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<front>
<journal-meta>
<journal-id journal-id-type="redalyc">693</journal-id>
<journal-title-group>
<journal-title specific-use="original" xml:lang="es">Revista MVZ Córdoba</journal-title>
<abbrev-journal-title abbrev-type="publisher" xml:lang="es">Rev. MVZ Córdoba</abbrev-journal-title>
</journal-title-group>
<issn pub-type="ppub">0122-0268</issn>
<issn pub-type="epub">1909-0544</issn>
<publisher>
<publisher-name>Universidad de Córdoba</publisher-name>
<publisher-loc>
<country>Colombia</country>
<email>revistamvz@gmail.com</email>
</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="art-access-id" specific-use="redalyc">69353273003</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Artículos</subject>
</subj-group>
</article-categories>
<title-group>
<article-title xml:lang="en">
<bold>Molecular identification of tick-borne hemoparasites in equines from Northwestern Colombia</bold>
</article-title>
<trans-title-group>
<trans-title xml:lang="es">
<bold>Identificación molecular de hemoparásitos transmitidos por garrapatas en equinos del Noroeste de Colombia</bold>
</trans-title>
</trans-title-group>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="no">
<name name-style="western">
<surname>Agudelo-Ruíz</surname>
<given-names>Yeison</given-names>
</name>
<xref ref-type="aff" rid="aff1"/>
<email>leidy.acevedo@udea.edu.co</email>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name name-style="western">
<surname>Acevedo-Gutiérrez</surname>
<given-names>Leidy</given-names>
</name>
<xref ref-type="corresp" rid="corresp1"/>
<xref ref-type="aff" rid="aff2"/>
<email>leidy.acevedo@udea.edu.co</email>
</contrib>
<contrib contrib-type="author" corresp="no">
<name name-style="western">
<surname>Montoya-Sanchéz</surname>
<given-names>Andrés</given-names>
</name>
<xref ref-type="aff" rid="aff3"/>
<email>leidy.acevedo@udea.edu.co</email>
</contrib>
<contrib contrib-type="author" corresp="no">
<name name-style="western">
<surname>Paternina</surname>
<given-names>Luis</given-names>
</name>
<xref ref-type="aff" rid="aff4"/>
<email>leidy.acevedo@udea.edu.co</email>
</contrib>
</contrib-group>
<aff id="aff1">
<institution content-type="original">Universidad de Antioquia, Grupo de investigación en Ciencias Veterinarias Centauro; Calle 70 No. 52-21, Medellín, Colombia</institution>
<institution content-type="orgname">Universidad de Antioquia</institution>
<country country="CO">Colombia</country>
</aff>
<aff id="aff2">
<institution content-type="original">Universidad de Antioquia, Grupo de investigación en Ciencias Veterinarias Centauro; Calle 70 No. 52-21, Medellín, Colombia</institution>
<institution content-type="orgname">Universidad de Antioquia</institution>
<country country="CO">Colombia</country>
</aff>
<aff id="aff3">
<institution content-type="original">Universidad de Antioquia, Grupo de investigación en Ciencias Veterinarias Centauro; Calle 70 No. 52-21, Medellín, Colombia</institution>
<institution content-type="orgname">Universidad de Antioquia</institution>
<country country="CO">Colombia</country>
</aff>
<aff id="aff4">
<institution content-type="original">Universidad de Sucre, Grupo investigaciones Biomédicas; Carrera. 14 No. 16B-32, Sincelejo, Colombia</institution>
<institution content-type="orgname">Universidad de Sucre</institution>
<country country="CO">Colombia</country>
</aff>
<author-notes>
<corresp id="corresp1">
<email>leidy.acevedo@udea.edu.co</email>
</corresp>
</author-notes>
<pub-date pub-type="epub-ppub">
<year>2017</year>
</pub-date>
<volume>22</volume>
<supplement/>
<fpage>6004</fpage>
<lpage>6013</lpage>
<history>
<date date-type="received" publication-format="dd mes yyyy">
<day>16</day>
<month>08</month>
<year>2016</year>
</date>
<date date-type="accepted" publication-format="dd mes yyyy">
<day>18</day>
<month>01</month>
<year>2017</year>
</date>
</history>
<permissions>
<ali:free_to_read/>
</permissions>
<abstract xml:lang="en">
<title>Abstract</title>
<p>
<bold> Objective</bold>. To detect and identify Anaplasmataceae agents and piroplasms in equines from the slaughterhouse “La Rinconada” at Rionegro municipality in Antioquia. <bold>Materials and methods</bold>. A descriptive cross-sectional study was carried out on equines selected by convenience during a period of 2015. Information about species, sex, age and origin of the animals. Whole blood was collected for DNA extraction procedure, and a PCR targeting a 360bp of Anaplasmataceae 16S ribosomal gene and 450bp of 18S ribosomal gene of Piroplasm were used for detection. PCR amplicons selected were submitted to direct sequencing for identification of hemoparasites through genetic analysis <bold>Results</bold>.135 equine samples from Antioquia, Cordoba y Sucre were analyzed. 78% were horses, 16% were donkeys and 6% were mules. Anaplasmataceae agents were not detected in any sample, meanwhile 13% were positive to piroplasm PCR. Sequence analysis reveals the circulation of Theileria equi in northwestern Colombia. <bold>Conclusions.</bold> This work presents the first molecular evidence of at least three genotypes of T. equi in equines of northwestern Colombia. </p>
</abstract>
<trans-abstract xml:lang="es">
<title>Resumen</title>
<p>
<bold> Objetivo.</bold> Detectar e identificar agentes de la familia Anaplasmataceae y piroplasmas en equinos colombianos que llegan a la planta de beneficio La Rinconada ubicada en el municipio de Rionegro, Antioquia. <bold>Materiales y métodos</bold>. Se realizó un estudio descriptivo de corte transversal durante parte del 2015 a equinos seleccionados por conveniencia. Se recopiló información tal como especie, sexo, edad y localidad de procedencia. Se obtuvieron muestras de sangre para extracción de ADN, y se amplificó un fragmento de 360pb del gen 16S ribosomal de Anaplasmataceae y un fragmento de 450 pb del gen 18S ribosomal de piroplasmas para detección de hemoparásitos. Amplicones de PCR fueron sometidos a secuenciación para identificación de los hemoparásitos a través de análisis genético. Resultados.Se analizaron 135 equinos provenientes de los departamentos de Antioquia, Córdoba y Sucre. Un 78% eran caballos, un 16% eran asnos y un 6% eran mulas. El 100% de los animales fueron negativos para agentes de la familia Anaplasmataceae y un 13% fueron positivos para piroplasmas. Se identificó por secuenciación la circulación de Theileria equi en la zona norte de Colombia. <bold>Conclusiones</bold>.Se presenta la primera evidencia molecular de al menos tres genotipos de T. equi infectando equinos del norte del país. </p>
