the identification of piroplasms, a fragment of the 571-bp region of the 18S ribosomal gene (18S-rDNA) was amplified with the primers BAB01 (5′CCGTGCTAATTGTAGGGCTAATACA3′) and BAB02 (5′GCTTGAAACACTCTARTTTTCTCAAAG 3′) as described previously (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....
; Sarma et al., 2019Sarma K, Nachum-Biala Y, Kumar M, Baneth G. Molecular investigation of vector-borne parasitic infections in dogs in Northeast India. Parasit Vectors 2019; 12(1): 122. http://dx.doi.org/10.1186/s13071-019-3389-8. PMid:30909966.
http://dx.doi.org/10.1186/s13071-019-338...
). Genomic DNA was extracted from 100 μL of whole blood using the QIAampDNA Minikit (Qiagen, Germany). Amplification product were submitted for purification and sequencing at Macrogen Inc., Korea, and the obtained sequence was deposited in GenBank under accession number: OM530520. Subsequently, the sequence was compared with those available in GenBank using the Basic Local Alignment Search Tool (BLASTn tool). The BLAST analysis revealed the highest nucleotide identity (i.e.,100% and 99.2%) with reference sequences of Babesia bigemina deposited in GenBank (OK605299, MH050387) reported in cattle and tick Rhipicephalus microplus from China and India. Additionally, sequence generated in this study and those of other Babesia species deposited in GenBank were aligned using the algorithm MUSCLE in MEGA 11. Subsequently, a phylogenetic reconstruction using the Maximum likelihood method was performed, also in MEGA 11 (Kumar et al., 2018Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 2018; 35(6): 1547-1549. http://dx.doi.org/10.1093/molbev/msy096. PMid:29722887.
http://dx.doi.org/10.1093/molbev/msy096...
). Branch support was estimated using 1,000 non-parametric bootstraps. The phylogenetic analysis supported the finding of B. bigemina. The sequence generated in this work were grouped with those of B. bigemina in a monophyletic group with support values that varied from 95-100 (Figure 2).

Figure 1
(a) Dorsal view of the female Amblyomma mixtum; (b) Photomicrograph of the paired intra-erythrocytic pyriform identified on Giemsa-stained thin blood smear suggested as Babesia sp.
Table 1
Hematological and biochemical analyses in a dog with B. bigemina infection during treatment with imidocard dipropionate.
Figure 2
Maximum-likelihood (ML) phylogenetic reconstruction generated with Tamura-Nei model (TN93). Constructed phylogenetic tree based on 571 pb of the 18S rDNA gene of genus Babesia. Sequence recovered in this study are marked with solid figures (red). The numbers at the nodes correspond to bootstrap values higher than 50% obtained with 1000 replicates. Theileria equi was used as outgroup.

The dog was treated with imidocarb dipropionate (two doses each 0.5 ml/10 kg b.w. at an interval of 14 days, intramuscularly) and fluid therapy. Additionally, a single dose of a chewable tablet that contained afoxolaner (2.5-5 mg/kg) and milbemycin oxime (0.5-1 mg/kg) NexGard Spectra ® was given orally. On day 7 of treatment, clinical signs in this patient were mostly reduced, with a rapid resolution. On day 20, the dog underwent physical examination. Red blood analysis showed increased values in RBC, Hb and HT compared to day 0, indicating recovery from anaemia. In day 30, a PCR was carried out again to assess the efficacy of the treatment, and Babesia DNA was no longer detectable. The treatment showed good tolerance and safety, with scarce adverse events observed. The case resolved favorably, and the patient was discharged.

In this report, we describe the first record and characterisation of B. bigemina in a dog with clinical and haematological abnormalities suggestive of Babesia infection in Mexico. Previous records in Mexico have shown that dogs in rural areas can be infested by several hard tick species such as Amblyomma mixtum, Amblyomma ovale, Amblyomma parvum, Ixodes affinis, Rhipicephalus microplus, Rhipicephalus sanguineus s.l. and Amblyomma oblongoguttatum. The tick A. mixtum, detected in this case, is the same as that previously reported attached to dogs in rural communities in Yucatan (Ojeda‐Chi et al., 2019Ojeda‐Chi MM, Rodriguez‐Vivas RI, Esteve‐Gasent MD, Pérez de León AA, Modarelli JJ, Villegas‐Perez SL. Ticks infesting dogs in rural communities of Yucatan, Mexico and molecular diagnosis of rickettsial infection. Transbound Emerg Dis 2019; 66(1): 102-110. http://dx.doi.org/10.1111/tbed.12990. PMid:30102850.
http://dx.doi.org/10.1111/tbed.12990...
). Additionally, A. mixtum parasitises a wide range of hosts and can take advantage of the nutritional resources present in the area (Gúzman-Cornejo et al., 2011Guzmán-Cornejo C, Robbins RG, Guglielmone AA, Montiel-Parra G, Pérez TM. The Amblyomma (Acari: Ixodida: Ixodidae) of Mexico: identification keys, distribution and hosts. Zootaxa 2011; 2998(1): 16-38. http://dx.doi.org/10.11646/zootaxa.2998.1.2.
http://dx.doi.org/10.11646/zootaxa.2998....
). For this reason, it is likely that this tick can be a potential transmitter of Babesia species and exchanges several pathogens between domestic animals and wildlife.

