Camer Gerry Amor, Oikawa Yuki, Omaki Hitomi, Endoh Daiji
University of Eastern Philippines, Department of Clinical Sciences - College of Veterinary Medicine, Catarman, Northern Samar 6400 Philippines.
Rakuno Gakuen University, Department of Radiation Biology-School of Veterinary Medicine, Ebetsu, 069-8501 Hokkaido, Japan.
Future Sci OA. 2018 Nov 13;5(1):FSO353. doi: 10.4155/fsoa-2018-0081. eCollection 2019 Jan.
To produce synthetic nucleotides of notifiable dengue virus (1-4 types), Japanese encephalitis, yellow fever and Zika flaviviruses. These notifiable flaviviruses, particularly dengue and Zika, are problematic mosquito-borne infections in the Philippines, as well as in those countries with tropical and subtropical climates.
An algorithmic design formulation of overlap extension - polymerase chain reaction (OE-PCR) was performed to propagate 50-60 oligomer lengths of select notifiable flaviviral RNAs to DNA nucleotides via the two-step process of OE-PCR.
Algorithmic OE-PCR design formulation efficiently produced 253-256 bp of notifiable flaviviruses. Comparing the newly designed algorithmic OE-PCR with existing executable programs demonstrated it to be efficient and useful in generating accurate sequences of synthetic flaviviral nucleotides.
The efficiently and accurately produced novel synthetic nucleotides of notifiable dengue virus 1-4, Japanese encephalitis, yellow fever and Zika flaviviruses using OE-PCR is useful in understanding the dynamics of flaviviral species and holds potential for the development of synthetic nucleotide-based immunogens.
制备法定报告的登革病毒(1 - 4型)、日本脑炎病毒、黄热病毒和寨卡病毒的合成核苷酸。这些法定报告的黄病毒,特别是登革病毒和寨卡病毒,在菲律宾以及那些热带和亚热带气候的国家中,是由蚊子传播的、难以解决的感染源。
进行重叠延伸聚合酶链反应(OE-PCR)的算法设计配方,通过OE-PCR的两步过程将选定的法定报告黄病毒RNA的50 - 60个寡聚物长度扩增为DNA核苷酸。
算法OE-PCR设计配方有效地产生了253 - 256 bp的法定报告黄病毒。将新设计的算法OE-PCR与现有的可执行程序进行比较,证明其在生成合成黄病毒核苷酸的准确序列方面是高效且有用的。
使用OE-PCR高效且准确地制备出法定报告的登革病毒1 - 4型、日本脑炎病毒、黄热病毒和寨卡病毒的新型合成核苷酸,有助于理解黄病毒物种的动态变化,并具有开发基于合成核苷酸的免疫原的潜力。