4.3 Article

Leek Yellow Stripe Virus Can Adjust for Host Adaptation by Trimming the N-Terminal Domain to Allow the P1 Protein to Function as an RNA Silencing Suppressor

Journal

PLANT PATHOLOGY JOURNAL
Volume 38, Issue 4, Pages 383-394

Publisher

KOREAN SOC PLANT PATHOLOGY
DOI: 10.5423/PPJ.FT.06.2022.0077

Keywords

alliums; leek yellow stripe virus; P1 protein; garlic; RNA silencing suppressor

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The length of the P1 protein of leek yellow stripe virus (LYSV) isolates in Japan varies, with the S-type P1 being shorter than the N-type P1. Both N-type and S-type P1 sequences can be found in mixed infections in garlic fields in Hokkaido. LYSV-S is detected more frequently in Allium spp. plants other than garlic in Honshu, suggesting a wider host range compared to LYSV-N. The P1 protein of LYSV has RNA silencing suppressor (RSS) activity, with the S-type P1 showing stronger RSS activity than the N-type P1.
In Japan, the P1 protein (S-type) encoded by leek yel-low stripe virus (LYSV) isolates detected in Honshu and southward is shorter than the P1 (N-type) of LYSV isolates from garlic grown in Hokkaido due to a large deletion in the N-terminal half. In garlic fields in Hok-kaido, two types of LYSV isolate with N-and S-type P1s are sometimes found in mixed infections. In this study, we confirmed that N-and S-type P1 sequences were present in the same plant and that they belong to different evolutionary phylogenetic groups. To investi-gate how LYSV with S-type P1 (LYSV-S) could have invaded LYSV with N-type P1 (LYSV-N)-infected gar-lic, we examined wild Allium spp. plants in Hokkaido and found that LYSV was almost undetectable. On the other hand, in Honshu, LYSV-S was detected at a high frequency in Allium spp. other than garlic, suggesting that the LYSV-S can infect a wider host range of Al-liumspp. compared to LYSV-N. Because P1 proteins of potyviruses have been reported to promote RNA silenc-ing suppressor (RSS) activity of HC-Pro proteins, we analyzed whether the same was true for P1 of LYSV. In onion, contrary to expectation, the P1 protein itself had RSS activity. Moreover, the RSS activity of S-type P1 was considerably stronger than that of N-type P1, sug-gesting that LYSV P1 may be able to enhance its RSS activity when the deletion is in the N-terminal half and that acquiring S-type P1 may have enabled LYSV to expand its host range.

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