PMID- 18971368 OWN - NLM STAT- MEDLINE DCOM- 20090202 LR - 20220408 IS - 1098-660X (Electronic) IS - 0095-1137 (Print) IS - 0095-1137 (Linking) VI - 47 IP - 1 DP - 2009 Jan TI - Phenotypic and genotypic analysis of enterotoxigenic Escherichia coli in samples obtained from Egyptian children presenting to referral hospitals. PG - 189-97 LID - 10.1128/JCM.01282-08 [doi] AB - Hospital surveillance was established in the Nile River Delta to increase the understanding of the epidemiology of diarrheal disease among Egyptian children. Between September 2000 and August 2003, samples obtained from children less than 5 years of age who had diarrhea and who were seeking hospital care were cultured for enteric bacteria. Colonies from each culture with a morphology typical of that of Escherichia coli were tested for the heat-labile (LT) and heat-stable (ST) toxins by a GM-1-specific enzyme-linked immunosorbent assay and colonization factor (CF) antigens by an immunodot blot assay. Enterotoxigenic E. coli (ETEC) isolates were recovered from 320/1,540 (20.7%) children, and ETEC isolates expressing a known CF were identified in 151/320 (47%) samples. ST CFA/I, ST CS6, ST CS14, and LT and ST CS5 plus CS6 represented 75% of the CFs expressed by ETEC isolates expressing a detectable CF. Year-to-year variability in the proportion of ETEC isolates that expressed a detectable CF was observed (e.g., the proportion that expressed CFA/I ranged from 10% in year 1 to 21% in year 3); however, the relative proportions of ETEC isolates expressing a CF were similar over the reporting period. The proportion of CF-positive ETEC isolates was higher among isolates that expressed ST. ETEC isolates expressing CS6 were isolated significantly less often (P < 0.001) than isolates expressing CFA/I in children less than 1 year of age. Macrorestriction profiling of CFA/I-expressing ETEC isolates by using the restriction enzyme XbaI and pulsed-field gel electrophoresis demonstrated a wide genetic diversity among the isolates that did not directly correlate with the virulence of the pathogen. The genome plasticity demonstrated in the ETEC isolates collected in this work suggests an additional challenge to the development of a globally effective vaccine for ETEC. FAU - Shaheen, H I AU - Shaheen HI AD - U.S. Naval Medical Research Unit No. 3, Cairo, Egypt. hind.shaheen.eg@med.navy.mil FAU - Abdel Messih, I A AU - Abdel Messih IA FAU - Klena, J D AU - Klena JD FAU - Mansour, A AU - Mansour A FAU - El-Wakkeel, Z AU - El-Wakkeel Z FAU - Wierzba, T F AU - Wierzba TF FAU - Sanders, J W AU - Sanders JW FAU - Khalil, S B AU - Khalil SB FAU - Rockabrand, D M AU - Rockabrand DM FAU - Monteville, M R AU - Monteville MR FAU - Rozmajzl, P J AU - Rozmajzl PJ FAU - Svennerholm, A M AU - Svennerholm AM FAU - Frenck, R W AU - Frenck RW LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20081029 PL - United States TA - J Clin Microbiol JT - Journal of clinical microbiology JID - 7505564 RN - 0 (Bacterial Toxins) RN - 0 (DNA, Bacterial) RN - 0 (Enterotoxins) RN - 0 (Escherichia coli Proteins) RN - 0 (colonization factor antigens) RN - 0 (heat stable toxin (E coli)) RN - 147680-16-8 (Fimbriae Proteins) RN - D9K3SN2LNY (heat-labile enterotoxin, E coli) RN - EC 3.1.21.- (endodeoxyribonuclease XBAI) RN - EC 3.1.21.4 (Deoxyribonucleases, Type II Site-Specific) SB - IM MH - Bacterial Toxins/biosynthesis MH - Child, Preschool MH - Cluster Analysis MH - DNA Fingerprinting MH - DNA, Bacterial/metabolism MH - Deoxyribonucleases, Type II Site-Specific/metabolism MH - Diarrhea/epidemiology/*microbiology MH - Egypt/epidemiology MH - Electrophoresis, Gel, Pulsed-Field MH - Enterotoxigenic Escherichia coli/classification/*genetics/isolation & purification/*metabolism MH - Enterotoxins/biosynthesis MH - Escherichia coli Infections/epidemiology/*microbiology MH - Escherichia coli Proteins/biosynthesis MH - Fimbriae Proteins/biosynthesis MH - Genetic Variation MH - Hospitals MH - Humans MH - Infant MH - Infant, Newborn MH - Molecular Epidemiology MH - Polymorphism, Restriction Fragment Length PMC - PMC2620865 EDAT- 2008/10/31 09:00 MHDA- 2009/02/03 09:00 PMCR- 2009/07/01 CRDT- 2008/10/31 09:00 PHST- 2008/10/31 09:00 [pubmed] PHST- 2009/02/03 09:00 [medline] PHST- 2008/10/31 09:00 [entrez] PHST- 2009/07/01 00:00 [pmc-release] AID - JCM.01282-08 [pii] AID - 1282-08 [pii] AID - 10.1128/JCM.01282-08 [doi] PST - ppublish SO - J Clin Microbiol. 2009 Jan;47(1):189-97. doi: 10.1128/JCM.01282-08. Epub 2008 Oct 29.