Previous Article | Next Article 
Journal of Clinical Microbiology, August 2002, p. 3086-3088, Vol. 40, No. 8
0095-1137/02/$04.00+0 DOI: 10.1128/JCM.40.8.3086-3088.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Chronic Diarrhea, Hemorrhagic Colitis, and Hemolytic-Uremic Syndrome Associated with HEp-2 Adherent Escherichia coli in Adults Infected with Human Immunodeficiency Virus in Bangui, Central African Republic
Christian Mossoro,1 Philippe Glaziou,2 Simon Yassibanda,3 Nguyen Thi Phuong Lan,1 Claudine Bekondi,1 Pierre Minssart,4 Christine Bernier,5 Chantal Le Bouguénec,5 and Yves Germani1*
Unité des Maladies Infectieuses Opportunistes, Institut Pasteur de Bangui,1
Service de Gastroentérologie, Hôpital de l'Amitié,3
Service de Médecine, Hôpital Communautaire, Bangui, Central African Republic,4
Unité d'Epidémiologie, Institut Pasteur du Cambodge, Phnom Penh, Cambodia,2
Unité de Pathogénie Bactérienne des Muqueuses, Institut Pasteur, Paris, France5
Received 2 January 2002/
Returned for modification 21 March 2002/
Accepted 7 May 2002

ABSTRACT
In human immunodeficiency virus (HIV)-infected adults from the
Central African Republic, the occurrence of chronic diarrhea
due to HEp-2 adherent
Escherichia coli (EAEC) harboring virulence
markers (
eaeA, BFP, EAF,
astA determinant of EAST/1, positive
FAS test, enteropathogenic
E. coli O serogroup) was shown to
be associated with AIDS. We also show that EAEC that produce
verotoxin (Stx2) but do not harbor the genetic markers for classical
enterohemorrhagic
E. coli are involved in hemorrhagic colitis
and hemolytic-uremic syndrome in patients with HIV.

TEXT
The Central African Republic is strongly affected by the human
immunodeficiency virus (HIV) epidemic (
24). Nearly 72% of the
adults hospitalized with AIDS present initially with chronic
diarrhea (CD) (
14). Between 1996 and 1999 we used phenotypic
(
14) and genotypic assays to study 88 HIV-infected adults hospitalized
in Bangui and their matched controls to determine the clinical
significance of diarrheagenic
Escherichia coli (
7,
8,
9,
10,
12,
16,
22,
25,
27,
29,
31,
32,
34,
35). The methods were as
previously described (
14). To be included in the study, the
patients had to be HIV positive and aged 18 or over, have CD
(3 or more loose watery stools per day for at least 14 days
[
3]), have
E. coli in a stool sample, and give informed consent.
Each patient was matched with a control recruited from among
the neighbors and family members of the patient. The matching
criteria dictated that the control be aged within 5 years of
the patient's age and of the same sex. The recruitment criteria
for the matched controls were as follows: testing positive for
HIV antibodies, having had no diarrhea on the day of recruitment
or during the previous month, and having
E. coli in their stools
on the day of recruitment. All controls gave informed consent
to participate.
HEp-2 adherent E. coli (EAEC) (5, 28) with localized adherent (LA), aggregative adherent (AA), or diffuse adherent (DA) patterns were more common in the patients (P < 10-5) than in the controls (Table 1). Some EAEC exhibited a strong LA pattern (16 patients versus no control) in which >20% of the randomly selected cells had attached bacteria (11, 19). These LA strains with a strong LA pattern were associated with CD, especially when the assays used to identify enteropathogenic E. coli (EPEC) virulence factors yielded positive results (eaeA, EPEC adherence factor [EAF] plasmid, bundle-forming pili [BFP] PCR, and fluorescent actin staining [FAS] test) (P < 10-5), and all belonged to known EPEC O serogroups (P = 0.0001). The isolation of enteroaggregative E. coli (EAggEC) was strongly correlated with the presentation of CD (P < 10-5). The difference in the isolation rates of EAEC strains exhibiting DA between patients and controls was only significant when the presence of the astA gene encoding EAST/1 was considered (P = 0.016); astA was located on 7- to 40-kb plasmids.
