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On-line version ISSN 1678-4782
J. Pediatr. (Rio J.) vol.85 no.4 Porto Alegre Aug. 2009
Lactobacilli and bifidobacteria in the feces of schoolchildren of two different socioeconomic groups: children from a favela and children from a private school
Ricardo M. P. de MelloI; Mauro B. de MoraisII; Soraia TahanIII; Lígia C. F. L. MelliIV; Mirian S. do Carmo RodriguesIV; Carolina S. MelloV; Isabel C. A. ScaletskyVI
IBiomédico. Mestre, Programa de
Pós-Graduação em Pediatria e Ciências Aplicadas à Pediatria, Disciplina de Gastroenterologia
Pediátrica, Departamento de Pediatria, Universidade Federal de São Paulo (UNIFESP),
São Paulo, SP, Brazil.
IIProfessor associado, livre-docente e chefe, Disciplina de Gastroenterologia Pediátrica, Departamento de Pediatria, UNIFESP, São Paulo, SP, Brazil.
IIIMédica. Doutora, Disciplina de Gastroenterologia Pediátrica, Departamento de Pediatria, UNIFESP, São Paulo, SP, Brazil. Professora, Instituto de Pesquisa Unolab, Departamento de Ciências da Saúde, Centro Universitário Fundação e Instituto de Educação de Osasco (UNIFIEO), Osasco, SP, Brazil. Professora, Instituto de Pesquisa Unolab, Departamento de Ciências da Saúde, UNIFIEO, Osasco, SP, Brazil.
IVProfessora, Instituto de Pesquisa Unolab, Departamento de Ciências da Saúde, UNIFIEO, Osasco, SP, Brazil.
VNutricionista. Mestre, Programa de Pós-Graduação em Pediatria e Ciências Aplicadas à Pediatria, Disciplina de Gastroenterologia Pediátrica, Departamento de Pediatria, UNIFESP, São Paulo, SP, Brazil.
VIProfessora adjunta, livre-docente, Disciplina de Microbiologia, Departamento de Microbiologia, Imunologia e Parasitologia, UNIFESP, São Paulo, SP, Brazil.
OBJECTIVE: To determine the number of
lactobacillus and bifidobacterium colonies in the feces of schoolchildren from
two different socioeconomic levels.
METHODS: We analyzed fecal samples of children aged 6 to 10 years without gastrointestinal symptoms or recent use of antimicrobials. The first group included 86 children living in a favela in the city of Osasco, state of São Paulo, southeastern Brazil. The second group included 36 children attending a private school in the same city. Body mass index (BMI) was used to assess nutritional status according to the reference values of the National Center for Health Statistics (NCHS). Specific anaerobic culture media were used for isolation of colonies for 48 and 72 hours at 37 °C. The number of colonies was determined using the plate-counting method.
RESULTS: The mean lactobacillus (1.125 x 109 colony-forming units, CFU/g) and bifidobacterium (1.675 x 109 CFU/g) counts in the private school group were higher (p < 0.001) than those in the favela group: 0.250 x 109 and 0.350 x 109 CFU/g, respectively. In the favela group, children with BMI z score < -1.0 standard deviation (SD) (n = 28) showed lower mean (p < 0.05) lactobacillus (0.100 x 109 CFU/g) and bifidobacterium (0.095 x 109 CFU/g) counts than the children with BMI > -1.0 SD (n = 57): 0.350 x 109 and 0.420 x 109 CFU/g, respectively.
CONCLUSION: The microbiota of schoolchildren living in unfavorable environmental conditions shows lower numbers of fecal lactobacillus and bifidobacterium colonies, especially in children with lower BMI values.
Keywords: Lactobacillus, bifidobacterium, socioeconomic factors, nutritional status, environmental exposure, enteropathies.
