The discovery of cholera--like enterotoxins produced by Escherichia coli causing secretory diarrhoea in humans.
Non-vibrio cholera has been recognized as a clinical entity for as
long as cholera was known to be caused by Vibrio cholerae. Until 1968,
the aetiologic agent of this syndrome was not known. Following a series
of studies in patients with non-vibrio cholera it was found that these
patients had large concentrations of Escherichia coli in the small bowel
and stools which produced cholera toxin-like enterotoxins, and had fluid
and electrolyte transport abnormalities in the small bowel similar to
patients with documented cholera. Furthermore, these patients developed
antibodies to the cholera-like enterotoxin. Later studies showed that
these strains, when fed to volunteers produced a cholera-like disease
and that two enterotoxins were found to be produced by these organisms:
a heat-labile enterotoxin (LT) which is nearly identical to cholera
toxin, and a heat-stable enterotoxin (ST), a small molecular weight
polypeptide. E. coli that produced one or both of these enterotoxins
were designated enterotoxigenic E. coli (ETEC). ETEC are now known not
only to cause a severe cholera-like illness, but to be the most common
bacterial cause of acute diarrhoea in children in the developing world,
and to be the most common cause of travellers' diarrhoea in persons
who visit the developing world.
Key words Cholera--diarrhoea--enterotoxin--non-cholera diarrhoea
Enterotoxins (Identification and classification)
Escherichia coli (Identification and classification)
|Author:||Sack, R. Bradley|
|Publication:||Name: Indian Journal of Medical Research Publisher: Indian Council of Medical Research Audience: Academic Format: Magazine/Journal Subject: Biological sciences; Health Copyright: COPYRIGHT 2011 Indian Council of Medical Research ISSN: 0971-5916|
|Issue:||Date: Feb, 2011 Source Volume: 133 Source Issue: 2|
|Geographic:||Geographic Scope: United States Geographic Code: 1USA United States|
Scope of this review
The review covers the following:
1. The development of the rabbit ileal loop (RIL) method by Dr S.N. De in 1953.
2. The use of the RIL to study live cultures of Escherichia coli isolated from stools of patients with cholera- like disease.
3. The clinical characterization of non-vibrio cholera during an unusual epidemic in 1963.
4. The demonstration that E. coli produced a cholera toxin-like enterotoxin in patients with cholera-like disease in 1968.
5. The rapid development of studies in the first 5 years after the findings of enterotoxigenic E. coli (ETEC) was published. These include: (i) the recognition that both heat-labile and heat-stable enterotoxins (LT and ST) were separate enterotoxin, (ii) the recognition of ETEC as an important pathogen in parts of the U.S., (iii) the discovery of pili (fimbria) as a critically important virulence factor for ETEC, and (iv) the important role of ETEC in the diarrhoea of travellers.
Work of Dr S.N. De
De developed the RIL in 1953 (1), and used it to study Vibrio cholerae infections and to discover the cholera toxin in 1959 (2). In 1956, he also used it to study E. coli isolated from the stools of adult patients with cholera-like symptoms but from whom V. cholerae could not be found (3). He used the RIL to test a live single colony culture of E. coli from each of 20 patients with non-vibrio cholera and 20 controls. About 65 per cent of the patients and 15 per cent of the controls gave a positive RIL. These data suggested that these E. coli may be the cause of the diarrhoea. Unfortunately, he did not test the cell-free filtrates of these E. coli.
De's work was published in 19563. The results of a representative positive RIL is shown in Fig. 1. Unfortunately, this paper was "hidden" in the medical literature of the day; at that time there was no easy way to search for specific areas of research. (We did not know of its existence until after publishing our first papers on ETEC).
In 1959 De, using the RIL, was the first to discover cholera enterotoxin and to publish a book "Cholera, its Pathology and Pathogenesis (4). The RIL developed by De was used in several laboratories for the study of enteropathogenic serotypes of E. coli from children with diarrhoea living in the developed world (5). The results were equivocal, and no one other than De had examined E. coli from adults with the non-vibrio cholera syndrome.
