皮膚常在真菌マラセチアの新たな病原メカニズムを発見―乳酸菌が腸管バリア障害を軽減する可能性―

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2026-09-15 京都大学

皮膚常在真菌マラセチア・フルフルの病原性を、線虫Caenorhabditis elegansを用いて解析した研究である。マラセチアを摂取した線虫では寿命が短縮し、腸管バリア機能も障害されることが明らかになった。さらに遺伝子解析から、病原体に対する自然免疫に関わるNSY-1/SEK-1経路がマラセチア防御に重要であることを特定した。一方、乳酸菌Lacticaseibacillus rhamnosusを同時に与えると、マラセチアによる寿命短縮と腸管バリア障害が部分的に軽減された。皮膚に常在する真菌が宿主の腸管機能にも影響し得る可能性を示すとともに、乳酸菌などの有用微生物を利用した感染・疾患予防戦略につながる知見として期待される。

皮膚常在真菌マラセチアの新たな病原メカニズムを発見―乳酸菌が腸管バリア障害を軽減する可能性―
本研究の概略図(作成者:岸田千穂、谷本佳彦)

<関連情報>

代替宿主である線⾍(Caenorhabditis elegans)におけるマラセチア・フルフル(Malassezia furfur)の病原性および腸管バリア破壊能は、ラクティカセイバチルス・ラムノサス(Lacticaseibacillus rhamnosus)によって部分的に軽減される Pathogenicity and intestinal barrier disruptive ability of Malassezia furfur in an alternative model host Caenorhabditis elegans is partially alleviated by Lacticaseibacillus rhamnosus

Chiho Kishida,Kanamu Chikuba,Chinatsu Yamamura,Himari Kanatani,Ayano Tsuru,Satoka Takabayashi,Xueyang Wu,Misaki Okahata,Yoshihiko Tanimoto,Eriko Kage-Nakadai
FEMS Microbes  Published:08 September 2026
DOI:https://doi.org/10.1093/femsmc/xtag049

Abstract

Malassezia furfur is fungi associated with various diseases; however, the mechanisms underlying its pathogenicity and the relationship between probiotics and fungi remain largely unknown. In the present study, Caenorhabditis elegans was used as the model host to evaluate M. furfur pathogenicity. Additionally, effects of lactic acid bacteria against M. furfur pathogenicity were evaluated. Compared to Escherichia coli OP50 (OP, control), both live and heat-killed M. furfur reduced the lifespan and body size of C. elegans, although heat-killed M. furfur was less effective than live M. furfur in lifespan shortening. Furthermore, unlike heat-killed M. furfur, live M. furfur disrupted the nematode intestinal barrier. Loss-of-function mutants of nsy-1 and sek-1, which encode components of the MAPK signaling pathway, were susceptible to M. furfur, suggesting their involvement in the defense against M. furfur infection. Expression of genes involved in host defense and of those coding for C-type lectin domain-containing proteins and antimicrobial peptides was upregulated in M. furfur-infected C. elegans. Lacticaseibacillus rhamnosus (LR) significantly ameliorated lifespan shortening and body size reduction in M. furfur-infected C. elegans and protected against intestinal barrier disruption, suggesting that LR protects nematodes from M. furfur virulence. This study highlights M. furfur pathogenicity and intestinal barrier disruptive ability in C. elegans and suggests that the M. furfur virulence is partially attenuated by LR.

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