1 / 55

ENTEROPATHOGENIC ESCHERICHIA COLI I

ENTEROPATHOGENIC ESCHERICHIA COLI I. Hin-chung Wong Department of Microbiology Soochow University. Content. INTRODUCTION HEAT-LABILE ENTEROTOXINS General Characteristics Gene and Regulation Mode of Action HEAT-STABLE ENTEROTOXINS

edwardbradley
Télécharger la présentation

ENTEROPATHOGENIC ESCHERICHIA COLI I

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. ENTEROPATHOGENICESCHERICHIA COLII Hin-chung Wong Department of Microbiology Soochow University

  2. Content • INTRODUCTION • HEAT-LABILE ENTEROTOXINS • General Characteristics • Gene and Regulation • Mode of Action • HEAT-STABLE ENTEROTOXINS • General Characteristics • Mode of Action and Regulation • ENTEROTOXIN PLASMIDS • SHIGA-LIKE TOXINS • Purification and Structure • Mode of Action • Production and Regulation • Genetics • Role in Disease • HEMOLYSINS • Production and Purification • Characteristics • Genetics • Role in Virulence and Mode of Action

  3. Content • ADHERENCE • In Enterotoxigenic E. coli • In Enteropathogenic E. coli • In Enterohemorrhagic E. coli • INVASIVENESS • DETECTION • Using glucuronidase assay • Animal Tissue Culture • Animal Assays • Immunological Methods • Enzymatic bio-nanotransduction • Nucleic Acid Probes • Using polymerase chain reaction

  4. INTRODUCTION • E. coli is usually considered to be an opportunistic pathogen which constitutes a large portion of the normal intestinal flora of humans • This organism can, however, contaminate, colonize, and subsequently cause infection of extraintestinal sites and is a major cause of septicemia, peritonitis, abscesses, meningitis, and urinary tract infections in humans

  5. INTRODUCTION • E. coli was first incriminated as an enteropathogen in 1945, responsible for an outbreak of infantile diarrhea • Enteropathogenic E. coli (EEC) has been associated with diarrhea in developing countries and localities having poor sanitation • In the developed countries, EEC has been historically associated primarily with infantile diarrhea, but it was later recognized that adults also may suffer from the illness • E. coli are also enteropathogenic in animals

  6. INTRODUCTION • E. coli O157:H7 causes severe illneses (hemorrhagic) and it does possess distinguishing characteristics, e.g. does not ferment sorbitol within 24 h, does not possess α-glucuronidase activity, and does not grow well at all at 44-45.5C

  7. INTRODUCTION • There are several subgroups of EEC • (A) enterotoxigenic (ETEC) • (B) enteroinvasive (EIEC) • (C) hemorrhagic (EHEC) • (D) enteropathogenic (EPEC) strains • Some authors classify them into six different pathotypes: ETEC, EIEC, EPEC, enteroaggregative E. coli, diffusely adherent E. coli, and Shiga toxin-producing E. coli (STEC)

  8. INTRODUCTION • In 1995, the enteropathogenic E. coli (EPEC) pathotype is divided into two groups, typical EPEC (tEPEC) and atypical EPEC (aEPEC) • The property that distinguishes these two groups is the presence of the EPEC adherence factor plasmid (pEAF), which is only found in tEPEC • aEPEC strains are emerging enteropathogens that have been detected worldwide • The large variety of serotypes and genetic virulence properties of aEPEC strains from nonclassical EPEC serogroups makes it difficult to determine which strains are truly pathogenic

  9. INTRODUCTION • Humans are thought to be the principal if not the only reservoir of toxigenic and invasive strains of E. coli, contaminating foods via contact with food or via contact of processing equipment with water contaminated by human feces • In contrast, animals are reservoirs of the hemorrhagic strain (O157:H7); hence, foods of animal origin may become contaminated via slaughter procedures or post-processing recontamination • However, when E. coli is isolated from foods, pathogenic serotypes are usually absent or represent a very low percentage of the total isolates