[FIGURE 1 OMITTED]
Clinical studies during a non-vibrio cholera epidemic
During the spring of 1963 an epidemic of non-vibrio cholera occurred in Kolkata, India and Dhaka, Bangladesh (then East Pakistan) which provided us with the opportunity to study these patients clinically and physiologically (6,7). These detailed observations showed that the concentrations of electrolytes in the blood and stools were nearly identical to those in patients with V. cholerae induced cholera. The intravenous fluid used to effectively treat cholera was equally effective in these patients.
The clinical picture of the patients with non-vibrio cholera-like diarrhoea, and their details compared to those with cholera, is shown in the Table. It was clear that patients with non-vibrio cholera appeared in the hospital with the same symptoms of cholera, but their illness was of much shorter duration and required less fluid replacement. It should be noted that although tetracycline reduced stool output in patients with cholera, this response was not seen in those with non-vibrio cholera. Unfortunately, because we were not aware of De's previous studies of E. coli, we did not do any tests on the large concentration of E. coli seen in the stool of these patients. As will be seen later, the non-vibrio cholera patients that we studied in 1968 had the same clinical picture as those studied in 1963, but without bacteriological confirmation of E. coli being involved.
In 1965, the first conference of the new U.S.-Japan Cooperative Science Program was held in Honolulu, Hawaii (8). Some of us from Johns Hopkins University were at the meeting, and noted that many papers were presented that used the RIL in studies of V. cholerae. Unfortunately De was not able to attend and there were no papers on the testing of E. coli by the RIL at this time. Fortunately at that meeting, I met Dr William Burrows, who later sent a colleague of his to teach me a modified RIL, which I later used in Kolkata.
The discovery of enterotoxigenic E. coli
In 1968, I was part of a team of four clinical scientists from the Johns Hopkins University School of Medicine who came to Kolkata as part of an International Center for Medical Research and Training (ICMRT), funded by the United States National Institutes of Health to study cholera, at the Calcutta School of Tropical Medicine and the Infectious Diseases Hospital. The cholera and ETEC team included Drs R. Bradley Sack, Sherwood Gorbach, John Banwell and Nathaniel Pierce from the Johns Hopkins University Center for Medical Research and Training, Baltimore, MD; Drs Benedicta Jacobs and B.D. Chetterjee from the Calcutta School of Tropical Medicine; and Drs Rupak Mitra and A. Mondal from the Infections Diseases Hospital, Calcutta (now Kolkata) during 1967-1970. Dr Sherwood Gorbach came to examine the microbiologic flora of the intestinal tract in patients with cholera. Dr John Banwell and Dr Nathaniel Pierce came to study the fluid and electrolyte movement in the small bowel of patients with cholera and their therapeutic implications, using intubation techniques. I came with the RIL to study the action of cholera toxin.
Our study patients were adults admitted to the Infectious Disease Hospital with watery stool and severe dehydration and a presumptive diagnosis of cholera. Our research team got "side-tracked" because of the unexpected finding of seeing large concentrations of E. coli rather than V. cholerae in the small bowel of many of these patients thought to have cholera. It soon became clear that we were seeing many cholera patients who had only E. coli in their small bowel and stool. Small bowel samples were found to have a pure growth of E. coli, with concentrations of 10 (6) to 10 (8) colony forming units (cfu) per ml. Stool samples also showed a predominance of E. coli at similar concentrations. This strongly suggested that E. coli may be an aetiologic agent of this syndrome. We immediately used the RIL test to determine whether they caused distention of the ileal loops, not only as live cultures but as culture filtrates. We were very excited to find that loops inoculated with either live cultures or culture filtrates caused distention of the loops, in the same way as cholera toxin was known to do. Furthermore the filtrates could be diluted up to 1:100 and still produce a positive RIL. The E. coli "diarrhoea factor" was quickly characterized and found to be non-dialyzable, heat-labile (when heated to 56[degrees]C for 30 min) and precipitated with 40 per cent ammonium sulphate. A picture of the positive RIL is shown in Fig. 2.
These data were first presented in November, 1968 at the US-Japan Cooperative Medical Science program in Unzen, Japan (9). During the discussion (which was printed in those early days of the program) investigators from both the US and Japan indicated that they had examined enteropathogenic serotypes of E. coli from local children with diarrhoea, and found them to be negative (9). At that time no one had tested E. coli from patients with severe cholera-like syndromes. Clinically, these patients harbouring enterotoxin-producing E. coli (ETEC) had the same findings as those studied in 1963. They had an abrupt onset of rice-water stools, and rapid onset of severe dehydration. Their illness lasted only 18 to 36 h with a low volume of stool, compared to cholera patients. They responded well to both intravenous and oral rehydration therapy. They had the same alteration in fluid and electrolyte movements in the small bowel, similar to patients with cholera.
