Detection for dengue virus infection using suckling mice as a biological amplification system and enzymeimmunoassay
1
Issued Date
2024
Copyright Date
1992
Resource Type
Language
eng
File Type
application/pdf
No. of Pages/File Size
xiv, 123 leaves : ill.
Access Rights
open access
Rights
ผลงานนี้เป็นลิขสิทธิ์ของมหาวิทยาลัยมหิดล ขอสงวนไว้สำหรับเพื่อการศึกษาเท่านั้น ต้องอ้างอิงแหล่งที่มา ห้ามดัดแปลงเนื้อหา และห้ามนำไปใช้เพื่อการค้า
Rights Holder(s)
Mahidol University
Bibliographic Citation
Thesis (M.Sc. (Pathobiology))--Mahidol University, 1992
Suggested Citation
Marisa Kemapunmanus Detection for dengue virus infection using suckling mice as a biological amplification system and enzymeimmunoassay. Thesis (M.Sc. (Pathobiology))--Mahidol University, 1992. Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/99102
Title
Detection for dengue virus infection using suckling mice as a biological amplification system and enzymeimmunoassay
Alternative Title(s)
การตรวจหาการติดเชื้อไวรัสไข้เลือดออกโดยการใช้หนูแรกเกิดเป็นระบบการเพิ่มจำนวนไวรัสและวินิจฉัยด้วยวิธีเอ็นซัยม์อิมมิวโน
Author(s)
Advisor(s)
Abstract
Detection for dengue viral proteins in patients sera with dengue virus infection was investigated by using suckling mouse as a biological amplification system evaluated in conjunction with the Viral antigens strip/ enzymeim munoassay (VAS/EIA). Dengue viral proteins can not be detected directly from patientssera by VAS/EIA method due to the high concentration of other serum proteins in human plasma. Therefore, an additional step must be inserted in order to facilitate the use of VAS/EIA. C lassi ical amplification system using dengue type 2 virus inoculated intracerebrally to suckling mouse brain was used as the first step to amplify the number of vision circulated in patients sera. Dengue type 2, New Guinea C strain, was employed for titration. Two groups of patients sera with clinical diagnosis of dengue infection collected from Ramathibodi hospital were tested for this study. Three dilutions, 1:1, 1:3 and 1:10 of patients sera were compared to select the proper serum dilution for an inoculation. The signs and symptoms of infected mice were closely observed. After inoculation, they were sacrified on day 5, 6, and 7. Infected mouse organs including the brain, spleen, liver, and also plasma were examined for the presence of dengue viral proteins by VAS/EIA. The best dilution for serum specimen to be use for an inoculation was found to be at 1:1 ratio, and the positive brain collected on day 7th clearly showed dengue viral proteins, even though the mice had no sign of infection which was used previously to indicate the establishment of dengue virus in mouse brain. Rabbit antidengue sera, dengue human hyperimmune sera, specific polyclonal anti-D2 (NS3), and MAb-D2 (E) were used as the specific primary antibody to identify dengue viral proteins. Hu man sera was found to be the most useful antibody for this purpose. Dengue viral proteins from each positive case revealed different patterns which were useful for further typing of dengue virus strains in another study which was done at this laboratory. Besides the brain, dengue viral proteins were also detected in the liver, but not in the spleen and plasma. However, the intensities of protein bands appeared after immunoenzymatic assay from infected liver specimens showed lower reaction than from infected brain of the same animal.
Description
Pathobiology (Mahidol University 1992)
Degree Name
Master of Science
Degree Level
Master's degree
Degree Department
Faculty of Science
Degree Discipline
Pathobiology
Degree Grantor(s)
Mahidol University