Abstract
Tick-borne diseases (TBD) cause enormous losses for farmers. Backyard raising comprises majority of the livestock population in the Philippines, but TBD information in backyard livestock is scarce. In this study, 48 cattle and 114 water buffalo samples from Quezon province, Philippines were molecularly screened for tick-borne pathogens. Anaplasma marginale (16.67%) and hemoplasma (20.99%) were detected in the samples. A. marginale infection (P=0.0001) was significantly higher in cattle, while hemoplasma infection (P=0.011) was significantly higher in water buffaloes. A. marginale isolates from this study were highly similar to previous isolates from the Philippines while Mycoplasma wenyonii and Candidatus Mycoplasma haemobos were the identified hemoplasma species. Our findings reveal additional information on the TBD situation of Philippine backyard livestock.
Keywords: Anaplasma, hemoplasma, Philippines, Quezon, tick-borne
The livestock industry is a significant contributor to the agriculture sector of the Philippines, accounting for 17.65% of the total agricultural production value in 2018 [18]. Backyard raising by smallholder farmers has been the predominant practice in livestock farming, particularly for large ruminants. Cattle are commonly raised as source of meat and milk, while water buffaloes (carabaos) are indispensable as draft animals providing labor power for small-scale crop production [7]. Unlike animals raised in commercial farms, field cattle and water buffaloes are often neglected, thus receiving inadequate nutrient supplements and health care [10]. Costly veterinary expense is also seen as additional economic burden for subsistence backyard livestock farmers.
Tick infestation is commonly observed in cattle and water buffalo in the field causing hide damage and tick worry. These ticks transmit numerous pathogens that negatively impact large ruminant health. Among the most economically important tick-borne pathogens (TBPs) are protozoan parasites Babesia and Theileria and bacteria Anaplasma and hemotropic Mycoplasma (hemoplasma), all of which were previously reported in the Philippines [23]. Anemia is the typical clinical sign associated with the diseases caused by these TBPs leading to decreased meat and milk production, reduced draft power, and in more severe cases, mortality [3, 4, 14, 19].
Most of the previous tick-borne disease (TBDs) investigations in livestock in the country focused on animals raised in commercial and semi-commercial farms and on imported breeds. This study aimed to detect TBPs in backyard-raised cattle and water buffaloes and to evaluate animal profile and hematological parameters related to TBDs in Quezon province, Philippines.
The animal handling procedures performed in this study observed the Philippine Animal Welfare Act (R.A. 8485 as amended by R.A. 10631). Permission for conducting animal experiments (permit no. 29-69) and DNA use (permit no. 1723-1724) were obtained from Obihiro University of Agriculture and Veterinary Medicine, Obihiro, Hokkaido, Japan. Sampling was done in 7 different municipalities in the east district of Quezon province, Luzon area, Philippines (Fig. 1). Blood samples were collected from a total of 162 apparently healthy cattle (N=48) and water buffaloes (N=114) in October 2018. Animal profile (sex, breed and presence or absence of ticks) was recorded (Table 1). About 2 ml of blood were collected from the jugular vein into EDTA-coated vacutainers. Approximately 1 ml of each blood sample was kept at −20°C for DNA extraction while the remaining blood samples were used for the complete blood count (CBC) test. Extraction of DNA was done using QIAamp® DNA Blood Mini Kit (QIAGEN, Hilden, Germany), following the manufacturer’s instructions. Hematological values, namely red blood cell (RBC) count, white blood cell (WBC) count, hemoglobin (Hgb) and packed cell volume (PCV), were obtained using KT-6180 3-part Hematology Analyzer (Shenzen Uniper Medical Technology, Shenzen, China).
Fig. 1.
Map of sampling sites in Quezon province, Philippines.
