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Acute melanization of silkworm hemolymph by peptidoglycans of the human commensal bacterium Cutibacterium acnes
Yasuhiko Matsumoto1, Eri Sato1, Takashi Sugita1
1Department of Microbiology, Meiji Pharmaceutical University, Kiyose, Tokyo, Japan.
Abstract:
Cutibacterium acnes is a pathogenic bacterium that cause inflammatory diseases of the skin and intervertebral discs. The immune activation induced by C. acnes requires multiple cellular responses in the host. Silkworm, an invertebrate, generates melanin by phenoloxidase upon recognizing bacterial or fungal components. Therefore, the melanization reaction can be used as an indicator of innate immune activation. A silkworm infection model was developed for evaluating the virulence of C. acnes, but a system for evaluating the induction of innate immunity by C. acnes using melanization as an indicator has not yet been established. Here we demonstrated that C. acnes rapidly causes melanization of the silkworm hemolymph. On the other hand, Staphylococcus aureus, a gram-positive bacterium identical to C. acnes, does not cause immediate melanization. Even injection of heat-killed C. acnes cells caused melanization of the silkworm hemolymph. DNase, RNase, and protease treatment of the heat-treated C. acnes cells did not decrease the silkworm hemolymph melanization. Treatment with peptidoglycan-degrading enzymes, such as lysostaphin and lysozyme, however, decreased the induction of melanization by the heat-treated C. acnes cells. These findings suggest that silkworm hemolymph melanization may be a useful indicator to evaluate innate immune activation by C. acnes and that C. acnes peptidoglycans are involved in the induction of innate immunity in silkworms.
Insights
Silkworm melanization indicates innate immune activation by Cutibacterium acnes (C. acnes). Peptidoglycans from C. acnes trigger this response, offering a new method to study immune activation.
Area of Science:
- Invertebrate immunology
- Microbial pathogenesis
- Biochemical assays
Background:
- Cutibacterium acnes (C. acnes) causes inflammatory diseases.
- Silkworm melanization, mediated by phenoloxidase, serves as an indicator of innate immune activation.
- A system to evaluate C. acnes-induced innate immunity using silkworm melanization is needed.
Purpose of the Study:
- To establish a silkworm melanization assay for evaluating innate immune activation by C. acnes.
- To identify the C. acnes components responsible for inducing melanization.
Main Methods:
- Infection of silkworms with C. acnes and Staphylococcus aureus.
- Treatment of heat-killed C. acnes with DNase, RNase, protease, lysostaphin, and lysozyme.
- Observation of silkworm hemolymph melanization.
Main Results:
- C. acnes rapidly induced silkworm hemolymph melanization, unlike S. aureus.
- Heat-killed C. acnes also induced melanization.
- Melanization induction was reduced by peptidoglycan-degrading enzymes (lysostaphin, lysozyme), but not by DNase, RNase, or protease treatments.
Conclusions:
- Silkworm hemolymph melanization is a potential indicator for evaluating innate immune activation by C. acnes.
- C. acnes peptidoglycans are key inducers of innate immunity in silkworms.
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