  10. HEAT-LABILE ENTEROTOXINS • Probably the most common type of EEC strains is the enterotoxigenic type. Heat-labile (LT) and heat-stable (ST) enterotoxins are produced. • Two partially cross-reacting antigenic variants of plasmid-coded LT, designated LTh and LTp, have been described in E. coli • LTh is associated with E. coli isolates from humans, and LTp is associated with E. coli isolates from pigs • The LT family from restricted geographical region exhibited a segregated pattern of dissemination that was revealed by a restriction enzyme site polymorphism

  11. HEAT-LABILE ENTEROTOXINS • Another heat-labile enterotoxin was discovered in extracts of E. coli SA53, a strain isolated from water buffalo • It activated adenylate cyclase. • Hyperimmune antisera prepared against LTh and LTp or CT do not neutralize the crude LT-like toxin in Y1 adrenal cell assays

  12. HEAT-LABILE ENTEROTOXINS • Subcloning and minicell experiments indicated that the toxin is composed of two polypeptide subunits that are encoded by two genes • The two toxin subunits exhibited mobilities on PAGE gels that are similar to those of CT and LT

  13. HEAT-LABILE ENTEROTOXINS

  14. HEAT-LABILE ENTEROTOXINS • The LT gene was cloned into E. coli and two proteins of molecular weights 11,500 (B subunit) and 25,500 (A subunits) were produced • The LT A subunit structureal gene (eltA) was sequenced and the amino acid sequence deduced

  15. HEAT-LABILE ENTEROTOXINS • It is proposed by Pickett et al. that the LTp and LTh (antigenic variants of LT will both be included in serogroup I and should be designated LTp-I and LTh-I and the LT-like toxin will be the prototype for serogroup II enterotoxins and should be renamed LT-II. • Two distinct members of the LT-II family, LT-IIa and LT-IIb, are now known, and both have A and B subunits which are similar in size to those of CT and LT-I

  16. HEAT-LABILE ENTEROTOXINS • It starts with methionine, ends with leucine, and comprises 254 amino acids • The computed molecular weight of LT A is 29,673. • The A subunit genes of CT and LT (LT-I) are 78.6% homologous, and the B subunit genes are 78% homologous • The NH2-terminal regions exhibit the highest degree of homology (91%) as compared with CT subunit A, while the COOH-terminal region, containing the sole cystine residue in each toxin is less conserved (52%) • Alignment of homologous residues in the COOH-terminal regions of LT A and CT A indicates that a likely site for proteolytic cleavage of LT A is after Arg residue 188

  17. HEAT-LABILE ENTEROTOXINS • The gene of LT-IIa was studied. It is organized in a transcriptional unit similar to those of CT and LT-I • The A subunit gene of LT-IIa was found to be 57% homologous with the A subunit gene of LTh-I and 55% homologous with the A gene of CT • Most of the homology derived from the region of the A gene which encodes the A1 fragment • The B gene of LT-IIa was not homologous with the B gene of LTh-I or CT

  18. HEAT-LABILE ENTEROTOXINS • The LT-IIb gene was also cloned and analysed. • The A genes of LT-IIa and LT-IIb exhibited 71% DNA sequence homology with each other and 55 to 57% homology with the A genes of CT and LT-I. • The B subunits of LT-IIa and LT-IIb differ from the LT-I in their carbohydrate-binding specificities. • The B genes of LT-IIa and LT-IIb were 66% homologous, but neither had significant homology with the B genes of CT and LT-Is. • The A subunits of the heat-labile enterotoxins also have limited homology with other ADP-ribosylating toxins, including pertussis toxin, diphtheria toxin, and Pseudomonas aeruginosa exotoxin A ADP-ribosylation is the addition of one or more ADP-ribose moieties to a protein

  19. HEAT-LABILE ENTEROTOXINS • The carboxy-terminal domain of EtxB (encodes B subunit) mediates A subunit-B subunit interaction • The gene encoding the B subunit of LT was mutated at its 3' end by targeted addition of random nucleotide sequences • The functional and structural properties of the gene products were analysed, that these mutants were defective in their ability to associate stably with A subunits and form holotoxin

