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Staphylococcal enterotoxins G and I, a cause of severe but reversible neonatal enteropathy.

Staphylococcal enterotoxins G and I, a cause of severe but reversible neonatal enteropathy. Research Abstract Details 

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  • Staphylococcal enterotoxins G and I, a cause of severe but reversible neonatal enteropathy. Abstract Text:

    sandhia naikSandhia Naik,fabienne smithFabienne Smith,john hoJohn Ho,nicholas m croftNicholas M Croft,paola domizioPaola Domizio,elisabeth priceElisabeth Price,ian r sandersonIan R Sanderson,nigel j meadowsNigel J Meadows,sandhia naikSandhia Naik,fabienne smithFabienne Smith,john hoJohn Ho,nicholas m croftNicholas M Croft,paola domizioPaola Domizio,elisabeth priceElisabeth Price,ian r sandersonIan R Sanderson,nigel j meadowsNigel J Meadows,

    BACKGROUND & AIMS: Staphylococcus aureus is recognized to produce toxins A-E and toxic shock syndrome toxin-1 associated with food poisoning and toxic shock syndrome. Enterotoxins G and I co-exist in the same S aureus strains (staphylococcal enterotoxin G and staphylococcal enterotoxin I) and are implicated in scarlet fever and toxic shock. We report these enterotoxins as causative agents of 2 cases of neonatal intractable diarrhea with enteropathy. METHODS: We used a note review for this study. Stool culture, multiplex polymerase chain reaction for enterotoxin, duodenal biopsy specimens for H&E, periodic acid-Schiff staining, and electron microscopy were used. RESULTS: Infant 1 had diarrhea from age 2 weeks and was referred at age 5 weeks with weight less than the 0.4th percentile. Infant 2 was referred at age 7 weeks with 4 weeks' of diarrhea, weight less than the 0.4th percentile. Both infants were severely malnourished. Elemental feeds were not tolerated and total parenteral nutrition was required. S aureus producing staphylococcal enterotoxin G and staphylococcal enterotoxin I was isolated in stools from both infants. Clinical improvement occurred after intravenous flucloxacillin and parenteral nutrition. Histology showed subtotal villous atrophy (H&E) with abnormal brush border (periodic acid-Schiff). Electron microscopy showed severe microvilli destruction, dilated mitochondria, and lysosomes containing cellular debris. Repeat histology was normal in infant 2, age 3 months, off parenteral nutrition, showed return to normal. Currently, both infants are 2 years of age and are thriving on a normal diet. CONCLUSIONS: Staphylococcal enterotoxin G- and I-induced enteropathy is a life-threatening condition, causing reversible disruption of enterocyte ultrastructure that responds well to supportive treatment with flucloxacillin and parenteral nutrition This condition should be a differential diagnosis of neonatal early onset diarrhea.

    Staphylococcal enterotoxins G and I, a cause of severe but reversible neonatal enteropathy. Publishing Authors By Initials

    s naikS Naik,f smithF Smith,j hoJ Ho,nm croftNM Croft,p domizioP Domizio,e priceE Price,ir sandersonIR Sanderson,nj meadowsNJ Meadows,s naikS Naik,f smithF Smith,j hoJ Ho,nm croftNM Croft,p domizioP Domizio,e priceE Price,ir sandersonIR Sanderson,nj meadowsNJ Meadows,

    For similar abstracts research abstracts see: abstracts research

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    Staphylococcal enterotoxins G and I, a cause of severe but reversible neonatal enteropathy. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Clinical gastroenterology and hepatology : the off

    VOLUME: 6

    Page Numbers: 251-4

    Journal Abbreviation: Clin. Gastroenterol. Hepatol.

    ISSN: 1542-7714

    DAY: 11

    MONTH: 12

    YEAR: 2007

    Staphylococcal enterotoxins G and I, a cause of severe but reversible neonatal enteropathy. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 101160775

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    Grant and Affiliation Information for Staphylococcal enterotoxins G and I, a cause of severe but reversible neonatal enteropathy.

    AFFILIATION: Department of Paediatric Gastroenterology, Barts and the London NHS Trust, London, United Kingdom. Sandhia.naik@bartsandthelondon.nhs.uk

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Clin Gastroenterol Hepatol

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