European multicentre evaluation of a commercial system for identification of methicillin-resistant Staphylococcus aureus.

A commercial system for the rapid detection of methicillin-resistant Staphylococcus aureus, the BBL Crystal MRSA test (C-MRSA ID; Becton Dickinson, USA), was evaluated prospectively and compared with a polymerase chain reaction test for the presence of the mecA gene. Ten European centres tested a total of 676 isolates of Staphylococcus aureus from blood cultures. The system correctly identified 661 (97.8%) isolates within 4 h. All but three mecA gene-negative isolates (99.4% specificity) yielded a negative C-MRSA ID reaction, and 158 of 170 mecA gene-positive isolates were accurately detected (92.9% sensitivity). After repeated testing of discrepant results, sensitivity and specificity increased to 99% and 100%, respectively.

Lytic activities, protein profiles and morphologic characteristics of new bacteriophages isolated from canine and human Staphylococcus aureus strains.

The lytic activity, protein profile and morphology of five newly isolated phages from canine Staphylococcus aureus strains and one from a human S. aureus strain were compared with those of selected phages in the international phage sets (IPS). Five canine phages lysed 57 (76.0%) of 75 canine isolates of Staphylococcus aureus from Nigeria at routine test dilution (RTD) while 34 (IPS) phages typed only 31 (41.3%) strains at RTD or/and 100-RTD. The new human phage lysed 11 (14.7%) of 75 strains isolated from human diarrhoea. The new phages were readily propagated, specific in activity and stable during storage at 4 degrees C. Prominent proteins detected by SDS-PAGE indicated similarities between some of the phages but one canine phage was distinctly different, as was its morphology which was an isometric head with a short tail compared to oval heads and long tails which characterized others. IPS phages in the same serologic group had similar protein profiles but no correlation was observed with lytic groups. The use of protein profile and electron micrographs allowed classification of the phages into serogroups. It is concluded that the newly isolated canine phages could be very useful in typing Nigerian canine strains of S. aureus.

[Electronenmicroscopic Studies on Cells of Listeria monocytogenes Treated with Enterocin (author's transl)]. / Elektronenmikroskopische Untersuchungen von Enterocinbehandelten Listeria monocytogenes-Zellen

Purified enterocin E1A, a bacteriocin produced by Streptococcus faecium E1, had a strong bactericidal activity on susceptible cells of Listeria monocytogenes. Electronmicroscopic observation of thin sections of L. monocytogenes, treated with enterocin E1A at a concentration that gave 0.1% survivors, revealed that the predominant features of morphological alterations concern the partial dissolution of the cell content and the damage of the cell envelope which enabled an efflux of cell-material. Not frequently intact protoplasts and greatly elongated cells were observed.

Effects of enterocin E1A on the ultrastructure of Streptococcus faecium.

Streptococcus faecium 158 cells were examined by electron microscopy at sequential intervals after addition of enterocin E1A, a bacteriocin produced by Streptococcus faecium E1. After addition of enterocin E1A, the nuclear material began to concentrate into distinct areas at the center of the bacteria. In a later stage, extensive condensation of the nuclear filaments left a small cluster of dense granules within a cytoplasmic vacuole, and 10-20% of the cells underwent a complete lysis.