Of these Anaplasma species, A. marginale, A. centrale, and A. ovis are prominent pathogens in ruminants worldwide [3,10,11]. In particular, A. marginale and A. ovis have considerable economic importance in tropical and subtropical areas [4]. A. marginale is known to be highly pathogenic in cattle, while A. centrale is less pathogenic. A. ovis is moderately pathogenic in sheep, goats, and wild ruminants [1,12] and causes acute disease in animals exposed to stress or other predisposing factors such as hot weather, deworming, tick infestation, and animal movement [13].

The importance of anaplasmosis in small ruminants in the Republic of Korea (ROK) is not yet known. The infection in sheep and goats is usually asymptomatic; however, it can sporadically cause hemolytic anemia and hemoglobinuria. Anaplasma infection may likely be neglected because of its low economic importance in the goat production industry of the ROK. Although there have been previous reports of Anaplasma infection in Korean native goats (Capra aegagrus hircus) [14,15], epidemiological studies on Anaplasma infection in these animals have not been well reported. Therefore, the objective of this study was to investigate Anaplasma infection in Korean native goats pastured on Jeju Island where ticks are most widely distributed and to perform molecular characterization of Anaplasma species detected on Jeju Island.

Whole blood samples from 39 Korean native goats on Jeju Island, ROK, were collected in April 2014. This herd typically grazed in the pasture for at least 1 season every year; that is, the animals were housed in stables in the cooler months (November-April), whereas in the warmer months (May-October), they grazed in the pasture. All goats were clinically healthy and no blood-sucking ticks were found on them. Blood samples were collected and immediately frozen at -80˚C until DNA extraction was performed.

Genomic DNA was extracted from whole blood samples using the DNeasy Blood & Tissue Kit (Qiagen, Valencia, California, USA) according to the manufacturer’s instructions. For the detection of Anaplasma infection, PCR was performed using the AccuPower^® Rickettsiales 3-Plex PCR Kit (Bioneer, Daejeon, Korea). Specific primer sets targeting the 16S rRNA were used to detect species belonging to Anaplasma (F, 5´-TACCTCTGTGTTGTAGCTAACGC-3´; R, 5´-CTTGCGACATTGCAACCTATTGT-3´), Ehrlichia (F, 5´-CGGAATTCCTAGTGTAGAGG-3´; R, 5´-AGGAGGGATACGACCTTC AT-3´), and Rickettsia (F, 5´-TAGGGGATGATGGAATTCCTA-3´; R, 5´-CCCCCGTCA ATTCCTTTGAG-3´). The predicted sizes of the amplified PCR products for Anaplasma, Ehrlichia, and Rickettsia were 429 bp, 340 bp, and 252 bp, respectively. The following cycling conditions were used: 95˚C for 15 min; 40 cycles of 95˚C for 10 sec, 58˚C for 30 sec, and 72˚C for 30 sec; and final extension at 72˚C for 5 min. PCR products were separated by gel electrophoresis on 1.5% agarose gels and visualized by staining with ethidium bromide.

The PCR products were purified with the QIAquick PCR Purification Kit (Qiagen). The nucleotide sequences were determined by direct sequencing of the PCR products using the BigDye Terminator Cycle Sequencing Kit (Applied Biosystems, Foster City, California, USA) and analyzed on ABI PRISM^® DNA Analyzer (Applied Biosystems). The sequence data were aligned initially using the Clustal X program (version 1.8) [16]. Additional sequences from representative anaplasmosis isolates were obtained from the GenBank database and then integrated with each set of alignments. A phylogenetic tree based on the nucleotide alignment was constructed using the neighbor-joining method [17]. Bootstrap analysis was carried out with 1,000 replications and the tree was visualized using Tree-view.

Statistical analyses were performed by one-way ANOVA with IBM SPSS Statistics (version 19.0) and GraphPad Prism (version 6.0). In all statistical tests, P-value of <0.05 were considered significant.

Anaplasma infection was analyzed in a population of 39 Korean native goats; blood samples from 7 animals (17.9%) tested positive for Anaplasma by 16S rRNA gene-based PCR. Infections with Ehrlichia and Rickettsia were not detected. None of the goats exhibited any clinical signs of illness, and no ticks were found on these animals. Additionally, no hematological abnormalities were observed. The incidence of Anaplasma infection in Korean native goats in all age groups and in male and female goats was investigated. Anaplasma infection was detected in female goats only (29.2%; Table 1), and the incidence was 38.9% in goats of 12 months of age (Table 2). Anaplasma infection was not detected in male goats or in other age groups.

Seven 16S rRNA gene sequences of Anaplasma sp. (GenBank Accession No. KR024571-KR024577) were obtained from the 7 Anaplasma-positive blood samples after direct sequencing. The sequence analysis of these 7 samples led to the identification of Anaplasma sp. The phylogenetic tree analysis revealed that there were 3 main clusters for the established Anaplasma spp.: A. marginale, A. ovis, and A. centrale clusters. The 7 sequences obtained from Korean native goats on Jeju Island formed a fourth, separate cluster, that is, Anaplasma sp., which diverged from A. marginale, A. centrale, and A. ovis, but was closely related to A. centrale (Fig. 1). These isolates had a 98% similarity with A. centrale, 96.4-97.5% similarity with A. ovis, and 96.9-97.8% similarity with A. marginale. The phylogenetic analyses showed that the 7 Anaplasma sp. identified in Korean native goats could potentially be new species, mainly because they clustered separately from the 3 established species, A. marginale, A. centrale, and A. ovis. Our 7 sequences are quite similar to the species isolated from goats in China (EU709493 and FJ389576), which also belong to Anaplasma sp., and are clustered in the same group. To our knowledge, this is the first study to identify Anaplasma sp. infection in Korean native goats by PCR.

Although anaplasmosis is one of the most widespread tick-borne diseases, very little is known about Anaplasma infection and its distribution in the ROK. Most studies concerning Anaplasma in the ROK have addressed ticks and humans [18,19], while the role of Anaplasma in goat pathology has not yet been described. In our study, a high prevalence of Anaplasma infection was observed in female and adult goats although it was not statistically significant. This result indicates that adult goats may have more opportunities for exposure to ticks carrying the pathogen than younger animals. Additionally, our findings suggest the presence of Anaplasma infection in Korean native goats on Jeju Island, which has a subtropical climate and a much higher distribution of ticks than other regions in the ROK. These conditions increase the possibility of tick-borne diseases spreading to livestock, wild animals, and humans.

In the present study, PCR and sequence analyses based on the 16S rRNA provided evidence of a new Anaplasma sp. infecting Korean native goats; these isolates were closely related to the previously reported Chinese isolates. The pathogenicity and role of Anaplasma sp. was not determined in Korean native goats; however, infection with this protozoan may have an impact on the health of these animals and consequently on their milk and meat production. Evidence of infection with a new Anaplasma sp. infection in Korean native goats would be very important, as the pathogens could considerably affect animal production, and outbreaks may occur under specific conditions. Accordingly, these findings indicate infection with a new species from the genus Anaplasma among Korean native goats on Jeju Island, ROK.

The current study demonstrates the presence of infection with Anaplasma sp. in Korean native goats, although none of the animals in our study exhibited clinical symptoms. Since the sample size was not sufficiently large to determine the incidence of Anaplasma infection, more studies are necessary to investigate epidemiological data and to elucidate the pathogenicity of Anaplasma sp. in these animals.