</trans-abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>Anaplasma</kwd>
<kwd>Ehrlichia</kwd>
<kwd>Theileria</kwd>
<kwd>Babesia</kwd>
<kwd>PCR</kwd>
<kwd>Filogenética (Mesh)</kwd>
</kwd-group>
<kwd-group xml:lang="es">
<title>Palabras clave</title>
<kwd>Anaplasma</kwd>
<kwd>Ehrlichia</kwd>
<kwd>Theileria</kwd>
<kwd>Babesia</kwd>
<kwd>PCR</kwd>
<kwd>Filogenética (Mesh)</kwd>
</kwd-group>
<counts>
<fig-count count="3"/>
<table-count count="2"/>
<equation-count count="0"/>
<ref-count count="30"/>
</counts>
</article-meta>
</front>
<body>
		
		<sec sec-type="intro">
            <title>
<bold>INTRODUCTION</bold>
</title>
			
			
		<p>Equine granulocytic anaplasmosis (EGA) and equine piroplasmosis (EP) are sidesases tramsitted by ticks, and affects equines in several places worldwide (<xref ref-type="bibr" rid="redalyc_69353273003_ref1">1</xref>,<xref ref-type="bibr" rid="redalyc_69353273003_ref2">2</xref>). EGA is caused by Anaplasma phagocytophilum, a bacteria of the Anaplasmataceae family, comprised by 4 genuses: Ehrlichia, Anaplasma, Wolbachia and Neorickettsia.all of them are obligate intracellular bacteria that replicate in small vacuoles derived from the host cell membrane. Each species may replicate inside vertebrate hosts, with the exception of Wolbachia, which has not been reported infecting mammals. Vectors for each species have been well studied, generally ticks or trematodes; however, the study of Wolbachia has not been clear due to the wide variety of invertebrate hosts where it has been found (<xref ref-type="bibr" rid="redalyc_69353273003_ref3">3</xref>). </p>
<p>Within the Anaplasmataceae, family, Ehrlichia y Anaplasma have been reported as the main pathogens in various types of wild and domestic mammals, including humans (<xref ref-type="bibr" rid="redalyc_69353273003_ref4">4</xref>,<xref ref-type="bibr" rid="redalyc_69353273003_ref5">5</xref>). Depending on the species, such genuses affect different blood cell types, to wit: neutrophils, monocytes, erythrocytes, macrophages, platelets, and endothelial cells of host mammals. Ehrlichiosis and anaplasmosis are recognized as emergent and re-emergent diseases with veterinary and human medical relevance (<xref ref-type="bibr" rid="redalyc_69353273003_ref3">3</xref>). </p>
<p>From the geographic standpoint within the Anaplasma genus, A. phagocytophilum is the most widely spread, and it has been reported in Asia, Europe, and America (<xref ref-type="bibr" rid="redalyc_69353273003_ref4">4</xref>). A. phagocytophilum has been long recognized as a pathogen in domestic ruminants in Europe and equines in the USA, but it has recently been detected in several species of mammals, including humans. Molecular studies suggest that some strains of these bacteria, pathogenic for humans and domestic animals, circulate in nature through different hosts (<xref ref-type="bibr" rid="redalyc_69353273003_ref2">2</xref>,<xref ref-type="bibr" rid="redalyc_69353273003_ref6">6</xref>).</p>
<p>Equines infected with A. phagocytophilum show clinical signs such as fever, depression, anorexia, petechial hemorrhages and jaundice. It is believed that the incubation period of these bacteria is close to 14 days, with clinical manifestations starting at day 7 (<xref ref-type="bibr" rid="redalyc_69353273003_ref5">5</xref>). EGA is a disease of veterinary relevance, and, with the appearance of human anaplasmosis caused by the same bacteria, there is an increasing interest in its effects on public health. This pathogen has been reported affecting sheep and bovine cattle in countries such as Scotland, Ireland, Austria, Switzerland, Spain, and France (<xref ref-type="bibr" rid="redalyc_69353273003_ref3">3</xref>). Evidence of agents causing equine ehrlichiosis y anaplasmosis in America has been reported (<xref ref-type="bibr" rid="redalyc_69353273003_ref7">7</xref>). </p>
<p>On the other hand, EP is caused by hemoparasites Theileria equi and Babesia caballi of the Apicomplexa phylum, which includes a large number of obligated intracellular eukaryote microorganisms in vertebrates and invertebrates. The common characteristic between these microorganisms is an apical complex which contains organelles deemed important in the invasion or establishment of the microorganism in the host cell. The phylum is divided into 4 main groups: Coccidia (subclass), Gregarinasida (subclass), Haemosporida (order), and piroplasmida (order). Piroplasmida order has two main genuses, Babesia and Theileria, which are responsible for major animal diseases and economic losses (<xref ref-type="bibr" rid="redalyc_69353273003_ref8">8</xref>).</p>
<p>Piroplasmosis is a disease with high economic, medical, and veterinary relevance and it is the second most common parasitic disease found in the blood of mammals, after trypanosomes (<xref ref-type="bibr" rid="redalyc_69353273003_ref9">9</xref>). Clinical symptoms in animals infected with this disease include fever, anemia, dyspnea, jaundice, splenomegaly and hepatomegaly, edema, intravascular hemolysis, hemoglobinuria, mucosa hemorrhage, and finally, death. Piroplasma affect animal health causing loss of appetite, and reducing their work capabilities (<xref ref-type="bibr" rid="redalyc_69353273003_ref10">10</xref>). After suffering an acute infection, animals then enter into a chronic stage with no clinical signs, becoming reservoirs for the microorganisms (<xref ref-type="bibr" rid="redalyc_69353273003_ref11">11</xref>). </p>
<p>EP is distributed worldwide and it is endemic in most tropical, subtropical, and mild climate areas (<xref ref-type="bibr" rid="redalyc_69353273003_ref12">12</xref>); however, a few countries are considered EP-free, such as Canada, Japan, Auatraliam England, United States, and Ireland. One of the impacts of piroplasmosis is the impediment for international mobilization of seroreactive equine animals, since countries free of piroplasmosis assume the presence of its vectors (<xref ref-type="bibr" rid="redalyc_69353273003_ref13">13</xref>). </p>
