Avoid mixing biologicals with antimicrobials

Dr. Jay W. Pscheidt and Lisa Jones, Dept. of Botany and Plant Pathology, Oregon State University

Actinovate AG (Streptomyces lydicus WYEC 108) and many other biological products are used in the management of organic grapes. Tank mixing more than one product is both economical and time-saving but tank mix compatibilities with biological control products such as Actinovate have not been thoroughly evaluated. In 2016, we examined the tank mix compatibility of Actinovate AG with commonly used organic products.

Actinovate AG was prepared at a concentration of 0.1g/ml. A 300 ml solution of Actinovate was prepared in a 500 ml beaker then mixed with each material and allowed to stand for 30 minutes. The mixture was then plated onto agar and incubated for 7 days at room temperature. The number of colony-forming units (CFU) of S. lydicus exposed in each mix was assessed daily and compared to an Actinovate plus water only control. The percentage of S. lydicus CFU in each tank mix compared to the CFU in the Actinovate control was calculated.

An average of 3.2×105 S. lydicus CFU developed after 7 days incubation on the various media when Actinovate was just mixed with water. Several products inhibited the growth of S. lydicus when prepared in as a mixture in the laboratory. No growth of S. lydicus was observed on plates when Actinovate was mixed with Horticultural Vinegar, a high rate of Regalia, Rex Lime Sulfur, Serenade Optimum, or Solubor DF. Less than 10% of the S. lydicus CFU grew when Actinovate was mixed with Biomin Calcium, Botector, Neptune’s Harvest 2-4-1 fish fertilizer, or Thuricide. Significantly fewer S. lydicus CFU grew when Double Nickel, the low rate of Regalia, Serenade Max, the high rate of Stimplex or Toggle were mix with Actinovate. There was no significant difference in the number of S. lydicus CFU that grew when Zen-O-Spore was mixed with Actinovate. The number of S. lydicus CFU was greater than double (219%) or quadruple (482%) that of the Actinovate control when mixed with Nitrozyme or the low rate of Stimplex, respectively.

Many of the biological products in this study grew quicker than S. lydicus under laboratory conditions. These fungi or bacteria generally outcompeted S. lydicus for space and resources on the agar plates. The fungus found in Zen-O-Spore was slower to grow and did not outcompete S. lydicus during the 7-day incubation.

This data does not imply a lack of or enhanced disease control in the field. For example, blueberry field trials over a 2-year period where Actinovate was mixed with Simplex did not result in disease control that was different than when either product was used alone. The data does indicate incompatibility between various products used in organic production.

For a complete data set please visit: http://sites.science.oregonstate.edu/bpp/Plant_Clinic/Fungicidebooklet/2016/Blueberry3.pdf

What’s New with Malolactic Fermentation

Dr. James Osborne, Associate Professor and Enology Extension Specialist, OSU

The malolactic fermentation (MLF) is a vital step in the production of cool climate red wines as well as some white wines. But despite its importance, MLF often gets taken for granted and just considered a step to reduce wine acidity. However, MLF is much more than just a biological de-acidification process and can have a number of other impacts on wine quality. Our lab has been conducting a number of projects over recent years investigating various aspects of MLF. One project is investigating interactions between Oenococcus oeni and the spoilage yeast Brettanomyces bruxellensis. An interesting result from this study was discovering that some O. oeni strains were capable of increasing the concentration of the volatile phenol precursors p-coumaric acid and ferulic acid. These pre-cursor compounds are found in grapes and wine mainly bound to a tartaric acid and in this form are not utilized by Brettanomyces. However, some O. oeni strains can remove the tartaric acid through the action of an enzyme, cinnamic esterase, and release free p-coumaric and ferulic acid that Brettanomyces can then metabolize to 4-ethylphenol and 4-ethyl guaiacol. This finding has led to the labelling of many commercial O. oeni strains as either cinnamic esterase (+) or (-) with the recommendation being to avoid use of cinnamic esterase (+) strains in situations where the wine may be at risk for Brettanomyces spoilage.

