Prevotella intermedia Synergistically Exacerbates Pneumonia Induced by Oral Streptococci

Hiroki Ashizawa, Naoki Iwanaga, Kazuki Nemoto, Tatsuro Hirayama, Masataka Yoshida, Kazuaki Takeda, Shotaro Ide, Masato Tashiro, Naoki Hosogaya, Takahiro Takazono, Kosuke Kosai, Noriho Sakamoto, Koichi Izumikawa, Mariko Naito, Yoshimasa Tanaka, Katsunori Yanagihara, Kazuhiro Yatera, Hiroshi Mukae
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Abstract

Background The precise mechanisms of respiratory infection caused by oral anaerobic bacteria remain elusive. Unexpectedly, bacterial microbiota analysis using 16S rRNA revealed “hidden” mixed infections of anaerobic bacteria and commensal oral Streptococcus species in patients with community-acquired pneumonia (CAP). The study aimed to elucidate the mechanisms by which Prevotella intermedia exacerbates oral streptococcal pneumonia. Methods Oral streptococci were oropharyngeally administered with the culture supernatants of P. intermedia (PiSup) in mice to assess survival, microbial burden, inflammatory responses, and host response using unbiased bulk RNA sequencing. Additionally, genetically engineered strains of P. intermedia were used to identify pathogenic factors. Results Seven-week-old female C57BL/6J mice treated with the combination of Streptococcus spp. and PiSup exhibited significantly worse survival and increased microbial burden in the lungs and spleen compared to Streptococcus spp. and control medium. RNA sequencing of whole lung revealed disruption of neutrophilic bactericidal activity due to NADP downregulation, accompanied by reduced myeloperoxidase production in mixed infections, leading to dysfunctional neutrophil accumulation in the lungs. Notably, PiSup from strains bearing mutations in the type IX secretion pathway (ΔporT or ΔporK) failed to worsen the mixed infection. Conclusions Prevotella intermedia exacerbates pneumonia caused by commensal oral streptococci by inducing neutrophilic dysfunction in mixed infection. Products of type IX secretion system should be investigated as novel targets independent of reported virulence factors.
中普雷沃氏菌协同加重口服链球菌引起的肺炎
背景口腔厌氧菌引起呼吸道感染的确切机制尚不清楚。出乎意料的是,使用16S rRNA进行细菌微生物群分析,发现社区获得性肺炎(CAP)患者中存在厌氧菌和共生口腔链球菌的“隐藏”混合感染。本研究旨在阐明中普雷沃氏菌加重口腔链球菌肺炎的机制。方法将小鼠口腔链球菌与中间媒介P.培养上清液(PiSup)一起经口咽部注射,使用无偏散装RNA测序技术评估小鼠的存活率、微生物负担、炎症反应和宿主反应。此外,利用基因工程菌株鉴定病原菌。结果7周龄C57BL/6J雌性小鼠经链球菌与PiSup联合处理后,其存活率明显低于对照组,肺和脾脏微生物负荷明显增加。全肺RNA测序显示,在混合性感染中,由于NADP下调,中性粒细胞杀菌活性被破坏,并伴有髓过氧化物酶生成减少,导致肺部中性粒细胞积聚功能失调。值得注意的是,来自IX型分泌途径突变菌株(ΔporT或ΔporK)的PiSup未能使混合感染恶化。结论中普雷沃氏菌通过诱导中性粒细胞功能障碍加重口腔共生链球菌所致肺炎。IX型分泌系统的产物应作为独立于已报道的毒力因子的新靶点进行研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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