-
Je něco špatně v tomto záznamu ?
Distinct gut microbiota profiles in patients with primary sclerosing cholangitis and ulcerative colitis
L. Bajer, M. Kverka, M. Kostovcik, P. Macinga, J. Dvorak, Z. Stehlikova, J. Brezina, P. Wohl, J. Spicak, P. Drastich,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu srovnávací studie, časopisecké články
Grantová podpora
NV15-28064A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Free Medical Journals
od 1998
Freely Accessible Science Journals
od 1998
PubMed Central
od 1997
Europe PubMed Central
od 1997
PubMed
28740343
DOI
10.3748/wjg.v23.i25.4548
Knihovny.cz E-zdroje
- MeSH
- Bacteria genetika izolace a purifikace MeSH
- dospělí MeSH
- dysbióza etiologie mikrobiologie MeSH
- feces mikrobiologie MeSH
- kolon mikrobiologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- RNA ribozomální 16S izolace a purifikace MeSH
- sekvenční analýza RNA MeSH
- senioři MeSH
- sklerozující cholangitida komplikace mikrobiologie MeSH
- střevní mikroflóra * MeSH
- střevní sliznice mikrobiologie MeSH
- ulcerózní kolitida komplikace mikrobiologie MeSH
- zdraví dobrovolníci pro lékařské studie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- srovnávací studie MeSH
AIM: To characterize the gut bacterial microbiota of patients with primary sclerosing cholangitis (PSC) and ulcerative colitis (UC). METHODS: Stool samples were collected and relevant clinical data obtained from 106 study participants, 43 PSC patients with (n = 32) or without (n = 11) concomitant inflammatory bowel disease, 32 UC patients, and 31 healthy controls. The V3 and V4 regions of the 16S ribosomal RNA gene were sequenced on Illumina MiSeq platform to cover low taxonomic levels. Data were further processed in QIIME employing MaAsLin and LEfSe tools for analysis of the output data. RESULTS: Microbial profiles in both PSC and UC were characterized by low bacterial diversity and significant change in global microbial composition. Rothia, Enterococcus, Streptococcus, Veillonella, and three other genera were markedly overrepresented in PSC regardless of concomitant inflammatory bowel disease (IBD). Rothia, Veillonella and Streptococcus were tracked to the species level to identify Rothia mucilaginosa, Streptococcus infantus, S. alactolyticus, and S. equi along with Veillonella parvula and V. dispar. PSC was further characterized by decreased abundance of Adlercreutzia equolifaciens and Prevotella copri. Decrease in genus Phascolarctobacterium was linked to presence of colonic inflammation regardless of IBD phenotype. Akkermansia muciniphila, Butyricicoccus pullicaecorum and Clostridium colinum were decreased in UC along with genus Roseburia. Low levels of serum albumin were significantly correlated with enrichment of order Actinomycetales. CONCLUSION: PSC is associated with specific gut microbes independently of concomitant IBD and several bacterial taxa clearly distinguish IBD phenotypes (PSC-IBD and UC).
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18024799
- 003
- CZ-PrNML
- 005
- 20201020154659.0
- 007
- ta
- 008
- 180709s2017 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3748/wjg.v23.i25.4548 $2 doi
- 035 __
- $a (PubMed)28740343
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Bajer, Lukas $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 245 10
- $a Distinct gut microbiota profiles in patients with primary sclerosing cholangitis and ulcerative colitis / $c L. Bajer, M. Kverka, M. Kostovcik, P. Macinga, J. Dvorak, Z. Stehlikova, J. Brezina, P. Wohl, J. Spicak, P. Drastich,
- 520 9_
- $a AIM: To characterize the gut bacterial microbiota of patients with primary sclerosing cholangitis (PSC) and ulcerative colitis (UC). METHODS: Stool samples were collected and relevant clinical data obtained from 106 study participants, 43 PSC patients with (n = 32) or without (n = 11) concomitant inflammatory bowel disease, 32 UC patients, and 31 healthy controls. The V3 and V4 regions of the 16S ribosomal RNA gene were sequenced on Illumina MiSeq platform to cover low taxonomic levels. Data were further processed in QIIME employing MaAsLin and LEfSe tools for analysis of the output data. RESULTS: Microbial profiles in both PSC and UC were characterized by low bacterial diversity and significant change in global microbial composition. Rothia, Enterococcus, Streptococcus, Veillonella, and three other genera were markedly overrepresented in PSC regardless of concomitant inflammatory bowel disease (IBD). Rothia, Veillonella and Streptococcus were tracked to the species level to identify Rothia mucilaginosa, Streptococcus infantus, S. alactolyticus, and S. equi along with Veillonella parvula and V. dispar. PSC was further characterized by decreased abundance of Adlercreutzia equolifaciens and Prevotella copri. Decrease in genus Phascolarctobacterium was linked to presence of colonic inflammation regardless of IBD phenotype. Akkermansia muciniphila, Butyricicoccus pullicaecorum and Clostridium colinum were decreased in UC along with genus Roseburia. Low levels of serum albumin were significantly correlated with enrichment of order Actinomycetales. CONCLUSION: PSC is associated with specific gut microbes independently of concomitant IBD and several bacterial taxa clearly distinguish IBD phenotypes (PSC-IBD and UC).
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a Bacteria $x genetika $x izolace a purifikace $7 D001419
- 650 _2
- $a sklerozující cholangitida $x komplikace $x mikrobiologie $7 D015209
- 650 _2
- $a ulcerózní kolitida $x komplikace $x mikrobiologie $7 D003093
- 650 _2
- $a kolon $x mikrobiologie $7 D003106
- 650 _2
- $a dysbióza $x etiologie $x mikrobiologie $7 D064806
- 650 _2
- $a feces $x mikrobiologie $7 D005243
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 12
- $a střevní mikroflóra $7 D000069196
- 650 _2
- $a zdraví dobrovolníci pro lékařské studie $7 D064368
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a střevní sliznice $x mikrobiologie $7 D007413
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a RNA ribozomální 16S $x izolace a purifikace $7 D012336
- 650 _2
- $a sekvenční analýza RNA $7 D017423
- 655 _2
- $a srovnávací studie $7 D003160
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kverka, Miloslav $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 700 1_
- $a Kostovcik, Martin $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 700 1_
- $a Macinga, Peter $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 700 1_
- $a Dvorak, Jiri $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 700 1_
- $a Stehlikova, Zuzana $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 700 1_
- $a Brezina, Jan $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 700 1_
- $a Wohl, Pavel $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 700 1_
- $a Spicak, Julius $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 700 1_
- $a Drastich, Pavel $u Lukas Bajer, Peter Macinga, Jan Brezina, Pavel Wohl, Julius Spicak, Pavel Drastich, Department of Gastroenterology and Hepatology, Institute for Clinical and Experimental Medicine, 14021 Prague, Czech Republic.
- 773 0_
- $w MED00006918 $t World journal of gastroenterology $x 2219-2840 $g Roč. 23, č. 25 (2017), s. 4548-4558
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28740343 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20180709 $b ABA008
- 991 __
- $a 20201020154655 $b ABA008
- 999 __
- $a ok $b bmc $g 1316930 $s 1021720
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 23 $c 25 $d 4548-4558 $i 2219-2840 $m World journal of gastroenterology $n World J Gastroenterol $x MED00006918
- GRA __
- $a NV15-28064A $p MZ0
- LZP __
- $a Pubmed-20180709