Initially, the E. coli enterotoxin was produced using methods that resulted in toxin production by V. cholerae: i.e., growing the organisms in Syncase media in shallow culture flasks for 48 h, followed by centrifugation, filtering through a 0.22 [mu] Millipore filter, dialyzing for 3 days, lyophilizing and storing at 5[degrees]C.
[FIGURE 2 OMITTED]
Clearly, serotyping of the E. coli strain was of great importance because of determining whether these ETEC were of similar serotypes and whether they were of the known enteropathogenic serotypes. In fact, the ETEC were found to be several different serogroups: the most frequent were O6, O15, O25, O78, and O126 (10,11). None was found to be an enteropathogenic serotype. Enterotoxin production by the ETEC was found to be stable after many passages. In fact, we have some of these strains in our laboratories after 41 years. Another strain, H1O4O7, first isolated in Bangladesh (then East Pakistan) in 1975 is presently being used in volunteer challenges during ETEC vaccine development. To determine whether enterotoxins from different strains of E. coli were identical, rabbits were immunized parenterally with a single crude enterotoxin preparation. The resultant serum antibodies neutralized crude preparations of toxin from several different E. coli strains, using the RIL, indicating the similarity of the enterotoxins (12). Immunological studies were done on 29 patients who had either ETEC-induced diarrhoea or cholera (13). Convalescent sera neutralized both enterotoxins to some degree (higher titres in patients with the homologous infections) indicating the immunologic similarity between the two toxins.
We compared the potency of the crude E. coli enterotoxin with a preparation of cholera toxin made by Wyeth Laboratories, and found it to be 1:10 to 1:100 as potent, using the RIL. A comparison of three preparations of crude E. coli enterotoxin with our own preparation of cholera toxin from strain V. cholerae 569B indicated the same differences in potency (14) (Fig. 3).
[FIGURE 3 OMITTED]
[FIGURE 4 OMITTED]
In September 1970 these data were presented at the US-Japan Cholera Conference in Yamanashi, Japan (15). Twenty seven isolates of ETEC were obtained from 17 patients, one of whom was from the Cholera Hospital in Dhaka, Bangladesh (East Pakistan). In April, 1971, three papers describing our experience with the discovery of ETEC were published simultaneously (10,16,17) (unfortunately, none of these papers included a reference to De's 1956 studies indicating our unawareness of his studies). Data from the same 17 patients were reported in each of the three publications. Details of the ETEC enterotoxin were given by Sack et al (10). Additional ETEC were described, along with the microbial flora of the entire intestinal tract in patients with cholera and ETEC- induced diarrhoea by Gorbach et al (16). Fluid and electrolyte movement in the small bowel of patients with cholera or ETEC-induced diarrhoea were described by Banwell et al (17).
Initially there were differences of opinion in the heat-stability of the crude enterotoxin preparations. Some investigators thought all preparations contained both heat-labile toxin (LT) and another heat-stable enterotoxin (ST). This was clarified by using other assays: the infant mouse assay was used to identify ST only and the RIL test was shown to measure a response to ST at 6 h and LT at 18 h (18) (Fig. 4). The Thiry-Vella loop assay in dogs clearly differentiated the time course of the secretory response to a crude E. coli enterotoxin preparation, showing an early and late response to ST and LT, respectively as compared to the late response of cholera toxin (19) (Fig. 5). Until about 1973 there was confusion about differentiating LT and ST. During these early days, only the RIL at 18 h was used, so that only LT would be detected. These questions were clarified when E. coli strains were found that produced only LT or ST.
One additional assay should be mentioned, the vascular permeability factor. This factor is assayed in guinea pig or rabbit skin (20) (Fig. 6). It was known to be produced by V. cholerae, and could be used for assaying toxin or antitoxins. The same property was seen in heat labile preparations of E. coli enterotoxin. This was used in early experiments as an assay for LT. (Interestingly, it can be seen that hair growth occurred much more rapidly in the spots where the enterotoxin had been injected).
