Lactobacillus johnsonii N6.2 Mitigates the Development of Type 1 Diabetes in BB-DP Rats

Background The intestinal epithelium is a barrier that composes one of the most immunologically active surfaces of the body due to constant exposure to microorganisms as well as an infinite diversity of food antigens. Disruption of intestinal barrier function and aberrant mucosal immune activation have been implicated in a variety of diseases within and outside of the gastrointestinal tract. With this model in mind, recent studies have shown a link between diet, composition of intestinal microbiota, and type 1 diabetes pathogenesis. In the BioBreeding rat model of type 1 diabetes, comparison of the intestinal microbial composition of diabetes prone and diabetes resistant animals found Lactobacillus species were negatively correlated with type 1 diabetes development. Two species, Lactobacillus johnsonii and L. reuteri, were isolated from diabetes resistant rats. In this study diabetes prone rats were administered pure cultures of L. johnsonii or L. reuteri isolated from diabetes resistant rats to determine the effect on type 1 diabetes development. Methodology/Principal Findings Results Rats administered L. johnsonii, but not L. reuteri, post-weaning developed type 1 diabetes at a protracted rate. Analysis of the intestinal ileum showed administration of L. johnsonii induced changes in the native microbiota, host mucosal proteins, and host oxidative stress response. A decreased oxidative intestinal environment was evidenced by decreased expression of several oxidative response proteins in the intestinal mucosa (Gpx1, GR, Cat). In L. johnsonii fed animals low levels of the pro-inflammatory cytokine IFNγ were correlated with low levels of iNOS and high levels of Cox2. The administration of L. johnsonii also resulted in higher levels of the tight junction protein claudin. Conclusions It was determined that the administration of L. johnsonii isolated from BioBreeding diabetes resistant rats delays or inhibits the onset of type 1 diabetes in BioBreeding diabetes prone rats. Taken collectively, these data suggest that the gut and the gut microbiota are potential agents of influence in type 1 diabetes development. These data also support therapeutic efforts that seek to modify gut microbiota as a means to modulate development of this disorder.

[1]  J. Doré,et al.  Low counts of Faecalibacterium prausnitzii in colitis microbiota , 2009, Inflammatory bowel diseases.

[2]  G. Lorca,et al.  Biochemical Properties of Two Cinnamoyl Esterases Purified from a Lactobacillus johnsonii Strain Isolated from Stool Samples of Diabetes-Resistant Rats , 2009, Applied and Environmental Microbiology.

[3]  S. Zeissig,et al.  Epithelial Tight Junctions in Intestinal Inflammation , 2009, Annals of the New York Academy of Sciences.

[4]  J. Hillebrands,et al.  Prevention of diabetes by a hydrolysed casein-based diet in diabetes-prone BioBreeding rats does not involve restoration of the defective natural regulatory T cell function , 2009, Diabetologia.

[5]  P. Desjardins,et al.  Direct Evidence for Central Proinflammatory Mechanisms in Rats with Experimental Acute Liver Failure: Protective Effect of Hypothermia , 2009, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[6]  G. Casella,et al.  Culture-independent identification of gut bacteria correlated with the onset of diabetes in a rat model , 2009, The ISME Journal.

[7]  Kazumasa Matsumoto,et al.  Establishment of an Analytical System for the Human Fecal Microbiota, Based on Reverse Transcription-Quantitative PCR Targeting of Multicopy rRNA Molecules , 2009, Applied and Environmental Microbiology.

[8]  D. Portetelle,et al.  Quantification of Bifidobacterium spp. and Lactobacillus spp. in rat fecal samples by real-time PCR. , 2008, Microbiological research.

[9]  R. Tang,et al.  Development of a real‐time PCR method for Firmicutes and Bacteroidetes in faeces and its application to quantify intestinal population of obese and lean pigs , 2008, Letters in applied microbiology.

[10]  J. Doré,et al.  Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients , 2008, Proceedings of the National Academy of Sciences.

[11]  J. Neu,et al.  The “Perfect Storm” for Type 1 Diabetes , 2008, Diabetes.

[12]  J. Neu,et al.  Neonatal Formula Feeding Leads to Immunological Alterations in an Animal Model of Type 1 Diabetes , 2008, Pediatric Research.

[13]  N. Charoenphandhu,et al.  Chronic metabolic acidosis upregulated claudin mRNA expression in the duodenal enterocytes of female rats. , 2007, Life sciences.

[14]  L. Augenlicht,et al.  STAT1-independent inhibition of cyclooxygenase-2 expression by IFNγ; a common pathway of IFNγ-mediated gene repression but not gene activation , 2007, Oncogene.

[15]  L. Augenlicht,et al.  STAT1-independent inhibition of cyclooxygenase-2 expression by IFNgamma; a common pathway of IFNgamma-mediated gene repression but not gene activation. , 2007, Oncogene.

[16]  Feiqi Zhu,et al.  Berberine chloride can ameliorate the spatial memory impairment and increase the expression of interleukin-1beta and inducible nitric oxide synthase in the rat model of Alzheimer's disease , 2006, BMC Neuroscience.

[17]  J. Neu,et al.  Comment on: Brugman S et al. (2006) Antibiotic treatment partially protects against type 1 diabetes in the Bio-Breeding diabetes-prone rat. Is the gut flora involved in the development of type 1 diabetes? Diabetologia 49:2105–2108 , 2006, Diabetologia.

