{"title":"Prevotella intermedia Synergistically Exacerbates Pneumonia Induced by Oral Streptococci","authors":"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","doi":"10.1093/infdis/jiaf278","DOIUrl":null,"url":null,"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.","PeriodicalId":501010,"journal":{"name":"The Journal of Infectious Diseases","volume":"40 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Infectious Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/infdis/jiaf278","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.