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1.
PLoS Negl Trop Dis ; 10(11): e0005102, 2016 11.
Article in English | MEDLINE | ID: mdl-27893750

ABSTRACT

The human mutilating disease chromoblastomycosis is caused by melanized members of the order Chaetothyriales. To assess population diversity among 123 clinical strains of agents of the disease in Brazil we applied sequencing of the rDNA internal transcribed spacer region, and partial cell division cycle and ß-tubulin genes. Strains studied were limited to three clusters divided over the single family Herpotrichiellaceae known to comprise agents of the disease. A Fonsecaea cluster contained the most important agents, among which F. pedrosoi was prevalent with 80% of the total set of strains, followed by 13% for F. monophora, 3% for F. nubica, and a single isolate of F. pugnacius. Additional agents, among which two novel species, were located among members of the genus Rhinocladiella and Cyphellophora, with frequencies of 3% and 1%, respectively.


Subject(s)
Ascomycota/isolation & purification , Chromoblastomycosis/microbiology , Ascomycota/classification , Ascomycota/genetics , Brazil/epidemiology , Chromoblastomycosis/epidemiology , DNA, Fungal/genetics , DNA, Ribosomal Spacer/genetics , Humans , Molecular Epidemiology , Mycological Typing Techniques , Phylogeny
2.
Microb Ecol ; 67(3): 624-34, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24658546

ABSTRACT

The sequence of bacterial events that occurs during the colonization of the gastrointestinal tract may affect the future health of the host. A clear understanding of the colonization process of the human neonatal gut in developing countries is lacking because the few available studies were mostly performed using culture techniques. Using molecular approaches, this study analyzed the fecal microbiota of children of low socioeconomic status in São Paulo, Brazil, during their first year of life. We collected fecal samples of healthy children at 3, 6, and 12 months of life. Total DNA was extracted directly from feces, and the bacteria-specific primers 27F-1492R were used to construct 16S rRNA libraries. Clones were randomly selected and partially sequenced. The main phylogenetic groups identified at 3 months were Streptococcus, unidentified bacteria, and Escherichia. At 6 months, Escherichia remained predominant, while the unidentified bacterial population increased significantly. At 12 months, a more complex composition of fecal microbiota was observed, represented by unidentified bacteria and microorganisms found at low rates at earlier ages. The genus Escherichia remained the most abundant microorganism (34% relative abundance and 75% prevalence). Principal component analysis (PCA) revealed changes in the composition of the microbiota at 6 months and an increase of diversity at 12 months of life. Bifidobacterium was identified by quantitative PCR (qPCR) and showed a high incidence in the microbiota at 3 months. The present results corroborate the global observation of inter-individual variability with an early establishment of microbial complexity at the end of the first year of life and highlight the presence of the Escherichia as abundant in microbiota composition of this group of children.


Subject(s)
Escherichia coli/physiology , Feces/microbiology , Bifidobacterium/genetics , Bifidobacterium/isolation & purification , Brazil , Escherichia coli/genetics , Escherichia coli/isolation & purification , Female , Humans , Infant , Male , Molecular Sequence Data , Phylogeny , RNA, Ribosomal, 16S/genetics , Real-Time Polymerase Chain Reaction , Sequence Analysis, DNA
3.
Vaccine ; 31(51): 6150-4, 2013 Dec 09.
Article in English | MEDLINE | ID: mdl-23747454

ABSTRACT

The ten-pneumococcal conjugate vaccine (PCV10) was introduced into the national immunization program for childhood vaccination schedules by the Brazilian Health Public Service in March 2010. The aim of this study was to compare Streptococcus pneumoniae serotype distribution, antibiotic resistance patterns, and potential coverage before (January 2006-June 2010) and after (July 2010-September 2012) PCV10 introduction. The incidence of invasive pneumococcal disease (IPD), patient demographics, and disease characteristics were recorded. This study was conducted at the University Hospital of Sao Paulo University in Brazil from January 2006 to September 2012. Serotyping was performed using multiplex PCR typing, and antimicrobial sensitivity by Clinical and Laboratory Standards Institute (CLSI). A total of 259 S. pneumoniae strains were isolated from patients with IPD. The ages of the patients ranged from 3 months to 95 years old. The strains were isolated from cerebrospinal fluid, pleural fluid, and blood. The incidence of IPD among patients at HU-USP changed after the introduction of PCV10. The overall incidence of IPD was 3.42 cases per 1000 admissions in the vaccine pre- implementation period and of 2.99 cases per 1000 admissions in the vaccine post-implementation period. The incidence of IPD among children<2 y.o. attended at HU-USP changed significantly after the introduction of PCV10, from 20.30 to 3.97 of incidence. The incidence of PCV10- serotypes decrease from 16.47 to 0.44 in the same age, before and after PC10 implementation, respectively. Moreover, it was possible to realize the sensitivity to penicillin among isolates increased significantly in the post-vaccine period. Data from this study suggest that PCV10 contributed to decrease with PID rate among children less than 2 y.o. The resistance rate among pneumococcal isolates also could be observed since serotypes with greater resistance to beta lactam antibiotics were not easily isolated after vaccination.


