| Literature DB >> 35807671 |
Mónica Rivadeneira1, Marta Zulema Galván1,2, Marina Abán1,2, Rosa Elena Semke3, Josefina Rivadeneira1,2, Melisa Lanza Volpe4, Sebastián Gomez Talquenca4.
Abstract
This study aimed to survey the occurrence of eight grapevine viruses in commercial vineyards located in the Calchaquíes Valleys in the northwest region of Argentina. A total of 103 samples of mature canes of vines showing either none or some viral-like symptoms were randomly collected. The samples were tested by RT-PCR/PCR-based assays for the screening of the following viruses: Grapevine fanleaf virus (GFLV), Grapevine leafroll-associated viruses (GLRaV-1, -2, -3, -4), Grapevine virus A (GVA), Grapevine rupestris stem pitting-associated viruses (GRSPaV), and Grapevine red blotch virus (GRBV). Sixty percent of the analyzed samples showed infection with some of the analyzed viruses, except GRBV. GLRaV-3 and GFLV were the most frequent viruses, present in 34% and 21% of the positive samples, respectively. This study represents the first survey report of the presence of grapevine viruses in the region of the Calchaquíes Valleys and contributes to the knowledge to maintain the sanitary status of commercial vineyards in Argentina.Entities:
Keywords: Calchaquíes Valleys; Vitis vinifera; grapevine viruses
Year: 2022 PMID: 35807671 PMCID: PMC9268931 DOI: 10.3390/plants11131720
Source DB: PubMed Journal: Plants (Basel) ISSN: 2223-7747
Figure 1Map showing the sampling localities for the grapevine virus survey in northwestern Argentina. (A) Map highlighting the location of northwestern Argentina. (B) Map of northwestern Argentina showing sampled provinces. (C) Sampled locations (▲) and geographic distribution of viruses detected among localities (bar charts). The viruses shared between sites are represented by the same color. Percentage of positive samples is indicated on the y axis. Dotted lines represent 20% increments.
Figure 2Virus and virus mixed infections detected in the grapevines from northwestern Argentina studied.
Number of positive samples detected for each grapevine virus analyzed by locality.
| Location | N a |
| GLRaV-1 c | GLRaV-2 | GLRaV-3 | GLRaV-4 | GRBV | GFLV | GRSPaV | GVA |
|---|---|---|---|---|---|---|---|---|---|---|
| Cachi | 27 | - | 3 | 4 | 6 | 1 | 0 | 5 | 0 | 6 |
| Molinos | 27 | - | 1 | 2 | 1 | 1 | 0 | 4 | 1 | 1 |
| San Carlos | 5 | - | 0 | 0 | 3 | 1 | 0 | 1 | 0 | 2 |
| Cafayate | 22 | + | 6 | 1 | 22 | 0 | 0 | 6 | 2 | 4 |
| Tafí del Valle | 22 | - | 1 | 1 | 3 | 0 | 0 | 6 | 0 | 0 |
| Total | 103 | 11 | 8 | 35 | 3 | 0 | 22 | 3 | 13 |
a Number of samples; b Presence (+) or absence (-) of Planococus ficus; c GLRaV: Grapevine leafroll-associated virus, GRBV: Grapevine red blotch virus, GFLV: Grapevine fanleaf virus, GRSPaV: Grapevine rupestris stem pitting-associated virus, and GVA: Grapevine virus A.
Primer sequences used in the RNA analysis for screening of eight grapevine viruses.
| Target | Primer sequences (5′-3′) | Location | Product Size (bp) | Gene | Reference |
|---|---|---|---|---|---|
| 18S rRNA | F: CGCATCATTCAAATTTCTGC | 215-234 | 844 | Internal control | [ |
| GLRaV-1 | F: TCTTTACCAACCCCGAGATGAA | 7245-7266 | 232 | Coat protein | [ |
| GLRaV-2 | F: GGTGATAACCGACGCCTCTA | 6745-6764 | 543 | Coat protein | [ |
| GLRaV-3 | F: TACGTTAAGGACGGGACACAGG | 13383-13404 | 336 | Coat protein | [ |
| GLRaV-4 | F: TGAGGTCCCATGTCATGAC | 7499-7517 | 457 | RNA-dependent RNA polimerase | [ |
| GVA | F: GAGGTAGATATAGTAGGACCTA | 6591-6612 | 272 | Coat protein | [ |
| GFLV | F: ATGCTGGATATCGTGACCCTGT | 5506-5527 | 118 | RNA-dependent RNA polimerase | [ |
| RSPaV | F: TGAAGGCTTTAGGGGTTAG | 7708-7726 | 905 | Coat protein | [ |
| GRBaV | F: CAAGTCGTTGTAGATTGAGGACGTATTGG | 2567-2595 | 318 | Replication-associated protein gene fragment (Rep) | [ |
GLRaV: Grapevine leafroll associated virus; GFLV: Grapevine fanleaf virus; GVA: Grapevine virus A; GRBaV: Grapevine red blotch-associated virus; RSPaV: Grapevine rupestris stem pitting-associated viruses. F: Forward primer; and R: Reverse primer.