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Journal of Clinical Microbiology, July 2002, p. 2606-2608, Vol. 40, No. 7
0095-1137/02/$04.00+0     DOI: 10.1128/JCM.40.7.2606-2608.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Prevalence of Enterotoxigenic Escherichia coli Strains Harboring the Longus Pilus Gene in Brazil

Lucilia S. Nishimura,1 Jorge A. Girón,2* Solange L. Nunes,1 and Beatriz E. C. Guth1

Departamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de São Paulo Escola Paulista de Medicina, UNIFESP, São Paulo, Brazil,1 Centro de Investigaciones en Ciencias Microbiológicas Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Puebla, México2

Received 11 February 2002/ Returned for modification 31 March 2002/ Accepted 11 April 2002


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ABSTRACT
 
The longus type IV pilus gene (lngA) was highly prevalent (32.8%) among Brazilian enterotoxigenic Escherichia coli strains producing both heat-labile and heat-stable enterotoxins and bearing the CFA/I, CS1CS3, or CS6 antigen. Furthermore, lngA was more often found in strains isolated from children with diarrhea than in strains isolated from children without diarrhea.


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TEXT
 
Enterotoxigenic Escherichia coli (ETEC) is a major cause of acute childhood diarrhea in developing countries (15). The production of heat-labile enterotoxin (LT) and/or heat-stable enterotoxin (ST) is responsible for the loss of fluids in the intestine. In addition, another important characteristic of these strains is the ability to colonize the small intestine, mediated by appendages called colonization factors (CFs). A spectrum of different surface filaments has been described among ETEC strains on the basis of their biochemical and immunological properties (3). Longus is a type IV pilus produced by human ETEC strains and is closely related to the CFA/III antigen (4, 13). Type IV pili are observed in a variety of gram-negative bacterial pathogens including Vibrio cholerae and enteropathogenic E. coli (5, 7, 25). It has been proposed that the most prevalent CFs are the best components for oral ETEC-based vaccines (2, 29). However, the prevalence of CFs among clinical ETEC isolates differs considerably depending on the geographic region of the world where the isolates are recovered (1, 11, 17, 20, 23, 26).

ETEC strains are important pathogens in São Paulo, Brazil, and are responsible for 7 to 20% of cases of infantile diarrheal (8, 21). Different studies have shown that CFs occur in 43 to 29% of the strains isolated, but a considerable number of ETEC strains isolated from patients with diarrhea still do not produce any of the known CFs (11, 16, 21). No data concerning the frequency of occurrence of longus pilus-producing strains in São Paulo are available. In the present study, the occurrence of the longus pilus was sought in a collection of 140 ETEC strains isolated from patients with or without diarrheal disease during several studies conducted in São Paulo from 1985 to 1990 (8, 10, 11). The toxigenic phenotypes, serotypes, and CF profiles of these strains have been determined previously (11, 16). Sera with polyclonal antibodies against CFA/I, CFA/II (CS1CS2, CS1CS3, CS2), CS8, and CFA/IV (CS6) (11) and CS18 (kindly provided by Glória Viboud [28]) or monoclonal antibodies (MAbs) against CS3, CS4, CS5, CS7, CS12, CS14, and CS17 (kindly provided by Ann-Mari Svernnerholm [27]) were used in dot blot enzyme-linked immunosorbent assays for CF identification. ETEC strain E9034A, which carries a 90-kbp plasmid with the CS3 and longus pilus genes, and strain E9034P, a plasmidless derivative of E9034A that is unable to produce the longus pilus, were used as positive and negative controls, respectively.

Colony blot hybridization and PCR were used to detect the longus pilin gene (lngA). Two specific probes, a 1.0-kbp EcoRV fragment from plasmid pOG140 containing the entire structural subunit lngA gene (9) and a 0.6-kbp EcoRI fragment from plasmid pZG1, were labeled with [{alpha}-32P]dCTP and used in colony hybridization experiments as described previously (14). Oligonucleotides JG1 (5'-CGGAATTCATGAGCCTGCTGGAAGTTATCA-3') and JG2 (5'-CGGAATTCCGGCTACCTAAAGTAATTGAGT-3') were used to amplify a 630-bp amplicon representing the entire lngA gene. Bacterial lysates were obtained from colonies on MacConkey agar that had been suspended in distilled H2O and boiled for 10 min. The amplification conditions were applied as described previously (12).

The longus pilus-related sequence (lngA) was identified in 32.8% (46 of 140) of the ETEC strains studied, and it was mainly observed among LT type I (LT-I)- and ST type I (ST-I)-producing strains and ST-I-producing strains (Table 1). This frequency is higher than those described for strains from other geographic regions such as Bangladesh, Chile, and Argentina, where it varies from 8.5 to 28%, but it was similar to the ones identified for strains from Egypt (31%) and Mexico (36.5%) (6, 12, 18). lngA has mostly been associated in previous studies with ST-I-producing strains (40 to 64.4%), and this percentage is in agreement with the one found in the present study. However, in this study the highest prevalence of lngA was observed among LT-I- and ST-I-producing strains (75%).


