scholarly journals Enteroaggregative Escherichia coli strain in a novel weaned mouse model: exacerbation by malnutrition, biofilm as a virulence factor and treatment by nitazoxanide

2013 ◽  
Vol 62 (6) ◽  
pp. 896-905 ◽  
Author(s):  
David T. Bolick ◽  
James K. Roche ◽  
Raquel Hontecillas ◽  
Josep Bassaganya-Riera ◽  
James P. Nataro ◽  
...  

Enteroaggregative Escherichia coli (EAEC) is increasingly recognized as a common cause of diarrhoea in healthy, malnourished and immune-deficient adults and children. There is no reproducible non-neonatal animal model for longitudinal studies of disease mechanism or therapy. Using two strains of human-derived EAEC to challenge weaned C57BL/6 mice, we explored an in vivo model of EAEC infection in mice, in which disease was monitored quantitatively as the growth rate, stool shedding and tissue burden of organisms; nutritional status was varied, and a new class of therapeutics was assessed. A single oral challenge of EAEC strain 042 resulted in significant growth shortfalls (5–8 % of body weight in 12 days), persistent shedding of micro-organisms in stools [>103.2 c.f.u. (10 mg stool)−1 for at least 14 days] and intestinal tissue burden [~103 c.f.u. (10 mg tissue)−1 detectable up to 14 days post-challenge]. Moderate malnourishment of mice using a ‘regional basic diet’ containing 7 % protein and reduced fat and micronutrients heightened all parameters of infection. Nitazoxanide in subMIC doses, administered for 3 days at the time of EAEC challenge, lessened growth shortfalls (by >10 % of body weight), stool shedding [by 2–3 logs (10 mg stool)−1] and tissue burden of organisms (by >75 % in the jejunum and colon). Thus, weaned C57BL/6 mice challenged with EAEC is a convenient, readily inducible model of EAEC infection with three highly quantifiable outcomes in which disease severity is dependent on the nutritional status of the host, and which is modifiable in the presence of inhibitors of pyruvate ferredoxin oxidoreductase such as nitazoxanide.

Author(s):  
Eva Diansari ◽  
Edy Suwarso ◽  
Aminah Dalimunthe

Objective: Kecapi bark (Sandoricum koetjape Merr.) is a plant of the Meliaceae family that is often used by people to treat diarrhea and abdominal pain. This study aims to determine the effects of antidiarrheal from the ethanol extract of the Kecapi stem bark on induced with castor oil and bacteria Escherichia coli.Methods: Before the in vivo on male guinea pig test was switched first, then 10 ml of castor oil was induced and 7.7 ml of E. coli male guinea pig was induced, then each male guinea was given a variation of dose ethanol extract kecapi stem bark and loperamide as the comparison. Parameters measured in this study were the start time of diarrhea, consistency of feces, frequency, and duration of diarrhea.Result: The results obtained showed that ethanol extract of kecapi bark antidiarrheal effect on guinea pigs induced castor oil (dose of 800 mg/kg body weight) and E. coli.Conclusion: Ethanol extract of Kecapi bark has an activity of antidiarrheal..


2012 ◽  
Vol 1 (4) ◽  
pp. 27 ◽  
Author(s):  
Roseline Ekiomado Uzeh ◽  
Chinwe Amaka Okolo ◽  
Bamidele Abiodun Iwalokun

<p>This study was undertaken to isolate <em>Escherichia coli </em>O157:H7 from salad vegetables, determine its pathogenicity and effect on the gastrointestinal tract of mice and sensitivity to probiotics; <em>Lactobacillus lactis </em>ATCC12315 and <em>Lactobacillus acidophilus </em>ATCC4356 in-vivo. Twenty seven samples made up of eight different types of salad vegetables which includes carrot, cabbage, cucumber, lettuce, peas, green pepper, green beans and spring onions were collected from different locations; markets, farm and street vendors in Lagos, Nigeria. Sampling was done between 13<sup>th</sup> October 2009 and 17<sup>th</sup> March 2010. In all experiments with mice the protocol for care of animal was carried out according to National Institute of Health (NIH). The mice given only <em>E. coli </em>O157:H7 developed diarrhea which led to loss of body weight and death of majority of them. On the other hand mice that were not given any microbial suspension (control), those given only probiotics, combination of <em>E. coli</em> O157:H7 and probiotics showed no symptom of diarrhea and there was increase in their body weight. The histopathology of the intestines of this group of mice showed that their intestines were not damaged, while those given only <em>E. coli</em> O157:H7 showed lymphoid hyperplasia, mucosal sloughing and inflammation (enteritis). The maintenance of good health by probiotics has again been re-emphasized.</p>


1974 ◽  
Vol 52 (10) ◽  
pp. 854-866 ◽  
Author(s):  
Theodore C. Y. Lo ◽  
M. Khalil Rayman ◽  
B. D. Sanwal