Early attempts to purify the LT enterotoxin were made using specific ganglioside agarose affinity columns, and also affinity columns using specific anti-cholera toxin antibodies. One of these investigators was Peter Agre, who was a medical student at Johns Hopkins School of Medicine at the time (21) and later became a Nobel Laureate in 2003 for the discovery of aquaporins.
[FIGURE 5 OMITTED]
[FIGURE 6 OMITTED]
E. coli enterotoxins in animals
Beginning in 1967, veterinary scientists examined E. coli isolates from young animals, particularly pigs, using the ileal loops of pigs, dogs, and rabbits (22-24). During the next few years, they were able to identify enterotoxins (LT and ST) and colonization factors carried in plasmids of E. coli from these young animals with diarrhoea. It should be pointed out that although the enterotoxins from animal strains are closely related or identical to those from humans, animal strains of ETEC do not infect humans, this primarily due to the differences in colonization factors.
Subsequent studies with ETEC
(i) The first volunteer challenge studies with ETEC
This was reported in 1971 by DuPont and colleagues (25), using two E. coli strains obtained from two American soldiers in Vietnam who had been diagnosed with "colitis", probably similar to what we know as travellers' diarrhoea. They did not have a cholera-like illness. These strains were found to produce LT, using the RIL. One of the strains (O148H28) was antigenically similar to the strain that had been identified in 1970 during an outbreak of travellers' diarrhoea among 19 of 38 British soldiers deployed in Aden (26).
The study was done in healthy volunteers at the Maryland House of Correction. At high doses of inoculum (1x10 (10) cfu), 7 of 10 volunteers developed a cholera-like illness and an antibody response to LT was seen in 6 volunteers. (Many years later volunteers' studies were done with E. coli that produced either LT or ST or both enterotoxins).
(ii) ETEC diarrhoea in the United States
In 1972 a search was made for ETEC in the stools of children hospitalized with diarrhoea at Cook County Hospital, Chicago (27). Studies were done in 29 children with diarrhoea in whom no other enteric pathogen could be isolated. Using the Infant Rabbit Test, 24 of these children (83%) were positive. This high rate of positive results was not found in other studies, and is probably related to variations in the ETEC assays. In 1973, my colleagues and I (28) conducted a search for ETEC in 59 children with acute diarrhoea who were under 4 years of age, living in the White Mountain Apache Tribe in Arizona, an area known to have high rates of diarrhoea in children. The assays used to detect ETEC were: RIL, infant rabbits, infant mice, and an adrenal cell assay. Eleven children had small bowel intubation performed in addition to routine stool cultures. The number of children with LT-producing ETEC in their stool was 10/59 (17%). No ST-producing ETEC was found. All of the intubated children had high concentrations of ETEC (10 (3) to 10 (9) cfu) in the small bowel. Antibodies to LT, using the adrenal cell assay, were studied in this general population and an increase in level of these antibodies with age was found (29). These data demonstrate the importance of ETEC as a cause of diarrhoea in this population.
(iii) The discovery of pili (fimbria) in ETEC in 1975
Pili have been known to occur in E. coli for many years. In 1955, Duguid and his colleagues (30) found "non-flagellar filamentous appendages (fimbria) and haemaglutination activity in Bacterium coli" These E. coli were not particularly related to illness, but were clearly demonstrated by electron microscopy (30).
In 1975, a colonization factor was first identified on ETEC by Evans and colleagues (31) (Fig. 7). It was found to be a transmissible surface-associated colonization factor (pili), which was shown to be a critically important virulence factor. E. coli strain H10407 was isolated from a woman with cholera-like diarrhoea hospitalized in the Cholera Hospital in Dhaka, Bangladesh. This strain and an identical strain without fimbria were tested in infant rabbits; only the fimbriated strain was virulent. (Many later studies also clearly showed the importance of fimbria in the virulence of ETEC.) Today there are at least 23 ETEC colonization factors that are antigenically distinct. A colonization factor was not recognized in V. cholerae until about 10 yr later.
