2021, Number 2
<< Back Next >>
Rev Cubana Med Trop 2021; 73 (2)
Adherence patterns in HEp-2 cells of Escherichia coli strains isolated from contaminated rivers in Havana
Romeu ÁB, Salazar JEP, Rojas HNM, Eslava CCA
Language: Spanish
References: 31
Page: 1-11
PDF size: 326.12 Kb.
ABSTRACT
Introduction:
Adherence is crucial to the development of most Escherichia coli infections. Three different adherence patterns have been described for pathotypes of this species: localized, diffuse and aggregative adherence, based on the specific clinical pathogenic processes they bring about. However, few studies have been conducted about in vitro adherence phenotypes of E. coli isolated from the environment.
Objective:
Determine the adherence phenotypes of E. coli strains isolated from freshwater ecosystems in Havana.
Methods:
An analysis was conducted of 108 E. coli strains isolated from the rivers Almendares, Quibú and Luyanó in Havana. Determination was made of the adherence pattern by adherence assays in HEp-2 cell line cultures, as well as of the serotype for each strain.
Results:
Of the E. coli strains isolated, 25% were adherent and 75% were not. Twenty-two strains displayed the typical diffusely adherent pattern and five displayed aggregative adherence. Strains exhibiting the two adherence patterns were found in the three rivers evaluated. The strains contained 24 different serotypes.
Conclusions:
The environmental E. coli strains circulating in these ecosystems were found to have adherent characteristics whose pathogenicity implies a potential risk to human health, particularly in childhood.
REFERENCES
Ríos D, Cerna JF, Morán N, Meza M, Estrada T. Escherichia coli enterotoxigénica y enteroagregativa: prevalencia, patogénesis y modelos múridos. Gac Med Mex. 2019;155 410-16.
Gómez OG. Enfermedad diarreica aguda por Escherichia coli patógenas en Colombia. Rev Chilena Infectol. 2014;31(5):577-86.
Nataro JP, Kaper JB. Diarrheagenic Escherichia coli. Clin Microbiol Rev. 1998;11(1):142-201.
Rodríguez G. Principales características y diagnóstico de los grupos patógenos de Escherichia coli. Rev Salud Pública de México. 2002;44(5):464-75.
Croxen MA, Law RJ, Scholz R, Keeney KM, Wlodarska M, Finlay BB. Recent advances in understanding enteric pathogenic Escherichia coli. Clin Microbiol Rev. 2013;26(4):822-80.
Cravioto A, Gross RJ, Scotland SM, Rowe B. An adhesive factor found in strains of Escherichia coli belonging to the traditional infantile enteropathogenic serotypes. Curr Microbiol. 1979;3:95-9.
Zamora J, Reinhardt G, Polette M, Orellana CM. Escherichia coli aislada de fecas de cerditos diarreicos. Patrones de adherencia a células HEp-2. Arch Med Vet. 2000;32(2):245-51.
Orskov F, Orskov I. Serotyping of Escherichia coli. Meth Microbiol. 1984;14(3):43-112.
Spano LC, Sadovsky AD, Segui PN, Saick KW, Kitagawa SM, Pereira FE. Age-specific prevalence of diffusely adherent Escherichia coli in Brazilian children with acute diarrhoea. J Med Microbiol. 2008;57(10):359-63.
Servin A. Pathogenesis of Afa/Dr diffusely adhering Escherichia coli. Clin Microbiol Rev. 2005;18(2):264-92.
Le Bouguénec C, Servin AL. Diffusely adherent Escherichia coli strains expressing Afa/Dr adhesins (Afa/Dr DAEC): hitherto unrecognized pathogens. FEMS Microbiol Lett. 2006;256(2):185-94.
Lopes LM, Fabbricotti SH, Ferreira AJP, Kato MAMF, Michalski J, Scaletsky ICA. Heterogeneity among strains of diffusely adherent Escherichia coli isolated in Brazil. J Clin Microbiol. 2005;43(4):1968-72.
Tozzoli R y Scheutz F. Diarrhoeagenic Escherichia coli infections in humans. En: Morabito S. Pathogenic Escherichia coli. Molecular and Cellular Microbiology. Norfolk, UK: Caister Academic Press; 2014. p 1-18.
Blanco JE, Blanco M, Alonso MP, Mora A, Dahbi G, Coira MA, et al. Serotypes, virulence genes, and intimin types of Shiga toxin (verotoxin)-producing Escherichia coli isolates from human patients: prevalence in Lugo, Spain, from 1992 through 1999. J Clin Microbiol. 2004;42:311-9.
