YUDHI RATNA NUGRAHENI, BAMBANG ARIYADI, ROCHMADIYANTO ROCHMADIYANTO, NINING KESUMANINGRUM, KUSWARI IMRAN, BAYU PRIYO KARTIKO, NUR ROHMI FARHANI, SUCI NURANI, ANA SAHARA, AAN AWALUDIN
{"title":"印度尼西亚日惹市牛中巴贝斯虫感染的分子检测","authors":"YUDHI RATNA NUGRAHENI, BAMBANG ARIYADI, ROCHMADIYANTO ROCHMADIYANTO, NINING KESUMANINGRUM, KUSWARI IMRAN, BAYU PRIYO KARTIKO, NUR ROHMI FARHANI, SUCI NURANI, ANA SAHARA, AAN AWALUDIN","doi":"10.13057/biodiv/d240759","DOIUrl":null,"url":null,"abstract":"Abstract. Nugraheni YR, Ariyadi B, Rochmadiyanto, Kesumaningrum N, Imran K, Kartiko BP, Farhani NR, Nurani S, Sahara A, Awaludin A. 2023. Molecular detection of Babesia infection in cattle in Yogyakarta, Indonesia. Biodiversitas 24: 4192-4198. Babesiosis is a tick-borne disease caused by hemoprotozoa that poses a significant threat to livestock production worldwide, including in Indonesia. This study aimed to assess the prevalence and molecular characterization of Babesia sp., the causative agent of babesiosis, in cattle from multiple regions in Central Java, Indonesia. The disease has had substantial negative economic impacts, highlighting the need for accurate prevalence data and effective disease control measures. A total of 13 blood samples were collected from cattle exhibiting symptoms of hematuria and babesiosis. The samples were obtained from smallholder farmers who reported these cases to local veterinarians in various regions of Yogyakarta, Indonesia. The farmers were selected based on their proximity to veterinary clinics and willingness to participate in the study. Upon sample collection, each blood sample was subjected to microscopic examination using Giemsa-stained blood smears. The examination aimed to identify the presence of Babesia parasites within the red blood cells. Positive samples, indicating the presence of Babesia infection, were further analyzed by molecular assay. Molecular tests were performed using Polymerase Chain Reaction (PCR) to detect the DNA of Babesia sp. Two specific genes were targeted: cytochrome b oxidase (cytb) and 18S small subunit ribosomal RNA (18S rRNA). PCR amplification was carried out following established protocols, and the resulting products were visualized using gel electrophoresis to confirm the presence of Babesia DNA. Statistical analysis was conducted to compare the sensitivity and efficacy of the two PCR methods (cytb and 18S rRNA). The data obtained from this study contributes to our understanding of the occurrence of babesiosis in Central Java's cattle population. The findings underscore the need for comprehensive babesiosis disease surveys to obtain accurate prevalence estimates and facilitate the development of effective disease control strategies. Moreover, the more sensitive amplification targeting the cytb gene holds promise for improved diagnostic and surveillance efforts. 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Babesiosis is a tick-borne disease caused by hemoprotozoa that poses a significant threat to livestock production worldwide, including in Indonesia. This study aimed to assess the prevalence and molecular characterization of Babesia sp., the causative agent of babesiosis, in cattle from multiple regions in Central Java, Indonesia. The disease has had substantial negative economic impacts, highlighting the need for accurate prevalence data and effective disease control measures. A total of 13 blood samples were collected from cattle exhibiting symptoms of hematuria and babesiosis. The samples were obtained from smallholder farmers who reported these cases to local veterinarians in various regions of Yogyakarta, Indonesia. The farmers were selected based on their proximity to veterinary clinics and willingness to participate in the study. Upon sample collection, each blood sample was subjected to microscopic examination using Giemsa-stained blood smears. The examination aimed to identify the presence of Babesia parasites within the red blood cells. Positive samples, indicating the presence of Babesia infection, were further analyzed by