[FIGURE 7 OMITTED]
(iv) ETEC as a cause of "Travellers'Diarrhoea"(TD)
In 1970, an outbreak of TD inAden was investigated by Rowe and colleagues (26) who found a predominance of a single serotype of E.coli, (O148:H28). Unfortunately, testing for enterotoxins was not available at that time. One year later in England, a laboratory technician working with this strain developed severe diarrhoea from which this same serotype was isolated. Furthermore, one of the strains used in the volunteer studies had the same serotype that was isolated from soldiers in Vietnam and was found to produce LT and a cholera-like syndrome in the volunteers (26). Although not completely documented this appears to be the first recognized outbreak of TD caused by ETEC. In 1974, Shore and colleagues (32) studied 28 travellers from Boston who had visited developing countries. Eleven developed TD, of which 4 (14%) had ETEC isolated from stool specimens. The assay used to detect ETEC was the infant mouse technique, so that only ST-producing E. coli could be recognized. In 1975, Gorbach and colleagues (33) studied American students travelling to Mexico. Thirty eight of 123 (29%) developed TD. ETEC were found in 72 per cent of those with TD and in 15 per cent of students who were healthy. The assay used for detecting ETEC was the rabbit skin permeability factor which detects LT. No assays for ST were done. This study demonstrates the great importance of LT-producing E. coli in the aetiology of TD. In 1976, Merson and colleagues (34) studied a group of 73 physicians and their families visiting Mexico to attend a Gastroenterology Conference. Of the 107 travellers, 59 (49%) developed TD; ETEC was isolated from 21 (36%) of those with TD. The methods used to detect ETEC were the adrenal cell assay, the Chinese hamster ovarian cell assay, the infant mouse and the RIL. In this study both LT and ST-producing E. coli were identified. Since that time there has been a large number of published studies verifying the role of ETEC as the most frequent cause of TD.
(v) Diagnosis of ETEC diarrhoea and cholera
ETEC diarrhoea is less severe than cholera, but may present exactly the same early clinical appearance. ETEC diarrhoea is relatively short-lived and requires less fluid replacement. Cholera can be treated effectively with antibiotics while ETEC diarrhoea has not clearly been shown to respond to antibiotics in endemic setting. In later studies antibiotics are clearly shown to be effective in the treatment of TD. ETEC has no phenotypic characteristics to make it recognizable in a plate of E. coli. V. cholerae can easily be recognized with the use of inhibitory media, such as thiosulphate citrate bile salts sucrose (TCBS) agar. For these reasons ETEC cannot be detected in minimally-equipped laboratories, whereas cholera can be easily diagnosed. As a result there have been relatively a few epidemiologic studies of ETEC diarrhoea.
(vi) Clinical understanding of ETEC diarrhoea in 2009
ETEC are the most common bacterial cause of diarrhoea in children living in the developing world. It is estimated that as many as 500,000 children may die annually. ETEC are the most frequent cause of TD among travellers from developed countries to developing countries. Thus association must be clear. Travellers are much like children living in those areas; both groups are immunologically naive and therefore lacking in resistance to infection by ETEC (35). The most important ongoing studies of ETEC are: (i) developing an effective, low-cost vaccine that can be used in children living in the developing world, as well as tourists visiting these areas, (ii) configuration of ST to make it antigenic, and (iii) developing a simpler test to identify ST. (The many rapid genetic tests for ETEC are available only in limited areas).
Nine years after the discovery of cholera enterotoxin by S.N. De in 19593 the discovery of enterotoxigenic E. coli in 19689 in patients with non-vibrio cholera was another major milestone in our understanding of aetiologies of acute infectious diarrhoeal diseases. From initial studies using rabbit ileal loops, the two enterotoxins of E. coli have now been identified at the molecular level, and pili, the other critical virulence factor, has been identified and now is known to consist of at least 23 different antigenic types. In the last 42 years ETEC has been extensively studied, microbiologically, clinically, genetically and epidemiologically. It is now known that ETEC are the most common bacterial agents of diarrhoea of children living in the developing world, and also the most common cause of "Travellers' diarrhoea" among visitors from the developed world travelling to the developing world. Although the improvement in water and sanitation is the ultimate long term goal for prevention of diarrhoeal illness, in the near future the development of an oral ETEC vaccine as a short term solution should be possible.
