Investigations were made in respect of the biological properties, the drug resistance, and the phagetype on 1171 strains of Staphylococcus which were isolated from various materials collected, from Feb. 1964 to Jun. 1965, at the Central Clinical Laboratory of the Affiliated Hospital of the Jikei University School of Medicine.
The stressing point was laid, in this paper, on properties related with coagulase activity and drug resistance.
Results are summed up as follows:
1) Materials and coagulase activity: Of total 1171 strains, 653 (55.7%) were coagulase positive, 518 (44.3%), negative. Of 440 pus-derived strains, 384 (87.3%) were coagulase positive, 56 (12.7)% were negative but considered to be pathogenic. On the contraly, of 486 urine-derived strains, 388 (79.8%) were coagulase negative and considered to be including many non-pathogenic strains, the contaminants from anteriol nare of urethra.
2) Biological properties related with coagulase activity: Mannitol fermentation activity, gelatin liquifaction activity, fibrinolysin producing activity, hemolytic activity on rabbit erythrocytes were seen in 97.1%, 94.3%, 86.0%, 83.6% of coagulase positive strains respectively. These properties were also seen in roughly 50% of coagulase negative strains except that fibrinolysin producing activity was seen in 15% of them. So, in general., comparatively paralleled relation is seen between coagulase and fibrinolysin producing activity.
3) Drug resistance: Penicillin-G (PC-G), Tetracycline (TC), Streptomycin (SM), Erythromycin (EM), Chloramphenicol (CP), Kanamycin (KM), Dimethoxyphenyl-penicillin (DMP-PC) were employed in this series. Marked increase of (EM)-resistant strains was noticed compared to others' data in 1957-1960. The incidence of resistant strains to (PC-G), (TC), (SM), or (EM) was 10-30% higher in coagulase positive strains than in negatve ones. Contrarily, to (CP), it was 14% higher in negative ones. To (KM) and (DMP-PC), however, it was only 2-3% regardless coagulase activity. As to the drug multiplicity in drug resistance, the pattern prevailing over single-drug-resistance in coagulase positive strains was (PC-G)-resistance. In duple-, or more drug-resistance, the combination of (PC-G)-(TC), (PC-G)-(TC)-(SM), (PC-G)-(TC)-(SM)-(EM), (PC-G)-(TC)-(SM)-(EM)-(CP) were predominant. Especially in quadruple-, or more drug-resistance, the latter two patterns rapidly increased. Furthermore, this tendency was more conspicuous in phage-typable strains than untypables. The multiple-drug-resistant strains, belonging to above patterns mostly belonged to the phage type Group 1 and subordinately to Group “miscellaneous”. On the other hand, the drug resistance pattern in coagulase negative strains covered comparatively wide range of drugs. It was noteworthy that the greater part of single-drugresistance was (PC-G)- resistance as seen in coagulase positive strains, while the combinations as (PC-G)-(TC), (PC-G)-(TC)-(CM), (PC-G)-(TC)-(CP)-(EM), (PC-G)-(TC)-(CM)-(EM)-(SM) were encountered very often, (CP) being replacing (SM) of triple-, and qaudruple-drug pattern in coagulase positive ones. From the results concerning the drug resistance and phage type, it can be conceivable that the phage typable strains with the drug resistance of (PC-G)-(TC)-(SM)-(EM) pattern obtained from natural world, include a large number of strains which were given the drug resistance by the transduction activity of phage.
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