Table 1. Association of tick-borne pathogen positivity with profile parameters of backyard cattle and water buffaloes in Quezon province, Philippines.
| Parameter | N |
Mycoplasma spp. |
Anaplasma marginale
|
|||
|---|---|---|---|---|---|---|
| No. of positives (%) | P valuea) | No. of positives (%) | P valuea) | |||
| Location | ||||||
| Atimonan | 12 | 1 (8.33) | n.a. | 1 (8.33) | n.a. | |
| Calauag | 21 | 6 (28.57) | 1 (4.76) | |||
| Guinayangan | 21 | 9 (42.86) | 1 (4.76) | |||
| Gumaca | 23 | 5 (21.74) | 0 | |||
| Lopez | 4 | 0 | 0 | |||
| Plaridel | 37 | 4 (10.81) | 2 (5.41) | |||
| Tagkawayan | 44 | 9 (20.45) | 2 (6.82) | |||
| Host | ||||||
| Water buffalo | 114 | 30 (26.32) | 0.011b) | 0 | 0.0001c) | |
| Cattle | 48 | 4 (8.33) | 8 (16.67) | |||
| Sex | ||||||
| Female | 133 | 26 (19.55) | 0.33 | 6 (4.51) | 0.63 | |
| Male | 29 | 8 (27.59) | 2 (6.90) | |||
| Breed | ||||||
| Native | 148 | 32 (21.62) | 0.74 | 6 (4.05) | 0.15 | |
| Crossbred or imported | 14 | 2 (14.29) | 2 (14.29) | |||
| Tick infestation | ||||||
| Yes | 19 | 1 (5.26) | 0.13 | 3 (15.79) | 0.053 | |
| No | 143 | 33 (23.08) | 5 (3.50) | |||
| Total | 162 | 34 (20.99) | 8 (4.94) | |||
a) Analyzed by Fisher’s exact or χ2 test; b) P<0.05; c) P<0.001. n.a.: not analyzed.
Previously established polymerase chain reaction-based assays were used in evaluating the presence of Babesia bovis, B. bigemina, Theileria spp., Anaplasma marginale and hemoplasma in the blood samples. Genes targeted were spherical body protein (SBP)-2 [1], rhoptry-associated protein (RAP)-1a [20], 18S rRNA [5], groEL heat-shock operon [21] and 16S rRNA [6], respectively. A final volume of 10 µl consisting of 4.85 µl of double-distilled water, 1 mM of dNTP solution mix (New England Biolabs, Ipswich, MA, USA), 1 µl of 10x ThermoPol® buffer (New England Biolabs), 10 µM of each primer, 0.05 µl of Taq DNA polymerase (New England Biolabs) and 2 µl of gDNA was used. Thermocycling conditions were performed for each pathogen as before, except for the extension and final extension temperatures, which were set at 68°C. Double-distilled water was used as negative control and cloned positive DNA samples were used as positive controls. After electrophoresis and staining with ethidium bromide, amplicons were visualized in 1.5% agarose gel under UV light. Amplicons of hemoplasma (N=7) and A. marginale (N=8) were purified using NucleoSpin® Gel and PCR Clean-up (Macherey-Nagel, Düren, Germany) and were directly sequenced using BigDye™ Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, CA, USA) and ABI Prism 3100 Genetic Analyzer (Applied Biosystems). Sequences were manually trimmed and submitted to the NCBI GenBank database. Species of obtained isolates were confirmed with BLASTn search while shared identity among isolates was determined by EMBOSS Matcher. Fisher’s exact and Pearson’s χ2 tests were used to assess the association between animal profile parameters and PCR positivity while differences in hematological values were evaluated by Mann-Whitney U test. Statistically significant P value was <0.05.
