आईएसएसएन: 2476-2024

डायग्नोस्टिक पैथोलॉजी: ओपन एक्सेस

खुला एक्सेस

हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।

ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं

में अनुक्रमित
  • गूगल ज्ञानी
  • RefSeek
  • हमदर्द विश्वविद्यालय
  • ईबीएससीओ एज़
  • पबलोन्स
  • यूरो पब
  • आईसीएमजेई
इस पृष्ठ को साझा करें

अमूर्त

Host Specific Eimeria Genus Diagnosis and QPCR Development in Sheeps and Goats

Shijie Li, Yichen Jian, Kaihui Zhang, Xiaoying Li, Rongjun Wang, Longxian Zhang, Fuchun Jian

Coccidiosis of sheep and goats is caused by protozoa in the genus Eimeria. These protozoa mainly affect young animals, causing a decrease in production and consequent economic losses. Routine diagnosis is made through morphological observation of the oocysts, which has several limitations. The objective of the present study was to develop a real-time PCR (qPCR) technique for the diagnosis of Eimeria spp. in sheep and goats. For this purpose, the 18S rRNA region of the DNA of these parasites was selected because it is a region with low variability among Eimeria spp. The qPCR technique was developed using SYBR Green, resulting in a PCR with high sensitivity, and the ability to amplify samples containing only one oocyst of an Eimeria spp. There was no cross-reaction with other intestinal protozoa, such as Blastocystis, Microsporidia, Cryptosporidium, and Giardia duodenum. The repeatability test showed that the coefficient of variation was less than 2%. This indicated that this method has good sensitivity, specificity, and reproducibility. Thus, the feasibility of using qPCR in the diagnosis of the genus Eimeria was demonstrated in this study. This technique was less laborious and required less skill and diagnostic training compared with the micromorphometry technique conventionally used for this diagnosis