Seroprevalence and Genotypic Analysis of Ehrlichia canis Infection in Dogs and Humans in Cauca, Colombia

Author:

Forero-Becerra Elkin1,Patel Jignesh2,Martínez-Díaz Heidy-C3,Betancourt-Ruiz Paola3,Benavides Efraín4,Durán Steven4,Olaya-Másmela Luz-A5,Bolaños Eliana6,Hidalgo Marylin3,McBride Jere W.2

Affiliation:

1. 1Research Training Program, Fogarty International Center (Code 1 D43), University of Texas Medical Branch at Galveston, Galveston, Texas;

2. 2Department of Pathology, University of Texas Medical Branch at Galveston, Galveston, Texas;

3. 3Grupo de Enfermedades Infecciosas, Departamento de Microbiología, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá D.C., Colombia;

4. 4Grupo de Investigación Epidemiología y Salud Pública, Facultad de Ciencias Agropecuarias, Universidad de La Salle, Bogotá, D.C., Colombia;

5. 5Programa de Medicina, Facultad de Ciencias de La Salud, Universidad Libre - Cali, Sede Valle del Lili, Santiago de Cali, Colombia;

6. 6Secretaría de Salud del Departamento del Cauca, Popayán, Colombia

Abstract

ABSTRACTEhrlichia canis infections have been reported in humans in Venezuela and Costa Rica. In this study, 506 healthy residents and 114 dogs from four municipalities (Cauca, Colombia) were surveyed and blood samples collected. Antibodies to E. canis in human and canine sera were evaluated using the Tandem repeat protein 19 (TRP19) peptide ELISA and indirect immunofluorescence assay (IFA). Ehrlichia canis TRP19 antibodies were detected in only 1/506 human sera, but the single positive sample was negative by IFA. The majority (75/114; 66%) of dogs surveyed had antibodies to the E. canis TRP19 peptide by ELISA, and eight randomly selected sera were further confirmed by E. canis IFA. Genomic DNA samples obtained from 73 E. canis TRP19 ELISA–positive dog blood samples were examined by PCR targeting the 16S ribosomal ribonucleic acid (rRNA) gene. Ehrlichia canis 16S rRNA was amplified in 30 (41%) of the dogs, and 16 amplicons were selected for DNA sequencing, which confirmed that all were E. canis. A second PCR was performed on the 16 confirmed E. canis 16S rRNA PCR–positive samples to determine the TRP36 genotype by amplifying the trp36 gene. TRP36 PCR amplicon sequencing identified nine dogs infected with the U.S. E. canis TRP36 genotype (56%), one dog with the Brazilian genotype (6%), and six dogs with the Costa Rican genotype (38%). Moreover, these molecular genotype signatures were consistent with serologic analysis using TRP36 genotype–specific peptides. Notably, there was no serologic evidence of E. canis infection in humans, suggesting that E. canis infection in dogs in Cauca is not associated with zoonotic human infection.

Publisher

American Society of Tropical Medicine and Hygiene

Subject

Virology,Infectious Diseases,Parasitology

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