Mahmoud Hassan Y A H, Rady Abdelrahman A, Tanaka Tetsuya
Division of Infectious Diseases, Animal Medicine Department, Faculty of Veterinary Medicine, South Valley University, Qena 83523, Egypt.
Laboratory of Infectious Diseases, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.
Parasite Epidemiol Control. 2024 Feb 1;25:e00340. doi: 10.1016/j.parepi.2024.e00340. eCollection 2024 May.
Tick-borne diseases have a major adverse effect on livestock worldwide, causing enormous economic losses in meat and milk production as well threatening animal and public health. In this study, we aimed to detect and characterize piroplasms isolated from cattle and buffalo in southern Egypt, using molecular techniques. Three hundred blood samples were collected from cattle and buffalo in two governorates in southern Egypt. All 300 samples (100%) were confirmed to contain DNA, as they exhibited bands of bovine gene at the expected 227 bp for cattle and buffalo. The samples were analyzed by PCR for the presence of piroplasms, specifically , , and . Samples positive for the gene were further examined for two additional genes, gene, to provide an enhanced degree of specificity for the identification of and , and the gene for The infection rate for piroplasma spp. was 60/300 (20%). The positivity rates were 10.7% (32/300) for , 5.3% (16/300) for , and 4% (12/300) for . By host species, 42/150 (28%) cattle and 18/150 (12%) buffalo were positive for piroplasms. None of the isolates sequenced for the isolates from buffalo in this study showed 100% identity with any sequence deposited in GenBank for the gene (maximum identity value = 99.74%). Similarly, no gene sequence identified in this study exhibited 100% identity with any sequence deposited in GenBank (maximum identity value = 99.89%). The current study provides a partial sequence of the gene, as well as the and genes, in cattle and buffalo in southern Egypt, and is the first report on these piroplasma genes in cattle and buffalo in southern Egypt.
蜱传疾病对全球家畜有重大不利影响,在肉类和牛奶生产中造成巨大经济损失,同时也威胁动物和公众健康。在本研究中,我们旨在使用分子技术检测和鉴定从埃及南部牛和水牛中分离出的梨形虫。从埃及南部两个省份的牛和水牛中采集了300份血样。所有300份样本(100%)均被证实含有DNA,因为它们在牛和水牛预期的227 bp处显示出牛基因条带。通过PCR分析样本中是否存在梨形虫,具体为、和。对基因呈阳性的样本进一步检测另外两个基因,即基因,以提高鉴定和的特异性程度,以及用于的基因。梨形虫属的感染率为60/300(20%)。的阳性率为10.7%(32/300),的阳性率为5.3%(16/300),的阳性率为4%(12/300)。按宿主物种分类,42/150(28%)的牛和18/150(12%)的水牛梨形虫检测呈阳性。本研究中对水牛分离株进行测序的所有分离株,其基因与GenBank中存档的任何序列均未显示100%的同一性(最大同一性值 = 99.74%)。同样,本研究中鉴定的任何基因序列与GenBank中存档的任何序列均未显示100%的同一性(最大同一性值 = 99.89%)。本研究提供了埃及南部牛和水牛中基因以及和基因的部分序列,是关于埃及南部牛和水牛中这些梨形虫基因的首次报道。