<p>Very Little information is available in Colombia regarding the Anaplasmataceae family, although one clinical case of EGA was diagnosed in Florencia (Caquetá) through a clinical test and peripheral blood smear (<xref ref-type="bibr" rid="redalyc_69353273003_ref14">14</xref>). On the other hand, EP has been reported in some countries such as Costa Rica, Venezuela, and Brazil (<xref ref-type="bibr" rid="redalyc_69353273003_ref15">15</xref>,<xref ref-type="bibr" rid="redalyc_69353273003_ref16">16</xref>,<xref ref-type="bibr" rid="redalyc_69353273003_ref17">17</xref>); in Colombia, studies have been performed in the departments of Antioquia, Córdoba, and Santander (<xref ref-type="bibr" rid="redalyc_69353273003_ref18">18</xref>,<xref ref-type="bibr" rid="redalyc_69353273003_ref19">19</xref>).</p>
<p>Regarding the diagnosis of these agents, it is noteworthy that clinic-based findings are non-specific, and peripheral blood smears have low sensitivity (<xref ref-type="bibr" rid="redalyc_69353273003_ref20">20</xref>). On the other hand, serological diagnosis depends on the production of antibodies during the acute phase of the disease, and shows a cross reaction with other closely related microorganisms (<xref ref-type="bibr" rid="redalyc_69353273003_ref21">21</xref>). Also, the above techniques do not allow, in most cases, to discriminate the species of these tick-transmitted agents. The purpose of this study was to detect agents of the Anaplasmataceae family and piroplasms in quines in a slaughterhouse in the municipality of Rionegro (Antioquia).</p>
</sec>
	<sec sec-type="materials|methods">
<title>
<bold>MATERIALS AND METHODS</bold>
</title>
<p>
<bold>Type of study and samples.</bold> A descriptive cross-sectional study was carried out on 135 equines during June, July, and August, 2015, at the “La Rinconada” slaughterhouse in the municipality of Rionegro (Antioquia), which processes animals from several municipalities of the department of Antioquia and other departments of the Caribbean region. Animals were selected by convenience. Information on species, age, sex, and department and municipality of origin was collected through the mobilization documents (<xref ref-type="bibr" rid="redalyc_69353273003_ref22">22</xref>). Animals were punctured in the jugular vein to draw 4 ml of whole blood with EDTA as an anticoagulant. The Ethics Committee for Animal Experimentation (CEEA, for its acronym in Spanish) of Universidad de Antioquia, Minute No. 89 of 2014 approved the procedures performed on the animals.</p>
<p>
<bold>Molecular tests</bold>. DNA was extracted from 100 µL of whole blood with EDTA. Extraction was performed using the DNeasy Blood and Tissue (QIAGEN, Valencia, CA) kit, following manufacturer recommendations. Concentration in DNA extracts was determined by udrop (Thermo Scientific Multiskan GO, μDrop TM Plate catalog N12391).From the DNA, a 259bp fragment of the β-actin constitutive gene was amplified for internal control. To search for the hemoparasites, we used the 16S rARN gene of the Anaplasmataceae family, and gene rARN 18S of piroplasms. </p>
<p>Amplification of the 360bp of the rARN 16S gene of Anaplasmataceae was made with Ehr-16SD/Ehr-16SR primers, and the amplification of a 450bp of the rARN 18S gene of piroplasms was made with PIRO A1/PIRO B primers. The sequences of all the primers used are shown in Table 1.</p>
<p>
<table-wrap id="gt2">
<label/>
<caption>
<title/>
</caption>
<alternatives>
<graphic xlink:href="69353273003_gt3.jpg" position="anchor" orientation="portrait"/>
</alternatives>
</table-wrap>
</p>
<p>For all three PCR tests, each reagent mix contained Buffer 10X [1X], deosynucleotide trifosphate (dNTPs) [0,4mM]), primers [0,4 pM], Magnesium Chloride (MgCl2) [1,6 mM], bovine seric albumin (BSA) [8 x 10 -6 mg/μL], DNAse-free water, and 200 ng of the extracted DNA. DNA of Ehrlichia canis and DNA of Babesia bigemina, donated by Dr. Santiago Nava of Instituto Nacional de Tecnología Agropecuaria (INTA) de Rafaela (Argentina) was used as positive control; DNAse-free water was used as negative control.</p>
<p>PCR amplification was made in a Veriti (Applied Biosystems, Austin, TX, USA) thermocycler, and PCR product visualization was made by electrophoresis in a 2% agarose gel stained with EZ vision® (Amresco, USA) and using a 100bp molecular weight marker (Invitrogen, USA). Gels were ran for 45 minutes at 100 volts.</p>
<p>
<bold>Genetic analysis</bold>. The PCRT products that showed the highest band intensity and quality in the gels were sent for sequencing. Sequences were edited and assembled in the GeneStudio 2.2.0.0 program. The sequences obtained in this work were compared to the GenBank references through the Basic Local Alignment Research Tool (BLASTn) of the National Center for Biotechnology Information (NCBI). The study and reference sequences of hemoparasites obtained from GenBank were aligned with the Clustal W algorithm, and then we created a Neighbor Joining sequence dendrogram with patristic distances and 1000 bootstrap replicates in MEGA 7 (<xref ref-type="bibr" rid="redalyc_69353273003_ref23">23</xref>).</p>
<p>
<bold>Statistical analysis</bold>. The data obtained was subject to a univariate and bivariate descriptive analysis (equine species, sex, age, department, municipality of origin) with respect to its positivity to hemoparasites. Data analysis was made in the InfoStat statistics program.</p>
</sec>
<sec sec-type="results">
<title>
<bold>RESULTS</bold>
</title>
<p>
<bold>General results</bold>. Out of the 135 equines selected for the study, 78% (n=105) were horses (Equus caballus, Ec), 16% (n=22) were donkeys (Equus asinus, Ea), and 6% (n=8) were mules (E. caballus x E. asinus). The predominating sex was male with 54% (n=73), while females accounted for 46% (n=62). We found animals of various age groups, adults (ages 5 to 18) were the most frequent, 80% (n=108), followed by young animals (&lt;5 years) accounting for 15% (n=20), and elderly animals (&gt;18 years) with 5% (n=7) (Table 1).</p>
<p>As for the origin of the animals, equines came from the departments of Córdoba accounted for 63% (n=90), Antioquia 24% (n=32), and Sucre 10% (n=13). In Antioquia, we received samples from the municipalities of Anzá, Caucasia, Mutatá, Planeta Rica, and Urrao. Equines from Córdoba came from the municipalities of Montería, Planeta Rica and Sahagún, and those from Sucre were brought from Tolú and Tolúviejo (Figure 1 and Table 1).</p>
<p>
<fig id="gf5">
<graphic xlink:href="69353273003_gf4.jpg" position="anchor" orientation="portrait"/>
