Dry- down probe free qPCR for detection of KFD in resource limited settings

• Published in: PloS one Vol. 18; no. 5; p. e0284559
• Main Authors: Yadav, Pooja, Sharma, Shashi, Dash, Paban Kumar, Dhankher, Suman, V K, Sandhya, Kiran, S K
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 10.05.2023
• Subjects: Arachnids; Assaying; Biology and Life Sciences; Cold storage; Defense research; Dengue fever; Diagnosis; Disease spread; Encephalitis Viruses, Tick-Borne - genetics; Env gene; Enzymes; Evaluation; Forest resources; Format; Health care; Humans; India - epidemiology; Infections; Kyasanur Forest Disease; Laboratories; Manufacturers; Medicine and Health Sciences; People and Places; Pest outbreaks; Polymerase chain reaction; R&D; Reagents; Real time; Real-Time Polymerase Chain Reaction; Research & development; Research and Analysis Methods; Resource-Limited Settings; Risk factors; Sensitivity; Sensitivity and Specificity; Stability; Temperature fluctuations; Tick-borne diseases; Ticks; Vaccines; Vectors; Viruses; West Nile virus; India; United States > US; Germany
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0284559

Kyasanur Forest Disease is a tick-borne flavivirus is endemic in the Southern India. The recent expansion and resurgence of sporadic outbreaks in southern parts of country is the most important concern. Although only formalin inactivated vaccine is available for treatment with limited efficacy the early detection and timely identification is a only way to prevent spread of cases. If the disease can be identified prior to infection in humans like in forest areas from ticks and vectors the disease spread supposed to be managed quickly. Here we have standardized a single tube ready to use dry-down probe free real time RT-PCR targeted against virus envelope gene for detection of KFDV infection. The assay was standardized in liquid format first, later it was converted into dry-down format with addition of stabilizers with a similar sensitivity and specificity (10RNA Copies/rxn). The sensitivity was comparable to the most widely used and accepted diagnostic platform i.e. TaqMan qRT-PCR. However as the reported assay here omit the need of probes makes it cost effective and dry-down reagents makes more stability to the developed assay in this study if compare to TaqMan qPCR. The assay was evaluated with KFD positive samples and healthy sample panel which revealed high concordance with TaqMan qRT-PCR. Stability was unaffected by temperature fluctuations during transportation even in cold chain free conditions, thus reduce the maintenance of strict cold storage. These findings demonstrated that the reported assay is convenient with 100% sensitivity and specificity to TaqMan qPCR. Thus this assay has the potential usefulness for diagnosis KFDV for routine surveillance in resource limited laboratory settings omitting the use costly and heat sensitive TaqMan qRT-PCR reagents without compromising the sensitivity and specificity of the diagnosis assay.