Multi-omics analysis reveals indicator features of microbe-host interactions during colonization and subsequent infection.

INTRODUCTION

gastrointestinal (GI) colonization is crucial for the onset of invasive disease. This research encompassed 31 patients diagnosed with spp. bloodstream infections during their admission to a university hospital in China.

METHODS

We explored risk factors associated with GI colonization and ensuing translocated infection. Animal models were established via gavage with clinical isolates of to induce GI tract colonization and subsequent kidney translocation infection. Our analysis is focused on 16S rRNA gene sequencing, metabolomics of colon contents, and transcriptomics of colon tissues, examining the intestinal barrier, inflammatory responses, and immune cell infiltration.

RESULTS

This study observed that down-regulation of programmed cell death 1 (PD-1) in colon tissues is likely linked to the progression from colonization to translocated infection. Notably, reductions in abundance and Short-chain fatty acids (SCFA) levels, coupled with increases in and D-erythro-imidazolylglycerol phosphate, were indicator features during the advancement to translocated invasive infection in hosts with rectal colonization by and lower serum protein levels.

CONCLUSION

Given the similarity in intestinal bacterial communities and metabolome profiles, antifungal treatment may not be necessary for patients with nonpathogenic colonization. The reduced expression of PD-1 in colon tissues may contribute to the transition from colonized to subsequent translocated infection. The indicator features of decreased Dubosiella abundance and SCFA levels, coupled with increased Mucispirillum and D-erythro-imidazolylglycerol phosphate, are likely linked to the development of translocated invasive infection in hosts colonized rectally by with lower serum protein levels.

IMPORTANCE

invasive infections pose a significant challenge to contemporary medicine, with mortality rates from such fungal infections remaining high despite antifungal treatment. Gastrointestinal colonization by potential pathogens is a critical precursor to the development of translocated infections. Consequently, there is an increasing demand to identify clinical risk factors, multi-omics profiles, and key indicators to prevent the progression to translocated invasive infections in patients colonized rectally by .