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Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera
Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera
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Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera
Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera

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Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera
Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera
Journal Article

Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera

2012
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Overview
The microsporidium Nosema ceranae is a newly prevalent parasite of the European honey bee (Apis mellifera). Although this parasite is presently spreading across the world into its novel host, the mechanisms by it which affects the bees and how bees respond are not well understood. We therefore performed an extensive characterization of the parasite effects at the molecular level by using genetic and biochemical tools. The transcriptome modifications at the midgut level were characterized seven days post-infection with tiling microarrays. Then we tested the bee midgut response to infection by measuring activity of antioxidant and detoxification enzymes (superoxide dismutases, glutathione peroxidases, glutathione reductase, and glutathione-S-transferase). At the gene-expression level, the bee midgut responded to N. ceranae infection by an increase in oxidative stress concurrent with the generation of antioxidant enzymes, defense and protective response specifically observed in the gut of mammals and insects. However, at the enzymatic level, the protective response was not confirmed, with only glutathione-S-transferase exhibiting a higher activity in infected bees. The oxidative stress was associated with a higher transcription of sugar transporter in the gut. Finally, a dramatic effect of the microsporidia infection was the inhibition of genes involved in the homeostasis and renewal of intestinal tissues (Wnt signaling pathway), a phenomenon that was confirmed at the histological level. This tissue degeneration and prevention of gut epithelium renewal may explain early bee death. In conclusion, our integrated approach not only gives new insights into the pathological effects of N. ceranae and the bee gut response, but also demonstrate that the honey bee gut is an interesting model system for studying host defense responses.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject

Acids

/ Alkaline Phosphatase - metabolism

/ Animals

/ Antioxidants

/ Antioxidants (Nutrients)

/ Apis mellifera

/ Bayesian analysis

/ Bees

/ Bees - enzymology

/ Bees - microbiology

/ Biochemistry

/ Bioinformatics

/ Biology

/ Cellular Biology

/ Degeneration

/ Detoxification

/ Digestive system

/ Digestive tract

/ DNA microarrays

/ Drosophila

/ Enzymes

/ Epidemiology

/ Epithelium

/ European honeybee

/ Gastrointestinal tract

/ Gastrointestinal Tract - microbiology

/ Gastrointestinal Tract - pathology

/ Gene expression

/ Gene Expression Profiling

/ Gene Expression Regulation - genetics

/ Gene Expression Regulation - physiology

/ Gene Regulatory Networks - genetics

/ Genetic aspects

/ Genomes

/ Genomics

/ Glutathione

/ Glutathione Peroxidase - metabolism

/ Glutathione reductase

/ Glutathione Reductase - metabolism

/ Glutathione transferase

/ Glutathione Transferase - metabolism

/ Histological Techniques

/ Homeostasis

/ Honey

/ Infection

/ Infections

/ Insects

/ Intestine

/ Laboratories

/ Life Sciences

/ Microarray Analysis

/ Microorganisms

/ Microsporidia

/ Midgut

/ Nosema

/ Oxidative stress

/ Oxidative Stress - genetics

/ Oxidative Stress - physiology

/ Parasites

/ Pathological effects

/ Pathology

/ Phosphatase

/ Reductases

/ Regulation

/ Senescence

/ Signal transduction

/ Signal Transduction - genetics

/ Signal Transduction - physiology

/ Signaling

/ Statistics, Nonparametric

/ Sugar

/ Superoxide

/ Superoxide Dismutase - metabolism

/ Superoxides

/ Tiling

/ Tissues

/ Transcription

/ Transcriptome - genetics

/ Transcriptome - physiology

/ Wnt protein

/ Wnt Signaling Pathway - genetics

/ Wnt Signaling Pathway - physiology