One of the main clinical findings observed in canine babesiosis is anaemia. Some reports state that oxidative stress and lipid peroxidation play a role in the pathogenesis of anaemia in some hemoprotozoan diseases (Maharana et al., 2016Maharana BR, Tewari AK, Saravanan BC, Sudhakar NR. Important hemoprotozoan diseases of livestock: Challenges in current diagnostics and therapeutics: an update. Vet World 2016; 9(5): 487-495. http://dx.doi.org/10.14202/vetworld.2016.487-495. PMid:27284225.
http://dx.doi.org/10.14202/vetworld.2016...
). In biological membranes, these mechanisms induce disturbances of the structural integrity, leading to the rupture of the membrane and the release of red blood cell contents, which causes lysis (Holovakha et al., 2018Holovakha VI, Piddubnуak ОV, Bakhur TI, Vovkotrub NV, Antipov AA, Anfiorova MV, et al. Changes in erythrocytopoesis indices in dogs with babesiosis. Regul Mech Biosyst 2018; 9(3): 379-383. http://dx.doi.org/10.15421/021856.
http://dx.doi.org/10.15421/021856...
). However, in babesiosis anaemia is caused by multifactorial components, including direct parasite damage to the erythrocyte membrane, splenic removal of damaged and parasitized erythrocytes, as well as activation of the immune system such as complement cascade and/or presence of anti-erythrocyte antibodies (Köster et al., 2015Köster LS, Lobetti RG, Kelly P. Canine babesiosis: a perspective on clinical complications, biomarkers, and treatment. Vet Med 2015; 6: 119-128. http://dx.doi.org/10.2147/VMRR.S60431. PMid:30155438.
http://dx.doi.org/10.2147/VMRR.S60431...
). Other clinical signs of canine babesiosis include fever, anorexia, depression and lethargy (Crnogaj et al., 2010Crnogaj M, Petlevski R, Mrljak V, Kis I, Torti M, Kucer N, et al. Malondialdehyde levels in serum of dogs infected with Babesia canis. Vet Med 2010; 55(4): 163-171. http://dx.doi.org/10.17221/77/2010-VETMED.
http://dx.doi.org/10.17221/77/2010-VETME...
), which coincide with our case. The abnormalities in the elevation of white blood cells could be related to the Babesia infection, with the likely exception of the peripheral eosinophilia. However, absolute eosinophilia cannot be considered a marker of babesiosis, considering that it is not a specific alteration of the infection in dogs but a common finding secondary to several helminths parasitic or allergic diseases (Chidumayo, 2018Chidumayo NN. Epidemiology of canine gastrointestinal helminths in sub-Saharan Africa. Parasit Vectors 2018; 11(1): 100. http://dx.doi.org/10.1186/s13071-018-2688-9. PMid:29458421.
http://dx.doi.org/10.1186/s13071-018-268...
). Low platelet count is well described in canine babesiosis as well as in other hemoprotozoan diseases, such as malaria and trypanosomiasis (Karasová et al., 2022Karasová M, Tóthová C, Víchová B, Blaňarová L, Kisková T, Grelová S, et al. Clinical efficacy and safety of Malarone®, azithromycin and artesunate combination for treatment of Babesia gibsoni in naturally infected dogs. Animals 2022; 12(6): 708. http://dx.doi.org/10.3390/ani12060708. PMid:35327106.
http://dx.doi.org/10.3390/ani12060708...
). However, the mechanism of thrombocytopenia seen in babesiosis is not clear. The severity and rapid recovery of the platelet counts has led to the suggestion that immune-mediated mechanisms are involved (Rautenbach et al., 2018Rautenbach Y, Schoeman J, Goddard A. Prevalence of canine Babesia and Ehrlichia co-infection and the predictive value of haematology. Onderstepoort J Vet Res 2018; 85(1): e1-e5. http://dx.doi.org/10.4102/ojvr.v85i1.1626. PMid:30326715.
http://dx.doi.org/10.4102/ojvr.v85i1.162...
). Higher serum urea levels are not uncommon in dogs with babesiosis, and this elevation is often disproportionate to the rise in creatinine levels. This is probably due to increased protein catabolism and urea production resulting from gastrointestinal haemorrhage or protein catabolism due to the febrile inflammatory illness (Ullal et al., 2018Ullal T, Birkenheuer A, Vaden S. Azotemia and proteinuria in dogs infected with Babesia gibsoni. J Am Anim Hosp Assoc 2018; 54(3): 156-160. http://dx.doi.org/10.5326/JAAHA-MS-6693. PMid:29558219.
http://dx.doi.org/10.5326/JAAHA-MS-6693...
). Regarding treatment, imidocarb is the one of the main drugs used in the antiprozoal treatment of babesiosis and has direct action against the parasite DNA, causing nucleic acid damage and inhibition of cellular repair and replication; however, a few drugs and drug combinations are used in the treatment of canine babesiosis, often without complete parasite elimination, and the dogs usually become chronic carriers or present with recurrent episodes of acute infection (Baneth, 2018Baneth G. Antiprotozoal treatment of canine babesiosis. Vet Parasitol 2018; 254: 58-63. http://dx.doi.org/10.1016/j.vetpar.2018.03.001. PMid:29657012.
http://dx.doi.org/10.1016/j.vetpar.2018....
). In this new scenario, veterinarians should be aware of unexpected Babesia species in dogs that, as known for this species, may be even worse than in livestock, considering the rapid manifestation of the clinical signs. In conclusion, the spectrum of Babesia pathogens that infect dogs is gradually being elucidated with the aid of new molecular techniques and meticulous clinical investigation. Additionally, chemoprophylaxis should also be adopted for dogs living in an endemic area, with the primary means of prevention being tick control.