IntroductionLactobacilli and bifidobacteria are microorganisms of the intestinal microbiota, well-known for their beneficial effects for human health and therefore called probiotic bacteria. Probiotic bacteria predominantly colonize the colon, but might also have beneficial effects to the small intestine, as well as systemic effects via immune system.1,2 A great number of these bacteria can be found in the colon of exclusively breastfed infants.3-5 This is a very important aspect since the composition of the colonic microbiota is established in the first months of life and tends to remain stable throughout life. Mode of delivery (vaginal or cesarean),1-6 the first environmental influence on the intestinal microbiota, also plays an extremely important role. In later stages of life, exposure to inadequate environmental conditions may cause tropical (environmental) enteropathy. Tropical enteropathy can be defined as a diffuse subclinical atrophy of the villus architecture in the small intestine, associated with inflammatory T cell infiltration.7-9 In tropical enteropathy, bacteria overgrowth in the proximal small intestine and alterations in indicator tests for enteral function may also occur, reflecting mucosal lesions.10 It has been observed that, in areas at risk for environmental enteropathy, enteropathogens can be found even in the feces of children without diarrhea.11 However, little research has been devoted to evaluate the participation of lactobacilli and bifidobacteria in the composition of the intestinal microbiota in areas that are most likely to develop environmental enteropathy. Studies12,13 conducted in the 1970s, involving a small number of malnourished children, revealed changes in the colonic microbiota during nutritional therapy.
Therefore, the objective of this study was to evaluate the number of lactobacillus and bifidobacterium colonies in the feces of school-age children from two different socioeconomic levels. One of them consisted of children from a favela, an environment likely to expose them to the risk of environmental enteropathy. The number of lactobacillus and bifidobacterium colonies was also related to weight and height and the presence or not of diarrheagenic Escherichia coli in the feces.
This cross-sectional study, conducted between August 2006 and September 2007, analyzed fecal samples of 122 children: 86 children living in a favela and 36 children attending a private school. Our strategy intended to obtain two groups of two different socioeconomic levels. The project was approved by the Research Ethics Committee of Universidade Federal de São Paulo - Escola Paulista de Medicina (UNIFESP-EPM), and the children's parents or legal guardians signed a free informed consent form.
Eligibility criteria for both groups included the following: aged between 6 and 10 years and absence of diarrhea for over 30 days. Exclusion criteria were: use of antibiotics in the previous 15 days, clinical evidence of severe diseases, such as cardiopathy, nephropathy, chronic liver disease, immunodeficiencies, and chronic neuropathy, or hospitalization in the previous months.
The first group was formed in a favela popularly called "Morro do Socó", located in a neighborhood called Portal D'Oeste, on the outskirts of the city of Osasco, State of São Paulo, southeastern Brazil. Houses are sited on steep hillsides, in an area with difficult access, next to a sanitary landfill. Children were selected to compose a representative sample of this population. Residences in the area were selected by random numbers according to information obtained from Osasco Housing Department. A community leader identified the children in the randomly selected residences. Thus, a total of 100 children were selected for the study. Their parents or legal guardians were invited to participate in a meeting in which they were explained about all study procedures. Of the 100 children selected, 86 agreed to participate and performed complete laboratory examination. Therefore, this group represented a probability sample of children aged 6 to 10 years living in the area where the study was carried out.
The private school group comprised elementary students attending Oswaldo Cruz School in Osasco. The school committee of pedagogical coordination invited the students' parents or legal guardians to participate in the study. Of the 60 children whose parents or legal guardians showed interest in participating in the study, 43 actually agreed to participate. Of the 43 children seven (16.3%) did not perform all laboratory tests. Therefore, this group was composed of 36 children and is a convenience sample that includes all students who agreed to participate in the study.
Regarding sample size, we intended to have the same number of children in both groups, but this was not possible because private school students' parents showed little interest in participating in the study. Preliminary data from the pilot study allowed us to demonstrate that the number of children in the study was sufficient to identify a statistically significant difference for the main variable of the study, that is, the number of lactobacillus and bifidobacterium colonies in the feces of children from the two different socioeconomic groups.
