Abstract

Coconut is one of the main cash crop in Mozambique, which occupied the second position after Tanzania in coconut production in Africa. Coconut production was drastically affected by the occurrence of a devastating Coconut Lethal Yellowing Disease (CLYD) epidemics, which reduced significantly the coconut yields. CLYD symptoms triggered upon phytoplasma infection, i.e. premature fruit dropping, necrosis of the inflorescence and progressive yellowing of the leaves, are used to identify infected trees. However, the diagnostic based uniquely on symptoms is not conclusive to confirm infection, and needs to be confirmed by molecular methods. In this study, three previously described reference primers for phytoplasma detection were tested on infected samples collected in Mozambique. Since those primers gave incongruent results, 20 new primer pairs targeting the 16S rDNA region, were newly designed. To evaluate their performance in detecting coconut infecting phytoplasma, 108 samples were tested and selected positive samples confirmed by sequencing. Our results showed a new primer pair more accurate and reliable compared to the reference pairs for CLYD detection in Mozambique. Moreover, the new primer pair was able to detect a new putative phytoplasma variant in Mozambique. Therefore, this study makes an important contribution to CLYD phytoplasma molecular diagnostics and its causative agent, giving insights that may be applied to the study of CLYD phytoplasma infection systems.

Highlights

  • Our results showed a new primer pair more accurate and reliable compared to the reference pairs for Coconut Lethal Yellowing Disease (CLYD) detection in Mozambique

  • Coconut Lethal Yellowing Disease (CLYD) is a highly destructive disease associated with phytoplasmas (Weintraub and Beanland 2006)

  • Out of the 8 amplicons obtained by the P1/P7 primer pair, 4 showed 98–99% sequence identity to CLYD phytoplasma strain M-182

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Summary

Introduction

Coconut Lethal Yellowing Disease (CLYD) is a highly destructive disease associated with phytoplasmas (Weintraub and Beanland 2006). The analysis of the 16S rDNA region revealed great genetic diversity within the phytoplasmas, often reflecting geographical distribution of the strain (Lee et al 2000; Llauger et al 2002; Husain et al 2002). These evidences led to define a new genus denominated BCandidatus Phytoplasma^, which includes the CLYD infecting phytoplasma (Bai et al 2006)

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