Abstract

Background Tyrophagus putrescentiae (Acari: Astigmata) and Fusarium sp. co-occur in poorly managed grain. In a laboratory experiment, mite grazing resulted in significant reduction of fungal mycelium on cultivation plates. The destruction of mycelium appeared to be a result of an interaction between the mites, fungi and associated bacteria.Methodology and Principal FindingsA laboratory experiment was performed to simulate a situation of grain multiinfested by mites and Fusarium fungi. Changes of mite-associated bacterial community in T. putrescentiae were described in 3 habitats: (i) T. putrescentiae mites from a rearing diet prior to their transfer to fungal diet; (ii) fungal mycelium before mite introduction; (iii) mites after 7 day diet of each Fusarium avenaceum, F. culmorum, F. poae and F. verticillioides. Bacterial communities were characterized by 16 S rRNA gene sequencing. In total, 157 nearly full-length 16 S rRNA gene sequences from 9 samples representing selected habitats were analyzed. In the mites, the shift from rearing to fungal diet caused changes in mite associated bacterial community. A diverse bacterial community was associated with mites feeding on F. avenaceum, while feeding on the other three Fusarium spp. led to selection of a community dominated by Bacillaceae.Conclusions/SignificanceThe work demonstrated changes of bacterial community associated with T. putrescentiae after shift to fungal diets suggesting selection for Bacillaceae species known as chitinase producers, which might participate in the fungal mycelium hydrolysis.

Highlights

  • It is believed that ancestors of synanthropic mites penetrated gradually from soil habitats to bird and rodent nests and switched from fungal diet to utilization of debris [1]

  • The aim of the study was to describe changes in miteassociated bacterial community induced by feeding on the cultures of Fusarium spp. and to find whether bacterial taxa able to participate in the elimination of the fungal mycelium are selected

  • Bacterial communities associated with F. avenaceum, F. culmorum and F. verticillioides were formed only by bacteria related to Stenotrophomonas

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Summary

Introduction

It is believed that ancestors of synanthropic mites penetrated gradually from soil habitats to bird and rodent nests and switched from fungal diet to utilization of debris [1]. Fungivory seems to remain one of the feeding strategies of synanthropic mites, and may have important consequences to their successful survival in human habitats [4]. Such habitats contain plant debris, which are rich in carbohydrate sources but poor in nitrogen contents. The mites interact and vector microorganisms of medical importance [7,8]. The destruction of mycelium appeared to be a result of an interaction between the mites, fungi and associated bacteria

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