To evaluate socioeconomic conditions, the children's mothers or legal guardians were interviewed. We used a structured questionnaire concerning demographic data, materials used in the construction of houses and availability of water supply, public sewage system and garbage collection, in addition to information necessary to the application of the Brazilian Economic Classification Criterion (Critério de Classificação Econômica Brasil).14 This criterion classifies families in descending order, from A to E, according to possessions and schooling of the household head.
Nutritional status was assessed based on the children's weight and height (stature) measured according to the recommendation by Jelliffe.15 Participants in underwear were weighted on a FilizolaTM scale in a reserved place. Standing height was measured without shoes using a portable wall-mounted stadiometer, and attention was given to this step to ensure that spine and feet were in a straight line. Weight-for-age, height-for-age and body mass index (BMI) z scores16 were calculated using the Epi-Info software version 3.4.3,17 according to the reference values of the National Center for Health Statistics (NCHS).18
The number of lactobacillus and bifidobacterium colony-forming units (CFU) in the feces was determined in a fecal sample collected by spontaneous evacuation. Within a 2-hour interval, feces were homogenized, and 1.0 g was extracted and diluted 1:5 in saline solution (1.0 g of feces + 4.0 mL 0.9% saline). The saline diluted sample was then homogenized and diluted again (1:100). From the 1:100 dilution, successive dilutions were performed (10-1 to 10-5). For the cultivation 0.1 mL volume of each dilution was inoculated onto the surface of Rogosa SL (Difco) and Beerens agar plates for the cultivation of lactobacilli and bifidobacteria, respectively.19 Plates were incubated under anaerobiosis at 37 ºC for 48 and 72 hours. After incubation, the number of CFU/g was determined and one colony of each selective medium was selected for morphologic analysis, after Gram staining.
Isolation and identification of diarrheagenic Escherichia coli in the feces was performed by biochemical and serologic methods, complemented by hybridization tests with genetic probes. Research was conducted by the staff of the laboratory of UNIFESP-EPM Discipline of Microbiology, using traditional methods.20
Statistical analysis was performed using the SigmaStat 3.5 software version 7.1 for Windows,21 with a 5% significance level. Comparisons between groups were performed using the chi-square test or Fisher's exact test for the categorical variables and the Mann-Whitney test or Wilcoxon test for the continuous variables.
Table 1 shows comparisons of age, sex, socioeconomic class, living conditions, and nutritional status. Both groups were matched for age. Regarding sex, there were more girls in the private school group (p = 0.029). The Brazilian Economic Classification Criterion showed that most families in the favela group belonged to classes C, D and E. In the private school group, families belonged to classes A and B, except for one single family that belonged to class C. In the favela group, a large number of residences had illegal water supply connection, garbage disposal in the pit or open air and used open public garbage dumps. More than half (59.3%) of the houses in the favela were made of wood or wood and bricks. In contrast, all families in the private school group lived in brick-built houses, had legal water supply, garbage disposal in the public sewage system and garbage collection service available in the neighborhood.
The favela group had weight-for-age, height-for-age and BMI z scores lower (p < 0.05) than those observed in the private school group (Table 1).
Lactobacilli and bifidobacteria were not isolated in 8.1 (n = 7) and in 11.6% (n = 10), respectively, of the feces of the 86 children in the favela group, whereas lactobacilli and bifidobacteria were isolated in the samples of all children in the private school group. The proportion of children in the favela group with non-isolated fecal bifidobacteria (11.6%) was higher (p = 0.032, Fisher's exact test) than that of the private school group (0.0%). Lactobacillus and bifidobacterium colony counts (Table 2) were higher in the private school group in relation to the favela group (p < 0.001).
The Wilcoxon test showed that the number of bifidobacterium colonies was higher than that of lactobacillus colonies in both groups (favela, p = 0.007 and private school, p = 0.002). The Spearman coefficient showed a correlation between the number of lactobacillus and bifidobacterium colonies in each study group (favela, r = +0.824, p < 0.000 and private school, r = +0.605, p < 0.000).
To evaluate the relation between the number of lactobacillus and bifidobacterium colonies and nutritional status in the favela group, z scores were dichotomized at the cutoff point of -1.0 standard deviation (SD). As shown in Table 3, no statistically significant difference was observed in the number of lactobacillus and bifidobacterium colonies in children with weight-for-age and height-for-age z score < -1.0 SD, when comparing to those children with z score > -1.0 SD. In the favela group, children with BMI z score < -1.0 SD showed lower lactobacillus and bifidobacterium counts than those with BMI z score > -1.0 SD.
Table 4 shows the number of lactobacillus and bifidobacterium colonies according to the presence of diarrheagenic Escherichia coli, which were identified in 41 (51.9%) children in the favela group and in 6 (17.1%) children in the private school group. There was no statistically significant difference in the number of lactobacillus and bifidobacterium colonies, according to the presence or not of diarrheagenic Escherichia coli, between groups.
DiscussionIn the city of Osasco, between 1980 and 2000, a fall was observed in infant mortality rates and in proportional mortality due to diarrhea.22,23 However, groups living in unfavorable environmental conditions can still be detected in this city, including the region where the present study was carried out (Table 1).
The number of lactobacillus and bifidobacterium colonies in the feces of school-age children was lower in the children living in the favela than in those attending a private school. We could observe lower bacterial counts in the feces of children with BMI z score less than -1.0 SD.
Lactobacilli and bifidobacteria were isolated in all fecal samples collected in the private school. In the favela group, these bacteria were not isolated in the fecal samples of 10 (11.6%) of the 86 children. In Estonia and Sweden, lactobacilli and bifidobacteria were not found in the feces of 56.0 and 41.0%, respectively, of 27 allergic children at 2 years of age and in 40.0 and 29.0% of the 35 age-matched controls.24
These rates, both in the allergic and control groups, are higher than those observed in our study; however, age difference between the two samples should be taken into account.
Although the proportion of individuals without lactobacilli and bifidobacteria in our study was lower than that found in the literature, repeated attempts to search for lactobacilli and bifidobacteria in initially negative individuals were performed to discard technical problems or issues related to the period of time between evacuation and beginning of sample processing. Such attempts, basically, confirmed our initial results.
Regarding the number of lactobacillus and bifidobacterium colonies, the counts obtained in the private school group were similar to those observed in the children attending Rubens Sverner Day Nursery of Hospital Israelita Albert Einstein (HIAE), in the city of São Paulo.25 It is worth mentioning that only employees' children attended this nursery, i.e., this is not a charity day nursery, as other services offered by HIAE are, such as the outpatient clinic available to the population of the favela called "Paraisópolis". In this nursery, using a similar methodology for microbiological evaluation, the authors found between 0.86 and 1.30 x 109 CFU/g of lactobacilli and 1.20 and 1.30 x 109 CFU/g of bifidobacteria.25 In the present study, the mean lactobacillus count in the private school was 1.125 x 109 CFU/g, higher than that observed in 2-year-old non-allergic Swedish and Estonian children24 (median = 0.53 x 109 CFU/g), in 68 Japanese subjects26 under 20 years of age (0.48 x 109 CFU/g), and in 5 English children27 aged 16 months to 7 years. In addition, the mean number of bifidobacterium colonies (1.675 x 109 CFU/g) was also higher than that found in those studies: Swedish and Estonian24 (median = 0.93 x 109 CFU/g), Japanese26 (1.01 x 109 CFU/g) and English27 (0.98 x 109 CFU/g). Such difference might result from differences in the culture techniques employed and from age differences, taking into account that the number of colonies may vary in children, adults and elderly people.27 Other factors related to environment and life style may also affect the composition of the colonic microbiota. In the study conducted with Swedish and Estonian children, the (above mentioned) number of colonies in the controls was compared to that of allergic children, and no statistically significant difference was found.24 On the other hand, in the study carried out in Japan,26 children with atopic dermatitis showed less lactobacillus (0.527 x 109 and 0.489 x 109 CFU/g, respectively) and bifidobacterium (0.975 x 109 and 1.01 x 109 CFU/g) colonies than the controls, with statistically significant differences.