</fig>
</p>
<p>
<bold>Molecular results.</bold> Out of the total DNA samples extracted, (n=135), 100% were positive for the β-actin gene, demonstrating the amsence of PCR inhibitors in the samples (Figure 2). Also, all of the samples analyzed with 16S rARN gene primers for the Anaplasmataceae family were negative. The general infection frequency for piroplasm infection in the studied animals was 13.3% (18/135). We obtained positive samples in the animals from the departments of Antioquia and Córdoba, and even though the largest number of positive samples came from Córdoba, the department of Antioquia showed a higher percentage of positive samples (Table 2).</p>
<p>
<fig id="gf6">
<graphic xlink:href="69353273003_gf5.jpg" position="anchor" orientation="portrait"/>
</fig>
</p>
<p>We found that horses was the group of animals with the highest percentage of positive samples, with 83.3% (n=15), followed by donkeys with 11.1% (n=2), and finally mules, with 5.5% (n=1). The age group with the highest positive frequency was the adult group with 83.3% (15 animals out of 18 positives), followed by young animals with 16.6% (2animals out of 18 positives), while the elderly group showed no positive sample. The sex with the highest infection rate was females, with 55.5% (n=10) and males showed 45.5% (n=8) (Table 2).</p>
<p>
<table-wrap id="gt3">
<label/>
<caption>
<title/>
</caption>
<alternatives>
<graphic xlink:href="69353273003_gt4.jpg" position="anchor" orientation="portrait"/>
</alternatives>
</table-wrap>
</p>
<p>Five samples from horses (Ec) and donkeys (Ea) from Monteria were selected for direct DNA sequencing (Ea035, Ea036, Ec096, Ec121, Ec142). The BLASTn in samples Ea035, Ea036 and Ec096 indicates a full identity with Theileria equi from Brazil (100% with KU240068), whereas the BLASTn in Ec121 and Ec142 shows a high similarity with the same agent from Florida (USA) (97-99% with KU672386). The Neighbor Joining dendrogram confirms circulation of three genotypes (haplotypes of gene18S) of Theileria equi in equines from the northern Colombia with a high branch support (bootstrap 97%) (Figure 3).</p>
<p>
<fig id="gf7">
<graphic xlink:href="69353273003_gf6.jpg" position="anchor" orientation="portrait"/>
</fig>
</p>
</sec>
<sec sec-type="results|discussion">
<title>
<bold>DISCUSSION</bold>
</title>
<p>This work presents the first molecular evidence of at least three genotypes of Theileria equi infecting equines in the northern part of the country. A 13% general piroplamsa infection was detected in these animals, and genetic analysis demonstrate active circulation of Theileria equi in animals from the departments of Antioquia and Córdoba.</p>
<p>There is very few data in Colombia on Ep epidemiology, and the findings in this work demonstrate the active infection of this type of agents in the departments of Antioquia and Córdoba. The zones studies with parasite presence can be considered as having high risk of transmission to healthy animals whose zootechnical use involves activities in EP-free countries, given the mobility restrictions imposed on animals infected with or seropositive to these hemoparasites. </p>
<p>The results of this work are similar to those obtained in other studies in the country regarding piroplasma frequency in equines, but its innovation lies in the implementation of molecular techniques instead of the conventional peripheral blood smears and serological tests (<xref ref-type="bibr" rid="redalyc_69353273003_ref18">18</xref>,<xref ref-type="bibr" rid="redalyc_69353273003_ref19">19</xref>). Thus, while serological tests rely on the search for anti-piroplasma antibodies indicating -depending on the antibody isotype- that the animal experienced a recent or distant infection, this work demonstrates the direct presence of parasite DNA in peripheral blood. Even though there was already knowledge of the circulation of piroplasms in equines in Montería (<xref ref-type="bibr" rid="redalyc_69353273003_ref24">24</xref>), this is the first time in Colombia for molecular identification of these protozoan agents of great significance for the health of equines. </p>
<p>This study was not able to detect agents of the Anaplasmataceae family in equines, despite the broad spectrum of the methodology used. However, these rickettsial agents have been successfully reported in other Latin American countries. For example, O’Nion et al (<xref ref-type="bibr" rid="redalyc_69353273003_ref24">24</xref>) found serological evidence of infection in 51 out of 92 sampled animals (55%) in Nicaragua, and managed to obtain molecular evidence of a potentially new species of Ehrlichia in four of these seroreactive animals (<xref ref-type="bibr" rid="redalyc_69353273003_ref24">24</xref>). In Guatemala, there has been molecular evidence of A. phagocytophilum reported on 13% of 74 analyzed horses (<xref ref-type="bibr" rid="redalyc_69353273003_ref25">25</xref>). Probably, these agents may be circulating in equines in Colombia, but the study design and sample size may be constraints to detect such rickettsial agents in this study. </p>
<p>Colombia has the ideal abiotic conditions for the development of tick-borne diseases, due to its location in a tropical area where temperature, relative humidity and lighting factors are favorable for the survival of disease vectors. For that purpose, in order to clarify the epidemiological scenario of these hemoparasytes in Colombia, further studies are necessary with specific sampling designs and with representation of other regions of the country, also engaging in the analysis of their potential vectors. These searches can be addressed by using techniques that allow a more sensitive and specific diagnosis, such as the one that molecular tests provide.</p>
</sec>
<sec>
<title>
<bold>Acknowledgements</bold>
</title>
<p>To the CODI of Universidad de Antioquia for financing (project 321-2014). To Colciencias for their support to LAG and LPT through National Doctorates. To Rene Ramírez of Universidad CES and the staff of La Rinconada slaughterhouse for their logistic support</p>
</sec>
<sec>
<title>
<bold>Conﬂict of interest</bold>
</title>
<p>The authors hereby declare that they have no conflicts of interest.</p>
</sec>
</body>
<back>
<ref-list>
<title>
<bold>REFERENCES</bold>
</title>
<ref id="redalyc_69353273003_ref1">
<label>1</label>
