Emergence of Babesia conradae infection in coyote-hunting Greyhounds in Oklahoma, USA.


Journal

Parasites & vectors
ISSN: 1756-3305
Titre abrégé: Parasit Vectors
Pays: England
ID NLM: 101462774

Informations de publication

Date de publication:
14 Aug 2021
Historique:
received: 12 01 2021
accepted: 27 07 2021
entrez: 15 8 2021
pubmed: 16 8 2021
medline: 18 11 2021
Statut: epublish

Résumé

Babesia species are intraerythrocytic Apicomplexan parasites that infect a wide range of vertebrate hosts. These pathogens are typically transmitted either by tick vectors or by direct blood-to-blood contact, and may cause life-threatening clinical disease, such as thrombocytopenia, hemolytic anemia and acute renal failure, in canine hosts. While Babesia vogeli and Babesia gibsoni infections have both been reported in Oklahoma, reports of Babesia conradae infections have been limited to California. Four separate kennels of coyote-hunting dogs were identified in Oklahoma after the kennels had consulted with Oklahoma State University Boren Veterinary Medical Teaching Hospital (antemortem cases) or the Oklahoma Animal Disease Diagnostic Lab (postmortem cases). Upon owner consent, every accessible dog from each of the four kennels was briefly examined for ectoparasites, particularly ticks, and whole blood samples were collected in EDTA tubes. Clinically ill dogs were examined by a practicing veterinarian, and clinical signs included anorexia, vomiting, lethargy, fever and anemia. DNA was extracted from each blood sample, and a nested PCR was performed using general apicomplexan primers for the partial 18S rRNA gene. PCR products were electrophoresed in agarose matrix, and appropriately sized amplicons were sequenced. Sequences were compared to reference 18S rRNA gene sequences available in GenBank, and samples with > 98% homology to B. conradae (GenBank: AF158702) were considered positive. Babesia conradae-positive dogs were then treated with atovaquone (13.5 mg/kg three times per day) and azithromycin (10 mg/kg once daily) for 10 days and retested at 30 and 60 days post-treatment by PCR. Of 40 dogs tested, 15 (37.5%) were positive for B. conradae with 98-99% sequence homology to B. conradae from California. All positive cases were coyote-hunting Greyhounds. Ectoparasites were not identified on any of the dogs at the time of blood collection. Treatment of clinically ill dogs with atovaquone and azithromycin resulted in complete clinical recovery in all treated dogs with negative follow-up PCR at 30 and 60 days post-treatment. Collectively, this study (i) documents the occurrence of B. conradae in Oklahoma, (ii) highlights this pathogen as a differential to be considered when clinical signs are present, (iii) supports the use of atovaquone and azithromycin as effective treatment in these cases and (iv) demonstrates chronic subclinical carrier dogs serving as potential reservoirs of B. conradae infection to naïve dogs.

Sections du résumé

BACKGROUND BACKGROUND
Babesia species are intraerythrocytic Apicomplexan parasites that infect a wide range of vertebrate hosts. These pathogens are typically transmitted either by tick vectors or by direct blood-to-blood contact, and may cause life-threatening clinical disease, such as thrombocytopenia, hemolytic anemia and acute renal failure, in canine hosts. While Babesia vogeli and Babesia gibsoni infections have both been reported in Oklahoma, reports of Babesia conradae infections have been limited to California.
METHODS METHODS
Four separate kennels of coyote-hunting dogs were identified in Oklahoma after the kennels had consulted with Oklahoma State University Boren Veterinary Medical Teaching Hospital (antemortem cases) or the Oklahoma Animal Disease Diagnostic Lab (postmortem cases). Upon owner consent, every accessible dog from each of the four kennels was briefly examined for ectoparasites, particularly ticks, and whole blood samples were collected in EDTA tubes. Clinically ill dogs were examined by a practicing veterinarian, and clinical signs included anorexia, vomiting, lethargy, fever and anemia. DNA was extracted from each blood sample, and a nested PCR was performed using general apicomplexan primers for the partial 18S rRNA gene. PCR products were electrophoresed in agarose matrix, and appropriately sized amplicons were sequenced. Sequences were compared to reference 18S rRNA gene sequences available in GenBank, and samples with > 98% homology to B. conradae (GenBank: AF158702) were considered positive. Babesia conradae-positive dogs were then treated with atovaquone (13.5 mg/kg three times per day) and azithromycin (10 mg/kg once daily) for 10 days and retested at 30 and 60 days post-treatment by PCR.
RESULTS RESULTS
Of 40 dogs tested, 15 (37.5%) were positive for B. conradae with 98-99% sequence homology to B. conradae from California. All positive cases were coyote-hunting Greyhounds. Ectoparasites were not identified on any of the dogs at the time of blood collection. Treatment of clinically ill dogs with atovaquone and azithromycin resulted in complete clinical recovery in all treated dogs with negative follow-up PCR at 30 and 60 days post-treatment.
CONCLUSIONS CONCLUSIONS
Collectively, this study (i) documents the occurrence of B. conradae in Oklahoma, (ii) highlights this pathogen as a differential to be considered when clinical signs are present, (iii) supports the use of atovaquone and azithromycin as effective treatment in these cases and (iv) demonstrates chronic subclinical carrier dogs serving as potential reservoirs of B. conradae infection to naïve dogs.

