Molecular detection and characterization of Theileria annulata, Babesia bovis, and Babesia bigemina infecting cattle and buffalo in southern Egypt

IF 2 Q3 INFECTIOUS DISEASES Parasite Epidemiology and Control Pub Date : 2024-02-01 DOI:10.1016/j.parepi.2024.e00340
Hassan Y.A.H. Mahmoud , Abdelrahman A. Rady , Tetsuya Tanaka
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Abstract

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 β-actin gene at the expected 227 bp for cattle and buffalo. The samples were analyzed by PCR for the presence of piroplasms, specifically Babesia bovis, Babesia bigemina, and Theileria annulata. Samples positive for the piroplasma 18S ribosomal RNA gene were further examined for two additional genes, spherical body protein 4 gene, to provide an enhanced degree of specificity for the identification of B. bovis and B. bigemina, and the major merozoite surface antigen gene for T. annulata. The infection rate for piroplasma spp. was 60/300 (20%). The positivity rates were 10.7% (32/300) for T. annulata, 5.3% (16/300) for B. bovis, and 4% (12/300) for B. bigemina. By host species, 42/150 (28%) cattle and 18/150 (12%) buffalo were positive for piroplasms. None of the isolates sequenced for the B. bovis isolates from buffalo in this study showed 100% identity with any sequence deposited in GenBank for the small subunit ribosomal RNA gene (maximum identity value = 99.74%). Similarly, no T. annulata small subunit ribosomal RNA 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 T. annulata merozoite-piroplasm surface antigen gene, as well as the B. bovis and B. bigemina spherical body protein 4 genes, in cattle and buffalo in southern Egypt, and is the first report on these piroplasma genes in cattle and buffalo in southern Egypt.

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对埃及南部感染牛和水牛的环状沙雷氏菌、牛巴贝斯虫和大肠巴贝斯虫进行分子检测并确定其特征
蜱传疾病对全世界的牲畜造成了严重的负面影响,给肉类和牛奶生产造成了巨大的经济损失,并威胁着动物和公众健康。在这项研究中,我们旨在利用分子技术检测和鉴定从埃及南部的牛和水牛身上分离出来的蜱虫。我们从埃及南部两个省的牛和水牛身上采集了 300 份血液样本。所有 300 份样本(100%)都被证实含有 DNA,因为它们在牛和水牛的预期 227 bp 处显示出牛 β-肌动蛋白基因条带。通过聚合酶链式反应(PCR)对样本进行了分析,以确定是否存在牛皮癣菌,特别是牛巴贝斯虫、大肠巴贝斯虫和环状毛癣菌。对螺旋体 18S 核糖体 RNA 基因呈阳性的样本还进一步检测了另外两个基因,即球形体蛋白 4 基因,以提高鉴定牛巴贝斯虫和大肠巴贝斯虫的特异性,以及环状丝虫的主要裂殖体表面抗原基因。螺浆虫属感染率为 60/300(20%)。环斑蓟马的阳性率为 10.7%(32/300),鲍曼不动杆菌的阳性率为 5.3%(16/300),比格明纳虫的阳性率为 4%(12/300)。从宿主种类来看,42/150(28%)头牛和 18/150(12%)头水牛对螺盘虫呈阳性反应。在本研究中,从水牛中分离出的牛包虫病分离物的小亚基核糖体 RNA 基因与 GenBank 中保存的任何序列都没有 100%的同一性(最大同一性值 = 99.74%)。同样,本研究中发现的 T. annulata 小亚基核糖体 RNA 基因序列与 GenBank 中的任何序列都没有 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环状丝虫螺旋体表面抗原基因的部分序列,以及牛杆菌和大肠杆菌球形体蛋白 4 基因的部分序列,是有关埃及南部牛和水牛中这些螺旋体基因的首次报道。
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来源期刊
Parasite Epidemiology and Control
Parasite Epidemiology and Control Medicine-Infectious Diseases
CiteScore
5.70
自引率
3.10%
发文量
44
审稿时长
17 weeks
期刊介绍: Parasite Epidemiology and Control is an Open Access journal. There is an increasing amount of research in the parasitology area that analyses the patterns, causes, and effects of health and disease conditions in defined populations. This epidemiology of parasite infectious diseases is predominantly studied in human populations but also spans other major hosts of parasitic infections and as such this journal will have a broad remit. We will focus on the major areas of epidemiological study including disease etiology, disease surveillance, drug resistance and geographical spread and screening, biomonitoring, and comparisons of treatment effects in clinical trials for both human and other animals. We will also look at the epidemiology and control of vector insects. The journal will also cover the use of geographic information systems (Epi-GIS) for epidemiological surveillance which is a rapidly growing area of research in infectious diseases. Molecular epidemiological approaches are also particularly encouraged.
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