<mixed-citation>1. A, Zamen M, Bozorgi S. Microscopic and molecular detection of Theileria (Babesia) equi infection in equids of Kurdistan province, Iran. Iran J Parasitol 2016; 11(1):86–90.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Zamen</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Bozorgi</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title>Microscopic and molecular detection of Theileria (Babesia) equi infection in equids of Kurdistan province, Iran</article-title>
<source>Iran J Parasitol</source>
<year>2016</year>
<volume>11</volume>
<issue>1</issue>
<fpage>86</fpage>
<lpage>90</lpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref2">
<label>2</label>
<mixed-citation>2.	Dumler JS, Walker DH. Tick-borne ehrlichioses. Lancet Infect Dis 2001; 1:21–8.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Dumler</surname>
<given-names>JS</given-names>
</name>
<name>
<surname>Walker</surname>
<given-names>DH</given-names>
</name>
</person-group>
<article-title>Tick-borne ehrlichioses</article-title>
<source>Lancet Infect Dis</source>
<year>2001</year>
<volume>1</volume>
<fpage>21</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref3">
<label>3</label>
<mixed-citation>3.	Dumler JS, Barbet AF, Bekker CP, Dasch GA, Palmer GH, Ray SC, et al. Reorganization of genera in the families Rickettsiaceae and Anaplasmataceae in the order Rickettsiales: unification of some species of Ehrlichia with Anaplasma, Cowdria with Ehrlichia and Ehrlichia with Neorickettsia, descriptions of six new species combi. Int J Syst Evol Microbiol 2001; 51(6):2145–65.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Dumler</surname>
<given-names>JS</given-names>
</name>
<name>
<surname>Barbet</surname>
<given-names>AF</given-names>
</name>
<name>
<surname>Bekker</surname>
<given-names>CP</given-names>
</name>
<name>
<surname>Dasch</surname>
<given-names>GA</given-names>
</name>
<name>
<surname>Palmer</surname>
<given-names>GH</given-names>
</name>
<name>
<surname>Ray</surname>
<given-names>SC</given-names>
</name>
</person-group>
<article-title>Reorganization of genera in the families Rickettsiaceae and Anaplasmataceae in the order Rickettsiales: unification of some species of Ehrlichia with Anaplasma, Cowdria with Ehrlichia and Ehrlichia with Neorickettsia, descriptions of six new species combi</article-title>
<source>Int J Syst Evol Microbiol</source>
<year>2001</year>
<volume>51</volume>
<issue>6</issue>
<fpage>2145</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref4">
<label>4</label>
<mixed-citation>4.	Santos HA, Thomé SMG, Baldani CD, Silva CB, Peixoto MP, Pires MS, et al. Molecular epidemiology of the emerging zoonosis agent Anaplasma phagocytophilum (Foggie, 1949) in dogs and ixodid ticks in Brazil. Parasit Vectors 2013; 6:348.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Santos</surname>
<given-names>HA</given-names>
</name>
<name>
<surname>Thomé</surname>
<given-names>SMG</given-names>
</name>
<name>
<surname>Baldani</surname>
<given-names>CD</given-names>
</name>
<name>
<surname>Silva</surname>
<given-names>CB</given-names>
</name>
<name>
<surname>Peixoto</surname>
<given-names>MP</given-names>
</name>
<name>
<surname>Pires</surname>
<given-names>MS</given-names>
</name>
</person-group>
<article-title>Molecular epidemiology of the emerging zoonosis agent Anaplasma phagocytophilum (Foggie, 1949) in dogs and ixodid ticks in Brazil.</article-title>
<source>Parasit Vectors</source>
<year>2013</year>
<volume>6</volume>
<fpage>348</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref5">
<label>5</label>
<mixed-citation>5.	Uehlinger FD, Clancey NP, Lofstedt J. Granulocytic anaplasmosis in a horse from Nova Scotia caused by infection with Anaplasma phagocytophilum. Can Vet J 2011; 52(5):537–40.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Uehlinger</surname>
<given-names>FD</given-names>
</name>
<name>
<surname>Clancey</surname>
<given-names>NP</given-names>
</name>
<name>
<surname>Lofstedt</surname>
<given-names>J</given-names>
</name>
</person-group>
<article-title>Granulocytic anaplasmosis in a horse from Nova Scotia caused by infection with Anaplasma phagocytophilum</article-title>
<source>Can Vet J</source>
<year>2011</year>
<volume>52</volume>
<issue>5</issue>
<fpage>537</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref6">
<label>6</label>
<mixed-citation>6.	Stuen S, Granquist EG, Silaghi C. Anaplasma phagocytophilum--a widespread multi-host pathogen with highly adaptive strategies. Front Cell Infect Microbiol 2013; 3(7):31.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Stuen</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Granquist</surname>
<given-names>EG</given-names>
</name>
<name>
<surname>Silaghi</surname>
<given-names>C</given-names>
</name>
</person-group>
<article-title>Anaplasma phagocytophilum--a widespread multi-host pathogen with highly adaptive strategie</article-title>
<source>Front Cell Infect Microbiol</source>
<year>2013</year>
<volume>3</volume>
<issue>7</issue>
<fpage>31</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref7">
<label>7</label>
<mixed-citation>7.	Teglas M, Matern E, Lein S, Foley P, Mahan SM, Foley J. Ticks and tick-borne disease in Guatemalan cattle and horses. Vet Parasitol 2005; 131(1–2):119–27.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Teglas</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Matern</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Lein</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Foley</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Mahan</surname>
<given-names>SM</given-names>
</name>
<name>
<surname>Foley</surname>
<given-names>J</given-names>
</name>
</person-group>
<article-title>Ticks and tick-borne disease in Guatemalan cattle and horses.</article-title>
<source>Vet Parasitol</source>
<year>2005</year>
<volume>131</volume>
<issue>1–2</issue>
<fpage>119</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref8">
<label>8</label>
<mixed-citation>8.	Mans BJ, Pienaar R, Latif AA. A review of Theileria diagnostics and epidemiology. Int J Parasitol Parasites Wildl 2015; 4(1):104–18.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Mans</surname>
<given-names>BJ</given-names>
</name>
<name>
<surname>Pienaar</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Latif</surname>
<given-names>AA</given-names>
</name>
</person-group>
