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Table 1 - MDPI

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Name. Sequence (5'→ 3'). Position 1. Polarity 2 for cDNA cloning. MY-1F. ATTGTCTACCCGCGACGTAA. 45-64. +. MY-1R. ACGGTGGTGTGCCTCATAC. 1914- ...

Figure S1.

Figure S2.

Table S1. Oligonucleotide primers/adaptor used in this study. Name MY-1F MY-1R MY-2F MY-2R MY-3F MY-3R MY-4F MY-4R MY-F MY-R 110 (3’-adaptor) RC110A (primer) M-RT-F M-RT-R

Sequence (5’→ 3’) Position 1 for cDNA cloning ATTGTCTACCCGCGACGTAA 45-64 ACGGTGGTGTGCCTCATAC 1914-1932 ACGGAGACCAAGCAACGACTC 1820-1840 GGAGGATCGCAAACCACGG 3936-3954 TAATGCCTCAATAGGCTTCG 3880-3899 TCAGGGCGTCATTGCGTAGT 5758-5774 CTATGTTCGCTTACGACGCA 5475-5494 ATTCGGGACCTTGATCGGTG 7370-7389 TGAGCATGGAGAGACAGAT 7340-7358 AACGCGTTTACTCGAGGAGG 278-297 TATCTTATCGGCGTGTCCCCC to 3’-end of dsRNA GGGGGACACGCCGATAAGATA complementary to the adaptor 110A for RT-PCR detection TAATGCCTCAATAGGCTTCG 3880-3899 AGATGCTGCAACCGCACCATGCC 5136-5158

Polarity 2 + – + – + – + – + – +/– –/+

Positions for the PCR primers or the adaptor in the cDNA of Botrytis cinerea mymonavirus 1 (BcMyV1) were labeled in Figure S1. 2 Polarity refers to the positive strand (+) and the negative strand (–) of BcMyV1. 1

+ –