Abstract
Background:
Ehrlichiosis is an emerging tick-borne zoonotic disease caused by the family of Anaplasmatacea. Recently, outbreak of human monocytic ehrlichiosis was reported in northern part of Iran. Besides, serological evidence of canine monocytic ehrlichiosis caused by Ehrlichia canis was reported from southeastern of Iran but the epidemiology of this disease is almost undetermined in Iran. The present study was designed to use PCR for detection of Ehrlichia spp. in tick infested household dogs and determination of risks of disease transmission to dog’s owners.
Method:
Blood samples were prepared from 100 tick infested household dogs after complete clinical examination. Complete cell blood count was done for each sample. DNA extraction was done and PCR was carried out by a commercial kit afterwards. Regarding to PCR results, blood samples were collected from owners and family members who were exposed to infected and non-infected dogs. A similar method was utilized for DNA extraction and PCR in human samples.
Result:
Ehrlichial DNA was detected by PCR in six percent of Rhipicephalus sanguineus tick pools and 9% of the examined dogs. No positive sample was detected among the 67 examined human bloods.
Conclusion:
Ehrlichiosis could be considered as an emerging canine disease but owning a dog should not be considered a major risk factor for ehrlichiosis in humans. Further serological and molecular studies in different parts of Iran are required to clarify the epidemiology of ehrlichiosis in canine, ticks, and human population.
Keywords: Ehrlichiosis, Dog, Ownership risk, Tick, Iran
Introduction
Humans and dogs are both susceptible to tick-borne diseases. Whenever dogs have tick infestation, they could be considered as reservoirs for human pathogens, as definitive feeding hosts for vector ticks or as mechanical transporters. Borreliosis, ehrlichiosis and anaplasmosis, are the reported emerging zoonotic diseases, which create ownership risks for tick, infested pet dogs (Fritz 2009).
In the order Rickettsiales Anaplasma phagocytophilum, E. canis, E. chaffeensis, E. ewingii, Rickettsia rickettsii and R. conorii are zoonotic tick-borne pathogens, which expose dogs and their owners (Nicholson et al. 2010).
Ehrlichiosis is a life-threatening emerging human tick-borne zoonosis, caused by obligate intracellular Gram-negative bacteria named Ehrlichiae. The dog brown tick (R. sanguineus) is the main vector of disease in infested dogs (Beugnet et al. 2009).
Rhipicephalus sanguineus is the most prevalent tick in dogs, which has a worldwide distribution. This tick is a common vector of many dogs and human pathogens. This tick is well distributed in both urban and rural areas in tropical, subtropical and some temperate regions. Rhipicephalus sanguineus not only infests dogs but also is highly adapted to live within human dwellings (Dantas-Torres 2010). Recent studies have demonstrated that ticks exposed to high temperatures attach and feed on humans more rapidly. This observation suggests that the risk of human parasitism by R. sanguineus could increase in areas experiencing warmer and/or longer summers, consequently increasing the risk of transmission of zoonotic agents (Guglielmone et al. 2006, Shoorijeh et al. 2008).
The human parasitism by R. sanguineus is relatively common in Europe, particularly during the summer. In contrast, the human parasitism is much less common or maybe much less reported in South America and there is no report about Asian countries (Guglielmone et al. 2006).
Kerman is located in southeast of Iran with warm springs and hot summers which makes it a perfect condition for R. sanguineus activity. On the other hand, most of pet dogs in this area are kept outdoor as guard dogs predisposing them to ectoparasite infestation in warm seasons.
Since the major route of human infection with Ehrlichia spp. is transmission by a vector tick, the presence of infected ticks near humans could be the most important risk factor for human infection (Unver et al. 2001, Dantas-Torres et al. 2006). Dogs play an important role in transporting infected ticks into their surroundings and their owners (Shoorijeh et al. 2008).
In Iran, outbreak of human monocytic ehrlichiosis has been reported from northern part (Babamahmoodi 2004). On the other hand, serological evidences of canine monocytic ehrlichiosis were reported in Kerman and Khuzestan Provinces respectively (Akhtardanesh et al. 2010, Avizeh et al. 2010). Serological studies usually indicates exposure rather than active infection, and might mislead due to serological cross reactions with other closely related organisms, so the present study was designed to use the polymerase chain reaction assay to confirm presence of Ehrlichia spp. in tick infested client-owned dogs and their attached ticks and determine the risks of disease transmission to the dogs’ owners in Kerman City.
