Intestinal Klebsiella pneumoniae Contributes to Pneumonia by Synthesizing Glutamine in Multiple Myeloma.
Yihui WangQin YangYinghong ZhuXingxing JianJiaojiao GuoJingyu ZhangChunmei KuangXiangling FengGang AnLugui QiuGuancheng LiYanjuan HeWen ZhouPublished in: Cancers (2022)
Pneumonia accounts for a significant cause of morbidity and mortality in multiple myeloma (MM) patients. It has been previously shown that intestinal Klebsiella pneumonia ( K. pneumonia ) enriches in MM and promotes MM progression. However, what role the altered gut microbiota plays in MM with pneumonia remains unknown. Here, we show that intestinal K. pneumonia is significantly enriched in MM with pneumonia. This enriched intestinal K. pneumonia links to the incidence of pneumonia in MM, and intestinal colonization of K. pneumonia contributes to pneumonia in a 5TGM1 MM mice model. Further targeted metabolomic assays reveal the elevated level of glutamine, which is consistently increased with the enrichment of K. pneumonia in MM mice and patients, is synthesized by K. pneumonia , and leads to the elevated secretion of TNF-α in the lung normal fibroblast cells for the higher incidence of pneumonia. Inhibiting glutamine synthesis by establishing glnA -mutated K. pneumonia alleviates the incidence of pneumonia in the 5TGM1 MM mice model. Overall, our work proposes that intestinal K. pneumonia indirectly contributes to pneumonia in MM by synthesizing glutamine. Altogether, we unveil a gut-lung axis in MM with pneumonia and establish a novel mechanism and a possible intervention strategy for MM with pneumonia.
Keyphrases
- respiratory failure
- community acquired pneumonia
- randomized controlled trial
- end stage renal disease
- multiple myeloma
- gene expression
- rheumatoid arthritis
- type diabetes
- adipose tissue
- newly diagnosed
- chronic kidney disease
- dna methylation
- high throughput
- induced apoptosis
- cell proliferation
- peritoneal dialysis
- extracorporeal membrane oxygenation
- acute respiratory distress syndrome
- cell cycle arrest
- endoplasmic reticulum stress