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      Rapid and sensitive detection of potato virus X by one-step reverse transcription-recombinase polymerase amplification method in potato leaves and dormant tubers.

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          Abstract

          Potato virus X (PVX), is a serious threat to global potato production. A simple and rapid detection method is imperative for PVX diagnosis and early management. In this study, an isothermal one-step reverse transcription-recombinase polymerase amplification (RT-RPA) method was optimized for the quick and convenient detection of PVX in potato leaves and tubers. Our results revealed that this one-step RT-RPA method was highly efficient than the conventional reverse transcription-polymerase chain reaction (RT-PCR). The amplification reaction was free from cross-reactivity with other common potato viruses and completed within 30 min. Moreover, this RT-RPA assay did not require a thermocycler based specific temperature phase amplification and can be easily performed using a simple heating block or water bath at a temperature range of 39-42 °C. The sensitivity assay demonstrated that the developed one-step RT-RPA method was 100 times more sensitive than a routine one-step RT-PCR. Initially, the purified total RNA as the template isolated from infected leaves of potato was used for the detection of PVX. One-step RT-RPA was later performed using cellular disc paper-based simple RNA extract as a template that could detect the virus more efficiently than purified total RNA. The performance of the one-step RT-RPA assay was further evaluated using 500 field samples of leaves and tubers representing different cultivars and geographical regions. To our knowledge, this is the first report of rapid, sensitive, and reliable detection of PVX infection by one-step RT-RPA using cellular disc paper-based simple RNA extract from leaves and dormant tubers of potato. It is superior to the common RT-PCR assay in terms of its versatility, quickness, and independence of highly purified RNA template and can be adopted as a substitute to RT-PCR as an effective technique for seed potato certification, quarantine, breeding, and field surveys.

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          Author and article information

          Journal
          Mol Cell Probes
          Molecular and cellular probes
          Elsevier BV
          1096-1194
          0890-8508
          August 2021
          : 58
          Affiliations
          [1 ] ICAR-Central Potato Research Institute, Shimla, 171 001, H. P, India. Electronic address: chauhanravinder97@gmail.com.
          [2 ] ICAR-Central Potato Research Institute, Shimla, 171 001, H. P, India. Electronic address: priyanka_kaundal@yahoo.co.in.
          [3 ] ICAR-Central Potato Research Institute, Shimla, 171 001, H. P, India. Electronic address: rahultiwari226@gmail.com.
          [4 ] ICAR-Central Potato Research Institute, Shimla, 171 001, H. P, India. Electronic address: sundareshas8@gmail.com.
          [5 ] ICAR-Central Potato Research Institute, Shimla, 171 001, H. P, India. Electronic address: kittu819@gmail.com.
          [6 ] ICAR-Central Potato Research Institute, Shimla, 171 001, H. P, India. Electronic address: kailashnaga3j@gmail.com.
          [7 ] ICAR-Central Potato Research Institute, Shimla, 171 001, H. P, India. Electronic address: sanjeevsharma.cpri@gmail.com.
          [8 ] ICAR-Central Potato Research Institute, Regional Station, Modipuram, 250110, Uttar Pradesh, India. Electronic address: manojkumar0105@gmail.com.
          Article
          S0890-8508(21)00050-5
          10.1016/j.mcp.2021.101743
          34051280
          011b8bd4-07d7-400d-a92d-15ff6fe46c2f
          History

          DAS-ELISA,Potato,RT-PCR,RT-RPA,Sensitivity,Simple RNA extract
          DAS-ELISA, Potato, RT-PCR, RT-RPA, Sensitivity, Simple RNA extract

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