  20. HEAT-LABILE ENTEROTOXINS • Mode of Action • LT from E. coli is a protein of approximately 86,000 daltons that consists of one A polypeptide and five B polypeptides held together by noncovalent bonds • LT is closely related to cholera enterotoxin (CT) in structure, antigenicity, and mode of action. Both LT and CT bind to ganglioside GM1 receptors on eukaryotic target cells via their B subunits

  21. Ganglioside http://en.wikipedia.org/wiki/Ganglioside

  22. HEAT-LABILE ENTEROTOXINS • The A subunit of LT like CT undergoes a proteolytic cleavage that produces two fragments designated A1 and A2 • The A1 fragment catalyzes the NAD-linked ADP ribosylation of a regulatory subunit of adenylate cyclase in the plasma membrane of eucaryotic target cells, resulting in stimulation of adenylate cyclase activity • The activation of adenylate cyclase in mucosal cells in the small intestine causes secretion of fluid and electrolytes into the lumen and produces watery diarrhea.

  23. HEAT-LABILE ENTEROTOXINS • The LT-II, similar to CT and LT-I, increases cAMP by activating adenylate cyclase through the GTP-dependent ADP-ribosylation of specific membrane.

  24. HEAT-LABILE ENTEROTOXINS • Fibroblasts incubated with LT-II had an increased cAMP content (Fig. 2)

  25. HEAT-LABILE ENTEROTOXINS • as well as a fourfold elevation of membrane adenylate cyclase activity (Fig. 3).

  26. HEAT-LABILE ENTEROTOXINS • The B subunit of LTh (Human) is also hemagglutinating • Very strong hemagglutination of both neuraminidase- and pronase-treated human erythrocytes was induced by the B subunit of LTh. • Different blood groups reacted differently to such enhancement • Combining site of the B subunit may gain access to the receptor exposed on erythrocytes more easily by enzyme treatment. • Neuraminidase and pronase are suppose to convert major gangliosides to GM1 and/or expose masked receptors for the B subunit. Both CT and LT strongly react with ganglioside GM1.

  27. HEAT-LABILE ENTEROTOXINS • Separation of ETEC bacteria from target intestinal epithelial monolayers by semipermeable filters prevented activation of adenylate cyclase suggesting that pathogen-host cell contact is required for efficient toxin delivery • Likewise, a non-motile strain bearing a mutation in the flagellar fliD gene was deficient in delivery of LT relative to the ETEC prototype • Although LT secretion via the type II secretion system (T2SS) was responsive to a variety of environmental factors, neither toxin release nor delivery depended on transcriptional activation of genes encoding LT or the T2SS

  28. HEAT-LABILE ENTEROTOXINS • Enterotoxigenic E. coli LT-induced diarrhea is the leading cause of infant death in developing countries. • Ginger significantly blocked the binding of LT to cell-surface receptor G M1 (Fig. 4), resulting in the inhibition of fluid accumulation in the closed ileal loops of mice (Fig. 5).

  29. HEAT-LABILE ENTEROTOXINS

  30. HEAT-LABILE ENTEROTOXINS

  31. HEAT-LABILE ENTEROTOXINS • Biological-activity-guided searching for active components showed that zingerone (vanillylacetone) was the likely active constituent responsible for the antidiarrheal efficacy of ginger. • Further analysis of chemically synthesized zingerone derivatives revealed that compound 31 (2-[(4-methoxybenzyl)oxy] benzoic acid) significantly suppressed LT-induced diarrhea in mice via an excellent surface complementarity with the B subunits of LT(Fig. 6)

  32. HEAT-STABLE ENTEROTOXINS • The heat-stable enterotoxins are low-molecular-weight, heat-stable, nonantigenic proteins which do not cause intestinal secretion by activation of adenylate cyclase • At least two types have been described, one with biological activity in suckling mice and piglets (STa, or named as STh, or ST-I) due to stimulation of particulate intestinal guanylate cyclase and a second which induces secretion by an unknown mechanism only in piglets (STb, or known as STp, or ST-II).

  33. HEAT-STABLE ENTEROTOXINS • Generally STs are known to be small peptide toxins consisting of 18 (STb) or 19 (STa) amino acids. • The different STa (M.W. about 2,000) from different animal origins are remarkably homogeneous. • The amino acid composition of STa of porcine, bovine, and human origins were identical and consisted of 10 of the 18 amino acids usually present in proteins. • Six of the 18 amino acids were half-cystines which appear to be present as three disulfide bonds in the native form of the toxin. These disulfide bonds are important for toxic activity.