[18]  T. Asahara,et al.  Sensitive Quantitative Detection of Commensal Bacteria by rRNA-Targeted Reverse Transcription-PCR , 2006, Applied and Environmental Microbiology.

[19]  R. Robertson,et al.  Diabetes, glucose toxicity, and oxidative stress: A case of double jeopardy for the pancreatic islet beta cell. , 2006, Free radical biology & medicine.

[20]  H. Harmsen,et al.  Antibiotic treatment partially protects against type 1 diabetes in the Bio-Breeding diabetes-prone rat. Is the gut flora involved in the development of type 1 diabetes? , 2006, Diabetologia.

[21]  J. Mehta,et al.  Oxidative stress in diabetes: a mechanistic overview of its effects on atherogenesis and myocardial dysfunction. , 2006, The international journal of biochemistry & cell biology.

[22]  T. Jacques,et al.  Essential role for hematopoietic prostaglandin D2 synthase in the control of delayed type hypersensitivity. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[23]  M. Marinaro,et al.  Oral probiotic administration induces interleukin-10 production and prevents spontaneous autoimmune diabetes in the non-obese diabetic mouse , 2005, Diabetologia.

[24]  J. Neu,et al.  Changes in Intestinal Morphology and Permeability in the BioBreeding Rat Before the Onset of Type 1 Diabetes , 2005, Journal of pediatric gastroenterology and nutrition.

[25]  T. Osawa,et al.  Identification and quantification of Nɛ-(Hexanoyl)lysine in human urine by liquid chromatography/tandem mass spectrometry , 2004 .

[26]  D. Polk,et al.  Commensal bacteria in the gut: learning who our friends are , 2004, Current opinion in gastroenterology.

[27]  Y. Chung,et al.  Immunoregulatory Role of Nitric Oxide in Kilham Rat Virus-Induced Autoimmune Diabetes in DR-BB Rats1 , 2004, The Journal of Immunology.

[28]  M. Nadkarni,et al.  Quantitative Analysis of Diverse Lactobacillus Species Present in Advanced Dental Caries , 2004, Journal of Clinical Microbiology.

[29]  R. Elliott,et al.  Dietary protein: a trigger of insulin-dependent diabetes in the BB rat? , 1984, Diabetologia.

[30]  T. Tsuno,et al.  Antioxidant activity and hypoglycemic effect of ferulic acid in STZ‐induced diabetic mice and KK‐Ay mice , 2004, BioFactors.

[31]  T. Osawa,et al.  Identification and quantification of N(epsilon)-(Hexanoyl)lysine in human urine by liquid chromatography/tandem mass spectrometry. , 2004, Free radical biology & medicine.

[32]  Yuet-Kin Leung,et al.  Androgenic regulation of oxidative stress in the rat prostate: involvement of NAD(P)H oxidases and antioxidant defense machinery during prostatic involution and regrowth. , 2003, The American journal of pathology.

[33]  M. Gye Changes in the expression of claudins and transepithelial electrical resistance of mouse Sertoli cells by Leydig cell coculture. , 2003, International journal of andrology.

[34]  D. Fairlie,et al.  Comparative protection against rat intestinal reperfusion injury by a new inhibitor of sPLA2, COX‐1 and COX‐2 selective inhibitors, and an LTC4 receptor antagonist , 2003, British journal of pharmacology.

[35]  J. Strubbe,et al.  Short-term dietary adjustment with a hydrolyzed casein-based diet postpones diabetes development in the diabetes-prone BB rat. , 2003, Metabolism: clinical and experimental.

[36]  O. Simell,et al.  Cellular distribution and contribution of cyclooxygenase (COX)-2 to diabetogenesis in NOD mouse , 2002, Cell and Tissue Research.

[37]  J. Kalff,et al.  Colonic Postoperative Inflammatory Ileus in the Rat , 2002, Annals of surgery.

[38]  O. Simell,et al.  Expression of cyclooxygenase-2 in intestinal goblet cells of pre-diabetic NOD mice. , 2002, Acta physiologica Scandinavica.

[39]  J. Catravas,et al.  Molecular mechanisms of iNOS induction by IL-1 beta and IFN-gamma in rat aortic smooth muscle cells. , 2002, American journal of physiology. Cell physiology.

[40]  J. Catravas,et al.  Molecular mechanisms of iNOS induction by IL-1β and IFN-γ in rat aortic smooth muscle cells , 2002 .

[41]  I. Mackay Tolerance and autoimmunity , 2000, BMJ : British Medical Journal.

[42]  Derek W. Gilroy,et al.  New insights into the role of COX 2 in inflammation , 2000, Journal of Molecular Medicine.

[43]  K. Chadee,et al.  Intestinal mucins in colonization and host defense against pathogens. , 1999, The American journal of tropical medicine and hygiene.

[44]  M. Hollingsworth,et al.  Probiotics inhibit enteropathogenic E. coliadherence in vitro by inducing intestinal mucin gene expression. , 1999, American journal of physiology. Gastrointestinal and liver physiology.

[45]  H. Neumann,et al.  Interferon γ Gene Expression in Sensory Neurons: Evidence for Autocrine Gene Regulation , 1997, The Journal of experimental medicine.

[46]  M. Mcdaniel,et al.  Tyrosine kinase inhibitors prevent cytokine-induced expression of iNOS and COX-2 by human islets. , 1996, The American journal of physiology.

[47]  H. Kolb,et al.  Transcription and translation of inducible nitric oxide synthase in the pancreas of prediabetic BB rats , 1993, FEBS letters.