Interestingly, all of the enteric bacteria isolated from 42
patients (86% of the 49 patients with severe immunodepression)
harboring EAEC with virulence factors were
E. coli (Table
2).
In contrast, in the 39 patients who had no EAEC or harbored
EAEC with no virulence factor (Table
2) and in controls (data
not shown),
E. coli never represented more than 50% of the isolated
enteric bacteria. This strongly suggests that some EAEC strains
are diarrheagenic pathogens. Thus, colony hybridization assays
under high-stringency conditions were carried out retrospectively
on archived filters prepared from stools streaked onto nonselective
medium to determine the percentage of colonies that harbored
eaeA and
astA. These stool samples were taken from 24 patients
(7 carrying EPEC clones identified by the presence of
eaeA,
13 harboring
astA-positive EAggEC, and 4 harboring
astA-positive
diffusely adhering
E. coli [DAEC]) and 12 controls. No hybridization
was observed in controls. Results showed that 90 to 100% of
the isolated bacteria hybridized with the
eaeA probe (
18) in
the 7 patients carrying EPEC clones (100%) and with the
astA probe (
astA PCR product from EAggEC strain 17-2 [
31]) in the
22 patients harboring
astA-positive EAggEC or DAEC. Antimicrobial
susceptibility tests were carried out, and accordingly, the
22 patients harboring EAEC with virulence factors (9 with LA
strains, 8 with AA strains, and 5 with
astA-positive DA strains)
received fluoroquinolones for 14 days. Seven days after the
end of treatment, EAEC negativation of cultures was associated
with complete resolution of diarrhea in 17 patients (77%; 9
with LA strains, 5 with AA strains, and 5 with DA strains).
This observation provides additional evidence that these EAEC
were etiologic factors of CD.
View this table:
[in this window]
[in a new window]
|
TABLE 2. Semiquantitative assessment of E. coli isolated on nonselective BCP medium according to the immunosuppression and the diarrheagenic E. coli in stools
|
During this study, the Central African Republic was afflicted
with epidemics of hemorrhagic colitis (HC) and hemolytic-uremic
syndrome (HUS) (
13,
15). The eight patients afflicted with both
HC and HUS presented pure cultures of EAEC. Non-EPEC serogrouped
LA clones producing both verotoxin (
20) (Stx2 alone according
to PCR tests) and hemolysin were isolated from the stools of
one patient. All of the isolates were negative for the enterohemorrhagic
E. coli (EHEC) plasmid marker
ehec-hly (
33) and for the PCR
detection of EHEC and EPEC virulence genes. They did not hybridize
with the EHEC probe (
23) or the EAF probe (
26) even under low-stringency
conditions and were negative in the FAS test and for invasion
in the HeLa cell gentamicin protection assay (
2). They all harbored
two plasmids (5 and 70 kb) that did not hybridize with an
stx2 probe that reacts only with total cellular DNA. These results
indicated that the
stx2 gene was present on the chromosome.
In the seven other patients, we isolated EAEC that produced
the verotoxin (Stx2 alone according to the PCR analysis). These
clones showed a mixed adherence pattern, predominated by AA.
In six of these patients, isolates showed AA and also typical
LA, and isolates from two patients produced hemolysin and gave
negative results in the PCR analyses for the EHEC plasmid marker
ehec-hly (
33). In the seventh patient, isolates showed a combination
of AA and LA patterns and an intercalated DA pattern. All of
the clones gave negative results by PCR for the detection of
virulence markers associated with EHEC, EPEC, DAEC, and EAggEC.
They did not hybridize with the
eaeA (
18) or EHEC (
23) probes,
even under low-stringency conditions. Southern blot analysis
indicated that the
stx2 gene was present on the chromosome.
Plasmid profile analysis and antimicrobial susceptibility testing
indicated that strains from the seven patients were epidemiologically
unrelated.
Taq cycle sequencing (
21,
30) showed that the B-subunit
gene of the toxin
stx2 was 100% homologous to the
stx2 B gene
from the O157:H7 strain EDL933 (
17) and from the O157:H7 and
O157:H
- strains recently isolated in the region (
13,
15). Although
these isolates did not contain the classical EHEC markers (such
as the
eaeA gene) and were negative in the FAS test, they can
be classified as EHEC because they were all isolated from HC
and HUS and all produced an Stx2. In immunocompetent subjects,
Stx2 production alone does not confer human pathogenicity (
27).
The Stx2-positive EAEC described in this study are thought to
colonize the intestinal mucosa as efficiently as the
eaeA-positive
EHEC. This may involve unknown adhesins (the HEp-2 adherence
test is a useful tool in this case for identifying potential
virulent strains of
E. coli), or it may illustrate that Stx2-producing
E. coli with reduced virulence have a greater potential for
producing HC and HUS in HIV-infected persons with enteric immune
defects than in healthy individuals.

ACKNOWLEDGMENTS
This work was partially supported by grants ANRS no. 97085 and
ANRS/VIHPAL no. 1277 and by the Groupe d'Etude des Infections
Diarrhéiques (Réseau International des Instituts
Pasteur et Instituts Associés).

FOOTNOTES
* Corresponding author. Mailing address: Institut Pasteur de Bangui (Unité des Maladies Infectieuses Opportunistes) S/C de l'Institut Pasteur à Paris, 25-28 rue du Docteur ROUX, 75724 Paris Cedex 15, France. Phone: (236) 61 85 83. Fax: (236) 61 01 09. E-mail:
germani{at}intnet.cf.


REFERENCES
1 - Baudry, B., S. J. Savarino, P. Vial, J. B. Kaper, and M. M. Levine. 1990. A sensitive and specific DNA probe to identify enteroaggregative Escherichia coli, a recently discovered diarrhoeal pathogen. J. Infect. Dis. 161:1249-1251.[Medline]
2 - Benjamin, P., M. Federman, and C. A. Wanke. 1995. Characterization of an invasive phenotype associated with enteroaggregative Escherichia coli. Infect. Immun. 63:3417-3421.[Abstract]
3 - Black, E. B., and C. F. Lanata. 1995. Epidemiology of diarrheal diseases in developing countries, p.13-36. In M. J. Blaser, P. D. Smith, J. I. Ravdin, H. B. Greenberg, and R. L. Guerrant (ed.), Infections of the gastrointestinal tract. Raven Press, New York, N.Y.
4 - Centers for Disease Control and Prevention. 1993. Revised classification system for HIV infection and expanded surveillance case definition for AIDS among adolescent and adults. Morb. Mortal. Wkly. Rep. 41:1-19.
5 - Cravioto, A., R. J. Gross, S. M. Scotland, et al. 1979. An adhesive factor in strains of Escherichia coli belonging to the traditional infantile enteropathogenic serotypes. Curr. Microbiol. 3:95-99.[CrossRef]
6 - Czeculin, J. R., S. Balepur, S. Hicks, A. Philips, R. Hall, M. H. Kothary, F. Navarro-Garcia, and J. Nataro. 1997. Aggregative adherence fimbria II, a second fimbrial antigen mediating aggregative adherence in enteroaggregative Escherichia coli. Infect. Immun. 65:4135-4145.[Abstract]
7 - Franke, J., S. Franke, H. Schmidt, A. Schwarzkopf, L. H. Wieler, G. Baljer, L. Beutin, and H. Karch. 1994. Nucleotide sequence analysis of enteropathogenic Escherichia coli (EPEC) adherence factor probe and development of PCR for rapid detection of EPEC harboring virulence plasmids. J. Clin. Microbiol. 32:2460-2463.[Abstract/Free Full Text]
8 - Frankel, G., J. A. Giron, J. Valmassoi, and G. K. Schoolnik. 1989. Multi-gene amplification: simultaneous detection of three virulence genes in diarrhoeal stool. Mol. Microbiol. 3:1729-1734.[CrossRef][Medline]
9 - Fratamico, P. M., S. K. Sackitey, M. Wiedmann, and M. Y. Deng. 1995. Detection of Escherichia coli O157:H7 by multiplex PCR. J. Clin. Microbiol. 33:2188-2191.[Abstract]
10 - Gannon, V. P. J., M. Rashed, R. K. King, and E. J. Golsteyn Thomas. 1993. Detection and characterization of the eae gene of Shiga-like toxin-producing Escherichia coli by using polymerase chain reaction. J. Clin. Microbiol. 31:1268-1274.[Abstract/Free Full Text]
11 - Germani, Y., E. Bégaud, P. Duval, and C. Le Bouguénec. 1996. Prevalence of enteropathogenic, enteroaggregative, and diffusely adherent Escherichia coli among isolates from children with diarrhea in New Caledonia. J. Infect. Dis. 174:1124-1126.[Medline]
12 - Germani, Y., E. Bégaud, and C. Le Bouguénec. 1997. Detection of the Escherichia coli attaching and effacing gene (eae A) in enteropathogenic strains by polymerase chain reaction. Res. Microbiol. 148:177-181.[Medline]
13 - Germani, Y., P. Cunin, E. Tedjouka, J. Morvan, and P. Martin. 1998. Enterohaemorrhagic Escherichia coli in Ngoïla (Cameroon) during an outbreak of bloody diarrhoea. Lancet 352:625-626.
14 - Germani, Y., P. Minssart, M. Vohito, S. Yassibanda, P. Glaziou, D. Hocquet, P. Berthélémy, and J. Morvan. 1998. Etiologies of acute, persistent, and dysenteric diarrheas in adults in Bangui, Central African Republic, in relation to human immunodeficiency virus serostatus. Am. J. Trop. Med. Hyg. 59:1008-1014.[Abstract]
15 - Germani, Y., B. Soro, M. Vohito, O. Morel, and J. Morvan. 1997. Enterohaemorragic Escherichia coli in Central African Republic. Lancet 349:1670.
16 - Gunzburg, S. T., N. G. Tornieporth, and L. W. Riley. 1995. Identification of enteropathogenic Escherichia coli by PCR-based detection of the bundle-forming pilus gene. J. Clin. Microbiol. 33:1375-1377.[Abstract]
17 - Jackson, M. P., R. J. Neill, A. D. O'Brien, R. K. Holmes, and J. W. Newland. 1987. Nucleotide sequence analysis and comparison of the structural genes for Shiga-like toxin I and Shiga-like toxin II encoded by bacteriophages from Escherichia coli 933. FEMS Microbiol. Lett. 44:104-114.
18 - Jerse, A. E., J. Yu, B. D. Tall, and J. B. Kaper. 1990. A genetic locus of enteropathogenic Escherichia coli necessary for the production of attaching and effacing lesions on tissue culture cells. Proc. Nat. Acad. Sci. USA 87:7839-7843.[Abstract/Free Full Text]
19 - Knutton, S., A. D. Philipps, H. R. Smith, R. J. Gross, R. Shaw, P. Watson, and E. Price. 1991. Screening for enteropathogenic Escherichia coli in infants with diarrhea by the fluorescent-actin staining test. Infect. Immun. 59:365-371.[Abstract/Free Full Text]
20 - Konowalchuk, J., J. I. Speirs, and S. Stavric. 1977. Vero response to a cytotoxin of Escherichia coli. Infect. Immun. 18:775-779.[Abstract/Free Full Text]
21 - Krishnan, B. R., R. W. Blakesly, and D. E. Berg. 1991. Linear amplification DNA sequencing directly from single phage plaques and bacterial colonies. Nucleic Acids Res. 19:1153.[Free Full Text]
22 - Le Bouguénec, C., M. Archambaud, and A. Labigne. 1992. Rapid and specific detection of pap, afa, and sfa adhesin-encoding operons in uropathogenic Escherichia coli strains by polymerase chain reaction. J. Clin. Microbiol. 30:1189-1193.[Abstract/Free Full Text]
23 - Levine, M. M., J. Xu, J. B. Kaper, H. Lior, V. Prado, J. Nataro, H. Karch, and I. K. Wachsmuth. 1987. A DNA probe to identify enterohemorrhagic Escherichia coli O157:H7 and other serotypes that cause hemorrhagic colitis and hemolytic uremic syndrome. J. Infect. Dis. 156:175-182.[Medline]
24 - Massanga, M., J. Ndoyo, D. J. Hu, and C. P. Pau. 1996. A highly heterogeneous HIV-1 epidemic in the Central African Republic. Emerg. Infect. Dis. 2:222-224.[Medline]
25 - Moseley, S. L., J. W. Hardy, M. I. Huq, P. Echeverria, and S. Falkow. 1983. Isolation and nucleotide sequence determination of a gene encoding a heat-stable enterotoxin of Escherichia coli. Infect. Immun. 39:1167-1174.[Abstract/Free Full Text]
26 - Nataro, J. P., M. M. Baldini, J. B. Kaper, R. E. Black, N. Bravo, and M. M. Levine. 1985. Detection of an adherence factor of enteropathogenic Escherichia coli with a DNA probe. J. Infect. Dis. 152:560-565.[Medline]
27 - Nataro, J. P., and J. B. Kaper. 1998. Diarrheagenic Escherichia coli. Clin. Microbiol. Rev. 11:142-201.[Abstract/Free Full Text]
28 - Nataro, J. P., J. B. Kaper, R. Robins-Browne, et al. 1985. Patterns of adherence of diarrheagenic Escherichia coli to HEp-2 cells. Pediatr. Infect. Dis. J. 6:829-831.
29 - Pollard, D. R., W. M. Johnson, H. Lior, S. D. Tyler, and K. R. Rozee. 1990. Rapid and specific detection of verotoxin genes in Escherichia coli by the polymerase chain reaction. J. Clin. Microbiol. 28:540-545.[Abstract/Free Full Text]
30 - Russmann, H., E. Kothe, H. Schmidt, S. Franke, D. Harmsen, A. Caprioloi, and H. Karch. 1995. Genotyping of Shiga-like toxin genes in non-O157 Escherichia coli strains associated with hemolytic uremic syndrome. J. Med. Microbiol. 42:404-410.
31 - Savarino, S. J., A. Fasano, J. Watson, B. M. Martin, M. M. Levine, S. Guandalini, and P. Guerry. 1993. Enteroaggregative Escherichia coli heat-stable enterotoxin 1 represents another subfamily of E. coli heat-stable toxin. Proc. Natl. Acad. Sci. USA 90:3093-3097.[Abstract/Free Full Text]
32 - Savarino, S. J., P. Fox, D. Yikang, and J. P. Nataro. 1994. Identification and characterization of a gene cluster mediating enteroaggregative Escherichia coli aggregative adherence fimbria I biogenesis. J. Bacteriol. 176:4949-4957.[Abstract/Free Full Text]
33 - Schmidt, H., L. Beutin, and H. Karch. 1995. Molecular analysis of the plasmid-encoded hemolysin of Escherichia coli O157:H7 strain EDL933. Infect. Immun. 63:1055-1061.[Abstract]
34 - Venkatesan, M. M., J. M. Buysse, and D. J. Kopecko. 1989. Use of Shigella flexneri ipaC and ipaH sequences for the general identification of Shigella spp. and enteroinvasive Escherichia coli. J. Clin. Microbiol. 27:2687-2691.[Abstract/Free Full Text]
35 - Yamamoto, T., T. Tamura, and T. Yokota. 1984. Primary structure of heat-labile enterotoxin produced by Escherichia coli pathogenic for humans. J. Biol. Chem. 259:5037-5044.[Abstract/Free Full Text]
Journal of Clinical Microbiology, August 2002, p. 3086-3088, Vol. 40, No. 8
0095-1137/02/$04.00+0 DOI: 10.1128/JCM.40.8.3086-3088.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Martinez-Jehanne, V., du Merle, L., Bernier-Febreau, C., Usein, C., Gassama-Sow, A., Wane, A.-A., Gouali, M., Damian, M., Aidara-Kane, A., Germani, Y., Fontanet, A., Coddeville, B., Guerardel, Y., Le Bouguenec, C.
(2009). Role of Deoxyribose Catabolism in Colonization of the Murine Intestine by Pathogenic Escherichia coli Strains. Infect. Immun.
77: 1442-1450
[Abstract]
[Full Text]
-
Boisen, N., Ruiz-Perez, F., Scheutz, F., Krogfelt, K. A., Nataro, J. P.
(2009). High Prevalence of Serine Protease Autotransporter Cytotoxins among Strains of Enteroaggregative Escherichia coli. Am J Trop Med Hyg
80: 294-301
[Abstract]
[Full Text]
-
Boisen, N., Struve, C., Scheutz, F., Krogfelt, K. A., Nataro, J. P.
(2008). New Adhesin of Enteroaggregative Escherichia coli Related to the Afa/Dr/AAF Family. Infect. Immun.
76: 3281-3292
[Abstract]
[Full Text]