Identifiants

pubmed: 34391445
doi: 10.1186/s13071-021-04897-x
pii: 10.1186/s13071-021-04897-x
pmc: PMC8364010
doi:

Substances chimiques

RNA, Ribosomal, 18S 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

402

Informations de copyright

© 2021. The Author(s).

Références

J Vet Intern Med. 2018 Sep;32(5):1609-1617
pubmed: 30307638
Vet Parasitol. 2006 May 31;138(1-2):103-11
pubmed: 16524663
Am J Vet Res. 1993 Oct;54(10):1579-84
pubmed: 8250380
Vet Parasitol. 2012 Jun 8;187(1-2):23-7
pubmed: 22305297
Vet Parasitol. 2010 Sep 20;172(3-4):355-60
pubmed: 20541322
Vet Parasitol. 2000 Apr 28;89(3):241-8
pubmed: 10760414
Int J Parasitol. 2000 Dec;30(14):1501-5
pubmed: 11428342
Int J Parasitol. 2012 Apr;42(4):353-63
pubmed: 22429769
J Parasitol. 1997 Aug;83(4):575-83
pubmed: 9267395
Parasit Vectors. 2015 Apr 08;8:207
pubmed: 25890372
J Am Vet Med Assoc. 2002 Jan 15;220(2):185-9
pubmed: 12126127
Vet Parasitol. 2008 Feb 14;151(2-4):279-85
pubmed: 18160223
Vet Clin North Am Small Anim Pract. 2007 Mar;37(2):245-66, vi
pubmed: 17336674
J Vet Intern Med. 2010 Jan-Feb;24(1):127-31
pubmed: 20002547
Gene. 1988 Nov 30;71(2):491-9
pubmed: 3224833
J Parasitol. 2001 Apr;87(2):437-8
pubmed: 11318581
J Am Vet Med Assoc. 1991 Sep 1;199(5):601-5
pubmed: 1787120
J Vet Intern Med. 2004 Jul-Aug;18(4):494-8
pubmed: 15320586

Auteurs

Erin Stayton (E)

Oklahoma State University, 250 McElroy Hall, Stillwater, OK, USA.

Megan Lineberry (M)

Oklahoma State University, 250 McElroy Hall, Stillwater, OK, USA.

Jennifer Thomas (J)

Oklahoma State University, 250 McElroy Hall, Stillwater, OK, USA.

Tina Bass (T)

Vinita Veterinary Center, Vinita, OK, USA.

Kelly Allen (K)

Oklahoma State University, 250 McElroy Hall, Stillwater, OK, USA.

Ramaswamy Chandrashekar (R)

IDEXX Laboratories, Inc., Westbrook, ME, USA.

Gene Yost (G)

Crescent Veterinary Hospital, Crescent, OK, USA.

Mason Reichard (M)

Oklahoma State University, 250 McElroy Hall, Stillwater, OK, USA.

Craig Miller (C)

Oklahoma State University, 250 McElroy Hall, Stillwater, OK, USA. craig.miller@okstate.edu.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH