Autor(es):
Almeida, Carina 
; Azevedo, N. F. ; Keevil, C. W. ; Vieira, M. J.
Data: 2009
Identificador Persistente: http://hdl.handle.net/1822/17314
Origem: RepositóriUM - Universidade do Minho
Detalhes do Documento
Salmonella enterica adhesion to different surfaces in the presence of Echerichi...
Descrição
AIMS Salmonella species have shown a great ability to adhere to solid surfaces and form biofilms. These may serve as pathogens reservoirs enhancing the risk of public health issues. In nature, biofilms are not usually formed by a single-species and the presence of other organisms may affect Salmonella population dynamics on surfaces. In this study, the Salmonella enterica serovar Enteritidis ability to adhere to different surfaces when in pure culture or co-cultured with Escherichia coli, was investigated. METHODS E. coli ATCC 25922 and S. Enteritidis ATCC 13076 suspension of ~ 1×108 total cells/ml in TSB were prepared. For each suspension (single and two species) 6 ml were added to each well of a 6-well tissue culture plate containing coupons of different materials. The plate was incubated at 24ºC ±2 and samples were taken with time (2, 4,6,24 and 48h). Cells were detached using a sonication step for cultivability assessment, total counts (DAPI) and Salmonella counts using a species-specific peptide nucleic acid (PNA). Cells were also visualized in situ by PNA- Fluorescence in situ hybridization (FISH) counterstained with DAPI. Total biomass was quantified by crystal violet (CV). RESULTS For all seven materials tested results were similar whatever the nature of the adhesion material. Typically E.coli outnumbered S. enterica in the adhered population for all materials, except for copper that presented similar number of cells and CFU’s for both populations. Cultivability and CV data revealed that total adhesion in the two-species culture is faster than S. enterica adhesion in pure culture, occurring in the first hours and then stabilizing with time. The direct detection (PNA FISH) in biofilms presented some limitations for particular types of adhesion materials mainly related with the autofluorescence of the support material. This limitation was overcome by disrupting the biofilm sample followed by hybridization in suspension. Direct counts by PNA-FISH were compared with CFU´s counts and provided similar values. CONCLUSIONS The S. enterica co-inoculation with E. coli did not interfered with the total number of Salmonella cells adhered to each material. Nevertheless, E. coli was typically the outnumbered species. Comparing PNA-FISH counts with CFU´s confirmed that this method represents a reliable tool for mixed/natural biofilm study, allowing specific and direct detectionand providing spatial organization.
AIMS Salmonella species have shown a great ability to adhere to solid surfaces and form biofilms. These may serve as pathogens reservoirs enhancing the risk of public health issues. In nature, biofilms are not usually formed by a single-species and the presence of other organisms may affect Salmonella population dynamics on surfaces. In this study, the Salmonella enterica serovar Enteritidis ability to adhere to different surfaces when in pure culture or co-cultured with Escherichia coli, was investigated. METHODS E. coli ATCC 25922 and S. Enteritidis ATCC 13076 suspension of ~ 1×108 total cells/ml in TSB were prepared. For each suspension (single and two species) 6 ml were added to each well of a 6-well tissue culture plate containing coupons of different materials. The plate was incubated at 24ºC ±2 and samples were taken with time (2, 4,6,24 and 48h). Cells were detached using a sonication step for cultivability assessment, total counts (DAPI) and Salmonella counts using a species-specific peptide nucleic acid (PNA). Cells were also visualized in situ by PNA- Fluorescence in situ hybridization (FISH) counterstained with DAPI. Total biomass was quantified by crystal violet (CV). RESULTS For all seven materials tested results were similar whatever the nature of the adhesion material. Typically E.coli outnumbered S. enterica in the adhered population for all materials, except for copper that presented similar number of cells and CFU’s for both populations. Cultivability and CV data revealed that total adhesion in the two-species culture is faster than S. enterica adhesion in pure culture, occurring in the first hours and then stabilizing with time. The direct detection (PNA FISH) in biofilms presented some limitations for particular types of adhesion materials mainly related with the autofluorescence of the support material. This limitation was overcome by disrupting the biofilm sample followed by hybridization in suspension. Direct counts by PNA-FISH were compared with CFU´s counts and provided similar values. CONCLUSIONS The S. enterica co-inoculation with E. coli did not interfered with the total number of Salmonella cells adhered to each material. Nevertheless, E. coli was typically the outnumbered species. Comparing PNA-FISH counts with CFU´s confirmed that this method represents a reliable tool for mixed/natural biofilm study, allowing specific and direct detectionand providing spatial organization.
Tipo de Documento
Documento de conferência
Idioma Inglês
Idioma Inglês
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