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  		TABLE 1. Occurrence of lngA in ETEC strains with different toxigenic phenotypes isolated in São Paulo, Brazila

Most of the longus pilus-positive ETEC strains (69.5%) also harbor other CFs (Table 2), including CFA/I (53%), CS6 (21.8%), and CS1CS3 (18.7%). In other countries, lngA was most highly associated with CFA/II-producing strains and even with strains lacking any of the known CFs (6). In São Paulo, lngA was more prevalent among strains expressing CFA/I. Such an association was also found in ETEC strains isolated in Argentina (18). An association of CFs is not a common property of ETEC strains except for an association between CS6 and CFA/III, CS12, and CS22, but this association occurs at a low frequency. However, it should be mentioned that a high degree of association between CS6 and the longus pilus (21.8%) was observed in the present study, suggesting heterogeneity among the strains expressing CS6. Taking into consideration the frequencies of occurrence of the widespread CFs, such as CFA/I, CFA/II, and CFA/IV, which have varied from 23 to 43% in previous epidemiological studies conducted in São Paulo (11, 16, 21) and from 22 to 73% in studies conducted in other geographic regions (1, 17, 20, 23), the frequencies of occurrence of the longus pilin genes found here or described by others confirm the importance of the longus pilus as a widely distributed antigen among ETEC strains. Moreover, almost all (91%) of the lngA-positive ETEC strains identified in the present study were isolated from children with diarrhea, suggesting an association of the presence of lngA with disease. Girón et al. (6) have also observed an association between the presence of lngA and disease.


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  		TABLE 2. Frequency of occurrence of other CFs observed among lngA-positive ETEC strains identified in Brazila

Interesting observations were also made when the lngA-positive ETEC strains were further analyzed for toxigenic phenotypes, serotypes, and expression of CFs (Table 3). LT- and ST-producing lngA strains were associated with only CFA/I or CFA/II (CS1CS3, CS2CS3) production, and such strains were only of serotypes O6:H16 and O78:H12. In addition, all of the longus pilus- and CFA/II-positive strains produced LT and ST. This strong association could be explained by the fact that these factors could be encoded on the same plasmid or on compatible plasmids. lngA was distributed among several serotypes of ST-producing strains, but a close association with CFA/I or CS6 production was also detected. In other regions of the world, the relationship between lngA, enterotoxin production, and CFs has mainly been associated with LT and ST production plus CFA/II and ST production and CFA/I production (6, 12, 18). Despite the relation of longus pili and the production of other CFs that have been identified, lngA also occurred in a relevant percentage (30.5%) of ETEC strains that lack CFs, suggesting that the longus pilus is a rather common antigen among the ETEC strains isolated in our community.


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  		TABLE 3. Relationship between lngA and the toxin profiles, serotypes, and CFs of ETEC strains isolated in Brazil

All of the data discussed here point to the notion that the longus pilus frequently occurs among ETEC strains in different geographic regions, and this should be taken into consideration when strategies for the prevention of ETEC infections such as the use of pilus-based vaccines are considered. In addition, an antibody response against the longus pilus was detected in sera and fecal extracts of patients with diarrhea caused by ETEC (19), suggesting that this fimbria may be expressed in vivo. Since diarrheal disease due to ETEC is an important cause of childhood morbidity and mortality, prophylactic intervention to prevent infections with these strains should be discussed. It has been shown that CFs are good ETEC immunogens that can elicit a protective antibody response (22, 24). Thus, for the purpose of vaccine formulation studies, searches for the distribution and prevalence of CFs in areas of endemicity as well as further surveys of the human immune response against ETEC infections are essential.


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ACKNOWLEDGMENTS
 
This work was supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (grant 97/11284-5), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and Financiadora de Estudos e Projetos/Ministério Da Ciência e Tecnologia/Programa de Apoio a Núcleos de Excelência (FINEP/MCT/PRONEX). J. Girón received support from Conacyt of México (grant 32777-M).


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FOOTNOTES
 
* Corresponding author. Mailing address: Centro de Investigaciones en Ciencias Microbiológicas, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Edificio 76 Complejo de Ciencias, Ciudad Universitaria, Puebla, México. Phone: 52 222 2 33 20 10. Fax: 52 222 44 45 18. E-mail: jagiron{at}yahoo.com. Back


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Journal of Clinical Microbiology, July 2002, p. 2606-2608, Vol. 40, No. 7
0095-1137/02/$04.00+0     DOI: 10.1128/JCM.40.7.2606-2608.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.



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