<article-title>A review of Theileria diagnostics and epidemiology</article-title>
<source>Int J Parasitol Parasites Wildl</source>
<year>2015</year>
<volume>4</volume>
<issue>1</issue>
<fpage>104</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref9">
<label>9</label>
<mixed-citation>9.	Schnittger L, Rodriguez AE, Florin-Christensen M, Morrison DA. Babesia: A world emerging. Infect Genet Evol 2012; 12(8):1788–809.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Schnittger</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Rodriguez</surname>
<given-names>AE</given-names>
</name>
<name>
<surname>Florin-Christensen</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Morrison</surname>
<given-names>DA</given-names>
</name>
</person-group>
<article-title>Babesia: A world emerging</article-title>
<source>Infect Genet Evol</source>
<year>2012</year>
<volume>12</volume>
<issue>8</issue>
<fpage>1788</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref10">
<label>10</label>
<mixed-citation>10.	Machado RZ, Toledo CZP, Teixeira MCA, André MR, Freschi CR, Sampaio PH. Molecular and serological detection of Theileria equi and Babesia caballi in donkeys (Equus asinus) in Brazil. Vet Parasitol 2012; 186(3–4):461–5.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Machado</surname>
<given-names>RZ</given-names>
</name>
<name>
<surname>Toledo</surname>
<given-names>CZP</given-names>
</name>
<name>
<surname>Teixeira</surname>
<given-names>MCA</given-names>
</name>
<name>
<surname>André</surname>
<given-names>MR</given-names>
</name>
<name>
<surname>Freschi</surname>
<given-names>CR</given-names>
</name>
<name>
<surname>Sampaio</surname>
<given-names>PH</given-names>
</name>
</person-group>
<article-title>Molecular and serological detection of Theileria equi and Babesia caballi in donkeys (Equus asinus) in Brazil.</article-title>
<source>Vet Parasitol</source>
<year>2012</year>
<volume>186</volume>
<issue>3–4</issue>
<fpage>461</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref11">
<label>11</label>
<mixed-citation>11. 	Bashiruddin JB, Camma C, Rebelo E. Molecular detection of Babesia equi and Babesia caballi in horse blood by PCR amplification of part of the 16S rRNA gene. Vet Parasitol 1999; 84(1–2):75–83.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Bashiruddin</surname>
<given-names>JB</given-names>
</name>
<name>
<surname>Camma</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Rebelo</surname>
<given-names>E</given-names>
</name>
</person-group>
<article-title>Molecular detection of Babesia equi and Babesia caballi in horse blood by PCR amplification of part of the 16S rRNA gene.</article-title>
<source>Vet Parasitol</source>
<year>1999</year>
<volume>84</volume>
<issue>1–2</issue>
<fpage>75</fpage>
<lpage>83</lpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref12">
<label>12</label>
<mixed-citation>12.	Abutarbush SM, Alqawasmeh DM, Mukbel RM, Al-Majali AM. Equine Babesiosis: Seroprevalence, Risk Factors and Comparison of Different Diagnostic Methods in Jordan. Transbound Emerg Dis. 2012;59(1):72–8.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Abutarbush</surname>
<given-names>SM</given-names>
</name>
<name>
<surname>Alqawasmeh</surname>
<given-names>DM</given-names>
</name>
<name>
<surname>Mukbel</surname>
<given-names>RM</given-names>
</name>
<name>
<surname>Al-Majali</surname>
<given-names>AM</given-names>
</name>
</person-group>
<article-title>Equine Babesiosis: Seroprevalence, Risk Factors and Comparison of Different Diagnostic Methods in Jordan</article-title>
<source>Transbound Emerg Dis</source>
<year>2012</year>
<volume>59</volume>
<issue>1</issue>
<fpage>72</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref13">
<label>13</label>
<mixed-citation>13.	Schwint ON, Knowles DP, Ueti MW, Kappmeyer LS, Scoles G a. Transmission of Babesia caballi by Dermacentor nitens (Acari: Ixodidae) is restricted to one generation in the absence of alimentary reinfection on a susceptible equine host. J Med Entomol 2008; 45(6):1152–1155.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Schwint</surname>
<given-names>ON</given-names>
</name>
<name>
<surname>Knowles</surname>
<given-names>DP</given-names>
</name>
<name>
<surname>Ueti</surname>
<given-names>MW</given-names>
</name>
<name>
<surname>Kappmeyer</surname>
<given-names>LS</given-names>
</name>
<name>
<surname>Scoles</surname>
<given-names>G</given-names>
</name>
</person-group>
<article-title>Transmission of Babesia caballi by Dermacentor nitens (Acari: Ixodidae) is restricted to one generation in the absence of alimentary reinfection on a susceptible equine host</article-title>
<source>J Med Entomol</source>
<year>2008</year>
<volume>45</volume>
<issue>6</issue>
<fpage>1152</fpage>
<lpage>1155</lpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref14">
<label>14</label>
<mixed-citation>14.	Calderón LGR, Delgado PAM. Reporte de Caso Clínico de Ehrlichiosis Equina en el municipio de Florencia (Colombia). REDVET 2013; 14(1):1–12.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Calderón</surname>
<given-names>LGR</given-names>
</name>
<name>
<surname>Delgado</surname>
<given-names>PAM</given-names>
</name>
</person-group>
<article-title>Reporte de Caso Clínico de Ehrlichiosis Equina en el municipio de Florencia (Colombia)</article-title>
<source>REDVET</source>
<year>2013</year>
<volume>14</volume>
<issue>1</issue>
<fpage>1</fpage>
<lpage>12</lpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref15">
<label>15</label>
<mixed-citation>15.	Vera M De, Guillén AT, García F, Contreras R, Sierralta Á, León E. Seroprevalencia de la Babesiosis Equina en caballos pura sangre de carrera alojados en los hipódromos la Rinconada y Nacional de Valencia, Venezuela. Vet Trop 2006; 31:43–52.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>M</surname>
<given-names>Vera</given-names>
</name>
<name>
<surname>Guillén</surname>
<given-names>AT</given-names>
</name>
<name>
<surname>García</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Contreras</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Sierralta</surname>
<given-names>Á</given-names>
</name>
<name>
<surname>León</surname>
<given-names>E</given-names>
</name>
</person-group>
<article-title>Seroprevalencia de la Babesiosis Equina en caballos pura sangre de carrera alojados en los hipódromos la Rinconada y Nacional de Valencia, Venezuela</article-title>