In this study, differences between mean lactobacillus and bifidobacterium counts were more significant than those observed in the Japanese children26 with atopic dermatitis. Therefore, differences in colonic microbiota seem to be more intensely affected by the unfavorable favela environment than by influence associated with abnormalities in the immune system of individuals with atopic dermatitis. The present study was developed along with other projects28,29 targeting the assessment of additional health and nutritional aspects of children living in the favela. We observed that favela children without diarrhea, in relation to private school children, showed increased frequency of bacterial overgrowth in the small intestine (28.2 and 3.0%, respectively)28 and of diarrheagenic Escherichia coli (51.9 and 17.1%).29 Thus, a small number of lactobacillus and bifidobacterium colonies might, hypothetically, be a part of the intestine global response to unfavorable environmental conditions. However, within this setting, no difference was observed in the number of lactobacillus and bifidobacterium colonies concerning the presence or not of diarrheagenic Escherichia coli in the feces of children living in the favela (Table 4). In such situation, probiotic bacteria would be expected to compete with diarrheagenic Escherichia coli. Evidence from the literature suggests that the increased number of lactobacillus and bifidobacterium colonies in the gastrointestinal tract is beneficial, since these colonies might inhibit or prevent adhesion30-32 and provide a competition for receptors in the intestinal mucosa,33 as well as protection against cell lesions caused by enteropathogenic bacteria.34,35 Therefore, it was not possible to confirm such theory with the methods used in the present study, pointing out that the children were without diarrhea when the study was carried out. The questionnaire used in this project did not include specific questions about occurrence of atopic diseases. In this context, it is worth mentioning that there is no complete agreement among studies on the prevalence of allergic diseases in different socioeconomic groups.36,37 We assume that low socioeconomic status and intestinal parasitosis are likely to be associated with a reduced risk of allergic diseases, in which, hypothetically, lower lactobacillus and bifidobacterium counts would be expected.38,39 Therefore, the lower lactobacillus and bifidobacterium counts observed in the low-socioeconomic group in the present study seem not to confirm such hypothesis.24,26
Data shown in Table 3 demonstrate that children with BMI z score < -1.0 SD had less lactobacillus and bifidobacterium colonies, with a statistically significant difference. The choice of this cutoff point allowed a characterization of decreased counts of potentially probiotic bacteria in individuals with lower BMI values. This result could not be achieved if the traditional -2.0 SD cutoff point was adopted; taking into account the small number of children that would be included in this category (7 of 86: 8.2%, in the favela group, and 1 of 36: 2.8%, in the private school group results not shown). In an analysis of the past 10-year literature, we could not find information on colonic microbiota in protein-calorie malnourished children. In the 1970s, studies12,13 carried out in Guatemala evaluated the microbiota in the digestive tube of children with malnutrition associated or not with diarrhea. In one of these studies,12 the colonic microbiota of four children with severe protein-calorie malnutrition was prospectively evaluated before nutritional treatment, during the stabilization phase and in two time points of the recuperation phase. An increase in the number of colonies of colonic anaerobes, which included lactobacilli and bifidobacteria, was detected, reverting the inversion of the ratio anaerobes/aerobes observed in malnutrition.12 The other article,13 which evaluated children with acute diarrhea secondary to Shigella dysenteriae infection, demonstrated in eight patients an increase in the sum of lactobacillus and bifidobacterium colonies between the third and the tenth day of antibiotic therapy.
Over recent years, probiotics have been used in the prevention of gastrointestinal abnormalities and in malnutrition induced in experimental animals.40,41 On the other hand, findings from recent experimental studies in animals show that intestinal microbiota might interfere in the regulation of the energy balance.42 In Finland, a group of 25 overweight children aged 7 years showed a lower number of bifidobacterium colonies and a larger number of Staphylococcus aureus colonies in their colonic microbiota at the end of their first year of life, when compared to 24 normal-weight schoolchildren.43 In the present study, overweight was observed in 5 (13.9%) of the 36 children attending private school, although the number of lactobacillus and bifidobacterium colonies in the feces of these children did not differ significantly from that observed in normal-weight children in the same group (results not shown). This information, however, should be analyzed with caution, considering the small number of children included in the private school group.
In conclusion, the microbiota of school-age children living in unfavorable environmental conditions shows reduced numbers of fecal lactobacillus and bifidobacterium colonies, especially of those children with lower BMI values.
1. Morais MB, Jacob CM. The role of probiotics and prebiotics in pediatric practice. J Pediatr (Rio J). 2006;82:S189-97. [ Links ]
2. Penna FJ, Péret LA, Vieira LQ, Nicoli JR. Probiotics and mucosal barrier in children. Curr Opin Clin Nutr Metab Care. 2008;11:640-4. [ Links ]
3. Holzapfel WH, Haberer P, Snel J, Schillinger U, Huis in't Veld JH. Overview of gut flora and probiotics. Int J Food Microbiol. 1998;41:85-101. [ Links ]
4. Isolauri E, Kirjavainen PV, Salminen S. Probiotics: a role in the treatment of intestinal infection and inflammation? Gut. 2002;50 Suppl 3:III54-9. [ Links ]
5. Mountzouris KC, McCartney AL, Gibson GR. Intestinal microflora of human infants and current trends for its nutritional modulation. Br J Nutr. 2002;87:405-20. [ Links ]
6. Parracho H, McCartney AL, Gibson GR. Probiotics and prebiotics in infant nutrition. Proc Nutr Soc. 2007;66:405-11. [ Links ]
7. Menzies IS, Zuckerman MJ, Nukajam WS, Somasundaram SG, Murphy B, Jenkins AP, et al. Geography of intestinal permeability and absorption. Gut. 1999;44:483-9. [ Links ]
8. Campbell DI, Murch SH, Elia M, Sullivan PB, Sanyang MS, Jobarteh B, et al. Chronic T cell-mediated enteropathy in rural west African children: relationship with nutritional status and small bowel function. Pediatr Res. 2003;54:306-11. [ Links ]
9. Kelly P, Menzies I, Crane R, Zulu I, Nickols C, Feakins R, et al. Responses of small intestinal architecture and function over time to environmental factors in a tropical population. Am J Trop Med Hyg. 2004;70:412-9. [ Links ]
10. dos Reis JC, de Morais MB, Oliva CA, Fagundes-Neto U. Breath hydrogen test in the diagnosis of environmental enteropathy in children living in an urban slum. Dig Dis Sci. 2007;52:1253-8. [ Links ]
11. Torres AL. Estudo microbiológico da diarréia aguda da criança em uma comunidade de favelados da cidade de São Paulo [tese]. São Paulo: Universidade Federal de São Paulo;1984. [ Links ]
12. Mata LJ, Jiménez F, Cordón M, Rosales R, Prera E, Schneider RE, et al. Gastrointestinal flora of children with protein-calorie malnutrition. Am J Clin Nutr. 1972;25:118-26. [ Links ]
13. Mata LJ, Mejicanos ML, Jiménez F. Studies on the indigenous gastrointestinal flora of Guatemalan children. Am J Clin Nutr. 1972;25:1380-90. [ Links ]