Received June 14, 2010
(1.) De SN, Chatterje DN. An experimental study of the mechanism of action of Vibrio cholerae on the intestinal mucous membrane. J Pathol Bacteriol 1953; 66 : 559-62.
(2.) De SN. Enterotoxicity of bacteria-free culture-filtrate of Vibrio cholerae. Nature 1959; 183 : 1533-4.
(3.) De SN, Bhattacharya K, Sarkar JK. A study of the pathogenicity of strains of Bacterium coli from acute and chronic enteritis. J Pathol Bacteriol 1956; 71 : 201-9.
(4.) De SN. Cholera: its pathology and pathogenesis. Edinburgh: Oliver and Boyd; 1961.
(5.) Taylor J, Bettelheim KA. The action of chloroform-killed suspensions of enteropathogenic Escherichia coli on ligated rabbit-gut segments. J Gen Microbiol 1966; 42 : 309-13.
(6.) Carpenter CC, Barua D, Wallace CK, Sack RB, Mitra PP, Werner AS, et al. Clinical and physiological observations during an epidemic outbreak of non- Vibrio cholera-like disease in Calcutta. Bull World Health Organ 1965; 33 : 665-71.
(7.) Lindenbaum J, Greenough WB 3rd, Benenson AS, Oseasohn R, Rizvi S, Saad A. Non-Vibrio cholera. Lancet 1965; 1 : 1081-3.
(8.) Proceedings of the Cholera Research Symposium. January 24-29, 1965, Honolulu, Hawaii. Washington D.C.: US Government Printing Office; 1965.
(9.) Sack RB. Diarrhea producing factors in cultures of Escherichia coli. Proceedings of the 4th Joint Conference, Japan-U.S. Cooperative Medical Science Program, Unzen, Japan; 1968. p. 23-5.
(10.) Sack RB, Gorbach SL, Banwell JG, Jacobs B, Chatterjee BD, Mitra RC. Enterotoxigenic Escherichia coli isolated from patients with severe cholera-like disease. J Infect Dis 1971; 123 : 378-85.
(11.) Orskov F, Orskov I, Evans DJ Jr, Sack RB, Sack DA, Wadstrom T. Special Escherichia coli serotypes among enterotoxigenic strains from diarrhoea in adults and children. Med Microbiol Immunol 1976; 162 : 73-80.
(12.) Sack RB, Froehlich JL. Antigenic similarity of heat-labile enterotoxins from diverse strains of Escherichia coli. J Clin Microbiol 1977; 5 : 570-2.
(13.) Sack RB, Jacobs B, Mitra R. Antitoxin responses to infections with enterotoxigenic Escherichia coli. J Infect Dis 1974; 129 : 330-5.
(14.) Sack RB. Human diarrheal disease caused by enterotoxigenic Escherichia coli. Annu Rev Microbiol 1975; 29 : 333-53.
(15.) Sack RB, Gorbach SL, Banwell JG, Jacobs B, Chatterjee BD, Mitra RC. Enterotoxigenic Escherichia coli isolated from patient with severe cholera-like disease. In: Proceedings of the 6th Joint Conference U.S.-Japan Cooperative Medical Science Program. Cholera panel. Lake Yamanaka,Yamanashi, Japan. 1970. p. 133-45.
(16.) Gorbach SL, Banwell JG, Chatterjee BD, Jacobs B, Sack RB. Acute undifferentiated human diarrhea in the tropics. I. Alterations in intestinal microflora. J Clin Invest 1971; 50 : 881-9.
(17.) Banwell JG, Gorbach SL, Pierce NF, Mitra R, Mondal A. Acute undifferentiated human diarrhea in the tropics. II. Alterations in intestinal fluid and electrolyte movements. J Clin Invest 1971; 50 : 890-900.
(18.) Evans DG, Evans DJ Jr, Pierce NF. Differences in the response of rabbit small intestine to heat-labile and heat-stable enterotoxins of Escherichia coli. Infect Immun 1973; 7 : 87380.
(19.) Sack RB, Johnson J, Pierce NF, Keren DF, Yardley JH. Challenge of dogs with live enterotoxigenic Escherichia coli and effects of repeated challenges on fluid secretion in jejunal Thiry-Vella loops. J Infect Dis 1976; 134 : 15-24.