Materials and Methods
Blood samples were randomly prepared from 100 owned tick infested dogs regardless of their age, sex and clinical status between April to October 2011. The animals were referred to the teaching veterinary hospital of Shahid Bahonar University of Kerman. Each animal was fully clinically examined and attached semi- or fully engorged ticks were collected from dogs using a forceps and transferred into the labeled holding tubes containing absolute ethanol individually. Then detailed questionnaire was filled for each animal and owner (or other family members) who were in close contact with pet dogs. Five milliliter of blood were collected from the cephalic vein of dogs which their owner provided verbal consent for attending in the study and divided in two tubes containing EDTA anticoagulant. Two-milliliter aliquot of blood was used for hematological evaluation and remaining three milliliter refrigerated at −18 °C for DNA extraction. The same method was used for the owner and family members who accepted to attend in a pathobiology laboratory for blood collection. Complete blood counts were performed by cell counter (Sysmex KX-21N™, USA) for all samples. The presence of hematological disorders such as anemia, leukopenia and thrombocytopenia was recorded in comparison with reference ranges (Tefferi et al. 2005, Willard et al. 2012).
In parasitology laboratory, collected ticks were taken from the absolute ethanol and their identification was carried out by observation with a binocular microscope (40 × magnifications). Ticks were classified into family, genus and species using the taxonomic and morphometric keys (Walker et al. 2003).
At least one to maximum five adult ticks collected from each dog and each species were pooled in sterile Eppendorf tubes and minced using a sterile scalpel blade. Specimens were incubated overnight after adding of 20-microliter proteinase K. Genomic DNA was extracted from specimens by using the QIAamp DNA Mini Kit (QIAGEN, Hilden, Germany) according to the manufacturer instructions. DNA extraction from dogs and human blood samples was carried out by viral gene-spin kits (VeTeK™, South Korea). Finally, PCR was done for all samples by VeTeK™ EHR Detection Kit (VeTeK™, South Korea) according to company instructions.
Ethics
The project underwent ethical review and was given approval by an institutional animal care and done by appropriately qualified scientific colleagues.
Results
A total of 408 ticks were collected from 100 selected dogs which all were identified as Rhipicephalus sanguineus regarding to specific characteristics including red-brown color, elongated body shape, and hexagonal basis capituli. Six of tick pools (6%) and 9% of examined dogs were positive for Ehrlichia spp. by PCR (Fig. 1). Three dogs were Ehrlichia spp. positive whereas their tick pools were negative. In dog population, infection rate was not significantly related to age (P value=0.627) and sex (P value=0.682) (Table 1). No significant changes were seen in owner’s complete blood count tests but some hematological alterations were seen in infected dogs. However, there was no significant difference between the infected and non-infected dogs in PCV level (P value= 0.242), WBC (P value=0.345), neutrophil (P value=0.643), lymphocyte (P value=0.408), eosinophil (P value=0.27) and monocyte count (P value=0.45) (Table 2).
Fig. 1.

Agarose gel electrophoresis for identification of Ehrlichia spp. DNA in ticks and dogs blood samples
L: 100 bp DNA ladder, Cr+: positive control (336 bp), NTC: negative control, lanes 1, 2 Positive dogs blood samples, lane 3, 4 positive tick samples.
Table 1.
Ehrlichia spp. infection status among studied dogs regarding to age and sex groups
| Parameters | Studied dogs population NO. (%) | PCR-positive dogs NO. (%) | |
|---|---|---|---|
| Age | >12 month | 25 (25) | 2(8) |
| 1–3 years | 33(33) | 3(9.1) | |
| >3 years | 42(42) | 4(9.5) | |
| Sex | Male | 58(58) | 5(8.6) |
| Female | 42(42) | 4(9.5) | |
Table 2.