Out of the 162 screened samples, 42 were positive for at least one TBP (25.93%). A. marginale was only found in cattle (16.67%) while hemoplasma was detected in both water buffalo (26.32%) and cattle (8.33%) (Table 1). A. marginale is the most prevalent and extensively reported TBP in the Philippines [23]. The 16.67% (8/48) bovine A. marginale detection rate in this survey was significantly lower compared to a recent study which reported a 100% Anaplasma spp. detection rate in 21 dairy cattle in the same area [8]. In the Philippines, hemoplasmas have only been reported in cattle and goats in Cebu [13, 22] and dairy cattle and water buffaloes (80%) in Bohol [24] in the Visayas area. The current study is the first report of livestock hemoplasma infection in the Luzon area. The lower infection rates of A. marginale and hemoplasma in this study might be due to the difference in the breeds of the animals and raising system. Native breeds, normally used for draft power or meat production, dominate backyard farms while dairy animals are commonly imported breeds or crossbreeds. Native breeds of cattle and water buffaloes are usually more resistant against TBPs such as A. marginale [15, 17]. In the current study, 97% of water buffaloes were Philippine carabao breed and 77% of cattle were Philippine native breed. While the breed was not associated with any detected TBPs (P>0.05) in this study (Table 1), the unequal proportion of native to imported or crossbred animals sampled may have affected this result.
Based on statistical analysis, A. marginale infection (P=0.0001) was significantly higher in cattle, while hemoplasma infection (P=0.011) was significantly higher in water buffaloes (Table 1). Although both ruminants are natural hosts, clinical anaplasmosis affects cattle more frequently, while water buffaloes act as reservoir hosts [12, 14]. On the other hand, there is little information on the susceptibility of water buffaloes to hemoplasma. Previous studies detected comparable rates of hemoplasma infection between water buffaloes and cattle [9, 24]. This finding is particularly interesting; hence, the extent of hemoplasma susceptibility of water buffaloes should be assessed in future studies.
There were 19 animals found to be tick-infested despite acaricide use of some farmers a week prior to the sampling, which might suggest emerging resistance of ticks to acaricides. The resistance of cattle-infesting Rhipicephalus microplus ticks to chemical acaricide was recently reported in Luzon area [11]. In this study, tick infestation (P>0.05) was neither associated with A. marginale nor hemoplasma infection (Table 2). Backyard-raised livestock, which are often pastured and tethered, have more exposure to blood-sucking arthropods which could transmit TBPs [22]. As both TBPs are not exclusively transmitted by ticks, mechanical transmission by other ectoparasites is a likely possibility.
Table 2. Hematological analysis of cattle positive for Anaplasma marginale and hemoplasma in Quezon province, Philippines.
| Hematological parameter | Hemoplasma infection (N=4) |
Hemoplasma negative (N=36) |
P valuea) |
A. marginale infection (N=5) |
A. marginale negative (N=35) |
P valuea) |
|---|---|---|---|---|---|---|
| Red blood cell (1012/l) | 5.80 | 6.24 | 0.25 | 6.06 | 6.22 | 0.92 |
| White blood cell (109/l) | 21.73 | 12.21 | 0.14 | 11.98 | 13.33 | 0.85 |
| Hemoglobin (g/dl) | 8.60 | 9.46 | 0.20 | 8.86 | 9.45 | 0.64 |
| Packed cell volume (%) | 35.75 | 40.80 | 0.12 | 37.94 | 40.63 | 0.42 |
a) Analyzed by Mann-Whitney U test.
The lack of clinical signs in animals positive for A. marginale and hemoplasma denotes persistent subclinical infection, a feature of Anaplasma and hemoplasma infections. Persistent A. marginale infection provides life-long protection against clinical anaplasmosis [14]. In the case of hemoplasma chronic infection, animals become pathogen carriers, and substantial losses in milk production are observed [19]. Only 147 samples (107 water buffaloes and 40 cattle) had hematological data, thus, samples with no information were excluded from the analysis (Tables 2 and 3). Overall, A. marginale and hemoplasma positivity did not cause significant changes in hematological values, indicating persistent subclinical infections which were also noted in past investigations [9, 19].
Table 3. Hematological analysis of hemoplasma-positive water buffaloes positive in Quezon province, Philippines.
| Hematological parameter | Hemoplasma infection (N=26) |
Hemoplasma negative (N=81) |
P valuea) |
|---|---|---|---|
| Red blood cell (1012/l) | 4.99 | 4.98 | 0.87 |
| White blood cell (109/l) | 9.93 | 9.17 | 0.29 |
| Hemoglobin (g/dl) | 9.57 | 9.84 | 0.61 |
| Packed cell volume (%) | 39.88 | 40.32 | 0.71 |
a) Analyzed by Mann-Whitney U test.