Subject(s)
Pneumococcal Infections/microbiology , Pneumococcal Vaccines/administration & dosage , Pneumococcal Vaccines/immunology , Serotyping , Streptococcus pneumoniae/classification , Adolescent , Adult , Anti-Bacterial Agents/pharmacology , Brazil/epidemiology , Child , Child, Preschool , Drug Resistance, Bacterial , Female , Humans , Incidence , Infant , Male , Pneumococcal Infections/epidemiology , Pneumococcal Infections/prevention & control , Streptococcus pneumoniae/drug effects , Streptococcus pneumoniae/immunology , Streptococcus pneumoniae/isolation & purification , Young Adult
4.
Clinics (Sao Paulo) ; 67(2): 113-23, 2012.
Article in English | MEDLINE | ID: mdl-22358235

ABSTRACT

OBJECTIVE: The establishment of the intestinal microbiota in newborns is a critical period with possible long-term consequences for human health. In this research, the development of the fecal microbiota of a group of exclusively breastfed neonates living in low socio-economic conditions in the city of São Paulo, Brazil, during the first month of life, was studied. METHODS: Fecal samples were collected from ten neonates on the second, seventh, and 30(th) days after birth. One of the neonates underwent antibiotic therapy. Molecular techniques were used for analysis; DNA was extracted from the samples, and 16S rRNA libraries were sequenced and phylogenetically analyzed after construction. A real-time polymerase chain reaction (PCR) was performed on the samples taken from the 30(th) day to amplify DNA from Bifidobacterium sp. RESULTS: The primary phylogenetic groups identified in the samples were Escherichia and Clostridium. Staphylococcus was identified at a low rate. Bifidobacterium sp. was detected in all of the samples collected on the 30(th) day. In the child who received antibiotics, a reduction in anaerobes and Escherichia, which was associated with an overgrowth of Klebsiella, was observed throughout the experimental period. CONCLUSION: The observed pattern of Escherichia predominance and reduced Staphylococcus colonization is in contrast with the patterns observed in neonates living in developed countries.


Subject(s)
Bacteria/isolation & purification , Breast Feeding , DNA, Bacterial/genetics , Feces/microbiology , Intestines/microbiology , RNA, Ribosomal, 16S/genetics , Bacteria/classification , Bacteria/genetics , Bifidobacterium/genetics , Bifidobacterium/isolation & purification , Brazil , Clostridium/genetics , Clostridium/isolation & purification , Colony Count, Microbial , Escherichia coli/genetics , Escherichia coli/isolation & purification , Female , Humans , Infant, Newborn , Male , Poverty , Sequence Analysis, DNA , Staphylococcus/genetics , Staphylococcus/isolation & purification
5.
Clinics ; 67(2): 113-123, 2012. ilus, graf, tab
Article in English | LILACS | ID: lil-614634

ABSTRACT

OBJECTIVE: The establishment of the intestinal microbiota in newborns is a critical period with possible long-term consequences for human health. In this research, the development of the fecal microbiota of a group of exclusively breastfed neonates living in low socio-economic conditions in the city of São Paulo, Brazil, during the first month of life, was studied. METHODS: Fecal samples were collected from ten neonates on the second, seventh, and 30th days after birth. One of the neonates underwent antibiotic therapy. Molecular techniques were used for analysis; DNA was extracted from the samples, and 16S rRNA libraries were sequenced and phylogenetically analyzed after construction. A real-time polymerase chain reaction (PCR) was performed on the samples taken from the 30th day to amplify DNA from Bifidobacterium sp. RESULTS: The primary phylogenetic groups identified in the samples were Escherichia and Clostridium. Staphylococcus was identified at a low rate. Bifidobacterium sp. was detected in all of the samples collected on the 30th day. In the child who received antibiotics, a reduction in anaerobes and Escherichia, which was associated with an overgrowth of Klebsiella, was observed throughout the experimental period. CONCLUSION: The observed pattern of Escherichia predominance and reduced Staphylococcus colonization is in contrast with the patterns observed in neonates living in developed countries.


Subject(s)
Female , Humans , Infant, Newborn , Male , Breast Feeding , Bacteria/isolation & purification , DNA, Bacterial/genetics , Feces/microbiology , Intestines/microbiology , /genetics , Brazil , Bacteria/classification , Bacteria/genetics , Bifidobacterium/genetics , Bifidobacterium/isolation & purification , Colony Count, Microbial , Clostridium/genetics , Clostridium/isolation & purification , Escherichia coli/genetics , Escherichia coli/isolation & purification , Poverty , Sequence Analysis, DNA , Staphylococcus/genetics , Staphylococcus/isolation & purification
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