The IL-10/IL-12 axis and regulation of DC-SIGN expression in HIV-infected human gut mucosa

2003 ◽  
Vol 124 (4) ◽  
pp. A155-A156
Author(s):  
Kevin Gurney ◽  
Julie Elliott ◽  
Hoorig Nassanian ◽  
Ian McGowan ◽  
Carol Song ◽  
...  
Keyword(s):  
2018 ◽  
Vol 101 (4) ◽  
pp. 1119-1126 ◽  
Author(s):  
Abdullah A Alyousef

Abstract The bacterium originally named Bacillus difficilis was later renamed Clostridium difficile because of the difficulty associated with its isolation in the laboratory. C. difficile causes human-associated diarrhea, which is now known as C. difficile infection (CDI), a major cause of nosocomial infection mainly occurring in developed countries. Changes in antibiotic patterns in its strains produce toxins that are responsible for the high mortality rates associated with CDI; therefore, the epidemiology and severity of CDI have recently changed. Apart from CDI, C. difficile also causes opportunistic infections of the human gut usually when the normal gut flora are disrupted by broad-spectrum antibiotics. By disrupting normal gut flora, spores of C. difficile germinate and traverse the gut mucosa through flagellar binding to the mucosal epithelium where several proteins are involved in the binding of C. difficile. Proper diagnostic techniques have to be applied to ensure early identification of CDI and prompt treatment administered because false results may lead to inappropriate treatment and increase risk of cross-infection. This review discusses the epidemiology and pathogenicity of this bacterium with concern for its changing pattern over the years. Further details on the diagnosis of CDI are elaborated upon, mainly focusing on the limits of and challenges in molecular diagnosis.


2009 ◽  
Vol 136 (7) ◽  
pp. 2214-2225.e3 ◽  
Author(s):  
Marco Metzger ◽  
Claire Caldwell ◽  
Amanda J. Barlow ◽  
Alan J. Burns ◽  
Nikhil Thapar

Lipids ◽  
1991 ◽  
Vol 26 (7) ◽  
pp. 492-494 ◽  
Author(s):  
Roger L. Gebhard ◽  
Stephen L. Ewing ◽  
Linda A. Schlasner ◽  
Donald B. Hunninghake ◽  
William F. Prigge

2005 ◽  
Vol 24 (3) ◽  
pp. 353-359 ◽  
Author(s):  
Stephane Lecleire ◽  
Moise Coeffier ◽  
Jonathan Leblond ◽  
Aurelie Hubert ◽  
Sabrina Lemoulan ◽  
...  
Keyword(s):  

Author(s):  
Emily W Sun ◽  
Alyce M Martin ◽  
David A Wattchow ◽  
Dayan deFontgalland ◽  
Philippa Rabbitt ◽  
...  
Keyword(s):  

1989 ◽  
Vol 97 (6) ◽  
pp. 1562-1584 ◽  
Author(s):  
P. Brandtzaeg ◽  
T.S. Halstensen ◽  
K. Kett ◽  
P. Krajči ◽  
D. Kvale ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Stefano Raimondi ◽  
Eliana Musmeci ◽  
Francesco Candeliere ◽  
Alberto Amaretti ◽  
Maddalena Rossi

AbstractMucins are large glycoproteins consisting of approximately 80% of hetero-oligosaccharides. Gut mucin degraders of healthy subjects were investigated, through a culture dependent and independent approach. The faeces of five healthy adults were subjected to three steps of anaerobic enrichment in a medium with sole mucins as carbon and nitrogen sources. The bacterial community was compared before and after the enrichment by 16S rRNA gene profiling. Bacteria capable of fermenting sugars, such as Anaerotruncus, Holdemania, and Enterococcaceae likely took advantage of the carbohydrate chains. Escherichia coli and Enterobacteriaceae, Peptococcales, the Coriobacteriale Eggerthella, and a variety of Clostridia such as Oscillospiraceae, Anaerotruncus, and Lachnoclostridium, significantly increased and likely participated to the degradation of the protein backbone of mucin. The affinity of E. coli and Enterobacteriaceae for mucin may facilitate the access to the gut mucosa, promoting gut barrier damage and triggering systemic inflammatory responses. Only three species of strict anaerobes able to grow on mucin were isolated from the enrichments of five different microbiota: Clostridium disporicum, Clostridium tertium, and Paraclostridium benzoelyticum. The limited number of species isolated confirms that in the gut the degradation of these glycoproteins results from cooperation and cross-feeding among several species exhibiting different metabolic capabilities.


2013 ◽  
Vol 6 (5) ◽  
pp. 985-992 ◽  
Author(s):  
M Ráki ◽  
A-C Røberg Beitnes ◽  
K E A Lundin ◽  
J Jahnsen ◽  
F L Jahnsen ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document