2009
DOI: 10.1111/j.1523-5378.2009.00692.x
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Presence of High Numbers of Transcriptionally Active Helicobacter pylori in Vomitus from Bangladeshi Patients Suffering from Acute Gastroenteritis

Abstract: We conclude that high numbers of transcriptionally active H. pylori are shed in vomitus, which indicates that new infections may be disseminated through vomiting.

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Cited by 19 publications
(15 citation statements)
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References 48 publications
(63 reference statements)
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“…Increased rates of H. pylori infection in developing nations such as Pakistan, Vietnam, Bangladesh and India, which combat poverty, poor sanitary conditions and overcrowding, indicate the role of environmental factors in the transmission of infection [17][18][19][20]. In 2007, Ahmed et al indicated that the risk of H. pylori infection can be reduced by improving personal hygiene and regular use of boiled drinking water [20].…”
Section: Resultsmentioning
confidence: 99%
“…Increased rates of H. pylori infection in developing nations such as Pakistan, Vietnam, Bangladesh and India, which combat poverty, poor sanitary conditions and overcrowding, indicate the role of environmental factors in the transmission of infection [17][18][19][20]. In 2007, Ahmed et al indicated that the risk of H. pylori infection can be reduced by improving personal hygiene and regular use of boiled drinking water [20].…”
Section: Resultsmentioning
confidence: 99%
“…For relative expression of imaA and ureA, transcript levels were normalized to the levels of groEL (69) in each sample. Transcripts were amplified with HP0289 For1.1 (For stands for forward) (5=-TAACGATCCAAAACGCT TCC) and HP0289 Rev1.1 (Rev stands for reverse) (5=-TCCCTTGAGGC GAGAGTGATT), UreA F1 and UreA R1 (36), and groEL F (JVO-529) and groEL R (JVO-5298) (69). Il8 (55) and TNF-␣ (84) expression levels from AGS cells were normalized to 18S (55) rRNA, and KC levels from mouse tissues were normalized to GAPDH (24).…”
Section: Methodsmentioning
confidence: 99%
“…Helicobacter pylori strains P12 and the Nicaraguan clinical isolate Nic25_A were cultured on Columbia blood agar plates under microaerophilic conditions (80% N 2 , 10% CO 2 , 10% H 2 ), which is standard for H. pylori (Janzon et al, 2009). The strains were replated and cultured for 24 h before the colony biomass was scraped from the plates and suspended in 500 μL of phosphate buffered saline.…”
Section: Methodsmentioning
confidence: 99%