The D-lactate oxidation dependent transport of succinate in membrane vesicles of an Escherichia coli strain lacking succinate dehydrogenase and fumarate reductase is inhibited by several categories of compounds. One category consists of compounds that are electron transport inhibitors (Amytal, Dicumarol, and mercurials), the second of compounds that act as competitive inhibitors of D-lactate dehydrogenase (oxamate and β-chlorolactate), the third of reagents that inhibit the Ca2+–Mg2+-activated ATPase (dicyclohexylcarbodiimide and pyrophosphate), and the fourth of compounds that tap off electrons from the respiratory chain (2,6-dichlorophenolindophenol). None of the succinate transport inhibitors, including mercurials like p-chloromercuribenzoate, interfere with the binding of succinate to the presumed membrane carriers.Membrane preparations from mutants of E. coli lacking D-lactate dehydrogenase are unable to transport succinate in the presence of D-lactate. Whole cells of these mutants, however, take up succinate normally. This observation suggests that D-lactate oxidation is not obligatorily linked in vivo to the uptake of succinate although the possibility is not excluded that transport in such mutants may be linked to some other dehydrogenase. Mutants having altered levels of ATPase, or membrane preparations made from such cells also have greatly reduced capacity to transport succinate. This observation coupled with the finding that ATPase inhibitors block dicarboxylate transport suggests involvement of ATPase in an unknown way in the concentrative uptake of succinate.With the exception of oxamate, β-chlorolactate (competitive inhibitors of D-lactate oxidation), and dicyclohexylcarbodiimide, all of the inhibitors of succinate uptake (including p-chloromercuribenzoate) cause an immediate efflux of preloaded succinate from membrane vesicles. Efflux is also caused by proton conducting reagents. The Km for efflux is 1.9 mM. This value is to be compared with the Km for influx, which is only about 0.02 mM.The weight of evidence favors the view that the active transport of succinate in vesicles occurs as a result of an energization of the membranes by the passage of electrons, although alternate oxidation and reduction of the succinate carrier as a mechanism for transport has not been definitely ruled out.


2002 ◽  
Vol 46 (7) ◽  
pp. 2310-2312 ◽  
Author(s):  
Qiu N. Sun ◽  
Laura K. Najvar ◽  
Rosie Bocanegra ◽  
David Loebenberg ◽  
John R. Graybill

ABSTRACT The in vivo activities of posaconazole, itraconazole, and amphotericin B in neutropenic mice with zygomycosis were compared. The in vitro MICs of posaconazole and itraconazole for the strains of Mucor spp. used in this study ranged from 0.125 to 8 μg/ml and 0.25 to 8 μg/ml, respectively. The in vitro MIC range for amphotericin B is 0.125 to 0.25 μg/ml. At twice-daily doses of ≥15 mg/kg of body weight, posaconazole prolonged the survival of the mice and reduced tissue burden.


2008 ◽  
Vol 100 (03) ◽  
pp. 530-541 ◽  
Author(s):  
Leo R. Fitzpatrick ◽  
Jeffrey Small ◽  
Robert A. Hoerr ◽  
Eileen F. Bostwick ◽  
Lynn Maines ◽  
...  

2013 ◽  
Vol 164 (2) ◽  
pp. 238-247 ◽  
Author(s):  
Shashank Ghanegaonkar ◽  
Jürgen Conrad ◽  
Uwe Beifuss ◽  
Georg A. Sprenger ◽  
Christoph Albermann
Keyword(s):  

1985 ◽  
Vol 25 (1A) ◽  
pp. 49-60 ◽  
Author(s):  
J. P. CHAPPUIS ◽  
Yvonne DUVAL-IFLAH ◽  
R. DUCLUZEAU ◽  
P. RAIBAUD ◽  
Marie-France OURIET ◽  
...  

1978 ◽  
Vol 174 (1) ◽  
pp. 1-7 ◽  
Author(s):  
G Delcuve ◽  
T Cabezón ◽  
A Herzog ◽  
M Cannon ◽  
A Bollen

A spontaneous mutant of Escherichia coli (strain AB2847), selected for resistance to the aminoglycoside antibiotic neamine, shows severe restriction of amber suppressors in vivo. Ribosomes isolated from the mutant exhibit only low misreading in vitro in the presence of the antibiotic. Genetic and biochemical analyses indicate that the neamine-resistant phenotype is the result of two distinct mutations. The first, res3128, appears to affect the gene (strA) coding for the ribosomal protein S12. Although it leads to a restrictive phenotype it does not, however, confer resistance to streptomycin. The second mutation, X3128, is located between the sirA and AROB loci and is lethal when segregated from the res3128 mutation. It may affect the ribosome at the level of a post-translational modification.


2005 ◽  
Vol 61 (3) ◽  
pp. 389-398 ◽  
Author(s):  
Michael Schultz ◽  
Sonja Watzl ◽  
Tobias A. Oelschlaeger ◽  
Heiko C. Rath ◽  
Claudia Göttl ◽  
...  

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