  • How to cite: Bravo-Ramos JL, Sánchez-Montes S, Ballados-González GG, Romero-Salas D, Gamboa-Prieto J, Olivares-Muñoz A. An atypical case of Babesia bigemina parasitising a dog from a rural area of eastern Mexico. Braz J Vet Parasitol 2022; 31(3): e006622. https://doi.org/10.1590/S1984-29612022039
  • Financial support: The authors declare that no funds, grants, or other support were received during the preparation of this manuscript.
  • Ethical Approval

    All applicable international, national, and/or institutional guidelines for the care and use of animals were followed. No approval was required. Anesthesia, euthanasia, or any other kind of animal sacrifice was not a part of the stud.

References

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    » http://dx.doi.org/10.1016/j.ttbdis.2012.02.003
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    » http://dx.doi.org/10.1186/s13071-015-0830-5
  • Baneth G, Nachum-Biala Y, Birkenheuer AJ, Schreeg ME, Prince H, Florin-Christensen M, et al. A new piroplasmid species infecting dogs: morphological and molecular characterization and pathogeny of Babesia negevi n. sp. Parasit Vectors 2020; 13(1): 130. http://dx.doi.org/10.1186/s13071-020-3995-5 PMid:32312309.
    » http://dx.doi.org/10.1186/s13071-020-3995-5
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    » http://dx.doi.org/10.1016/j.vetpar.2018.03.001
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    » http://dx.doi.org/10.1016/j.ttbdis.2021.101729
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    » http://dx.doi.org/10.1186/s13071-018-2688-9
  • Crnogaj M, Petlevski R, Mrljak V, Kis I, Torti M, Kucer N, et al. Malondialdehyde levels in serum of dogs infected with Babesia canis. Vet Med 2010; 55(4): 163-171. http://dx.doi.org/10.17221/77/2010-VETMED
    » http://dx.doi.org/10.17221/77/2010-VETMED
  • Guzmán-Cornejo C, Robbins RG, Guglielmone AA, Montiel-Parra G, Pérez TM. The Amblyomma (Acari: Ixodida: Ixodidae) of Mexico: identification keys, distribution and hosts. Zootaxa 2011; 2998(1): 16-38. http://dx.doi.org/10.11646/zootaxa.2998.1.2
    » http://dx.doi.org/10.11646/zootaxa.2998.1.2
  • Holovakha VI, Piddubnуak ОV, Bakhur TI, Vovkotrub NV, Antipov AA, Anfiorova MV, et al. Changes in erythrocytopoesis indices in dogs with babesiosis. Regul Mech Biosyst 2018; 9(3): 379-383. http://dx.doi.org/10.15421/021856
    » http://dx.doi.org/10.15421/021856
  • Karasová M, Tóthová C, Víchová B, Blaňarová L, Kisková T, Grelová S, et al. Clinical efficacy and safety of Malarone®, azithromycin and artesunate combination for treatment of Babesia gibsoni in naturally infected dogs. Animals 2022; 12(6): 708. http://dx.doi.org/10.3390/ani12060708 PMid:35327106.
    » http://dx.doi.org/10.3390/ani12060708
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    » http://dx.doi.org/10.2147/VMRR.S60431
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    » http://dx.doi.org/10.1093/molbev/msy096
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    » http://dx.doi.org/10.14202/vetworld.2016.487-495
  • 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, 1844, and Amblyomma sculptum Berlese, 1888 (Ixodida: ixodidae). Ticks Tick Borne Dis 2014; 5(3): 252-276. http://dx.doi.org/10.1016/j.ttbdis.2013.11.004 PMid:24556273.
    » http://dx.doi.org/10.1016/j.ttbdis.2013.11.004
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    » http://dx.doi.org/10.1016/j.micpath.2018.10.033
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    » http://dx.doi.org/10.1111/tbed.12990
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Publication Dates

  • Publication in this collection
    08 Aug 2022
  • Date of issue
    2022

History

  • Received
    26 Apr 2022
  • Accepted
    05 July 2022
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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