Silva Claudia Bezerra da, Santos Huarrisson Azevedo, Navarrete Maylín González, Ribeiro Carla Carolina Dias Uzedo, Gonzalez Belkis Corona, Zaldivar Maykelin Fuentes, Pires Marcus Sandes, Peckle Maristela, Costa Renata Lins da, Vitari Gabriela Lopes Vivas, Massard Carlos Luiz
Department of Animal Parasitology, Veterinary Institute, Federal Rural University of Rio de Janeiro, Br 465, km 7, Seropedica, Rio de Janeiro, 23897-000, Brazil.
Department of Epidemiology and Public Health, Veterinary Institute, Federal Rural University of Rio de Janeiro, Br 465, km 7, Seropedica, Rio de Janeiro, 23897-000, Brazil.
Ticks Tick Borne Dis. 2016 Jul;7(5):938-944. doi: 10.1016/j.ttbdis.2016.04.012. Epub 2016 Apr 22.
Canine cyclic thrombocytopenia, an infectious disease caused by Anaplasma platys is a worldwide dog health problem. This study aimed to detect and characterize A. platys deoxyribonucleic acid (DNA) in dogs and ticks from Cuba using molecular methods. The study was conducted in four cities of Cuba (Habana del Este, Boyeros, Cotorro and San José de las Lajas). Blood samples were collected from 100 dogs in these cities. The animals were inspected for the detection of tick infestation and specimens were collected. Genomic DNA was extracted from dog blood and ticks using a commercial kit. Genomic DNA samples from blood and ticks were tested by a nested polymerase chain reaction (nPCR) to amplify 678 base pairs (bp) from the 16S ribosomal DNA (rDNA) of A. platys. Positive samples in nPCR were also subjected to PCR to amplify a fragment of 580bp from the citrate synthase (gltA) gene and the products were sequenced. Only Rhipicephalus sanguineus sensu lato (s.l.) was found on dogs, and 10.20% (n=5/49) of these ticks plus sixteen percent (16.0%, n=16/100) of dogs were considered positive for A. platys by nPCR targeting the 16S rDNA gene. All analyzed gltA and 16S rDNA sequences showed a 99-100% identity with sequences of A. platys reported in around the world. Phylogenetic analysis showed two defined clusters for the 16S rDNA gene and three defined clusters for the gltA gene. Based on the gltA gene, the deduced amino acid sequence showed two mutations at positions 88 and 168 compared with the sequence DQ525687 (GenBank ID from Italian sample), used as a reference in the alignment. A preliminary study on the epidemiological aspects associated with infection by A. platys showed no statistical association with the variables studied (p>0.05). This is the first evidence of the presence of A. platys in dogs and ticks in Cuba. Further studies are needed to evaluate the epidemiological aspects of A. platys infection in Cuban dogs.
犬周期性血小板减少症是一种由血小板无浆体引起的传染病,是一个全球性的犬类健康问题。本研究旨在使用分子方法检测和鉴定古巴犬和蜱体内的血小板无浆体脱氧核糖核酸(DNA)。研究在古巴的四个城市(哈瓦那东部、博耶罗斯、科托罗和圣何塞德拉哈斯)进行。从这些城市的100只犬采集血液样本。检查动物是否有蜱虫寄生并收集标本。使用商业试剂盒从犬血液和蜱虫中提取基因组DNA。通过巢式聚合酶链反应(nPCR)检测血液和蜱虫的基因组DNA样本,以扩增血小板无浆体16S核糖体DNA(rDNA)的678个碱基对(bp)。nPCR阳性样本也进行PCR,以扩增柠檬酸合酶(gltA)基因的580bp片段,并对产物进行测序。在犬身上仅发现了血红扇头蜱指名亚属(Rhipicephalus sanguineus sensu lato,s.l.),通过针对16S rDNA基因的nPCR检测,这些蜱虫中有10.20%(n = 5/49)以及犬中有16.0%(n = 16/100)被认为血小板无浆体呈阳性。所有分析的gltA和16S rDNA序列与世界各地报道的血小板无浆体序列显示出99 - 100%的同一性。系统发育分析显示16S rDNA基因有两个明确的聚类,gltA基因有三个明确的聚类。基于gltA基因,与比对中用作参考的序列DQ525687(来自意大利样本的GenBank ID)相比推导的氨基酸序列在第88和168位显示出两个突变。一项关于与血小板无浆体感染相关的流行病学方面的初步研究表明,与所研究的变量无统计学关联(p>0.05)。这是古巴犬和蜱体内存在血小板无浆体的首个证据。需要进一步研究以评估古巴犬中血小板无浆体感染的流行病学方面。