scholarly journals Genotypic and Phenotypic Variation of Lewis Antigen Expression in Geographically Diverse Helicobacter pylori Isolates

Helicobacter ◽  
2011 ◽  
Vol 16 (6) ◽  
pp. 475-481 ◽  
Author(s):  
Mary Ann Pohl ◽  
William Zhang ◽  
Sunny N. Shah ◽  
Edgardo L. Sanabria-Valentín ◽  
Guillermo I. Perez-Perez ◽  
...  
2006 ◽  
Vol 20 (9) ◽  
pp. 1534-1536 ◽  
Author(s):  
Hans-Peter Wirth ◽  
Manqiao Yang ◽  
Edgardo Sanabria-Valentín ◽  
Douglas E. Berg ◽  
André Dubois ◽  
...  

2008 ◽  
Vol 46 (8) ◽  
pp. 2783-2785 ◽  
Author(s):  
G. Gonzalez-Valencia ◽  
L. Munoz-Perez ◽  
R. Morales-Espinosa ◽  
M. Camorlinga-Ponce ◽  
O. Munoz ◽  
...  

2004 ◽  
Vol 38 (1) ◽  
pp. 85-91 ◽  
Author(s):  
Ana Margarida Nogueira ◽  
Terezinha Marques ◽  
Paula Cristina M. Soares ◽  
Leonor David ◽  
Celso A. Reis ◽  
...  

2003 ◽  
Vol 71 (5) ◽  
pp. 2902-2906 ◽  
Author(s):  
Alain Lozniewski ◽  
Xavier Haristoy ◽  
David A. Rasko ◽  
Renée Hatier ◽  
François Plénat ◽  
...  

ABSTRACT The role of Helicobacter pylori lipopolysaccharide (LPS) Lewis antigens in infection is still not well known. We investigated the influence of Lewis antigen expression by H. pylori on its internalization by AGS cells and the epithelium of human gastric xenografts in nude mice using isogenic mutants in LPS biosynthetic genes. In vivo, colonization rates were unaffected by the change in H. pylori Lewis antigen expression, whereas the number of viable intracellular bacteria was significantly higher with wild-type H. pylori strains expressing Lewis antigens when compared to the isogenic mutants in both models. H. pylori strains expressing more Lewis X antigens (Lex) were internalized at a higher rate than those expressing less Lex, type II Lewis antigens (Lea or Leb) alone, or no Lewis antigens. Thus, Lewis antigens appear to be involved in the internalization of H. pylori by the gastric epithelium.


1991 ◽  
Vol 79 (3) ◽  
pp. 493-499 ◽  
Author(s):  
Niels C. Langkilde ◽  
Hans Wolf ◽  
Torben F. Ørntoft

1998 ◽  
pp. 477-483
Author(s):  
M. A. Apicella ◽  
M. Shero ◽  
G. A. Jarvis ◽  
J. M. Griffiss ◽  
Robert E. Mandrell ◽  
...  

2012 ◽  
Vol 80 (4) ◽  
pp. 1593-1605 ◽  
Author(s):  
Mary Ann Pohl ◽  
Sabine Kienesberger ◽  
Martin J. Blaser

ABSTRACTLewis (Le) antigens are fucosylated oligosaccharides present in theHelicobacter pylorilipopolysaccharide. Expression of these antigens is believed to be important forH. pyloricolonization, since Le antigens also are expressed on the gastric epithelia in humans. A galactosyltransferase encoded by β-(1,3)galTis essential for production of type 1 (Leaand Leb) antigens. The upstream genejhp0562, which is present in many but not allH. pyloristrains, is homologous to β-(1,3)galTbut is of unknown function. BecauseH. pyloridemonstrates extensive intragenomic recombination, we hypothesized that these two genes could undergo DNA rearrangement. A PCR screen and subsequent sequence analyses revealed that the two genes can recombine at both the 5′ and 3′ ends. Chimeric β-(1,3)galT-like alleles can restore function in a β-(1,3)galTnull mutant, but neither native nor recombinantjhp0562can. Mutagenesis ofjhp0562revealed that it is essential for synthesis of both type 1 and type 2 Le antigens. Transcriptional analyses of both loci showed β-(1,3)galTexpression in all wild-type (WT) and mutant strains tested, whereasjhp0562was not expressed injhp0562null mutants, as expected. Sincejhp0562unexpectedly displayed functions in both type 1 and type 2 Le synthesis, we asked whethergalT, part of the type 2 synthesis pathway, had analogous functions in type 1 synthesis. Mutagenesis and complementation analysis confirmed thatgalTis essential for Lebproduction. In total, these results demonstrate thatgalTandjhp0562have functions that cross the expected Le synthesis pathways and thatjhp0562provides a substrate for intragenomic recombination to generate diverse Le synthesis enzymes.


2007 ◽  
Vol 7 (1) ◽  
pp. 26 ◽  
Author(s):  
Justin G Hovey ◽  
Emily L Watson ◽  
Melanie L Langford ◽  
Ellen Hildebrandt ◽  
Sangeetha Bathala ◽  
...  

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