14. Associação Brasileira de Empresas de Pesquisa (ABEP). Critério de classificação econômica Brasil [página na Internet]. São Paulo; 2003 [citado 2006 Abr 28]. http://www.abep.org/codigosguias/ABEP_CCEB_2003.pdf. [ Links ]
15. Jelliffe DB. Evaluación del estado de nutrición de la comunidad (con especial referencia a las encuestas en las regiones en desarrollo. Ginebra: Organización Mundial de la Salud; 1968. [ Links ]
16. World Health Organization. Physical status: the use of and interpretation of anthropometry: report of a WHO expert committee. Geneva; WHO; 1995. [ Links ]
17. Epi-info [computer program]. Version 3.4.3. Atlanta (GA): Center of Disease Control and Prevention; 2007. [ Links ]
18. National Center for Infectious Diseases [homepage on the Internet]. Atlanta: Centers for Disease Control and Prevention (US); [Modified 2008 Aug 6]. 2000 CDC Growth Charts: United States; [reviewed 2008 May 16; cited 2008 Aug 6]. http://www.cdc.gov/growthcharts/. [ Links ]
19. Beerens H. Detection of bifidobacteria by using propionic acid as a selective agent. Appl Environ Microbiol. 1991;57:2418-9. [ Links ]
20. Scaletsky IC, Fabbricotti SH, Carvalho RL, Nunes CR, Maranhão HS, Morais MB, et al. Diffusely adherent Escherichia coli as a cause of acute diarrhea in young children in Northeast Brazil: a case-control study. J Clin Microbiol. 2002;40:645-8. [ Links ]
21. SigmaStat [computer program]. Version 3.5 for Windows. San Jose (CA): Systat Software Inc.; 2005. [ Links ]
22. Melli LC, Waldman EA. Temporal trends and inequality in under-5 mortality from diarrhea. J Pediatr (Rio J). 2009;85:21-7. [ Links ]
23. Victora CG. Diarrhea mortality: what can the world learn from Brazil? J Pediatr (Rio J). 2009; 85:3-5. [ Links ]
24. Björkstén B, Naaber P, Sepp E, Mikelsaar M. The intestinal microflora in allergic Estonian and Swedish 2-year-old children. Clin Exp Allergy. 1999;29:342-6. [ Links ]
25. Nóbrega FJ, Trabulsi LR, Keller R, Franzolin MR, Alves RC, Santos MF, et al. Efeitos do prebiótico (oligossacarídeo) em leite em pó modificado na flora intestinal: comparação com leite em pó modificado sem prebiótico em estudo duplo-cego. Rev Paul Pediatr. 2004;22:205-11. [ Links ]
26. Watanabe S, Narisawa Y, Arase S, Okamatsu H, Ikenaga T, Tajiri Y, et al. Differences in fecal microflora between patients with atopic dermatitis and healthy control subjects. J Allergy Clin Immunol. 2003;111:587-91. [ Links ]
27. Hopkins MJ, Sharp R, Macfarlane GT. Variation in human intestinal microbiota with age. Dig Liver Dis. 2002;34 Suppl 2:S12-8.28. [ Links ]
28. Mello CS. Estado nutricional e indicadores de enteropatia ambiental em escolares pertencentes a dois estratos socioeconômicos [dissertação]. São Paulo: Universidade Federal de São Paulo; 2008. [ Links ]
29. Souza TB. Pesquisa de Escherichia coli diarreiogênica nas fezes de crianças de diferentes níveis sociais do município de Osasco [dissertação]. São Paulo: Universidade Federal de São Paulo; 2008. [ Links ]
30. Forestier C, De Champs C, Vatoux C, Joly B. Probiotic activities of Lactobacillus casei rhamnosus: in vitro adherence to intestinal cells and antimicrobial properties. Res Microbiol. 2001;152:167-73. [ Links ]
31. Bernet MF, Brassart D, Neeser JR, Servin AL. Adhesion of human bifidobacterial strains to cultured human intestinal epithelial cells and inhibition of enteropathogen-cell interactions. Appl Environ Microbiol. 1993;59:4121-8. [ Links ]
32. Mack DR, Michail S, Wei S, McDougall L, Hollingsworth MA. Probiotics inhibit enteropathogenic E. coli adherence in vitro by inducing intestinal mucin gene expression. Am J Physiol. 1999;276:G941-50. [ Links ]
