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

被引:212
作者
Valladares, Ricardo [1 ]
Sankar, Dhyana [2 ]
Li, Nan [2 ]
Williams, Emily [1 ]
Lai, Kin-Kwan [1 ]
Abdelgeliel, Asmaa Sayed [1 ]
Gonzalez, Claudio F. [1 ]
Wasserfall, Clive H. [3 ]
Larkin, Joseph, III [1 ]
Schatz, Desmond [2 ]
Atkinson, Mark A. [3 ]
Triplett, Eric W. [1 ]
Neu, Josef [2 ]
Lorca, Graciela L. [1 ]
机构
[1] Univ Florida, Dept Microbiol & Cell Sci, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Pediat, Gainesville, FL USA
[3] Univ Florida, Dept Pathol Immunol & Lab Med, Gainesville, FL USA
来源
PLOS ONE | 2010年 / 5卷 / 05期
关键词
TREATMENT PARTIALLY PROTECTS; NITRIC-OXIDE SYNTHASE; OXIDATIVE STRESS; COMMENSAL BACTERIA; IFN-GAMMA; PRONE RAT; EXPRESSION; GUT; TRANSCRIPTION; CYCLOOXYGENASE-2;
D O I
10.1371/journal.pone.0010507
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 IFN gamma 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.
引用
收藏
页数:9
相关论文
共 44 条
[1]   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 [J].
Arumugam, TV ;
Arnold, N ;
Proctor, LM ;
Newman, M ;
Reid, RC ;
Hansford, KA ;
Fairlie, DP ;
Shiels, IA ;
Taylor, SM .
BRITISH JOURNAL OF PHARMACOLOGY, 2003, 140 (01) :71-80
[2]   Intestinal mucins in colonization and host defense against pathogens [J].
Belley, A ;
Keller, K ;
Göettke, M ;
Chadee, K .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1999, 60 (04) :10-15
[3]   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? [J].
Brugman, S. ;
Klatter, F. A. ;
Visser, J. T. J. ;
Wildeboer-Veloo, A. C. M. ;
Harmsen, H. J. M. ;
Rozing, J. ;
Bos, N. A. .
DIABETOLOGIA, 2006, 49 (09) :2105-2108
[4]   Quantitative analysis of diverse Lactobacillus species present in advanced dental caries [J].
Byun, R ;
Nadkarni, MA ;
Chhour, KL ;
Martin, FE ;
Jacques, NA ;
Hunter, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (07) :3128-3136
[5]   Neonatal formula feeding leads to immunological alterations in an animal model of type 1 diabetes [J].
Caicedo, Ricardo A. ;
Li, Nan ;
Des Robert, Clotilde ;
Scumpia, Philip O. ;
Hubsher, Chad P. ;
Wasserfall, Clive H. ;
Schatz, Desmond A. ;
Atkinson, Mark A. ;
Neu, Josef .
PEDIATRIC RESEARCH, 2008, 63 (03) :303-307
[6]   Oral probiotic administration induces interleukin-10 production and prevents spontaneous autoimmune diabetes in the non-obese diabetic mouse [J].
Calcinaro, F ;
Dionisi, S ;
Marinaro, M ;
Candeloro, P ;
Bonato, V ;
Marzotti, S ;
Corneli, RB ;
Ferretti, E ;
Gulino, A ;
Grasso, F ;
De Simone, C ;
Di Mario, U ;
Falorni, A ;
Boirivant, M ;
Dotta, F .
DIABETOLOGIA, 2005, 48 (08) :1565-1575
[7]   Chronic metabolic acidosis upregulated claudin mRNA expression in the duodenal enterocytes of female rats [J].
Charoenphandhu, Narattaphol ;
Wongdee, Kannikar ;
Tudpor, Kukiat ;
Pandaranandaka, Jantarima ;
Krishnamra, Nateetip .
LIFE SCIENCES, 2007, 80 (19) :1729-1737
[8]   Tyrosine kinase inhibitors prevent cytokine-induced expression of iNOS and COX-2 by human islets [J].
Corbett, JA ;
Kwon, G ;
Marino, MH ;
Rodi, CP ;
Sullivan, PM ;
Turk, J ;
McDaniel, ML .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (06) :C1581-C1587
[9]   Quantification of Bifidobacterium spp. and Lactobacillus spp. in rat fecal samples by real-time PCR [J].
Delroisse, Jean-Marc ;
Boulvin, Anne-Lise ;
Parmentier, Isabelle ;
Dauphin, Robin Dubois ;
Vandenbol, Micheline ;
Portetelle, Daniel .
MICROBIOLOGICAL RESEARCH, 2008, 163 (06) :663-670
[10]  
ELLIOTT RB, 1984, DIABETOLOGIA, V26, P297, DOI 10.1007/BF00283653