Abstract
Domestic farm animals (n=145) were sampled for the presence of ectoparasites in northwestern Peru during March, 2008. Ninety domestic animals (62%) were positive for the presence of an ectoparasite(s) and produced a total collection of the following: 728 ticks [Amblyomma maculatum, Anocentor nitens, Rhipicephalus (Boophilus) microplus, Rhipicephalus sanguineus, and Otobius megnini], 12 lice (Haematopinus suis), and 3 fleas (Ctenocephalides felis). A Rickettsia genus-specific qPCR assay was performed on nucleic acid preparations of the collected ectoparasites that resulted in 5% (37/743, 35 ticks and 2 fleas) of the ectoparasites positive for the presence of Rickettsia. DNA from the positive individual ticks was tested with 2 other qPCR assays for the presence of the ompB gene in Candidatus Rickettsia andeanae or Rickettsia parkeri. Candidatus R. andeanae was found in 25 A. maculatum ticks and in two Rh. sanguineus ticks, whereas R. parkeri was detected in 6 A. maculatum ticks. Two A. maculatum were co-infected with both Candidatus R. andeanae and R. parkeri. Rickettsia felis was detected in 2 fleas, Ctenocephalides felis, by multilocus sequence typing of the 17-kD antigen and ompA genes. These findings expand the geographic range of R. parkeri to include Peru as well as expand the natural arthropod vector of Candidatus R. andeanae to include Rhipicephalus sanguineus.
Introduction
Materials and Methods
Sample collections occurred in March, 2008, at 17 sites within 3 districts in the Department of Piura, Peru: Paimas (04°37’49”S and 79°56’85”W), Suyo (04°51’42”S and 80°00’42”), and Tambogrande (04°44’14”L and 80°17’69”W). A variety of domestic animals common to the typical rural farm were examined for external parasites. All visible ectoparasites to the unaided eye were removed with fine forceps, placed in appropriate containers, and later identified to species using morphological keys of Aragão and Fonseca (1961) and Guglielmone and Viñabal (1994). Specimens were transported alive to the laboratory, where they were flash-frozen and maintained at −80°C until DNA extraction. Each specimen was surface-sterilized using sequential washes of sodium hypochlorite (0.05%), benzalkonium chloride (0.5%), ethanol (70%), and distilled sterile water. The specimens were then dried on filter paper and cut in half with a sterile scalpel. One half was used for DNA extraction and PCR analysis and the other half stored for future analysis. Candidatus R. andeanae and R. parkeri were detected by species-specific qPCR, whereas R. felis was found by multilocus sequence typing of the 17-kD antigen and ompA genes. DNA extraction, PCR, and sequencing methodologies were performed according to Jiang et al. (2005).
Results
A total of 145 domestic farm animals were surveyed, of which 90 animals were found to have ectoparasites (Table 1). From these 90 animals, 743 ectoparasites were collected: 728 ticks, 3 fleas, and 12 lice. Percentages of ectoparasites collected in relation to the domestic animals were the following: 38.9% on horses, 34.6% on dogs, 22.5% on donkeys, 2.7% on pigs, and 1.3% on cows. Cats, chickens, goats, guinea pig, and sheep did not yield any ectoparasites. SFG rickettsiae were detected in ticks and fleas from 22 domestic animals (11/50 dogs, 5/25 horses, 4/26 donkeys, 1/12 pigs, and 1/13 cows), resulting in 5% (37/743) of the total ectoparasite specimens positive for the presence of a SFG rickettsiae. Positive ectoparasites were 2 Ctenocephalides felis (Bounché) fleas and 35 ticks: 34.7% (33/95) of the collected Amblyomma maculatum Koch and 0.9% (2/221) of the collected Rhipicephalus sanguineus (Latreille). No Rickettsia was found in the other 3 tick species collected, Anocentor nitens (Neumann), Rhipicephalus (Boophilus) microplus (Canestrini), Otobius megnini (Dugès), or in the 12 louse specimens, all identified as the hog louse Haematopinus suis (Linnaeus). Candidatus R. andeanae was found in 27 A. maculatum ticks (collected from 7 dogs, 5 horses, 4 donkeys, and 1 cow) and in 2 Rh. sanguineus ticks (from 2 dogs) (Table 2). Rickettsia parkeri was detected in 8 A. maculatum ticks (collected from 4 dogs, 3 horses, and 1 pig). Rickettsia felis was detected in the 2 positive fleas, Ct. felis (from 2 dogs). Two specimens of A. maculatum were found co-infected with Candidatus R. andeanae and R. parkeri (Table 2).
Discussion
In this study, we identified the presence of 3 species of SFG rickettsiae in ectoparasites collected in northwestern Peru. Two species of the SFG rickettsia, Candidatus R. andeanae and R. felis, were documented previously (Blair et al. 2004b). We now report the presence of R. parkeri in Peru. R. parkeri is commonly found in A. maculatum ticks in the southeastern United States (Paddock et al. 2010, Varela-Stokes et al. 2011), but an infected A. maculatum had not been documented in Peru until now. Two specimens of A. maculatum were detected with co-infections of Candidatus R. andeanae and R. parkeri, a mixed infection of the same tick with 2 species of Rickettsia that is not frequently reported in the literature. Also, our findings expand the number of tick species known to be infected with Candidatus R. andeanae to include Rh. sanguineus. We believe that this is the first report documenting detection of R. parkeri from within Peru and the first report of Candidatus R. andeanae from Rh. sanguineus.
Footnotes
Acknowledgments
We thank Dr. Rosario Mendez (San Martin de Porres University), Dany Viera (SRS Luciano Castillo Colona–Ministry of Health, Sullana), Leonardo Mendoza (National Institute of Health), and Christopher Cruz (NAMRU-6) for their assistance and support of this study. The views expressed in this article are those of the author(s) and do not necessarily reflect the official policy or position of the Department of the Navy, Department of Defense, or the US Government. This work was supported by DOD–Global Emerging Infection Surveillance, project number 847705.82000.25GB.A0074. The study protocol was approved by the Naval Medical Research Center Institutional Review Board in compliance with all applicable Federal regulations governing the protection of human subjects. This work was prepared as part of official duties of the lead author. Title 17 U.S.C. §105 provides that “Copyright protection under this title is not available for any work of the United States Government.”
Author Disclosure Statement
No competing financial interests exist.