<source>Vet Trop</source>
<year>2006</year>
<volume>31</volume>
<fpage>43</fpage>
<lpage>52</lpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref16">
<label>16</label>
<mixed-citation>16.	Vargas-Hernández G, André MR, Faria JLM, Munhoz TD, Hernandez-Rodriguez M, Machado RZ, et al. Molecular and serological detection of Ehrlichia canis and Babesia vogeli in dogs in Colombia. Vet Parasitol 2012; 186(3–4):254–60.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Vargas-Hernández</surname>
<given-names>G</given-names>
</name>
<name>
<given-names>MR</given-names>
</name>
<name>
<given-names>André</given-names>
</name>
<name>
<surname>Faria</surname>
<given-names>JLM</given-names>
</name>
<name>
<surname>Munhoz</surname>
<given-names>TD</given-names>
</name>
<name>
<surname>Hernandez-Rodriguez</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Machado</surname>
<given-names>RZ</given-names>
</name>
</person-group>
<article-title>Molecular and serological detection of Ehrlichia canis and Babesia vogeli in dogs in Colombia</article-title>
<source>Vet Parasitol</source>
<year>2012</year>
<volume>186</volume>
<issue>3–4</issue>
<fpage>254</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref17">
<label>17</label>
<mixed-citation>17.	Posada-Guzmán MF, Dolz G, Romero-Zúñiga JJ, Jiménez-Rocha AE. Detection of Babesia caballi and Theileria equi in Blood from Equines from Four Indigenous Communities in Costa Rica. Vet Med Int 2015; 2015(6):1–6.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Posada-Guzmán</surname>
<given-names>MF</given-names>
</name>
<name>
<surname>Dolz</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Romero-Zúñiga</surname>
<given-names>JJ</given-names>
</name>
<name>
<surname>Jiménez-Rocha</surname>
<given-names>AE</given-names>
</name>
</person-group>
<article-title>Detection of Babesia caballi and Theileria equi in Blood from Equines from Four Indigenous Communities in Costa Rica.</article-title>
<source>Vet Med Int</source>
<year>2015</year>
<volume>6</volume>
<fpage>1</fpage>
<lpage>6</lpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref18">
<label>18</label>
<mixed-citation>18.	León C, Ardila F, Celis J. Prevalencia de reactores seropositivos a Theileria equi (Babesia equi) en equinos del área rural del municipio de Floridablanca, Santander. Rev Spei Domus 2010; 6(12):54.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>León</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Ardila</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Celis</surname>
<given-names>J</given-names>
</name>
</person-group>
<article-title>Prevalencia de reactores seropositivos a Theileria equi (Babesia equi) en equinos del área rural del municipio de Floridablanca, Santander</article-title>
<source>Rev Spei Domus</source>
<year>2010</year>
<volume>6</volume>
<issue>12</issue>
<fpage>54</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref19">
<label>19</label>
<mixed-citation>19.	Calderón A, Cardona J, Vergara Ó. Frecuencia de Babesia spp. en caballos de Montería, Córdoba (Colombia). Rev UDCA Act Div Cient 2013; 16:451–8.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Calderón</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Cardona</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Vergara</surname>
<given-names>Ó</given-names>
</name>
</person-group>
<article-title>Frecuencia de Babesia spp. en caballos de Montería, Córdoba (Colombia)</article-title>
<source>Rev UDCA Act Div Cient</source>
<year>2013</year>
<volume>16</volume>
<fpage>451</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref20">
<label>20</label>
<mixed-citation>20.	Böse R, Jorgensen WK, Dalgliesh RJ, Friedhoff KT, de Vos AJ. Current state and future trends in the diagnosis of babesiosis. Vet Parasitol 1995; 57(1–3):61–74.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Böse</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Jorgensen</surname>
<given-names>WK</given-names>
</name>
<name>
<surname>Dalgliesh</surname>
<given-names>RJ</given-names>
</name>
<name>
<surname>Friedhoff</surname>
<given-names>KT</given-names>
</name>
<name>
<surname>de Vos</surname>
<given-names>AJ</given-names>
</name>
</person-group>
<article-title>Current state and future trends in the diagnosis of babesiosis</article-title>
<source>Vet Parasitol</source>
<year>1995</year>
<volume>57</volume>
<issue>1–3</issue>
<fpage>61</fpage>
<lpage>74</lpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref21">
<label>21</label>
<mixed-citation>21.	Vargas D, Bonet R, Oliva P, Campano S. Implementación de la técnica de PCR enla identificación de Babesia ssp en equinos. Parasitol Latinoam 2004; 59(3–4):179–82.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Vargas</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Bonet</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Oliva</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Campano</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title>Implementación de la técnica de PCR enla identificación de Babesia ssp en equinos</article-title>
<source>Parasitol Latinoam</source>
<year>2004</year>
<volume>59</volume>
<issue>3–4</issue>
<fpage>179</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref22">
<label>22</label>
<mixed-citation>22.	Practitioners AA of E. Official guide for determining the age of the horse. Fort Dodge Laboratories: Cornell University; 1981. URL Available from: https://books.google.com.co/books?id=jO5UAAAAYAAJ</mixed-citation>
<element-citation publication-type="webpage">
<person-group person-group-type="author">
<name>
<given-names>Practitioners AA of E</given-names>
</name>
</person-group>
<article-title>Official guide for determining the age of the horse. Fort Dodge Laboratories: Cornell University; 1981</article-title>
<source>https://books.google.com.co/books?id=jO5UAAAAYAA</source>
<year>1981</year>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref23">
<label>23</label>
<mixed-citation>23.	Kumar S, Stecher G, Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Mol Biol Evol 2016; 33(7):54.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Kumar</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Stecher</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Tamura</surname>
<given-names>K</given-names>
</name>
</person-group>
