Abstract

Brettanomyces bruxellensis is described as a wine spoilage yeast with many mainly strain-dependent genetic characteristics, bestowing tolerance against environmental stresses and persistence during the winemaking process. Thus, it is essential to discriminate B. bruxellensis isolates at the strain level in order to predict their stress resistance capacities. Few predictive tools are available to reveal intraspecific diversity within B. bruxellensis species; also, they require expertise and can be expensive. In this study, a Random Amplified Polymorphic DNA (RAPD) adapted PCR method was used with three different primers to discriminate 74 different B. bruxellensis isolates. High correlation between the results of this method using the primer OPA-09 and those of a previous microsatellite analysis was obtained, allowing us to cluster the isolates among four genetic groups more quickly and cheaply than microsatellite analysis. To make analysis even faster, we further investigated the correlation suggested in a previous study between genetic groups and cell polymorphism using the analysis of optical microscopy images via deep learning. A Convolutional Neural Network (CNN) was trained to predict the genetic group of B. bruxellensis isolates with 96.6% accuracy. These methods make intraspecific discrimination among B. bruxellensis species faster, simpler and less costly. These results open up very promising new perspectives in oenology for the study of microbial ecosystems.

Highlights

  • Random Amplified Polymorphic DNA (RAPD)-Polymerase Chain Reaction (PCR) was adapted here to assess its discriminating power and provide an accessible protocol to determine the genetic group of B. bruxellensis isolates

  • Assay was performed on 74 B. bruxellensis isolates with 3 different primers among those most used in the literature: OPA-02, OPA-03 and OPA-09 [19,21,31,33]

  • The reproducibility of the RAPD-PCR method adapted in this study was checked

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Summary

Introduction

The spoilage yeast Brettanomyces bruxellensis presents many strain dependent characteristics, such as volatile phenol production that contributes to the famous “Brett character” [1,2,3], or capacities to withstand many stresses associated with wine related environments (nutritional requirements, resistance to low pH values, capacity to enter in Viable But Not. Cultivable state and SO2 resistance) [4,5,6,7,8]. It is important to develop tools to further discriminate from the species level toward the strain level, and potentially, to predict spoilage-related phenotypes

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