(20.) Evans DJ Jr, Evans DG, Gorbach SL. Production of vascular permeability factor by enterotoxigenic Escherichia coli isolated from man. Infect Immun 1973; 8 : 725-30.
(21.) Agre P. Perspectives, lifeline. Lancet2008; 371 : 295.
(22.) Smith HW, Gyles CL. The effect of cell-free fluids prepared from cultures of human and animal enteropathogenic strains of Escherichia coli on ligated intestinal segments of rabbits and pigs. J Med Microbiol 1970; 3 : 403-9.
(23.) Moon HW, Whipp SC, Baetz AL. Comparative effects of enterotoxins from Escherichia coli and Vibrio cholerae on rabbit and swine small intestine. Lab Invest 1971; 25 : 133-40.
(24.) Moon HW, Whipp SC. Systems for testing the enteropathogenicity of Escherichia coli. Ann NY Acad Sci 1971; 176 : 197-211.
(25.) DuPont HL, Formal SB, Hornick RB, Snyder MJ, Libonati JP, Sheahan DG, et al. Pathogenesis of Escherichia coli diarrhea. N Engl J Med 1971; 285 : 1-9.
(26.) Rowe B, Taylor J, Bettelheim KA. An investigation of travellers' diarrhoea. Lancet 1970; 1 : 1-5.
(27.) Gorbach SL, Khurana CM. Toxigenic Escherichia coli: a cause of infantile diarrhea in Chicago. N Engl J Med 1972; 287 : 791-5.
(28.) Sack RB, Hirschhorn N, Brownlee I, Cash RA, Woodward WE, Sack DA. Enterotoxigenic Escherichia-coli-associated diarrheal disease in Apache children. N Engl J Med 1975; 292 :1041-5.
(29.) Sack RB, Hirschhorn N, Woodward WE, Sack DA, Cash RA. Antibodies to heat-labile Escherichia coli enterotoxin in Apaches in Whiteriver, Arizona. Infect Immun 1975; 12 : 1475-7.
(30.) Duguid JP, Smith IW, Dempster G, Edmunds PN. Non-flagellar filamentous appendages (fimbriae) and haemagglutinating activity in Bacterium coli. J Pathol Bacteriol 1955; 70 : 335-48.
(31.) Evans DG, Silver RP, Evans DJ Jr, Chase DG, Gorbach SL. Plasmid-controlled colonization factor associated with virulence in Escherichia coli enterotoxigenic for humans. Infect Immun 1975; 12 : 656-67.
(32.) Shore EG, Dean AG, Holik KJ, Davis BR. Enterotoxin producing Escherichia coli and diarrheal disease in adult travelers: a prospective study. J Infect Dis 1974; 129 : 577-82.
(33.) Gorbach SL, Kean BH, Evans DG, Evans DJ Jr, Bessudo D. Travelers' diarrhea and toxigenic Escherichia coli. N Engl J Med 1975; 292 : 933-6.
(34.) Merson MH, Morris GK, Sack DA, Wells JG, Feeley JC, Sack RB, et al. Travelers' diarrhea in Mexico. A prospective study of physicians and family members attending a congress. N Engl J Med 1976; 294 : 1299-305.
(35.) Qadri F, Svennerholm AM, Faruque AS, Sack RB. Enterotoxigenic Escherichia coli in developing countries: epidemiology, microbiology, clinical features, treatment, and prevention. Clin Microbiol Rev 2005; 18 : 465-83.
Reprint requests: Dr R. Bradley Sack, Department of International Health, Johns Hopkins University, Bloomberg School of Public Health 615 North Wolfe Street, Room W5953, Baltimore, Maryland, 21205, USA e-mail: email@example.com
R. Bradley Sack
Johns Hopkins University, Bloomberg School of Public Health, Baltimore, Maryland, USA
Table. Comparison of clinical characteristics in 97 patients with cholera or non-vibrio cholera Clinical characteristics Cholera Non-vibrio (n = 11) cholera (n = 86) IV fluids needed (l) 17 5 Stool volumes (l) 16 2 Length of illness (days) 4-5 2 Response to tetracycline + - Source: Data extracted from Ref. 6
|Gale Copyright:||Copyright 2011 Gale, Cengage Learning. All rights reserved.|