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Probing the expression and adhesion of glycans involved in Helicobacter pylori infection
Helicobacter pylori infects approximately half the human population and has an unusual infective niche of the human stomach. Helicobacter pylori is a major cause of gastritis and has been classified as a group 1 carcinogen by the WHO. Treatment involves triple or quadruple antibiotic therapy, but an...
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Published in: | Scientific reports 2024-04, Vol.14 (1), p.8587-8587, Article 8587 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Helicobacter pylori
infects approximately half the human population and has an unusual infective niche of the human stomach.
Helicobacter pylori
is a major cause of gastritis and has been classified as a group 1 carcinogen by the WHO. Treatment involves triple or quadruple antibiotic therapy, but antibiotic resistance is becoming increasingly prevalent.
Helicobacter pylori
expresses certain blood group related antigens (Lewis system) as a part of its lipopolysaccharide (LPS), which is thought to assist in immune evasion. Additionally,
H. pylori
LPS participates in adhesion to host cells alongside several adhesion proteins. This study profiled the carbohydrates of
H. pylori
reference strains (SS1 and 26695) using monoclonal antibodies (mAbs) and lectins, identifying interactions between two carbohydrate-targeting mAbs and multiple lectins. Atomic force microscopy (AFM) scans were used to probe lectin and antibody interactions with the bacterial surfaces. The selected mAb and lectins displayed an increased adhesive force over the surface of the curved
H. pylori
rods. Furthermore, this study demonstrates the ability of anti-carbohydrate antibodies to reduce the adhesion of
H. pylori
26695 to human gastric adenocarcinoma cells via AFM. Targeting bacterial carbohydrates to disrupt crucial adhesion and immune evasion mechanisms represents a promising strategy for combating
H. pylori
infection. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-024-59234-w |