Abstract

Plant in vitro vegetative propagation using classical semi-solid culture medium is limited due to the low degree of automation, suboptimal nutrient availability and induced physiological stress which often reduce its efficiency. Temporary Immersion System (TIS) emerged as an innovative approach to optimize and eliminate the drawbacks associated with the conventional system of micropropagation. In this study, both Dioscorea and Musa spp. were subjected to conventional semi-solid culture media, complete immersion in shaking liquid culture media and TIS using RITA bioreactor. In vitro grown plantlets were screened for possible vegetative changes using agro-morphological descriptors while genetic and methylation differences were assessed using amplified fragment length polymorphism (AFLP) and methylation-sensitive amplification polymorphism (MSAP). In vitro results showed that the number of shoots produced in Musa spp. varied significantly (P≤0.001) with the type of culture system. The highest mean shoot produced was observed with TIS (28.40) and the least using semi-solid culture medium (1.13). For Dioscorea spp., there was no significant interaction between the hormone combination and the culture system. However, the lowest mean shoot value (1.55) was observed in the semi-solid culture medium. Genetic analysis via AFLP using 15 primer pair combinations revealed that the 3 culture systems maintained genetic variation for Musa and Dioscorea spp. under in vitro and field conditions. Results showed 99% and 91% of the total bands were polymorphic under in vitro and field conditions respectively for Musa and 100% polymorphism for Dioscorea under in vitro and field conditions. Methylation investigation via MSAP using 12 primer pair combinations showed 25% and 46% polymorphic methylated-sensitive loci, 100% and 78% of non-methylated loci of the total bands generated under in vitro and field conditions respectively. Unmethylated (HPA+/MSP+) levels were highest in TIS (0.0842) as compared to CI (0.0227) and SS (0.0161) while full methylation or absence of target (HPA-/MSP-) was lowest in TIS (0.5890) and highest in SS (0.7138). For Dioscorea, 52% and 53% methylated sensitive loci and 100% non-methylated loci were polymorphic under in vitro and field conditions respectively. Although in vitro plant tissue culture techniques led to methylation at some loci of both species, there were no observable changes in the phenotype of both crops under field conditions. This also confirmed that not all methylation events lead to phenotypic changes.

Highlights

  • In vitro plant tissue culture is recognized as one of the most valuable biotechnology tools for rapid multiplication of disease-free and true-to-type genotypes

  • temporary immersion system (TIS) (RITA bioreactor) gave significantly higher shoot mean across the genotypes, followed by complete immersion in liquid media system with shaking while the least was observed with semi-solid medium (Fig 1)

  • The present study confirmed the advantage of temporary immersion system (TIS, RITA bioreactor) in improving the multiplication rate of polyshoot production in both Musa and Dioscorea spp

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Summary

Introduction

In vitro plant tissue culture is recognized as one of the most valuable biotechnology tools for rapid multiplication of disease-free and true-to-type genotypes. There are, some challenges related to formation of aberrant plantlets and low survival during acclimatization stages in the field [1,2,3] In both Dioscorea and Musa spp., in vitro clonal propagation can be used either for large scale propagation or conservation. Semi-solid and liquid culture are some of the common culture media systems used for in vitro plant propagation [10]. These methods have certain advantages but there are limitations too. The major disadvantages are asphyxiation, hyperhydricity, induced stress on agitated cultures, explant blackening (oxidation), poor diffusion rate and sub-optimal nutrient uptake which may lead to severe physiological disorder [10]

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