<article-title>MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets.</article-title>
<source>Mol Biol Evol</source>
<year>2016</year>
<volume>33</volume>
<issue>7</issue>
<fpage>54</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref24">
<label>24</label>
<mixed-citation>24.	O’Nion VL, Montilla HJ, Qurollo BA, Maggi RG, Hegarty BC, Tornquist SJ, et al. Potentially novel Ehrlichia species in horses, Nicaragua. Emerg Infect Dis 2015; 21(2):335–8.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>O’Nion</surname>
<given-names>VL</given-names>
</name>
<name>
<surname>Montilla</surname>
<given-names>HJ</given-names>
</name>
<name>
<surname>Qurollo</surname>
<given-names>BA</given-names>
</name>
<name>
<surname>Maggi</surname>
<given-names>RG</given-names>
</name>
<name>
<surname>Hegarty</surname>
<given-names>BC</given-names>
</name>
<name>
<surname>Tornquist</surname>
<given-names>SJ</given-names>
</name>
</person-group>
<article-title>Potentially novel Ehrlichia species in horses, Nicaragua</article-title>
<source>Emerg Infect Dis</source>
<year>2015</year>
<volume>21</volume>
<issue>2</issue>
<fpage>335</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref25">
<label>25</label>
<mixed-citation>25.	Teglas M, Matern E, Lein S, Foley P, Mahan SM, Foley J. Ticks and tick-borne disease in Guatemalan cattle and horses. Vet Parasitol 2005; 131:119–27.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Teglas</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Matern</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Lein</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Foley</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Mahan</surname>
<given-names>SM</given-names>
</name>
<name>
<surname>Fole</surname>
<given-names>J</given-names>
</name>
</person-group>
<article-title>Ticks and tick-borne disease in Guatemalan cattle and horses.</article-title>
<source>Vet Parasitol</source>
<year>2005</year>
<volume>131</volume>
<fpage>119</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref26">
<label>26</label>
<mixed-citation>26.	Alonso S, Minty A, Bourlet Y, Buckingham M. Comparison of three actin-coding sequences in the mouse; Evolutionary relationships between the actin genes of warm-blooded vertebrates. J Mol Evol 1986; 23(1):11–22.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Alonso</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Minty</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Bourlet</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Buckingham</surname>
<given-names>M</given-names>
</name>
</person-group>
<article-title>Comparison of three actin-coding sequences in the mouse; Evolutionary relationships between the actin genes of warm-blooded vertebrates</article-title>
<source>J Mol Evol</source>
<year>1986</year>
<volume>23</volume>
<issue>1</issue>
<fpage>11</fpage>
<lpage>22</lpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref27">
<label>27</label>
<mixed-citation>27.	László CF, Wu S. Mechanism of UV-Induced IκBα-Independent Activation of NF-κB. Photochem Photobiol 2008; 84(6):1564–8.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>László</surname>
<given-names>CF</given-names>
</name>
<name>
<surname>Wu</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title>Mechanism of UV-Induced IκBα-Independent Activation of NF-κB.</article-title>
<source>Photochem Photobiol</source>
<year>2008</year>
<volume>84</volume>
<issue>6</issue>
<fpage>1564</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref28">
<label>28</label>
<mixed-citation>28.	Inokuma H, Raoult D, Brouqui P. Detection of Ehrlichia platys DNA in brown dog ticks (Rhipicephalus sanguineus) in Okinawa island, Japan. J Clin Microbiol 2000; 38(11):4219–21.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Inokuma</surname>
<given-names>H</given-names>
</name>
<name>
<surname>Raoul</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Brouqui</surname>
<given-names>P</given-names>
</name>
</person-group>
<article-title>Detection of Ehrlichia platys DNA in brown dog ticks (Rhipicephalus sanguineus) in Okinawa island, Japan</article-title>
<source>J Clin Microbiol</source>
<year>2000</year>
<volume>38</volume>
<issue>11</issue>
<fpage>4219</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref29">
<label>29</label>
<mixed-citation>29.	Sanogo YO, Parola P, Shpynov S, Camicas JL, Brouqui P, Caruso G, et al. Genetic diversity of bacterial agents detected in ticks removed from asymptomatic patients in northeastern Italy. Ann N Y Acad Sci 2003; 990(33):182–90.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Sanogo</surname>
<given-names>YO</given-names>
</name>
<name>
<surname>Parola</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Shpynov</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Camicas</surname>
<given-names>JL</given-names>
</name>
<name>
<surname>Brouqui</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Caruso</surname>
<given-names>G</given-names>
</name>
</person-group>
<article-title>Genetic diversity of bacterial agents detected in ticks removed from asymptomatic patients in northeastern Italy</article-title>
<source>Ann N Y Acad Sci</source>
<year>2003</year>
<volume>990</volume>
<issue>33</issue>
<fpage>182</fpage>
</element-citation>
</ref>
<ref id="redalyc_69353273003_ref30">
<label>30</label>
<mixed-citation>30.	García A, De Mello A, Cerqueira F, O’Dwyer LH, De Barros Macieira D, Da Abreu S, et al. Detection and Molecular Characterization of Babesia canis vogeli From Naturally Infected Brazilian Dogs. Int J Appl Res Vet Med 2004; 4(2):163–8.</mixed-citation>
<element-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>García</surname>
<given-names>A</given-names>
</name>
<name>
<surname>De Mello</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Cerqueira</surname>
<given-names>F</given-names>
</name>
<name>
<surname>O’Dwyer</surname>
<given-names>LH</given-names>
</name>
<name>
<surname>De Barros Macieira</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Da Abreu</surname>
<given-names>S</given-names>
</name>
</person-group>
<article-title>Detection and Molecular Characterization of Babesia canis vogeli From Naturally Infected Brazilian Dogs</article-title>
<source>Int J Appl Res Vet Med</source>
<year>2004</year>
<volume>4</volume>
<issue>2</issue>
<fpage>163</fpage>
</element-citation>
</ref>
</ref-list>
</back>
</article>