molecular assay. Molecular tests were performed using Polymerase Chain Reaction (PCR) to detect the DNA of Babesia sp. Two specific genes were targeted: cytochrome b oxidase (cytb) and 18S small subunit ribosomal RNA (18S rRNA). PCR amplification was carried out following established protocols, and the resulting products were visualized using gel electrophoresis to confirm the presence of Babesia DNA. Statistical analysis was conducted to compare the sensitivity and efficacy of the two PCR methods (cytb and 18S rRNA). The data obtained from this study contributes to our understanding of the occurrence of babesiosis in Central Java's cattle population. 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引用次数: 0
摘要
摘要Nugraheni YR, Ariyadi B, Rochmadiyanto, kessumaningrum N, Imran K, Kartiko BP, Farhani NR, Nurani S, Sahara A, Awaludin A. 2023。印度尼西亚日惹市牛中巴贝斯虫感染的分子检测。生物多样性,24(4):492 - 498。巴贝斯虫病是一种由血原虫引起的蜱传疾病,对包括印度尼西亚在内的世界各地的畜牧业生产构成重大威胁。本研究旨在评估巴贝虫病病原巴贝虫sp.在印度尼西亚中爪哇多个地区的牛中的流行情况和分子特征。该疾病对经济产生了重大负面影响,因此需要准确的流行数据和有效的疾病控制措施。从表现出血尿和巴贝斯虫病症状的牛身上共采集了13份血液样本。这些样本是从向印度尼西亚日惹不同地区的当地兽医报告这些病例的小农那里获得的。选择农民的依据是他们离兽医诊所的距离和参与研究的意愿。样本收集后,每个血液样本都使用吉姆萨染色的血液涂片进行显微镜检查。检查的目的是确定巴贝斯虫寄生虫在红细胞内的存在。阳性样本表明巴贝虫感染的存在,进一步进行分子分析。采用聚合酶链式反应(PCR)技术对巴贝虫进行分子检测,筛选出细胞色素b氧化酶(cytb)和18S小亚基核糖体RNA (18S rRNA)两个特异性基因。按照既定方案进行PCR扩增,并用凝胶电泳对扩增结果进行可视化,以确认巴贝斯虫DNA的存在。比较两种PCR方法(cytb和18S rRNA)的敏感性和有效性。从这项研究中获得的数据有助于我们了解中爪哇牛群中巴贝斯虫病的发生情况。研究结果强调需要进行全面的巴贝斯虫病调查,以获得准确的患病率估计,并促进制定有效的疾病控制战略。此外,针对cytb基因的更敏感的扩增有望改善诊断和监测工作。这些见解对于防治巴贝斯虫病和减轻其对畜牧生产的经济影响至关重要。
Molecular detection of Babesia infection in cattle in Yogyakarta, Indonesia
Abstract. Nugraheni YR, Ariyadi B, Rochmadiyanto, Kesumaningrum N, Imran K, Kartiko BP, Farhani NR, Nurani S, Sahara A, Awaludin A. 2023. Molecular detection of Babesia infection in cattle in Yogyakarta, Indonesia. Biodiversitas 24: 4192-4198. Babesiosis is a tick-borne disease caused by hemoprotozoa that poses a significant threat to livestock production worldwide, including in Indonesia. This study aimed to assess the prevalence and molecular characterization of Babesia sp., the causative agent of babesiosis, in cattle from multiple regions in Central Java, Indonesia. The disease has had substantial negative economic impacts, highlighting the need for accurate prevalence data and effective disease control measures. A total of 13 blood samples were collected from cattle exhibiting symptoms of hematuria and babesiosis. The samples were obtained from smallholder farmers who reported these cases to local veterinarians in various regions of Yogyakarta, Indonesia. The farmers were selected based on their proximity to veterinary clinics and willingness to participate in the study. Upon sample collection, each blood sample was subjected to microscopic examination using Giemsa-stained blood smears. The examination aimed to identify the presence of Babesia parasites within the red blood cells. Positive samples, indicating the presence of Babesia infection, were further analyzed by molecular assay. Molecular tests were performed using Polymerase Chain Reaction (PCR) to detect the DNA of Babesia sp. Two specific genes were targeted: cytochrome b oxidase (cytb) and 18S small subunit ribosomal RNA (18S rRNA). PCR amplification was carried out following established protocols, and the resulting products were visualized using gel electrophoresis to confirm the presence of Babesia DNA. Statistical analysis was conducted to compare the sensitivity and efficacy of the two PCR methods (cytb and 18S rRNA). The data obtained from this study contributes to our understanding of the occurrence of babesiosis in Central Java's cattle population. The findings underscore the need for comprehensive babesiosis disease surveys to obtain accurate prevalence estimates and facilitate the development of effective disease control strategies. Moreover, the more sensitive amplification targeting the cytb gene holds promise for improved diagnostic and surveillance efforts. These insights are crucial for combating babesiosis and mitigating its economic impact on livestock production.