Observations On Infantile Diarrhea Caused by Enteropathogenic Escherichia Coli

2018 ◽  
pp. 57-56
Author(s):  
Ralph A. Giannella
Keyword(s):  
Escherichia Coli ◽  
Enteropathogenic Escherichia Coli ◽  
Infantile Diarrhea

scholarly journals Afa, a Diffuse Adherence Fibrillar Adhesin Associated with Enteropathogenic Escherichia coli

2002 ◽  
Vol 70 (5) ◽  
pp. 2681-2689 ◽  
Author(s):  
Rogéria Keller ◽  
Juana G. Ordoñez ◽  
Rosana R. de Oliveira ◽  
Luiz R. Trabulsi ◽  
Thomas J. Baldwin ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Virulence Genes ◽  
Chromosomal Region ◽  
Enzyme Electrophoresis ◽  
Enteropathogenic Escherichia Coli ◽  
Epec Strain ◽  
Infantile Diarrhea ◽  
E Coli ◽  
Multilocus Enzyme Electrophoresis ◽  
Typical Epec

ABSTRACT O55 is one of the most frequent enteropathogenic Escherichia coli (EPEC) O serogroups implicated in infantile diarrhea in developing countries. Multilocus enzyme electrophoresis analysis showed that this serogroup includes two major electrophoretic types (ET), designated ET1 and ET5. ET1 corresponds to typical EPEC, whilst ET5 comprises strains with different combinations of virulence genes, including those for localized adherence (LA) and diffuse adherence (DA). Here we report that ET5 DA strains possess a DA adhesin, designated EPEC Afa. An 11.6-kb chromosomal region including the DA adhesin operon from one O55:H− ET5 EPEC strain was sequenced and found to encode a protein with 98% identity to AfaE-1, an adhesin associated with uropathogenic E. coli. Although described as an afimbrial adhesin, we show that both AfaE-1 and EPEC Afa possess fine fibrillar structures. This is the first characterization and demonstration of an Afa adhesin associated with EPEC.

Attaching and Effacing Enteropathogenic Escherichia coli as a Cause of Infantile Diarrhea in Bangkok

1991 ◽  
Vol 164 (3) ◽  
pp. 550-554 ◽  
Author(s):  
P. Echeverria ◽  
F. Orskov ◽  
I. Orskov ◽  
S. Knutton ◽  
F. Scheutz ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Enteropathogenic Escherichia Coli ◽  
Infantile Diarrhea

scholarly journals Gut Digestive Function and Microbiome after Correction of Experimental Dysbiosis in Rats by Indigenous Bifidobacteria

2021 ◽  
Vol 9 (3) ◽  
pp. 522
Author(s):  
Lyudmila V. Gromova ◽  
Elena I. Ermolenko ◽  
Anastasiya L. Sepp ◽  
Yulia V. Dmitrieva ◽  
Anna S. Alekseeva ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Digestive Enzymes ◽  
Specific Activity ◽  
Control Group ◽  
Enteropathogenic Escherichia Coli ◽  
Beneficial Bacteria ◽  
Opportunistic Bacteria ◽  
Dyspeptic Symptoms ◽  
Specific Activities ◽  
Impaired Motor Function

In recent years, great interest has arisen in the use of autoprobiotics (indigenous bacteria isolated from the organism and introduced into the same organism after growing). This study aimed to evaluate the effects of indigenous bifidobacteria on intestinal microbiota and digestive enzymes in a rat model of antibiotic-associated dysbiosis. Our results showed that indigenous bifidobacteria (the Bf group) accelerate the disappearance of dyspeptic symptoms in rats and prevent an increase in chyme mass in the upper intestine compared to the group without autoprobiotics (the C1 group), but significantly increase the mass of chyme in the colon compared to the C1 group and the control group (healthy animals). In the Bf group in the gut microbiota, the content of opportunistic bacteria (Proteus spp., enteropathogenic Escherichia coli) decreased, and the content of some beneficial bacteria (Bifidobacterium spp., Dorea spp., Blautia spp., the genus Ruminococcus, Prevotella, Oscillospira) changed compared to the control group. Unlike the C1 group, in the Bf group there was no decrease in the specific activities of maltase and alkaline phosphatase in the mucosa of the upper intestine, but the specific activity of maltase was decreased in the colon chyme compared to the control and C1 groups. In the Bf group, the specific activity of aminopeptidase N was reduced in the duodenum mucosa and the colon chyme compared to the control group. We concluded that indigenous bifidobacteria can protect the microbiota and intestinal digestive enzymes in the intestine from disorders caused by dysbiosis; however, there may be impaired motor function of the colon.

scholarly journals Drug resistance among infantile enteropathogenic Escherichia coli strains isolated in the United Kingdom.

BMJ ◽  
1982 ◽  
Vol 285 (6340) ◽  
pp. 472-473 ◽  
Author(s):  
R J Gross ◽  
L R Ward ◽  
E J Threlfall ◽  
H King ◽  
B Rowe
Keyword(s):  
Escherichia Coli ◽  
Drug Resistance ◽  
United Kingdom ◽  
Enteropathogenic Escherichia Coli ◽  
The United Kingdom

scholarly journals The gut at war: the consequences of enteropathogenic Escherichia coli infection as a factor of diarrhea and malnutrition

2000 ◽  
Vol 118 (1) ◽  
pp. 21-29 ◽  
Author(s):  
Ulysses Fagundes-Neto ◽  
Isabel Cristina Affonso Scaletsky
Keyword(s):  
Escherichia Coli ◽  
Diarrheal Disease ◽  
Driving Forces ◽  
Public Health Problem ◽  
Clinical Aspects ◽  
Small Intestinal Mucosa ◽  
Enteropathogenic Escherichia Coli ◽  
Important Public Health Problem ◽  
The Impact

Diarrheal disease is still the most prevalent and important public health problem in developing countries, despite advances in knowledge, understanding, and management that have occurred over recent years. Diarrhea is the leading cause of death in children under 5 years of age. The impact of diarrheal diseases is more severe in the earliest periods of life, when taking into account both the numbers of episodes per year and hospital admission rates. This narrative review focuses on one of the major driving forces that attack the host, namely the enteropathogenic Escherichia coli (EPEC) and the consequences that generate malnutrition in an early phase of life. EPEC serotypes form dense microcolonies on the surface of tissue-culture cells in a pattern known as localized adherence (LA). When EPEC strains adhere to epithelial cells in vitro or in vivo they cause characteristic changes known as Attaching and Effacement (A/E) lesions. Surface abnormalities of the small intestinal mucosa shown by scanning electron microscopy in infants with persistent diarrhea, although non-specific, are intense enough to justify the severity of the clinical aspects displayed in a very young phase in life. Decrease in number and height of microvilli, blunting of borders of enterocytes, loss of the glycocalyx, shortening of villi and presence of a mucus pseudomembrane coating the mucosal surface were the abnormalities observed in the majority of patients. These ultrastructural derangements may be due to an association of the enteric enteropathogenic agent that triggers the diarrheic process and the onset of food intolerance responsible for perpetuation of diarrhea. An aggressive therapeutic approach based on appropriate nutritional support, especially the utilization of human milk and/or lactose-free protein hydrolyzate-based formulas and the adequate correction of the fecal losses, is required to allow complete recovery from the damage caused by this devastating enteropathogenic agent.

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