B. bovis, B. bigemina, and Theileria spp. were not detected in the current study. Previous studies in neighboring provinces like Batangas, Cavite and Laguna reported detection of B. bovis, B. bigemina and Theileria spp. in cattle [2, 16, 25]. The limited number of samples as well as the natural resistance of native animals might be attributed to the absence of these TBPs in the current survey. Despite non-detection, continuous surveillance of these economically TBPs should be conducted.
Eight A. marginale isolates (MN961201-MN961208) shared 99.1–100% identities with each other. A. marginale is considered an endemic TBP in the Philippines [23] and the high identities of current isolates with previous Philippine isolates corroborate past findings. Seven isolates of hemoplasma were confirmed as Mycoplasma wenyonii (MT241310–MT241312) and Candidatus Mycoplasma haemobos (MT241313–MT241316). M. wenyonii was earlier identified in cattle and water buffaloes in Bohol [22, 24] while CandidatusM. haemobos was detected in goats in Cebu [13]. Although both species can infect bovids, it was noted that CandidatusM. haemobos-infected cattle develop more severe clinical signs compared to M. wenyonii-infected cattle [19]. Nonetheless, prevention measures against hemoplasma infection in livestock should be implemented to minimize the economic impact caused by this tick-borne infectious disease.
In this study, A. marginale and hemoplasma were detected in backyard-raised cattle and water buffaloes in Quezon, Philippines. The current study is the first report of livestock hemoplasma infection in the Luzon area and the first confirmation of CandidatusM. haemobos in cattle and water buffaloes in the Philippines. Our findings reveal additional information on the diversity of TBPs in livestock in the country.
Acknowledgments
The authors thank the personnel at the Office of the Provincial Veterinarian of Quezon province, the farmers and livestock technicians for their assistance and cooperation during the sampling. This study was funded by a grant-in-aid for scientific research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan and a grant from the Japanese Society for Promotion of Science Core-to-Core Program.
REFERENCES
- 1.AbouLaila M., Yokoyama N., Igarashi I.2010. Development and evaluation of a nested PCR based on spherical body protein 2 gene for the diagnosis of Babesia bovis infection. Vet. Parasitol. 169: 45–50. doi: 10.1016/j.vetpar.2009.12.013 [DOI] [PubMed] [Google Scholar]
- 2.Belotindos L. P., Lazaro J. V., Villanueva M. A., Mingala C. N.2014. Molecular detection and characterization of Theileria species in the Philippines. Acta Parasitol. 59: 448–453. doi: 10.2478/s11686-014-0256-9 [DOI] [PubMed] [Google Scholar]
- 3.Bishop R., Musoke A., Morzaria S., Gardner M., Nene V.2004. Theileria: intracellular protozoan parasites of wild and domestic ruminants transmitted by ixodid ticks. Parasitology 129 Suppl: S271–S283. doi: 10.1017/S0031182003004748 [DOI] [PubMed] [Google Scholar]
- 4.Bock R., Jackson L., de Vos A., Jorgensen W.2004. Babesiosis of cattle. Parasitology 129 Suppl: S247–S269. doi: 10.1017/S0031182004005190 [DOI] [PubMed] [Google Scholar]
- 5.Cao S., Zhang S., Jia L., Xue S., Yu L., Kamyingkird K., Moumouni P. F., Moussa A. A. E. M., Zhou M., Zhang Y., Terkawi M. A., Masatani T., Nishikawa Y., Xuan X.2013. Molecular detection of Theileria species in sheep from northern China. J. Vet. Med. Sci. 75: 1227–1230. doi: 10.1292/jvms.13-0028 [DOI] [PubMed] [Google Scholar]
- 6.Criado-Fornelio A., Martinez-Marcos A., Buling-Saraña A., Barba-Carretero J. C.2003. Presence of Mycoplasma haemofelis, Mycoplasma haemominutum and piroplasmids in cats from southern Europe: a molecular study. Vet. Microbiol. 93: 307–317. doi: 10.1016/S0378-1135(03)00044-0 [DOI] [PubMed] [Google Scholar]
