Duodenal-Mucosal Bacteria Associated with Celiac Disease in Children

被引:125
作者
Sanchez, Ester [1 ]
Donat, Ester [2 ]
Ribes-Koninckx, Carmen [2 ]
Leonor Fernandez-Murga, Maria [1 ]
Sanz, Yolanda [1 ]
机构
[1] Natl Res Council IATA CSIC, Inst Agrochem & Food Technol, Microbial Ecol & Nutr Res Grp, Valencia, Spain
[2] Hosp Univ La Fe, Valencia, Spain
关键词
INFLAMMATORY-BOWEL-DISEASE; GRADIENT GEL-ELECTROPHORESIS; IMMUNE-RESPONSES; INTESTINAL MICROBIOTA; ULCERATIVE-COLITIS; HUMAN GUT; DIVERSITY; CELLS; BIFIDOBACTERIA; COMMUNITIES;
D O I
10.1128/AEM.00869-13
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Celiac disease (CD) is an immune-mediated enteropathy triggered by the ingestion of cereal gluten proteins. This disorder is associated with imbalances in the gut microbiota composition that could be involved in the pathogenesis of CD. The aim of this study was to characterize the composition and diversity of the cultivable duodenal mucosa-associated bacteria of CD patients and control children. Duodenal biopsy specimens from patients with active disease on a gluten-containing diet (n = 32), patients with nonactive disease after adherence to a gluten-free diet (n = 17), and controls (n = 8) were homogenized and plated on plate count agar, Wilkins-Chalgren agar, brain heart agar, or yeast, Casitone, and fatty acid agar. The isolates were identified by partial 16S rRNA gene sequencing. Renyi diversity profiles showed the highest diversity values for active CD patients, followed by nonactive CD patients and control individuals. Members of the phylum Proteobacteria were more abundant in patients with active CD than in the other child groups, while those of the phylum Firmicutes were less abundant. Members of the families Enterobacteriaceae and Staphylococcaceae, particularly the species Klebsiella oxytoca, Staphylococcus epidermidis, and Staphylococcus pasteuri, were more abundant in patients with active disease than in controls. In contrast, members of the family Streptococcaceae were less abundant in patients with active CD than in controls. Furthermore, isolates of the Streptococcus anginosus and Streptococcus mutans groups were more abundant in controls than in both CD patient groups, regardless of inflammatory status. The findings indicated that the disease is associated with the overgrowth of possible pathobionts that exclude symbionts or commensals that are characteristic of the healthy small intestinal microbiota.
引用
收藏
页码:5472 / 5479
页数:8
相关论文
共 54 条
[1]   Oral Findings and Salivary Parameters in Children with Celiac Disease: A Preliminary Study [J].
Acar, Sibel ;
Yetkiner, Arzu Aykut ;
Ersin, Nazan ;
Oncag, Ozant ;
Aydogdu, Sema ;
Arikan, Cigdem .
MEDICAL PRINCIPLES AND PRACTICE, 2012, 21 (02) :129-133
[2]   ANAEROBIC FACULTATIVE BACTERIA ISOLATED FROM THE GUT OF RABBITS FED DIFFERENT DIETS [J].
CANGANELLA, F ;
ZIRLETTA, G ;
GUALTERIO, L ;
MASSA, S ;
TROVATELLI, LD .
ZENTRALBLATT FUR MIKROBIOLOGIE, 1992, 147 (08) :537-540
[3]   Role of Intestinal Bacteria in Gliadin-Induced Changes in Intestinal Mucosa: Study in Germ-Free Rats [J].
Cinova, Jana ;
De Palma, Giada ;
Stepankova, Renata ;
Kofronova, Olga ;
Kverka, Miloslav ;
Sanz, Yolanda ;
Tuckova, Ludmila .
PLOS ONE, 2011, 6 (01)
[4]   Specific duodenal and faecal bacterial groups associated with paediatric coeliac disease [J].
Collado, M. C. ;
Donat, E. ;
Ribes-Koninckx, C. ;
Calabuig, M. ;
Sanz, Y. .
JOURNAL OF CLINICAL PATHOLOGY, 2009, 62 (03) :264-269
[5]   Pivotal Advance: Bifidobacteria and Gram-negative bacteria differentially influence immune responses in the proinflammatory milieu of celiac disease [J].
De Palma, G. ;
Cinova, J. ;
Stepankova, R. ;
Tuckova, L. ;
Sanz, Y. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2010, 87 (05) :765-778
[6]   Intestinal dysbiosis and reduced immunoglobulin-coated bacteria associated with coeliac disease in children [J].
De Palma, Giada ;
Nadal, Inmaculada ;
Medina, Marcela ;
Donat, Ester ;
Ribes-Koninckx, Carmen ;
Calabuig, Miguel ;
Sanz, Yolanda .
BMC MICROBIOLOGY, 2010, 10
[7]   Duodenal and faecal microbiota of celiac children: molecular, phenotype and metabolome characterization [J].
Di Cagno, Raffaella ;
De Angelis, Maria ;
De Pasquale, Ilaria ;
Ndagijimana, Maurice ;
Vernocchi, Pamela ;
Ricciuti, Patrizia ;
Gagliardi, Francesca ;
Laghi, Luca ;
Crecchio, Carmine ;
Guerzoni, Maria Elisabetta ;
Gobbetti, Marco ;
Francavilla, Ruggiero .
BMC MICROBIOLOGY, 2011, 11
[8]   Coeliac disease: an update for pathologists [J].
Dickson, B. C. ;
Streutker, C. J. ;
Chetty, R. .
JOURNAL OF CLINICAL PATHOLOGY, 2006, 59 (10) :1008-1016
[9]   Multiple common variants for celiac disease influencing immune gene expression [J].
Dubois, Patrick C. A. ;
Trynka, Gosia ;
Franke, Lude ;
Hunt, Karen A. ;
Romanos, Jihane ;
Curtotti, Alessandra ;
Zhernakova, Alexandra ;
Heap, Graham A. R. ;
Adany, Roza ;
Aromaa, Arpo ;
Bardella, Maria Teresa ;
van den Berg, Leonard H. ;
Bockett, Nicholas A. ;
de la Concha, Emilio G. ;
Dema, Barbara ;
Fehrmann, Rudolf S. N. ;
Fernandez-Arquero, Miguel ;
Fiatal, Szilvia ;
Grandone, Elvira ;
Green, Peter M. ;
Groen, Harry J. M. ;
Gwilliam, Rhian ;
Houwen, Roderick H. J. ;
Hunt, Sarah E. ;
Kaukinen, Katri ;
Kelleher, Dermot ;
Korponay-Szabo, Ilma ;
Kurppa, Kalle ;
MacMathuna, Padraic ;
Maki, Markku ;
Mazzilli, Maria Cristina ;
McCann, Owen T. ;
Mearin, M. Luisa ;
Mein, Charles A. ;
Mirza, Muddassar M. ;
Mistry, Vanisha ;
Mora, Barbara ;
Morley, Katherine I. ;
Mulder, Chris J. ;
Murray, Joseph A. ;
Nunez, Concepcion ;
Oosterom, Elvira ;
Ophoff, Roel A. ;
Polanco, Isabel ;
Peltonen, Leena ;
Platteel, Mathieu ;
Rybak, Anna ;
Salomaa, Veikko ;
Schweizer, Joachim J. ;
Sperandeo, Maria Pia .
NATURE GENETICS, 2010, 42 (04) :295-U42
[10]  
Dubreuil L, 1996, PATHOL BIOL, V44, P333