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. 2023 Jan 28;24(3):2511. doi: 10.3390/ijms24032511

Table 2.

Comparison and validation of potato leafroll virus (PLRV) detection methods, viz., one-step reverse-transcription recombinase polymerase amplification (RT-RPA) and reverse transcription-polymerase chain reaction (RT-PCR) of field-collected suspected plant parts of widely cultivated and popular potato cultivars across different agroecological zones in various states of India.

Field Sample No. One-Step RT-PCR [12] One Step RT-RPA with Primer Pair C (LRRPAF3/R3) under Heating Block/Water Bath One Step RT-RPA with Primer Pair C (LRRPAF3/R3) under Heating Block/Water Bath
Leaves Purified RNA Purified RNA Crude RNA (Cellular Disc-Mediated RNA Extract with Added 1.0%
Sodium Sulphite)
1 + + +
2 + + +
3 + +
4
5 + + +
6 + + +
7 + + +
8 + + +
9 + + +
10 + + +
11
12 + + +
13 + + +
14 + + +
15
Healthy Control
Negative Control
Positive Control + + +
Field Sample No. One-step RT-PCR [12] One-step RT-RPA with primer pair C (LRRPAF3/R3) under thermal
Cycler
One step RT-RPA with primer pair C (LRRPAF3/R3) under heating block/water bath
Tubers Purified RNA Purified RNA Purified RNA
1 + + +
2 + + +
3 + + +
4 + +
5
6 + + +
7 + + +
8 + + +
9 + + +
10 + + +
Healthy Control
Positive Control + + +

(+): PLRV positive; (−): PLRV negative.