- 7.Cruz L. C.2007. Trends in buffalo production in Asia. Ital. J. Anim. Sci. 6: 9–24. doi: 10.4081/ijas.2007.s2.9 [DOI] [Google Scholar]
- 8.Dela Cruz A. P., Galay R. L., Sandalo K. A. C., Pilapil-Amante F. M. I. R., Tanaka T.2019. Molecular detection of Anaplasma spp. in blood and milk of dairy cattle in the Philippines. Turk. J. Vet. Anim. Sci. 43: 540–545. doi: 10.3906/vet-1903-27 [DOI] [Google Scholar]
- 9.Díaz-Sánchez A. A., Corona-González B., Meli M. L., Álvarez D. O., Cañizares E. V., Rodríguez O. F., Rivero E. L., Hofmann-Lehmann R.2019. First molecular evidence of bovine hemoplasma species (Mycoplasma spp.) in water buffalo and dairy cattle herds in Cuba. Parasit. Vectors 12: 78. doi: 10.1186/s13071-019-3325-y [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Food and Agriculture Organization.2003. Status of the Philippines’ Animal Genetic Resources. http://www.fao.org/ag/againfo/programmes/en/genetics/documents/Interlaken/countryreports/Philippines.pdf [accessed on November 18, 2019].
- 11.Galay R. L., Alota S., Edquiban T. R., Evangelista J., Valera F. G. R., Sandalo K. A., Bernardo J. M., Tanaka T.2019. Detection of resistance to chemical acaricides in Rhipicephalus (Boophilus) microplus ticks from selected cattle farms in Luzon, Philippines. Paper presented at the 27th Conference of the World Association for the Advancement of Veterinary Parasitology, Wisconsin, USA, July 7–11, 2019. http://www.waavp2019.com/wp-content/uploads/2019/07/WAAVP2019-Abstract-Book.pdf [accessed on November 18, 2019].
- 12.Galon E. M. S., Adjou Moumouni P. F., Ybañez R. H. D., Ringo A. E., Efstratiou A., Lee S. H., Liu M., Guo H., Gao Y., Li J., Salces C. B., Maurillo B. C. A., Boldbaatar D., Ybañez A. P., Xuan X.2019a. First molecular detection and characterization of tick-borne pathogens in water buffaloes in Bohol, Philippines. Ticks Tick Borne Dis. 10: 815–821. doi: 10.1016/j.ttbdis.2019.03.016 [DOI] [PubMed] [Google Scholar]
- 13.Galon E. M. S., Adjou Moumouni P. F., Ybañez R. H. D., Macalanda A. M. C., Liu M., Efstratiou A., Ringo A. E., Lee S. H., Gao Y., Guo H., Li J., Tumwebaze M. A., Byamukama B., Li Y., Ybañez A. P., Xuan X.2019b. Molecular evidence of hemotropic mycoplasmas in goats from Cebu, Philippines. J. Vet. Med. Sci. 81: 869–873. doi: 10.1292/jvms.19-0042 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Kocan K. M., de la Fuente J., Blouin E. F., Coetzee J. F., Ewing S. A.2010. The natural history of Anaplasma marginale. Vet. Parasitol. 167: 95–107. doi: 10.1016/j.vetpar.2009.09.012 [DOI] [PubMed] [Google Scholar]
- 15.Mingala C. N., Konnai S., Cruz L. C., Onuma M., Ohashi K.2009. Comparative moleculo-immunological analysis of swamp- and riverine-type water buffaloes responses. Cytokine 46: 273–282. doi: 10.1016/j.cyto.2009.02.006 [DOI] [PubMed] [Google Scholar]
- 16.Ochirkhuu N., Konnai S., Mingala C. N., Okagawa T., Villanueva M., Pilapil F. M. I., Murata S., Ohashi K.2015. Molecular epidemiological survey and genetic analysis of vector-borne infections of cattle in Luzon Island, the Philippines. Vet. Parasitol. 212: 161–167. doi: 10.1016/j.vetpar.2015.05.019 [DOI] [PubMed] [Google Scholar]
- 17.Parker R. J., Shepherd R. K., Trueman K. F., Jones G. W., Kent A. S., Polkinghorne I. G.1985. Susceptibility of Bos indicus and Bos taurus to Anaplasma marginale and Babesia bigemina infections. Vet. Parasitol. 17: 205–213. doi: 10.1016/0304-4017(85)90032-9 [DOI] [PubMed] [Google Scholar]
- 18.Philippine Statistics Authority.2019. Selected Statistics on Agriculture 2019, Quezon City, Philippines. https://psa.gov.ph/sites/default/files/Selected%20Statistics%20on%20Agriculture%202019.pdf [accessed on November 18, 2019].