Hematological alteration in studied dogs regarding to Ehrlichia spp. infection status
| Parameter | Unit |
Ehrlichia spp. infection |
|
|---|---|---|---|
| PCR-positive* | PCR-negative* | ||
| PCV | % | 35.4 ± 3.12 | 38.5 ± 6.4 |
| WBC | ×103/ml | 11.2 ± 3.4 | 12.4 ± 4.3 |
| Neutrophil | ×103/ml | 7.3 ± 2.3 | 7.6 ± 2.8 |
| Lymphocyte | ×103/ml | 4.1 ± 1.1 | 4.9 ± 3.1 |
| Basophil | ×103/ml | 0 | 0 |
| Eosinophil | ×103/ml | 0 | 0.05 ± 0.01 |
| Monocyte | ×103/ml | 0.04 ± 0.01 | 0.01 ± 0.01 |
Data are Mean±SEM
Blood samples from 36 persons (owner and family members) that were in close contact with infected dogs (group 1) and 31 owners of non-infected dogs (group 2) were PCR negative. Demographic data for the participants are shown in Table 3. All owners were aware about their dog tick infestation but none of the participants reported a tick bite history.
Table 3.
Demographic data of owners
| Variable | Owners of infected dogs (n=36) | Owners of non-infected dogs (n=31) |
|---|---|---|
| Age(mean ± SEM)* | 35.4 ± 2.9 | 42.0 ± 3.6 |
| Sex NO (%) | ||
| Male | 23 (63.8) | 19 (62) |
| Female | 13 (36.1) | 12 (38) |
| Place of residence No (%) | ||
| Urban | 18 (50) | 28 (90.3) |
| Rural | 18 (50) | 3 (9.7) |
years
Discussion
The genus Ehrlichia consists of five recognized species, including E. canis, E. chaffeensis, E. ewingii, E. muris, and E. ruminantium. Nowadays Ehrlichia species are discovered in new areas and new tick species, which emphasize on wider distribution of these agents. Host population, migration, changes in climate and control failure is environmental factors, which have been known to exacerbate the spread of Ehrlichia species (Esemu et al. 2011).
Dogs can be infected with different Ehrlichia species of which E. canis, E. ewingi, and E. chaffeensis are considered zoonotic. Ehrlichia canis, which is the most prevalent species in dogs, has been shown to infect humans in Venezuela whereas R. sanguineus was a common ectoparasite on household dogs in both urban and rural areas (Perez et al. 1996, Perez et al. 2006).
Domestic dogs and ring-tailed lemurs are naturally exposed to E. chaffeensis and human granulocytic ehrlichiosis which caused by this organism have been reported in North America, Asia and Europe (Spolidorio et al. 2010).
Ehrlichia canis, E. chaffeensis and E. ewingii have been recently detected synchronously in dogs and their ticks. Ndip et al. suggest that R. sanguineus ticks which are primarily infected with E. canis, may get infected with other ehrlichial agents and transmit them to humans (Ndip et al. 2007).
Ehrlichia ewingii and A. phagocytophilum which has been identified as pathogens of both dogs and humans are chiefly granulocytotropic (Buller et al. 1999, Ganguly et al. 2008). Serosurvey showed that dogs be routinely guarded for assessing risk for human granulocytic ehrlichiosis in humans in Europe and North America (Cizman et al. 2000, Day 2011).
A. phagocytophilum reported to be prevalent in Ixodex ticks, which infest dogs, so it can easily, transmitted to humans (Nicholson et al. 2010). On the other hand, A. phagocytophilum was isolated from Ixodex ticks in northern parts of Iran, which creates risk of human infection in our country (Bashiribod 2004).
The presented data showed that dogs and their ticks can be part of the epidemiological cycle of ehrlichiosis all around the world and surveillance, diagnosis, treatment, and prevention of tick-borne diseases in humans and dogs can yield mutually beneficial information for public and veterinary health.
In this study, three dogs were Ehrlichia spp. positive whereas their tick pools were negative. It is not determined that after tick’s blood sucking, how long does it take that transmission of ehrlichiosis from infected dogs to naïve ticks occurs. On the other hand, the rickettsemia levels to which ticks are exposed during feeding may also impacts on the proportion of infected ticks, so non-infected ticks may not have enough time to achieve the infection from their infected hosts (Johnson et al. 1998).
