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Escherichia coli O.128 Causing Gastro-enteritis of Infants

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... Escherichia coli strains of serogroup 0128 were first isolated by Taylor and Charter from cases of infantile diarrhea (25). These authors described six serotypes (O:H types) in this serogroup: H-(nonmotile), H2 (most common), H8, H9, H10, and H12. ...
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Strains of three subgroups of Escherichia coli O128 were studied. Enterotoxin production was observed in 30 (91%) O128ac strains, whereas strains of subgroups O128ab and O128ad were not toxigenic. CFA/I was only found in two serotypes of subgroup O128ac, all of them producing heat-stable enterotoxin except for one which produced both toxins. None of the strains studied produced CFA/II. In a binding test with HeLa cells, localized adherence was found only in strains of subgroup O128ab; diffuse adherence occurred in strains of subgroup O128ac. As flagellar antigens were specific in subgroups ab and ac and toxin production was observed only in subgroup ac, the present results suggest that subgroup and serotype are useful markers for O128 strains that are enterotoxigenic or enteropathogenic.
... The remaining 42 isolates (which possessed eae alone) belonged to 25 serotypes and 11 intimin types. Several of the 42 eae , stx , and ehxA isolates, including isolates of serotypes O26:H (Int-), O55:H6 (Int-1), O86:H (Int-), O111:H (Int-), O126:H2 (Int-), O127:H (Int-1), and O128:H2 (Int-), were isolated prior to 1955 (25,33,34,(45)(46)(47); and the majority of these were from patients with infantile diarrhea. Thus, these isolates probably represent typical EPEC isolates, although further studies are needed to confirm this. ...
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The intimin gene eae, located within the locus of enterocyte effacement pathogenicity island, distinguishes enteropathogenic Escherichia coli (EPEC) and some Shiga toxin-producing E. coli (STEC) strains from all other pathotypes of diarrheagenic E. coli. EPEC is a leading cause of infantile diarrhea in developing countries, and intimin-positive STEC isolates are typically associated with life-threatening diseases such as hemolytic-uremic syndrome and hemorrhagic colitis. Here we describe the development of a PCR-restriction fragment length polymorphism (RFLP) assay that reliably differentiates all 11 known intimin types (alpha1, alpha2, beta, gamma, kappa, epsilon, eta, iota, lambda, theta, and zeta) and three new intimin genes that show less than 95% nucleotide sequence identity with existing intimin types. We designated these new intimin genes Int- micro, Int-nu, and Int-xi. The PCR-RFLP assay was used to screen 213 eae-positive E. coli isolates derived from ovine, bovine, and human sources comprising 60 serotypes. Of these, 82 were STEC isolates, 89 were stx-negative (stx(-)) and ehxA-positive (ehxA(+)) isolates, and 42 were stx(-) and ehxA-negative isolates. Int-beta, the most commonly identified eae subtype (82 of 213 [38.5%] isolates), was associated with 21 serotypes, followed by Int-zeta (39 of 213 [18.3%] isolates; 11 serotypes), Int-theta (25 of 213 [11.7%] isolates; 15 serotypes), Int-gamma (19 of 213 [8.9%] isolates; 9 serotypes), and Int-epsilon (21 of 213 [9.9%] isolates; 5 serotypes). Intimin subtypes alpha1, alpha2, kappa, lambda, xi, micro, nu, and iota were infrequently identified; and Int-eta was not detected. Phylogenetic analyses with the Phylip package of programs clustered the intimin subtypes into nine distinct families (alpha, beta-xi, gamma, kappa, epsilon-eta-nu, iota- micro, lambda, theta, and zeta). Our data confirm that ruminants are an important source of serologically and genetically diverse intimin-containing E. coli strains.
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Foram estudadas 103 cepas de Escherichia coli do sorogrupo O128, quanto às características fenotípicas e genotípicas associadas à virulência. Cinqüenta e nove cepas representantes de todos os sorotipos foram submetidas a ribotipagem. Os sorotipos mais freqüentes foram O128:H35 (41,7%), O128:H2 (14,6%), O128:H- (8,7%) e O128:H8 (6,8%). Diferentes grupos enteropatogênicos foram identificados. Somente as cepas do sorotipo O128:H2 foram positivas para as sondas eae and bfpA e apresentaram o padrão de adesão AL-like. Cepas do sorotipo O128:H8 e algumas imóveis reagiram apenas com a sonda eae e foram classificadas como EPEC atípicas. As cepas O128:H35 corresponderam à categoria enteroagregativa e os sorotipos O128:H7, O128:H21, O128:H27 e as cepas imóveis foram classificadas como enterotoxigênicas. Todas as cepas que apresentaram marcadores de virulência pertenciam ao grupo clonal A, enquanto que no grupo clonal B estavam incluídas as cepas desprovidas dos fatores de virulência pesquisados.
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In den Jahren 1957–1960 wurden am Hygiene-Institut Frankfurt am Main 8773 Stuhluntersuchungen auf D.-Colibakterien durchgefhrt, von denen 2470, das sind 28,60%, positiv waren. Die Hufigkeit der einzelnen Typen wird aufgezeigt. Besonders auffallend ist dabei der Rckgang der D.-Coli 0111:B4 und 055:B5 und der sprunghafte Anstieg des Typs 0127:B8, auf dessen klinische Bedeutung besonders hingewiesen wird. Ergnzend wird ber zwei 0127:B8-Krankenhausendemien berichtet.
