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Research Project
ECOLOGY AND PERSISTENCE OF LISTERIA MONOCYTOGENES IN FOOD ASSOCIATED ENVIRONMENTS RETAIL ESTABLISHMENTS AND KITCHENS FROM HOSPITALS AND ELDERLY LONG-TERM CARE INSTITUTIONS
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Biofilm formation among clinical and food isolates of Listeria monocytogenes
Publication . Barbosa, Joana; Borges, Sandra; Camilo, Ruth; Magalhães, Rui; Ferreira, Vânia; Santos, Isabel; Silva, Joana; Almeida, Gonçalo; Teixeira, Paula
Objective. A total of 725 Listeria monocytogenes isolates, 607 from various foods and 118 from clinical cases of listeriosis, were investigated concerning their ability to form biofilms, at 4°C during 5 days and at 37°C during 24 h. Methods. Biofilm production was carried out on polystyrene tissue culture plates. Five L. monocytogenes isolates were tested for biofilm formation after being exposed to acidic and osmotic stress conditions. Results. Significant differences ( ) between clinical and food isolates were observed. At 37°C for 24 h, most food isolates were classified as weak or moderate biofilm formers whereas all the clinical isolates were biofilm producers, although the majority were weak. At 4°C during 5 days, 65 and 59% isolates, from food and clinical cases, respectively, were classified as weak. After both sublethal stresses, at 37°C just one of the five isolates tested was shown to be more sensitive to subsequent acidic exposure. However, at 4°C both stresses did not confer either sensitivity or resistance. Conclusions. Significant differences between isolates origin, temperature, and sublethal acidic stress were observed concerning the ability to form biofilms. Strain, origin, and environmental conditions can determine the level of biofilm production by L. monocytogenes isolates.
Enrichment of acinetobacter spp. from food samples
Publication . Carvalheira, Ana; Ferreira, Vânia; Silva, Joana; Teixeira, Paula
Relatively little is known about the role of foods in the chain of transmission of acinetobacters and the
occurrence of different Acinetobacter spp. in foods. Currently, there is no standard procedure to recover
acinetobacters from food in order to gain insight into the food-related ecology and epidemiology of
acinetobacters. This study aimed to assess whether enrichment in Dijkshoorn enrichment medium followed
by plating in CHROMagar™ Acinetobacter medium is a useful method for the isolation of Acinetobacter
spp. from foods. Recovery of six Acinetobacter species from food spiked with these organisms
was compared for two selective enrichment media (Baumann's enrichment and Dijkshoorn's enrichment).
Significantly (p < 0.01) higher cell counts were obtained in Dijkshoorn's enrichment. Next, the
Dijkshoorn's enrichment followed by direct plating on CHROMagar™ Acinetobacter was applied to
detect Acinetobacter spp. in different foods. Fourteen different presumptive acinetobacters were recovered
and assumed to represent nine different strains on the basis of REP-PCR typing. Eight of these
strains were identified by rpoB gene analysis as belonging to the species Acinetobacter johnsonii, Acinetobacter
calcoaceticus, Acinetobacter guillouiae and Acinetobacter gandensis. It was not possible to identify
the species level of one strain which may suggests that it represents a distinct species
Prevalence of staphylococcus aureus from nares and hands on health care professionals in a portuguese hospital
Publication . Castro, A.; Komora, N.; Ferreira, Vânia; Lira, A.; Mota, M.; Silva, Joana; Teixeira, Paula
Aims: The main goal was to estimate the prevalence of methicillin-resistant
Staphylococcus aureus on hands and in nose of health care professionals.
Methods and Results: Detection of Staph. aureus on hands or in the nose of
169 individuals was performed. Nasal and hand carriage was found in 39 6 and
in 8 9% respectively. About 17 2% of the individuals were carriers of
methicillin-resistant Staph. aureus (MRSA) in the nose and 4 7% on hands.
The majority of nasal MRSA were resistant to b-lactams, erythromycin and
ciprofloxacin. All nasal MRSA were SCCmec type IV and Panton-Valentine
leukocidin (PVL) negative. One MRSA isolated from hand was SCCmec type
V. About 75 6% of MRSA isolates presented the same or closely related
restriction patterns. Sixty per cent of Staph. aureus from hands and from noses
from the same individual were the same strain.
Conclusions: MRSA nasal carriage was high considering healthy health care
professionals but in accordance with high level of MRSA infection in Portugal.
Isolates recovered in this study seemed to be different from major clones
previously isolated in other Portuguese hospitals.
Significance and Impact of the Study: These findings may have implications
on the knowledge of healthy health care workers as vehicles of MRSA
infections among the community. Presence of several virulence factors may
contribute to increased pathogenesis in case of infection.
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Funding agency
Fundação para a Ciência e a Tecnologia
Funding programme
FARH
Funding Award Number
SFRH/BPD/72617/2010