An additional area of research has been determining the effect of MLF on red wine color. We know that MLF changes wine pH which can cause a shift in red color, but were there other impacts on color due to MLF? Our lab demonstrated that independent of pH change, MLF results in a loss of color and lower formation of polymeric pigments. Results from a number of studies showed that this color loss was likely due to the metabolism of acetaldehyde by O. oeni. Acetaldehyde plays a key role in the development of polymeric pigments and so metabolism of acetaldehyde during MLF reduced formation of these color compounds. Delaying MLF was shown to help mitigate this color loss but delaying MLF for long periods is risky from a microbial spoilage point of view, as SO2 cannot be added to the wine until MLF is complete. Additional strategies to mitigate color loss due to MLF are currently being explored. One such strategy is the use of ML bacteria that do not metabolize acetaldehyde. To date, all O. oeni strains screened can metabolize acetaldehyde but other lactic acid bacterial species such as Lactobacillus look more promising. There has been renewed interest in using certain Lactobacillus species and strains to conduct MLF. In particular, homofermentative species of Lactobacillus have been studied as potential ML starter cultures. These bacteria do not produce acetic acid from glucose metabolism and so could be used for conducting concurrent alcoholic and malolactic fermentations without the risk of increased acetic acid. Currently, there are commercially produced L. platarum cultures available outside of the USA for use in winemaking. However, at this time these cultures are not available for winemaking use in the USA. The use of concurrent alcoholic and malolactic fermentation is one final area our lab has been studying. While there are obvious time advantages to conducting alcoholic and malolactic fermentation at the same time, there are still some concerns over the impact on wine quality, particularly for red wines. We recently completed a study investigating how the timing of MLF impacts Chardonnay aroma and mouthfeel and will be continuing work in this area focused on concurrent fermentations of red wines. As we continue to study malolactic bacteria, we are gaining a better appreciation for the impact they can have on wine quality and potential new strategies for their use. For additional information on any of the studies we have conducted on MLF please contact me at: james.osborne@oregonstate.edu

Pest Alert: Grape Cane Borer

Dr. Patty Skinkis, Professor and Viticulture Extension Specialist, OSU
Dr. Vaughn Walton, Professor and Horticultural Entomologist, OSU

There have been an increasing number of reports of grape cane borer presence and damage in vineyards throughout the Willamette Valley this winter. Typically these reports during the bud break period in April when adults are active and evidence of shoot dieback occurs. However, we have received numerous reports this January and early February as growers begin pruning. This observation may be due to various factors including more suitable weather conditions (winter and summer), higher levels of populations surviving, more suitable host plant materials, increased awareness and improved monitoring. The borers can have a long life cycle within the vine, living as larvae (grubs) within the shoot or cane for nearly one year. Adults lay eggs during early spring and hatch and develop into larvae that feed on the shoot tissues during the growing season. They remain in the wood as pupae during winter and may be found when pruning commences. Both pupae and adults have been reported in southern and mid-Willamette Valley vineyards this winter. This article covers the most salient points for your awareness this winter; please consult additional resources below for further details.

What to look for in the vineyard:
Galleries burrowed by larvae can be observed in cane tissue usually in older or dead wood, canes, spurs, or cordons. These holes are round, drill-like holes of ~0.4 mm diameter, and they are often accompanied with sawdust that was produced by the adult when burrowing into the shoot during late summer or early fall the year prior. Cutting into the wood near these holes during pruning will likely reveal a pupa that is 1-8 mm in length (<0.3 in).

Insecticide application is often difficult to apply during the dormancy period due to the difficulty for the application to reach the pest and the inability to get into the vineyard with equipment. There are biological controls, such as the Steinernema carpocapsae, an entomopathogenic nematode, that may be used, but care needs to be taken to ensure that the product is handled properly and applied to the entry points of the pest to be effective. In some cases, the best method will be to cut out any canes that have the burrow holes evident. Remove pruning wood, as the wood contains the pupae that will emerge in spring. Removing the pest from the vineyard will ensure that a population does not exist to allow new infestations into tissues.

For more information about the cane borer, please see the following resources: