Skip to main content
Elsevier - PMC COVID-19 Collection logoLink to Elsevier - PMC COVID-19 Collection
. 2004 Feb 4;5(4):192–198. doi: 10.1016/S1201-9712(01)90069-4

Ordinary and opportunistic enteropathogens associated with diarrhea in senegalese adults in relation to human immunodeficiency virus serostatus☆☆

Amy Gassama , Papa Salif Sow , Fatou Fall , Pathé Camara , Hovette Philippe , Aïssatou Guèye-N'diaye §, Rémonie Seng , Badara Samb , Souleymane M'Boup §, Yves Germani #, Awa Aïdara-Kane ∗,
PMCID: PMC7128624  PMID: 11953215

Abstract

Objectives: A survey was conducted in Dakar, Senegal, to identify major types and prevalences of bacteria, parasites, fungi, and Rotaviruses associated with diarrhea in relation to human immunodeficieny virus (HIV) serostatus with the goal to provide guidance to physicians for case management.

Methods: Etiologic agents were identified in a case-control study: cases were HIV-infected patients with diarrhea (HIV+ D+) and HIV seronegative patients with diarrhea (HIV− D+); controls were HIV-infected patients without diarrhea (HIV+ D−) and seronegative controls without diarrhea (HID− D−). Ordinary enteric pathogens were identified by conventional methods. Different Escherichia coli pathotypes were characterized by polymerase chain reaction (PCR), identification of HEp-2 cell adherence pattern, Sereny test, GIvl1-ELISA, and the suckling mouse assay. Opportunistic parasites, such as Cryptosporidium and Microsporidium, were identified by the Kinyoun method and trichromic stain of Weber, respectively. Rotaviruses were identified with a commercial latex agglutination kit. Antimicrobial susceptibility testing was carried out by the disk diffusion method.

Results: Among the 594 patients examined, 158 were HIV+ D+, 121 were HIV− D+, 160 were HIV+ D−, and 155 were HIV− D−. The main etiologies of diarrhea were different according to HIV serostatus of patients. In immunocompetent adults the main causes of diarrhea were Shigella sp (12.4%), Entamoeba histolytica (10.7%), Salmonella enterica (6.6%), and Giardia (4.9%). In the immunocompromised host the more frequent pathogens were enteroaggregative E. coli (19.6%), Microsporidium (9.4%), Cryptosporidium sp (8.2%), Rotavirus (8.2%), Shigella sp (7.6%), Candida albicans (7.6%), E. histolytica (5.1%), S. enterica (4.4%), and Isospora belli (4.4%). Also, Blastocystis hominis has to be considered as an opportunistic parasite, because it was identified only in HIV-infected patients, with higher prevalence in adults with diarrhea (2.5% in HIV+ D+ patients; 0.6% in HIV+ D− patients). High level of asymptomatic carriage of Ascaris lumbricoides and Trichuris trichiura and some cases of multiple infections were observed. Fungi, Cryptosporidium sp and Microsporidium sp, were often identified in patients with low CD4 counts (range, 79–250 cells/mL). Independently from HIV-serostatus, CD4 count was lower in diarrheic persons, suggesting that diarrhea is a debilitating illness and that effective management of diarrhea can prevent immunosuppression. Isolated enteropathogenic strains displayed high resistance to most antibiotics used in Senegal for treating diarrhea (ampicillin, tetracycline, cotrimoxazole); they were susceptible to amikacin, gentamicin, and norfloxacin.

Conclusion: These epidemiologic data suggest that guidelines for the management of diarrhea during HIV infection in Dakar should be updated.

Keywords: Dakar, diarrhea, etiologies, HIV, Senegal

Footnotes

Presented in part at the 8th International Congress on Infectious Diseases. Boston, Massachusetts, May 15–18,1998.

☆☆

Supported by a grant of the French Agence National de Recherche sur le SIDA (ANRS grant N° 98080) and the General Delegation of the Pasteur Institute Network (Action Concertée Inter Institut Pasteur 1996).

References

  • 1.Bartlett J.G., Belistos P.C., Sears C.L. AIDS enteropathy. Clin Infect Dis. 1992;15:726–735. doi: 10.1093/clind/15.4.726. [DOI] [PubMed] [Google Scholar]
  • 2.O'Keefe E.A., Wood R. AIDS in Africa. Scand J Gastroenterol Suppl. 1996;220:147–152. doi: 10.3109/00365529609094768. [DOI] [PubMed] [Google Scholar]
  • 3.Johanson J.E. Diagnosis and management of AIDS-related diarrhea. Can J Gastroenterol. 1996;10:461–468. doi: 10.1155/1996/739845. [DOI] [PubMed] [Google Scholar]
  • 4.Framm S.R., Soave R. Agents of diarrhea. Med Clin North Am. 1997;81:427–447. doi: 10.1016/s0025-7125(05)70525-3. [DOI] [PubMed] [Google Scholar]
  • 5.Weber R., Bryan R.T., Owen R.L., Wilcox C.M., Gorelkin L., Visvesvara G.S. Improved light microscopical detection of Microsporidia spores in stool and duodenal aspirates. N Engl J Med. 1992;;326:161–166. doi: 10.1056/NEJM199201163260304. [DOI] [PubMed] [Google Scholar]
  • 6.Murray P.R., Barron E.J., Pfaffer M.A., Tenover F.C., Yolken R.H. 6th ed. American Society for Microbiology; Washington, DC: 1995. Manual of clinical microbiology. [Google Scholar]
  • 7.Tornieporth N.G., John J., Salgado K. Differentiation of pathogenic E. coli strains in Brazilian children by PCR. J Clin Microbiol. 1995;33:1371–1374. doi: 10.1128/jcm.33.5.1371-1374.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Frankel G., Giron J.A., Valmossoi J., Schoolnick G.K. Multi-gene amplification: simultaneous detection of three virulence gene in diarrhoeal stool. Mol Microbiol. 1989;3:1729–1734. doi: 10.1111/j.1365-2958.1989.tb00158.x. [DOI] [PubMed] [Google Scholar]
  • 9.Riley L.W. Infection diseases associated with Escherichia coli. In: Balows A., Hausler W.J., Ohashi M., Turano A., editors. 1st ed. Vol 1. Springer-Verlag; New York: 1988. pp. 237–261. (Laboratory diagnosis of infectious diseases. Principles and practice). [Google Scholar]
  • 10.Yamamoto T., Tamura T., Yokota T. Primary structure of heatlabile enterotoxin produced by Escherichia coli pathogenic for humans. J Biol Chem. 1984;259:5037–5044. [PubMed] [Google Scholar]
  • 11.Giannella R.A. Suckling mouse model for detection of heatstable Escherichia coli enterotoxin: characteristics of the model. Infect Immun. 1976;14:95–99. doi: 10.1128/iai.14.1.95-99.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Dean A.G., Ching Y.C., William R.G., Harden L.B. Test for Escherichia coli enterotoxin using infant mice: application in a study of diarrhea in children in Honolulu. J Infect Dis. 1972;125:407–411. doi: 10.1093/infdis/125.4.407. [DOI] [PubMed] [Google Scholar]
  • 13.Sereny B. Experimental keratoconjunctivitis shigellosis. Acta Microbiol Acad Sci Hung. 1957;4:367–376. [PubMed] [Google Scholar]
  • 14.Vial P.A., Robins-Browne R., Lior H. Characterization of enteroadherent-aggregative Escherichia coli, a putative agent of diarrheal disease. J Infect Dis. 1988;158:70–79. doi: 10.1093/infdis/158.1.70. [DOI] [PubMed] [Google Scholar]
  • 15.Bauer A.W., Kirby W.M., Sherris J.C., Turck M. Antibiotic susceptibility testing by a standardized single disk method. Ann J Clin Pathol. 1966;45:493–496. [PubMed] [Google Scholar]
  • 16.Mayer H.B., Wanke C.A. Enteroaggregative Escherichia coli as a possible cause of diarrhea in an HIV-infected patient. N Engl J Med. 1995;332:273–274. doi: 10.1056/NEJM199501263320417. [DOI] [PubMed] [Google Scholar]
  • 17.Polotsky Y., Nataro J.P., Kotler D., Barret T.J., Orenstein J.M. HEp2 cell adherence patterns, serotyping, and DNA analysis of Escherichia coli isolates from eight patients with AIDS and chronic diarrhea. J Clin Microbiol. 1997;35:1952–1958. doi: 10.1128/jcm.35.8.1952-1958.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Germani Y., Minssart P., Vohito M. 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. 1998;59:1008–1014. doi: 10.4269/ajtmh.1998.59.1008. [DOI] [PubMed] [Google Scholar]
  • 19.de Sola Earle C., Montiel Quezel-Guerraz N., Hidalgo Rojas L., Sanchez Cantos A., Garcia Alegria J. Severe acute gastroenteritis due to Aeromonas in a patient colectomized for Crohn's disease. Rev Esp Enferm Dig. 1997;89:48–50. [PubMed] [Google Scholar]
  • 20.Aïdara A., Koblavi S., Boye C.S. Phenotypic and genotypic characterization of Vibrio cholerae isolates from a recent cholera outbreak in Senegal: comparison with isolates from Guinea Bissau. Am J Trop Med Hyg. 1998;58:163–167. doi: 10.4269/ajtmh.1998.58.163. [DOI] [PubMed] [Google Scholar]
  • 21.Schmidt W., Schneider T., Heise W. Stool viruses, coinfections, and diarrhea in HIV-infected patients. Berlin Diarrhea/Wasting Syndrome Study Group. J Acquir Immune Defic Syndr Hum Retrovirol. 1996;13:33–38. doi: 10.1097/00042560-199609000-00006. [DOI] [PubMed] [Google Scholar]
  • 22.Gomez Morales M.A., Atzori C., Ludovici A., Rossi P., Scaglia M., Pozio E. Opportunistic and non-opportunistic parasites in HIV-positive and negative patients with diarrhoea in Tanzania. Trop Med Parasitol. 1995;46:109–114. [PubMed] [Google Scholar]
  • 23.Albrecht H., Stellbrink H.J., Koperski K., Greten H. Blastocystis hominis in human immunodeficiency virus-related diarrhea. Scand J Gastroenterol. 1995;30:909–914. doi: 10.3109/00365529509101600. [DOI] [PubMed] [Google Scholar]
  • 24.Navin T.R., Weber R., Vugia D.J. Declining CD4+ T-lymphocyte counts are associated with increased risk of enteric parasitosis and chronic diarrhea: results of a 3-year longitudinal study. J Acquir Immune Defic Syndr Hum Retrovirol. 1999;20:154–159. doi: 10.1097/00042560-199902010-00007. [DOI] [PubMed] [Google Scholar]
  • 25.Lloyd A. HIV infection and AIDS. P N G Med J. 1996;39:174–180. [PubMed] [Google Scholar]

Articles from International Journal of Infectious Diseases are provided here courtesy of Elsevier

RESOURCES