33. Marco ML, Pavan S, Kleerebezem M. Towards understanding molecular modes of probiotic action. Curr Opin Biotechnol. 2006;17:204-10. [ Links ]
34. Liévin-Le Moal V, Amsellem R, Servin AL, Coconnier MH. Lactobacillus acidophilus (strain LB) from the resident adult human gastrointestinal microflora exerts activity against brush border damage promoted by a diarrhoeagenic Escherichia coli in human enterocyte-like cells. Gut. 2002;50:803-11. [ Links ]
35. Resta-Lenert S, Barrett KE. Live probiotics protect intestinal epithelial cells from the effects of infection with enteroinvasive Escherichia coli (EIEC). Gut. 2003;52:988-97. [ Links ]
36. Gehring U, Pattenden S, Slachtova H, Antova T, Braun-Fahrländer C, Fabianova E, et al. Parental education and children's respiratory and allergic symptoms in the Pollution and the Young (PATY) study. Eur Respir J. 2006;27:95-107. [ Links ]
37. Almqvist C, Pershagen G, Wickman M. Low socioeconomic status as a risk factor for asthma, rhinitis and sensitization at 4 years in a birth cohort. Clin Exp Allergy. 2005;35:612-8. [ Links ]
38. Cooper PJ, Chico ME, Rodrigues LC, Strachan DP, Anderson HR, Rodriguez EA, et al. Risk factors for atopy among school children in a rural area of Latin America. Clin Exp Allergy. 2004;34:845-52. [ Links ]
39. Nascimento-Carvalho CM, Rocha H, Benguigui Y. Effects of socioeconomic status on presentation with acute lower respiratory tract disease in children in Salvador, Northeast Brazil. Pediatr Pulmonol. 2002;33:244-8. [ Links ]
40. Dock DB, Aguilar-Nascimento JE, Latorraca MQ. Probiotics enhance the recovery of gut atrophy in experimental malnutrition. Biocell. 2004;28:143-50. [ Links ]
41. Dock DB, Latorraca MQ, Aguilar-Nascimento JE, Gomes-da-Silva MH. Probiotics enhance recovery from malnutrition and lessen colonic mucosal atrophy after short-term fasting in rats. Nutrition. 2004;20:473-6. [ Links ]
42. DiBaise JK, Zhang H, Crowell MD, Krajmalnik-Brown R, Decker GA, Rittmann BE. Gut microbiota and its possible relationship with obesity. Mayo Clin Proc. 2008;83:460-9. [ Links ]
43. Kalliomäki M, Collado MC, Salminen S, Isolauri E. Early differences in fecal microbiota composition in children may predict overweight. Am J Clin Nutr. 2008;87:534-8. [ Links ]
Correspondence: Manuscript submitted Jan 15 2009, accepted for
publication Apr 15 2009. This study was conducted in the laboratory of
the Discipline of Microbiology, Department of Microbiology, Immunology and Parasitology,
and the Discipline of Pediatric Gastroenterology, Department of Pediatrics,
Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil.
Mauro Batista de Morais
Rua Pedro de Toledo, 441
CEP 04039-031 - São Paulo, SP - Brazil
Tel.: +55 (11) 5579.5834
Fax: +55 (11) 5579.5834
No conflicts of interest declared concerning the publication of this article.
Suggested citation: de Mello RM, de Morais MB, Tahan S, Melli LC, Rodrigues MS, Mello CS, et al. Lactobacilli and bifidobacteria in the feces of schoolchildren of two different socioeconomic groups: children from a favela and children from a private school. J Pediatr (Rio J). 2009;85(4):307-314.
Manuscript submitted Jan 15 2009, accepted for publication Apr 15 2009.
This study was conducted in the laboratory of
the Discipline of Microbiology, Department of Microbiology, Immunology and Parasitology,
and the Discipline of Pediatric Gastroenterology, Department of Pediatrics,
Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil.