TY - JOUR
T1 - The impact of gut microbiota on gender-specific differences in immunity
AU - Fransen, Floris
AU - van Beek, Adriaan A.
AU - Borghuis, Theo
AU - Meijer, Ben
AU - Hugenholtz, Floor
AU - van der Gaast-de Jongh, Christa
AU - Savelkoul, Huub F.
AU - de Jonge, Marien I.
AU - Faas, Marijke M.
AU - Boekschoten, Mark V.
AU - Smidt, Hauke
AU - Aidy, Sahar El
AU - de Vos, Paul
PY - 2017
Y1 - 2017
N2 - Males and females are known to have gender-specific differences in their immune system and gut microbiota composition. Whether these differences in gut microbiota composition are a cause or consequence of differences in the immune system is not known. To investigate this issue, gut microbiota from conventional males or females was transferred to germ-free (GF) animals of the same or opposing gender. We demonstrate that microbiota-independent gender differences in immunity are already present in GF mice. In particular, type I interferon signaling was enhanced in the intestine of GF females. Presumably, due to these immune differences bacterial groups, such as Alistipes, Rikenella, and Porphyromonadaceae, known to expand in the absence of innate immune defense mechanism were overrepresented in the male microbiota. The presence of these bacterial groups was associated with induction of weight loss, inflammation, and DNA damage upon transfer of the male microbiota to female GF recipients. In summary, our data suggest that microbiota-independent gender differences in the immune system select a gender-specific gut microbiota composition, which in turn further contributes to gender differences in the immune system.
AB - Males and females are known to have gender-specific differences in their immune system and gut microbiota composition. Whether these differences in gut microbiota composition are a cause or consequence of differences in the immune system is not known. To investigate this issue, gut microbiota from conventional males or females was transferred to germ-free (GF) animals of the same or opposing gender. We demonstrate that microbiota-independent gender differences in immunity are already present in GF mice. In particular, type I interferon signaling was enhanced in the intestine of GF females. Presumably, due to these immune differences bacterial groups, such as Alistipes, Rikenella, and Porphyromonadaceae, known to expand in the absence of innate immune defense mechanism were overrepresented in the male microbiota. The presence of these bacterial groups was associated with induction of weight loss, inflammation, and DNA damage upon transfer of the male microbiota to female GF recipients. In summary, our data suggest that microbiota-independent gender differences in the immune system select a gender-specific gut microbiota composition, which in turn further contributes to gender differences in the immune system.
KW - Gender
KW - Germ-free mice
KW - Gut microbiota
KW - Immunity
KW - Inflammation
U2 - 10.3389/fimmu.2017.00754
DO - 10.3389/fimmu.2017.00754
M3 - Article
AN - SCOPUS:85021765830
VL - 8
JO - Frontiers in Immunology
JF - Frontiers in Immunology
SN - 1664-3224
M1 - 754
ER -