Hassan Y.A.H. Mahmoud , Abdelrahman A. Rady , Tetsuya Tanaka
{"title":"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","authors":"Hassan Y.A.H. Mahmoud , Abdelrahman A. Rady , Tetsuya Tanaka","doi":"10.1016/j.parepi.2024.e00340","DOIUrl":null,"url":null,"abstract":"<div><p>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 <em>β-actin</em> gene at the expected 227 bp for cattle and buffalo. The samples were analyzed by PCR for the presence of piroplasms, specifically <em>Babesia bovis</em>, <em>Babesia bigemina</em>, and <em>Theileria annulata</em>. Samples positive for the <em>piroplasma 18S ribosomal RNA</em> gene were further examined for two additional genes, <em>spherical body protein 4</em> gene, to provide an enhanced degree of specificity for the identification of <em>B. bovis</em> and <em>B. bigemina</em>, and the <em>major merozoite surface antigen</em> gene for <em>T. annulata.</em> The infection rate for piroplasma spp. was 60/300 (20%). The positivity rates were 10.7% (32/300) for <em>T. annulata</em>, 5.3% (16/300) for <em>B. bovis</em>, and 4% (12/300) for <em>B. bigemina</em>. By host species, 42/150 (28%) cattle and 18/150 (12%) buffalo were positive for piroplasms. None of the isolates sequenced for the <em>B. bovis</em> isolates from buffalo in this study showed 100% identity with any sequence deposited in GenBank for the <em>small subunit ribosomal RNA</em> gene (maximum identity value = 99.74%). Similarly, no <em>T. annulata small subunit ribosomal RNA</em> 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 <em>T. annulata merozoite-piroplasm surface antigen</em> gene, as well as the <em>B. bovis</em> and <em>B. bigemina spherical body protein 4</em> genes, in cattle and buffalo in southern Egypt, and is the first report on these piroplasma genes in cattle and buffalo in southern Egypt.</p></div>","PeriodicalId":37873,"journal":{"name":"Parasite Epidemiology and Control","volume":null,"pages":null},"PeriodicalIF":2.0000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2405673124000047/pdfft?md5=b128e5a77b3f939f93fca61e3732415e&pid=1-s2.0-S2405673124000047-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Molecular detection and characterization of Theileria annulata, Babesia bovis, and Babesia bigemina infecting cattle and buffalo in southern Egypt\",\"authors\":\"Hassan Y.A.H. Mahmoud , Abdelrahman A. Rady , Tetsuya Tanaka\",\"doi\":\"10.1016/j.parepi.2024.e00340\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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 <em>β-actin</em> gene at the expected 227 bp for cattle and buffalo. The samples were analyzed by PCR for the presence of piroplasms, specifically <em>Babesia bovis</em>, <em>Babesia bigemina</em>, and <em>Theileria annulata</em>. Samples positive for the <em>piroplasma 18S ribosomal RNA</em> gene were further examined for two additional genes, <em>spherical body protein 4</em> gene, to provide an enhanced degree of specificity for the identification of <em>B. bovis</em> and <em>B. bigemina</em>, and the <em>major merozoite surface antigen</em> gene for <em>T. annulata.</em> The infection rate for piroplasma spp. was 60/300 (20%). The positivity rates were 10.7% (32/300) for <em>T. annulata</em>, 5.3% (16/300) for <em>B. bovis</em>, and 4% (12/300) for <em>B. bigemina</em>. By host species, 42/150 (28%) cattle and 18/150 (12%) buffalo were positive for piroplasms. None of the isolates sequenced for the <em>B. bovis</em> isolates from buffalo in this study showed 100% identity with any sequence deposited in GenBank for the <em>small subunit ribosomal RNA</em> gene (maximum identity value = 99.74%). Similarly, no <em>T. annulata small subunit ribosomal RNA</em> 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 <em>T. annulata merozoite-piroplasm surface antigen</em> gene, as well as the <em>B. bovis</em> and <em>B. bigemina spherical body protein 4</em> genes, in cattle and buffalo in southern Egypt, and is the first report on these piroplasma genes in cattle and buffalo in southern Egypt.</p></div>\",\"PeriodicalId\":37873,\"journal\":{\"name\":\"Parasite Epidemiology and Control\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2024-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2405673124000047/pdfft?md5=b128e5a77b3f939f93fca61e3732415e&pid=1-s2.0-S2405673124000047-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Parasite Epidemiology and Control\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2405673124000047\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Parasite Epidemiology and Control","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405673124000047","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Molecular detection and characterization of Theileria annulata, Babesia bovis, and Babesia bigemina infecting cattle and buffalo in southern Egypt
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.
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.