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SUMMARY : Hydrogen sulphide production by growing cultures and non-multi- plying suspensions was compared and the factors influencing the sensitivity of the tests were investigated. Cysteine hydrochloride (0.01 yo) was added to Lemco broth to provide a medium with a standard source of sulphur. H,S was detected with lead acetate papers more readily than by lead acetate agar. Suspensions were tested with cysteine, sodium thiosulphate and sodium sulphite ; the organisms investigated were mainly Bacteriaceae and seldom failed to produce H,S from cysteine ; sodium thiosulphate was less readily attacked ; sodium sulphite was unsuitable for this technique. Media commonly used for testing the capacity of bacteria to produce H,S are reviewed and the value of this test in bacterial classifica- tion discussed. Hydrogen sulphide was one of the earliest products of bacterial decomposition to be recognized. Orlowski (1895) described H2S production by the typhoid bacillus, and Burnet & Weissenbach (1915) and Jordan & Victorson (1917) in comparative studies used H,S production to distinguish between the para- typhoid and enteritidis groups. Sasaki & Otsuka (1912) and Burger (1914) showed that many different species of bacteria produced H2S from cystine but not from taurine. Tanner (1917) found that a large number of bacteria produced H2S from peptone or cystine, and some from thiourea and thio- sulphate, though none examined produced it from sulphate or sulphite. Myers (1920) and Tilley (1923a, b) found variations in H,S production from different peptones; Tilley concluded that this was not directly related to the cystine content of the peptone. He tested media reinforced with cystine, thiosulphate, sulphite and sulphate, and concluded that a thiosulphate medium was most useful for diagnostic use. Wilson (1922-3) showed that the typhoid and paratyphoid bacteria could produce H2S from sulphite in the presence of a fermentable carbohydrate and recommended an iron + sul- phite +glucose organic medium. Tarr (1933a, b) showed that the production of H2S from cystine and cysteine by washed suspensions of Proteus vulgaris and Chromobacterium prodigiosum was enzymic ; he obtained a cell-free preparation from Proteus (Tarr, 1934). He also found that the production of H2S by Proteus from cysteine and thiosulphate was additive and independent and therefore due to two distinct enzyme systems. The cysteine enzyme was shown to be highly specific and only attacked compounds containing the a-amino-P-thiolcarboxylic acid structure. Desnuelle & Fromageot (1939) obtained a cell-free enzyme preparation from Bacterium coli to which they gave the name cysteinase. This enzyme was investigated in a number of species by Desnuelle & Fromageot (1939) and by Desnuelle, Wookey & Fromageot (1940). Fromageot (1951) concluded that cysteinase occurs in all GM VIII 3 26
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Strains of Aerobacter aerogenes, A. cloacae and Escherichia coli, including mucoid capsulate, mucoid non-capsulate, smooth and rough variant forms, were grown on defined agar media. The polysaccharide content of the cultures was estimated by the anthrone method and related to the amount of growth as measured by the non-dialysable nitrogen content. Polysaccharide production, as measured by the polysaccharide : nitrogen ratio, was increased in all strains when growth was limited by a restricted supply of nitrogen source so that added carbohydrate remained in relative excess. A low incubation temperature, 15-20° instead of 35O, influenced polysaccharide production differently in the various strains and species ; thus it greatly increased production in E. coli strains, but decreased it in A. cloacae strains grown on certain media. The various strains showed considerable differences in the amount of polysaccharide production and in the distribution of the polysaccharide between the different possible sites of accumulation : i.e. intracellular, capsular and as loose slime. The mucoid strains produced the largest amounts of polysaccharide, most of which was present extracellularly as capsuIes or slime; the smooth strains produced much smaller amounts, almost entirely intracellular; a rough strain pro- duced least of all. The antigenic constitution of certain strains was examined, particularly that of a mucoid capsulate A. aerogenes and mucoid non-capsulate and non-mucoid smooth variants derived from it. The designation of such morphological and immunological variants is discussed. The amount of polysaccharide produced varies greatly with different strains and species of Enterobacteriaceae. Among twelve strains of Escherichia coli grown at 13-17' on glucose medium, Morgan & Beckwith (1939) found that the amount of polysaccharide produced, as indicated by the degree of mucoid- ness, was large in five strains, moderate in two strains and small in the remainder ; they found similar differences among salmonella strains. Mucoid, smooth and rough variants of the same strain may also show great differences in polysaccharide production. Boivin, Mesrobeanu, Magheru & Magheru (1936) measured the amount of a polysaccharide-containing substance, the ' complete antigen ', which was extracted with trichloroacetic acid from cultures of E. coli. Large amounts of this (0.41-0.98 mg./loo mg. moist culture) were found in all of six ' smooth ' strains which gave smooth colonies and were not agglutinable by trypaflavine, while none was found in five of
Serological Typing of the Colon Bacteria
  • Munksgaard
Munksgaard, Serological Typing of the Colon Bacteria. Acta J. gen. 281
Acta path. microbiol. scand
  • S D Henriksen
  • Henriksen, S.D.