Prevalence of E. canis in different tick species collected from dogs from Ardebil in North West of Iran was reported (16.66%) by Khazeni et al. (2013) while nested PCR detected ehrlichial DNA in 63.82% of R. Sanguineus ticks and these results warrant studying on vector competence of ticks for the ehrlichiosis agents.
All collected ticks in our study were R. sanguineus but results of present study suggest that owning an Ehrlichia infected dog should not be considered a major risk factor for human ehrlichiosis in Kerman. This finding must be interpreted cautiously due to the widespread distribution of R. sanguinus in hot seasons on owned dogs and increased risk of human parasitism by R. sanguineus in tropical areas like as Kerman.
Population at risk for ehrlichiosis are the elderly, immunosuppressed and infants patients and as all of the examined human populations in this study were healthy adults, the absence of association between dogs and human infections must be interpreted conservatively. Low incidence of disease in dogs’ population and small population of dog’s owners who attend in our study are other confinement factors in this study.
In conclusion, result of present study confirm the presence of ehrlichiosis as an emerging infectious disease in canine population and their collected ticks in Iran, but further research is needed to reveal the importance of pet dogs and their ticks in the cycle of human ehrlichiosis in our country.
Conclusion
Based on the result of the present study, ehrlichiosis could be considered as an emerging canine disease but owning a dog should not be considered a major risk factor for ehrlichiosis in humans. Although our data suggest that ownership of dogs, is not associated with increased risk of ehrlichiosis in human medicine but this finding must be interpreted cautiously due to the widespread distribution of R. sanguinus in hot seasons on owned dogs. Further serological and molecular studies in different parts of Iran are required to clarify the epidemiology of ehrlichiosis in canine, ticks, and human population.
Acknowledgements
The authors are grateful to Zoonosis Research Committee of Kerman University of Medical Sciences for the financial support with the grant No. 168/90 and Research Council of Shahid Bahonar University for technical and laboratory support. The authors declare that there is no conflict of interests.
References
- Akhtardanesh B, Ghanbarpour R, Blourizadeh H. (2010) Serological evidence of canine monocytic ehrlichiosis in Iran. Comp Clin Path. 19( 5): 469– 474. [Google Scholar]
- Avizeh R, Mosallanejad B, Razi Jalali M, Alborzi A. (2010) Seroprevalence of Ehrlichia canis in dogs referred to Veterinary Hospital of Shahid Chamran University of Ahvaz, Iran. Arc Razi Inst. 65( 1): 21– 26. [Google Scholar]
- Babamahmoodi F. (2004) First outbreak of human ehrlichiosis in Mazandaran Province. 12th Iranian Congress of Tropical Infectious Disease, 17–21 January 2004, Tehran, Iran. [Google Scholar]
- Bashiribod H. (2004) First Molecular Detection of Anaplasma phagocytophihim in Ixodes ricinus Ticks in Iran. J Med Sci. 4( 4): 282– 286. [Google Scholar]
- Beugnet F, Marie JL. (2009) Emerging arthropod-borne diseases of companion animals in Europe. Vet Parasitol. 163( 4): 298– 305. [DOI] [PubMed] [Google Scholar]
- Buller RS, Arens M, Hmiel SP, Paddock CD, Sumner JW. (1999) Ehrlichia ewingii, a newly recognized agent of human ehrlichiosis. N Engl J Med. 341( 3): 148– 155. [DOI] [PubMed] [Google Scholar]
- Cizman M, Avsic-Zupanc T, Petrovec M, Ruzic-Sabljic E, Pokorn M. (2000) Seroprevalence of ehrlichiosis, Lyme borreliosis and tick-borne encephalitis infections in children and young adults in Slovenia. Wien Klin Wochenschr. 112(19): 842– 845. [PubMed] [Google Scholar]
