2018
DOI: 10.1007/s12223-018-0665-5
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Intensive formation of coccoid forms as a feature strongly associated with highly pathogenic Helicobacter pylori strains

Abstract: The variability of Helicobacter pylori morphology and the heterogeneity of virulence factors expressed by these bacteria play a key role as a driving force for adaptation to the hostile stomach environment. The aim of the study was to determine the relationship between the presence of certain genes encoding virulence factors and H. pylori morphology. One reference and 13 clinical H. pylori strains with a known virulence profile ( … Show more

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Cited by 15 publications
(24 citation statements)
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“…Morphological variability in response to unfavorable environmental conditions is typical for many Gram-negative rods, including H. pylori [38]. This microorganism, in response to stressful conditions, most often undergoes a morphological transformation into spherical forms, for which increased survivability and participation in the failure of antimicrobial therapies are suggested [39,40,41]. In many studies defining the antibacterial activity of substances, the mechanism of H. pylori morphological conversion from the spiral to coccoid form was noticed [42,43,44].…”
Section: Discussionmentioning
confidence: 99%
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“…Morphological variability in response to unfavorable environmental conditions is typical for many Gram-negative rods, including H. pylori [38]. This microorganism, in response to stressful conditions, most often undergoes a morphological transformation into spherical forms, for which increased survivability and participation in the failure of antimicrobial therapies are suggested [39,40,41]. In many studies defining the antibacterial activity of substances, the mechanism of H. pylori morphological conversion from the spiral to coccoid form was noticed [42,43,44].…”
Section: Discussionmentioning
confidence: 99%
“…The strains were categorized as susceptible or resistant to antibiotics based on the EUCAST recommendations, i.e., amoxicillin (AMX, R > 0.125 μg/mL), clarithromycin (CLR, R > 0.5 μg/mL), tetracycline (TET, R > 1 μg/mL), and metronidazole (MTZ, > 8 μg/mL) [52]. Bacterial strains were kept in a Trypticase soy broth (TSB) (Oxoid, Le Pont de Claix, France) with the addition of 15% glycerol at −70 °C until testing [41]. After thawing, the bacteria were plated on Columbia agar (Difco, Lublin, Poland) with 7% hemolysed horse blood (CA+HB) and incubated for 3 days under microaerophilic conditions (Genbox microaer kits, BioMerieux, Marcy I’Etoile, France) at 37 °C.…”
Section: Methodsmentioning
confidence: 99%
“…Bacterial morphology was determined during the checkerboard method and time-killing assays [40]. Each time, 50 µL of bacterial suspension was dripped onto slides from each concentration and strain tested, and stained using the Gram's method.…”
Section: Light Microscopymentioning
confidence: 99%
“…Bacteria treated with certain concentrations of SER were fixed by adding a 2.5% glutaraldehyde solution (Sigma-Aldrich) [38,40]. After 24 h of fixing, bacteria were centrifuged at 600 g for 5 min and washed three times in 0.1 M cacodylate buffer (Sigma-Aldrich), centrifuging after each wash at 600 g for 5 min.…”
Section: Scanning Electron Microscopymentioning
confidence: 99%
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