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We commend Ding and colleagues for their innovative work investigating how high-fat diet-induced changes to the gut microbiome can alter spermatogenesis.1 This link between the gut microbiome and testicular function had earlier been suggested by studies that reported the consumption of probiotic bacteria could improve spermatogenesis and testosterone production in both mice and men.2 3 Furthermore, we had earlier published the Gut Endotoxin Leading to a Decline IN Gonadal function (GELDING) theory that outlined the scientific evidence behind why obesity related change in the gut microbiome, and the associated increase in intestinal permeability with passage of gut bacterial endotoxin (metabolic endotoxaemia, ME) into the systemic circulation, may impair testicular function.4 Since that publication we have gone on to show that obesity related ME is associated with low-grade systemic inflammation, reduction in testosterone production and impaired sperm quality5 6—all consistent with the probiotic studies2 3 and the experimental findings of Ding et al. 1
While we agree that Ding’s murine faecal transplant study does confirm that alteration of the gut microbiome and associated ME can disturb spermatogenesis independent of adiposity, we do not agree that their transfer of bacteria by repeated gastric lavage is an appropriate model for what happens in the obese state. Obesity and its associated lifestyle (high fat diet, minimal exercise) primarily produce colonic dysbiosis, with bacterial numbers still remaining low in the small intestine due to the inhibitory action of gastric acid and bile.4 In the Ding paper1 the authors delivered large numbers of faecal bacteria direct to the small intestine by gastric lavage over a 15-week period. While this did modify the recipient’s faecal (colonic) microbiome, it also resulted in very significant small intestinal inflammation suggestive of small intestinal bacterial overgrowth (SIBO). As SIBO is seen in only a fraction of obese men,7 it is questionable whether these findings are relevant to all obese men. Instead, we believe that Ding’s experimental work, plus our own preliminary findings described below, support a link between SIBO and impaired spermatogenesis.
The small intestine is particularly susceptible to migration of bacteria into the systemic circulation (ME) as it must exhibit permeability to other macro-molecules (digested food), and unlike the colon is not protected by a thick mucus barrier. In the presence of bacteria, the small intestine produces zonulin which increases intestinal permeability by triggering disengagement of epithelial tight junctions, thereby flushing out bacteria and preventing colonisation. Pilot data from our group confirms a significant positive correlation between serum zonulin production and ME, while a negative correlation exist between these two markers of intestinal permeability and serum testosterone (figure 1, table 1). While neither zonulin nor ME are conclusive for the presence of SIBO, these observations in the context of Ding’s findings,1 certainly support the concept that bacterial overgrowth in the small intestine may trigger an increase in intestinal permeability and ME, which then impairs testicular function.5 6
Proton pump inhibitors (PPI) are one of the most commonly prescribed medications, with PPI use being a significant risk factor for development of SIBO.8 Interestingly, PPI use has already been linked with impaired spermatogenesis and low serum testosterone in some studies.9 10 As such we call for more research and awareness of this possible link between the gut microbiome and testicular function, and we specifically caution gastroenterologists about this possible link between PPI use, SIBO and impaired male reproductive function.
Collaborators Amy Hill.
Contributors Both authors have read the Ding et al paper in Gut. KT wrote this letter to the editor response and KP reviewed it. Both authors were involved in the pilot research study contained in this letter.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; internally peer reviewed.
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