- 19.Tagawa M., Yamakawa K., Aoki T., Matsumoto K., Ishii M., Inokuma H.2013. Effect of chronic hemoplasma infection on cattle productivity. J. Vet. Med. Sci. 75: 1271–1275. doi: 10.1292/jvms.13-0119 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Terkawi M. A., Huyen N. X., Shinuo C., Inpankaew T., Maklon K., Aboulaila M., Ueno A., Goo Y. K., Yokoyama N., Jittapalapong S., Xuan X., Igarashi I.2011. Molecular and serological prevalence of Babesia bovis and Babesia bigemina in water buffaloes in the northeast region of Thailand. Vet. Parasitol. 178: 201–207. doi: 10.1016/j.vetpar.2011.01.041 [DOI] [PubMed] [Google Scholar]
- 21.Ybañez A. P., Sivakumar T., Ybañez R. H. D., Ratilla J. C., Perez Z. O., Gabotero S. R., Hakimi H., Kawazu S., Matsumoto K., Yokoyama N., Inokuma H.2013. First molecular characterization of Anaplasma marginale in cattle and Rhipicephalus (Boophilus) microplus ticks in Cebu, Philippines. J. Vet. Med. Sci. 75: 27–36. doi: 10.1292/jvms.12-0268 [DOI] [PubMed] [Google Scholar]
- 22.Ybañez A. P., Ybañez R. H., Tagawa M.2015. Molecular detection of hemoplasma species (Mycoplasma spp.) in cattle in Cebu, Philippines. J. Adv. Vet. Res. 5: 43–46. [Google Scholar]
- 23.Ybañez A. P., Mingala C. N., Ybañez R. H. D.2018. Historical review and insights on the livestock tick-borne disease research of a developing country: The Philippine scenario. Parasitol. Int. 67: 262–266. doi: 10.1016/j.parint.2017.11.009 [DOI] [PubMed] [Google Scholar]
- 24.Ybañez A. P., Ybañez R. H. D., Armonia R. K. M., Chico J. K. E., Ferraren K. J. V., Tapdasan E. P., Salces C. B., Maurillo B. C. A., Galon E. M. S., Macalanda A. M. C., Moumouni P. F. A., Xuan X.2019. First molecular detection of Mycoplasma wenyonii and the ectoparasite biodiversity in dairy water buffalo and cattle in Bohol, Philippines. Parasitol. Int. 70: 77–81. doi: 10.1016/j.parint.2019.02.004 [DOI] [PubMed] [Google Scholar]
- 25.Yu L., Terkawi M. A., Cruz-Flores M. J., Claveria F. G., Aboge G. O., Yamagishi J., Goo Y. K., Cao S., Masatani T., Nishikawa Y., Xuan X.2013. Epidemiological survey of Babesia bovis and Babesia bigemina infections of cattle in Philippines. J. Vet. Med. Sci. 75: 995–998. doi: 10.1292/jvms.12-0425 [DOI] [PubMed] [Google Scholar]