- Dantas-Torres F, Figueredo LA, Brandão-Filho SP. (2006) Rhipicephalus sanguineus (Acari: Ixodidae), the brown dog tick, parasitizing humans in Brazil. Rev Soc Bras Med Trop. 39 ( 1): 64– 67. [DOI] [PubMed] [Google Scholar]
- Dantas-Torres F. (2010) Biology and ecology of the brown dog tick, Rhipicephalus sanguineus. Parasit Vectors. 3( 2): 26– 37. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Day MJ. (2011) One health: the importance of companion animal vector-borne diseases. Parasit Vectors. 4: 49. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Esemu SN, Ndip LM, Ndip RN. (2011) Ehrlichia species, probable emerging human pathogens in sub-Saharan Africa: environmental exacerbation. Rev Environ Health. 26(4): 269– 279. [DOI] [PubMed] [Google Scholar]
- Fritz CL. (2009) Emerging tick-borne diseases. Vet Clin North Am Small Anim Pract. 39( 2): 265– 278. [DOI] [PubMed] [Google Scholar]
- Ganguly S, Mukhopadhayay S. (2008) Tick-borne ehrlichiosis infection in human beings. J Vector Borne Dis. 45( 4): 273– 280. [PubMed] [Google Scholar]
- Guglielmone A, Beati L, Barros-Battesti D, Labruna M, Nava S. (2006) Ticks (Ixodidae) on humans in South America. Exp Appl Acarol. 40(2): 83– 100. [DOI] [PubMed] [Google Scholar]
- Johnson E, Ewing S, Barker R, Fox J, Crow D. (1998) Experimental transmission of Ehrlichia canis (Rickettsiales: Ehrlichieae) by Dermacentor variabilis (Acari: Ixodidae). Vet Parasitol. 74( 2–4): 277– 288. [DOI] [PubMed] [Google Scholar]
- Khazeni A, Telmadarraiy Z, Oshaghi MA, Mohebali M, Zarei Z. (2013) Molecular detection of Ehrlichia canis in ticks population collected on dogs in Meshkin-Shahr, Ardebil Province, Iran. J Biomed Sci and Eng. 6: 1– 5. [Google Scholar]
- Ndip LM, Ndip RN, Ndive VE, Awuh JA, Walker DH. (2007) Ehrlichia species in Rhipicephalus sanguineus ticks in Cameroon. Vector Borne Zoonotic Dis. 7( 2): 221– 227. [DOI] [PubMed] [Google Scholar]
- Nicholson WL, Allen KE, McQuiston JH, Breitschwerdt EB, Little SE. (2010) The increasing recognition of rickettsial pathogens in dogs and people. Trends Parasitol. 26( 4): 205– 212. [DOI] [PubMed] [Google Scholar]
- Perez M, Bodor M, Zhang C, Xiong Q, Rikihisa Y. (2006) Human infection with Ehrlichia canis accompanied by clinical signs in Venezuela. Ann N Y Acad Sci. 1078( 1): 110– 117. [DOI] [PubMed] [Google Scholar]
- Perez M, Rikihisa Y, Wen B. (1996) Ehrlichia canis-like agent isolated from a man in Venezuela: antigenic and genetic characterization. J Clin Microbiol. 34( 9): 2133– 2139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shoorijeh SJ, Ghasrodashti AR, Tamadon A, Moghaddar N, Behzadi MA. (2008) Seasonal Frequency of Ectoparasite Infestation in Dogs from Shiraz, Southern Iran. Turk J Vet Anim Sci. 32( 4): 309– 313. [Google Scholar]
- Spolidorio MG, Labruna MB, Machado RZ, Moraes-Filho J, Zago AM. (2010) Survey for tick-borne zoonoses in the state of Espirito Santo, southeastern Brazil. Am J Trop Med Hyg. 83( 1): 201– 206. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tefferi A, Hanson CA, Inwards DJ. (2005) How to interpret and pursue an abnormal complete blood cell count in adults. Mayo Clin Proc. 80( 7): 923– 936. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Unver A, Perez M, Orellana N, Huang H, Rikihisa Y. (2001) Molecular and antigenic comparison of Ehrlichia canis isolates from dogs, ticks, and a human in Venezuela. J Clin Microbiol. 39: 2788– 2793. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walker AR, Bouattour A, Camicas J, Estrada-Pena A, Horak I. (2003) Ticks of domestic animals in Africa: a guide to identification of species. Bioscience reports Edinburgh, UK. [Google Scholar]
- Willard MD, Tvedten H, Turnwald GH. (2012) Small animal clinical diagnosis by laboratory methods. Appendix ll. WB Saunders Company, Philadelphia. [Google Scholar]
