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      Comment on Sofi et al. pH of Drinking Water Influences the Composition of Gut Microbiome and Type 1 Diabetes Incidence. Diabetes 2014;63:632–644

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      Diabetes
      American Diabetes Association

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          Abstract

          We read with interest the report by Sofi et al. (1) in Diabetes. This article is of practical interest to many groups who use the nonobese diabetic (NOD) mouse model. As this group observed, we have also observed that mice that are ordered from The Jackson Laboratory tend to get diabetes sooner than those bred in National Institutes of Health facilities. The results in this article suggest this is partly due to the use of acidic (pH 3.0–3.2) water. If true, it would be a relatively easy way to obtain a more consistent diabetes phenotype for experiments. However, another article was published with data suggesting that acidic water reduces diabetes incidence in NOD mice (2). Therefore, we decided to repeat the comparison of diabetes incidence with neutral or acidic water in our facility. NOD/ShiLtJt mice were purchased from The Jackson Laboratory and maintained under specific pathogen–free conditions and were fed autoclaved LabDiet JL Rat and Mouse/Auto 6F 5K67 diet, as well as sterile water. Water was acidified by adding hydrochloric acid to achieve a pH range of 3.0–3.3. Breeding pairs were spilt between neutral and acidified water, and all pups born from these breeding pairs were kept on their specific water. NOD female mice on acidic (n = 35) or neutral water (n = 37) were followed from 9 weeks old until 30 weeks old for the onset of diabetes, testing urine glucose once a week. A positive test was confirmed by a blood glucose measurement >250 mmol/L. At 30 weeks, 75.7% of NOD mice on neutral water mice became diabetic as compared with 77.1% of NOD mice on acidic water. Significance was calculated using either the Mantel-Cox test (P value = 0.9741) or the Gehan-Breslow-Wilcoxon test (P value = 0.9909). No difference in diabetes timing or incidence was observed. In addition, insulitis was measured in a separate cohort of mice, and no significant difference in insulitis score was observed at 9 weeks of age (average score 0.34 for neutral group and 0.26 for low-pH group, P value = 0.2). In conclusion, although Sofa et al. (1) reported an acceleration of diabetes in NOD mice on acidic water, this result is not universal across different animal facilities. Sofi et al. reported a change in microbiome as the mechanism for the effect of acidic water on diabetes development. One possibility is that the baseline commensals are different at different locations, and this may interact with the acidic water treatment, eliciting different results in different facilities.

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          pH of Drinking Water Influences the Composition of Gut Microbiome and Type 1 Diabetes Incidence

          Nonobese diabetic (NOD) mice spontaneously develop type 1 diabetes (T1D), progression of which is similar to that in humans, and therefore are widely used as a model for understanding the immunological basis of this disease. The incidence of T1D in NOD mice is influenced by the degree of cleanliness of the mouse colony and the gut microflora. In this report, we show that the T1D incidence and rate of disease progression are profoundly influenced by the pH of drinking water, which also affects the composition and diversity of commensal bacteria in the gut. Female NOD mice that were maintained on acidic pH water (AW) developed insulitis and hyperglycemia rapidly compared with those on neutral pH water (NW). Interestingly, forced dysbiosis by segmented filamentous bacteria (SFB)-positive fecal transfer significantly suppressed the insulitis and T1D incidence in mice that were on AW but not in those on NW. The 16S rDNA–targeted pyrosequencing revealed a significant change in the composition and diversity of gut flora when the pH of drinking water was altered. Importantly, autoantigen-specific T-cell frequencies in the periphery and proinflammatory cytokine response in the intestinal mucosa are significantly higher in AW-recipient mice compared with their NW counterparts. These observations suggest that pH of drinking water affects the composition of gut microflora, leading to an altered autoimmune response and T1D incidence in NOD mice.
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            Consumption of Acidic Water Alters the Gut Microbiome and Decreases the Risk of Diabetes in NOD Mice

            Infant formula and breastfeeding are environmental factors that influence the incidence of Type 1 Diabetes (T1D) as well as the acidity of newborn diets. To determine if altering the intestinal microbiome is one mechanism through which an acidic liquid plays a role in T1D, we placed non-obese diabetic (NOD)/ShiLtJt mice on neutral (N) or acidified H2O and monitored the impact on microbial composition and diabetes incidence. NOD-N mice showed an increased development of diabetes, while exhibiting a decrease in Firmicutes and an increase in Bacteroidetes, Actinobacteria, and Proteobacteria from as early as 2 weeks of age. NOD-N mice had a decrease in the levels of Foxp3 expression in CD4+Foxp3+ cells, as well as decreased CD4+IL17+ cells, and a lower ratio of IL17/IFNγ CD4+ T-cells. Our data clearly indicates that a change in the acidity of liquids consumed dramatically alters the intestinal microbiome, the presence of protective Th17 and Treg cells, and the incidence of diabetes. This data suggests that early dietary manipulation of intestinal microbiota may be a novel mechanism to delay T1D onset in genetically pre-disposed individuals.
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              Author and article information

              Journal
              Diabetes
              Diabetes
              diabetes
              diabetes
              Diabetes
              Diabetes
              American Diabetes Association
              0012-1797
              1939-327X
              August 2015
              16 July 2015
              : 64
              : 8
              : e19
              Affiliations
              Immune Tolerance Section, Diabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD
              Author notes
              Corresponding author: Kristin V. Tarbell, tarbellk@ 123456niddk.nih.gov .
              Article
              0321
              10.2337/db15-0321
              4512222
              26207042
              13412f7e-baeb-4bf5-bd0d-288415bad7bb
              © 2015 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered.
              History
              Page count
              Pages: 1
              Funding
              Funded by: National Institute of Diabetes and Digestive and Kidney Diseases http://dx.doi.org/10.13039/100000062
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              Endocrinology & Diabetes
              Endocrinology & Diabetes

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