The aim of this study was to verify the existence of synergistic antibacterial effect between four essential oils (Aniba rosaeodora, Melaleuca alternifolia, Origanum vulgare, and Pelargonium graveolens) individually combined with the antibacterial drug Gentamicin. We investigated the effectiveness in vitro of the association of essential oil/Gentamicin, against fifteen different strains of Gram positive and Gram negative bacteria. The antibacterial effects of these oils in combination with Gentamicin were evaluated by using the MHB microdilution method, while gas chromatography (GC) and GC/Mass spectrometry were used to analyze the chemical composition of the oils. A synergistic interaction was observed against all tested strains with the associations between the essential oils Aniba rosaeodora/Gentamicin and Pelargonium graveolens/Gentamicin. In particular a very strong synergistic interaction was observed against Acinetobacter baumannii ATCC 19606 (FIC index = 0.11). In contrast, the essential oils Origanum vulgare and Melaleuca alternifolia in association with Gentamicin were less effective on bacterial species growth. In vitro interaction can improve the antimicrobial effectiveness of the Gentamicin and may contribute to reduce its dose correlated to side effects.

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Infestazioni ed infezioni intestinali parassitari nel biennio 2006 -2007 nell'esperienza perugina SUMMARYBetween 2006-07 faecal specimens of 2.132 subjects (1.508 adults and 624 children) were examined for ova & parasites, using direct and after formalin-ethylacetate concentration microscopy, and permanent specific stains. 380 bubjects (17.8 %) were infected: 313 adults (20.8 %) and 67 children (10.7 %). 331 cases (15.5 %) were infected by pathogens, 275 adults (18.2 %) and 56 children (9.0 %). 389 pathogenic or not pathogenic protozoa (18.2 %) and 60 helminths (2.8 %) were identified, more among adults than children (21.0 % vs 11.5 % and 3.2 % vs 1.8 % respectively).Among protozoa, D. fragilis was in all observed in 145 cases (6.8 %), G. duodenalis in 74 cases (3.5 %), other were very rare.Among helminths nematodes were more frequent than trematodes and cestodes, with S. stercoralis (14 cases) and E. vermicularis (13 cases) the most frequent ones. 2.302 subjects (1.505 adults and 797 children) were examined for microbiological tests because affected by acute or prolonged diarrhoea. 82 cases (3.6 %) of protozoal infections were observed, 70 among adults (4.7 %) and 12 among children (1.5 %). D. fragilis was in all prevalent (2.0 %) in respect of G. duodenalis (1.0 %) or other ones (0.6 %). For S. stercoralis specific investigation, modified Baermann method / larvae colture were performed: 20/189 cases (10.6 %) od strongyloidiasis was diagnosed in adults. For E. vermicularis investigation, scotch test was performer: 43/179 cases (24.0%) of enterobiasis was diagnosed. The Authors underline the application of standard operative procedures for O & P with permanent specific stains in subject affected by enterites too, and the analysis of more specimens for each subjects for good diagnostical performances.

Valutazione del sistema GeneXpert ® per la rilevazione di Staphylococcus aureus meticillinoresistente in campioni clinici SUMMARY Infections caused by methicillin-resistant Staphyloccocus aureus strains (MRSA) have reached epidemic proportions globally, being the major cause of nosocomial infections. Rapid identification of MRSA in nasal swabs or in clinical samples is considered a useful strategy for control and treatment of these infections. GeneXpert system (Cepheid Europe,Vira-Solelch, Maurence-Scopont-France) can detect by real-time PCR in approximately one hour methicillin-resistant S. aureus or coagulase-negative staphylococci (CoNS) in clinical samples, in comparison with 24 hours for the culture or 48 hours for the antimicrobial susceptibility testing. In this study GeneXpert system was compared with traditional tests for MRSA detection in nasal swabs, bloodcultures and surgical wound swabs. Materials and methods. Eighteen nasal swabs, 23 blood-cultures and 13 surgical wound swabs were tested. The samples were cultured on blood-agar and mannitol-salt agar. Identification of isolates was carried out with traditional tests (Gram staining, catalase, coagulase) and automatic Phoenix system. Methicillin-susceptibility was evaluated according to 2010 CLSI guidelines. GeneXpert system was performed according to manufacturers instructions, by using the specific kits and methicillin-resistance was detected by amplification of the genic sequences spa, SCC e mecA. Results. The results showed a 100% accordance between GeneXpert system and traditional tests for detection of methicillin-resistant staphylococci. In particular, among 18 nasal swabs, no MRSA was detected, while 1 bloodculture (4.3%) and 4 surgical wound swabs (30.7%) were positive for MRSA. Conclusions. GeneXpert system allows a rapid detection of MRSA in clinical samples and shows the same sensitivity and specificity as traditional tests. Therefore, it represents a further effective diagnostic method for prevention and treatment of nosocomial infections due to methicillin-resistant staphylococci.