  34. HEAT-STABLE ENTEROTOXINS • STb is a heat-stable enterotoxin which does not cause intestinal fluid secretion in the suckling mouse as STa does, but does cause intestinal fluid secretion in pig intestinal loop assays. • It is insoluble in methanol, while STa is methanol-soluble

  35. HEAT-STABLE ENTEROTOXINS • Since STs are small peptides and are nonantigenic, fusion proteins (e.g. STa with outer membrane protein C, etc.) (Saarilahti et al., 1989) or synthetic ST peptide conjugated with ovalbumin could be use as the immunoprophylactic agents against diarrhea caused by STs.

  36. HEAT-STABLE ENTEROTOXINS • In a study, these two toxins were examined in terms of importance for piglets >1 week old with the construction of isogenic single- and double-deletion mutants and inoculation of 9-day-old F4ac receptor-positive gnotobiotic piglets. • Based on the postinoculation percent weight change per h and serum bicarbonate concentrations, the virulence of the STb- mutant (Delta estB) did not significantly differ from that of the parent. • However, deletion of the LT genes (Delta eltAB) in the STb(-) mutant resulted in a complete abrogation of weight loss, dehydration, and metabolic acidosis in inoculated pigs, and LT complementation restored the virulence of this strain.

  37. HEAT-STABLE ENTEROTOXINS • The cysteine residues were substituted in vivo by oligonucleotide-directed site-specific mutangenesis to dissociate each disulfide bond and examined the biological activitites of the resulting mutants (Fig.7, 8). • All three disulfide bonds formed at fixed positions are required for full expression of the biological activity of STb. • It has some fexibilities in its conformation to exert toxic activity and that the role of each disulfide bond in exerting toxic activity is not quite the same

  38. HEAT-STABLE ENTEROTOXINS

  39. HEAT-STABLE ENTEROTOXINS

  40. HEAT-STABLE ENTEROTOXINS • The STs share biologically active sequences which reside in the C-terminal 13 amino acid residues. Substitution of the asparagines residue at position 11 of STb by other amino acids resulted in significant decrease in enterotoxic activities, although the conformation was not changed (Okamoto et al., 1988). • The amino acid sequences and disulfide bonds of the heat-stable enterotoxins of E. coli, Yersinia enterocolitica, and Vibrio cholerae non-O1 are shown in Fig. 9

  41. HEAT-STABLE ENTEROTOXINS

  42. HEAT-STABLE ENTEROTOXINS • Analogs of ST were made, including the native 18-amino-acid ST, the 14-amino-acid carboxy terminus of this native peptide with a proline at position 12, and the 14-amino-acid carboxy terminus of in which the proline at position 12 was substituted with glycine (Table 1).

  43. HEAT-STABLE ENTEROTOXINS

  44. HEAT-STABLE ENTEROTOXINS • Each analog bound to the receptor in a dose-dependent fashion, native ST with the highest adherence (Fig. 10).

  45. HEAT-STABLE ENTEROTOXINS

  46. HEAT-STABLE ENTEROTOXINS • Similarly, these peptides maximally activated particulate guanylate cyclase and stimulate intestinal secretion in suckling mice, and native ST with the highest potency (Fig. 11, Table 2).

  47. HEAT-STABLE ENTEROTOXINS

  48. HEAT-STABLE ENTEROTOXINS

  49. HEAT-STABLE ENTEROTOXINS • It demonstrats that the four amino-terminal residues contribute significantly to the potency of these peptides. • In addition, the turn imposed by the proline residue at position 12 is not absolutely required for receptor occupancy or activation of the biochemical cascade that results in intestinal secretion. • However, it significantly increases the potency of the toxin

  50. HEAT-STABLE ENTEROTOXINS • The STb structural gene (estA) was cloned into high-expression vector pKC30 downstream from the strong PL promoter and the expression was studied • 10-20-fold increase in mRNA was produced by the recombinant strain.

More Related