Not known to transmit any human or animal pathogens.
Not known to vector any pathogens or other associated organisms.
Plum pox virus has been transmitted by at least 20 aphid species, although only a few are considered important vectors. The vectors that are considered important vectors in United States include: the black bean aphid (Aphis fabae), the spirea aphid (Aphis spiraecola), the black peach aphid (Brachycaudus persicae), and the green peach aphid (Myzus persicae).
| Method | Detail | NAPIS Survey Method |
|---|---|---|
| Tissue Sample | Follow National PPV Survey Plan. Also see Sampling PPV document below. | 3011 - General Tissue Sample |
Negative data should be entered into NAPIS at the species level (Potyvirus plumpoxi). New state positive records should be further identified, however, to the strain level. Unusual positive records (highly virulent pathogen, expanded host range, etc.) can be entered at the strain level if strain-level information is available. Please contact stcaps@usda.gov if you need assistance, have questions, or want to enter an unusual record into NAPIS.
No specific signs are present.
The best time to collect samples is in the spring, from the time new leaves are fully expanded until temperatures become too hot for reliable leaf samples to be collected. Virus antigen levels are significantly lower at 85°F and above. In warmer states, there may be a relatively narrow window in which samples can be collected.
Surveyors should perform visual surveys. Inspect host plants for symptoms and sample symptomatic tissue. Survey for leaves showing symptoms such as mild light green discoloration, chlorotic spots, bands or rings, vein clearing or yellowing, and leaf distortions.
Survey for PPV in apricots, cherry, nectarine, peach or plum trees.
Detection survey for PPV in orchards is based on the use of a hierarchical sampling method. This involves collecting 8 leaf samples from each of 25 percent of the trees in an orchard. Trees to be sampled are selected in groups of 4, with 32 leaves that are collected from the four trees being ELISA tested as four 8 leaf samples. To determine the total number of samples to be collected in an orchard being surveyed, the following formula can be used:
(Number of trees per acre) x (number of acres in the orchard) / 4
Thus, in a 9 acre orchard with a planting rate of 140 trees per acre, 315 eight leaf samples would be submitted for ELISA testing. Sampling at lower rates significantly reduces the likelihood of detecting PPV, and sampling at higher rates is only warranted if there are unusual risk factors present.
Fully expanded symptomatic leaves from the middle of the branch are preferred. However, if symptoms are not present, collect asymptomatic leaves from the same locations. Do not sample dead leaves.
Label the sealed bag with the name of the host (including cultivar) and identification code used in your records in case a positive result triggers additional sampling to confirm a positive PPV tree. Place the sealed plastic bag into a second bag and seal the second bag. DO NOT freeze the plant material. Instead, keep it cool by placing the samples into a cooler with a lid and freezer bags/cold packs.
PPV cannot be visually distinguished from other plant pathogens or abiotic symptoms. Molecular identification is necessary to confirm the presence of PPV. PPV may be confused with Taphrina deformans (peach leaf curl), Apple chlorotic leaf spot and Peach mosaic virus in peach, or Prunus necrotic ringspot in cherry. These diseases are present in the United States.
If you are unable to find a reference, contact STCAPS@usda.gov. See the CAPS Pest Datasheet for all references.