Bielaszewska M, Mellmann A, Zhang W, Köck R, Fruth A, Bauwens A, et al. Characterisation of the Escherichia coli strain associated with an outbreak of haemolytic uraemic syndrome in Germany, 2011: a microbiological study. Lancet Infect Dis. 2011;11(9):671-6.
Germani Y, Begaud E, Duval P, Le Bouguenec C. Prevalence of enteropathogenic, enteroaggregative, and diffusely adherent Escherichia coli among isolates from children with diarrhea in New Caledonia. J Infect Dis. 1996;174(5):1124-6.
Mohamed JA, Huang DB, Jiang ZD, Dupont HL, Nataro JP, Belkind-Gerson J, et al. Association of putative enteroaggregative Escherichia coli virulence genes and biofilm production in isolates from travelers to developing countries. J Clin Microbiol. 2007;45(1):121-6.
Pereira AL, Silva TN, Gomes AC, Araújo AC, Giugliano LG. Diarrhea-associated biofilm formed by enteroaggregative Escherichia coli and aggregative Citrobacter freundii: a consortium mediated by putative F pili. BMC Microbiol. 2010;10(57):1-10.
Dautin N. Serine protease autotransporters of enterobacteriaceae (SPATEs): biogenesis and function. Toxins (Basel). 2010;2(6):1179-206.
Ruiz-Pérez F, Nataro JP. Bacterial serine proteases secreted by the autotransporter pathway: classification, specificity, and role in virulence. Cell Mol Life Sci. 2013;10:1007-10.
Ruiz-Perez F, Wahid R, Faherty CS, Kolappaswamy K, Rodríguez L, Santiago A, et al. Serine protease autotransporters from Shigella flexneri and pathogenic Escherichia coli target a broad range of leukocyte glycoproteins. Proc Natl Acad Sci, USA. 2011;108(31):12881-6.
Blanco J. Escherichia coli enteroagregativa O104:H4-ST678 productora de Stx2a. ¡Diagnóstico microbiológico ya, de este y otros serotipos de STEC/VTEC! Enferm Infecc Microbiol Clin. 2012;30(2):84-9.
Rasko DA, Webster DR, Sahl JW, Bashir A, Boisen N, Scheutz F, et al. Origins of the E. coli strain causing an outbreak of Hemolytic-Uremic Syndrome in Germany. N Engl J Med. 2011;365:709-17.
Frank C, Werber D, Cramer JP, Askar M, Faber M, Heiden MA, et al. The HUS investigation Team. Epidemic profile of Shiga-Toxin-producing Escherichia coli O104:H4 Outbreak in Germany - Preliminary Report. N Engl J Med. 2011;22:1-10.
Mora A, Blanco M, Blanco JE, Dahbi G, López C, Justel P, et al. Serotypes, virulence genes and intimin types of Shiga toxin (verocytotoxin)-producing Escherichia coli isolates from minced beef in Lugo (Spain) from 1995 through 2003. BMC Microbiol. 2007;7:13.
Michino H, Araki K, Minami S, Takaya S, Sakai N, Miyazaki M, et al. Massive outbreak of Escherichia coli O157:H7 infection in school children in Sakai City, Japan, associated with consumption of white radish sprouts. Am J Epidemio.l 1999;150:787-96.
Itoh Y, Nagano I, Kunishima M, Ezaki T. Laboratory investigation of enteroaggregative Escherichia coli Ountypeable:H10 associated with amassive outbreak of gastrointestinal illness. J Clin Microbiol. 1997;35:2546-50.
Barton C, Jones TF, Vugia DJ, Long C, Marcus R, Smith K, et al. Deaths associated with bacterial pathogens transmitted commonly through food: foodborne diseases active surveillance network (FoodNet), 1996-2005. J Infect Dis. 2011;204(2):263-7.
Urbina D, Arzuza O, Young G, Parra E, Castro R, Puello M. Rotavirus type A and other enteric pathogens in stool samples from children with acute diarrhea on the Colombian northern coast. Int Microbiol. 2003;6(1):27-32.
Rúgeles LC, Bai J, Martínez AJ, Vanegas MC, Gómez-Duarte OG. Molecular characterization of diarrheagenic Escherichia coli strains from stools samples and food products in Colombia. Int J Food Microbiol. 2010;138(3):282-6.
Gavio B, Palmer-Cantillo S, Mancera JE. Historical analysis (2000-2005) of the coastal water quality in San Andrés Island, Sea Flower Biosphere Reserve, Caribbean Colombia. Mar Pollut Bull. 2010;60(7):1018-30.