Background The chaperone ClpB, a bacterial protein, is a conformational antigen-mimetic of α-melanocyte-stimulating hormone (α-MSH) implicated in body weight regulation in mice. We here investigated the potential associations of gut bacterial ClpB-like gene function with obesity status and gut microbiota in humans. Results Gut microbiota ClpB KEGG function was negatively associated with body mass index, waist circumference, and total fat mass (DEXA). The relative abundance (RA) of several phyla and families directly associated with ClpB was decreased in subjects with obesity. Specifically, the RA ofRikenellaceae,Clostridiaceaeand not assignedFirmicutes were lower in subjects with obesity and positively associated with gut bacterial ClpB-like gene function (not assignedFirmicutes(r =0.405, FDR = 2.93 × 10−2),Rikenellaceae(r =0.217, FDR = 0.031), andClostridiaceae(r =0.239, FDR = 0.017)). The gut bacterial ClpB-like gene function was also linked to specific plasma metabolites (hippuric acid and 3-indolepropionic acid) and fecal lupeol. The α-MSH-like epitope similar to that ofEscherichia coliClpB was also identified in some sequences of those bacterial families. After fecal transplantation from humans to mice, the families that more contributed to ClpB-like gene function in humans were also associated with ClpB-like gene function in mice after adjusting for the donor’s body mass index (not assignedFirmicutes(r =0.621,p =0.003),Prevotellaceae(r =0.725,p =4.1 × 10−7),Rikenellaceae(r =0.702,p =3.9 × 10−4), andRuminococcaceae(r =0.526,p =0.014)).Clostridiaceae(r =− 0.445,p =0.038) andPrevotellaceaeRA (r = −0.479,p =0.024) and were also negatively associated with weight gain in mice. The absolute abundance (AA) ofPrevotellaceaein mice was also positively associated with the gut bacterial ClpB-like gene function in mice. DESeq2 identified species ofPrevotellaceae, both negatively associated with mice’ weight gain and positively with gut bacterial ClpB-like gene function. Conclusions In summary, gut bacterial ClpB-like gene function is associated with obesity status, a specific gut microbiota composition and a plasma metabolomics profile in humans that could be partially transplanted to mice.
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Arnoriaga‐Rodríguez et al. (2020) studied this question.
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