TY - JOUR
T1 - Frequency and distribution of α- and β-haemolysin in Staphylococcus aureus of bovine and human origin
T2 - A comparison between pheno- and genotype
AU - Aarestrup, Frank Møller
AU - Larsen, H. D.
AU - Eriksen, N. H. R.
PY - 1999
Y1 - 1999
N2 - The phenotypic expression of haemolysins and the presence of genes encoding α and β-haemolysin were determined in 105 Staphylococcus aureus isolates from bovine mastitis, 100 isolates from the nostrils of healthy humans, and 60 isolates from septicaemia in humans. Furthermore, the possible change in expression of haemolysins after subcultivation in human and bovine blood and milk was studied in selected isolates, α-haemolysin was expressed phenotypically in 39 (37%) of the bovine isolates, in 59 (59%) of the human carrier isolates, and in 40 (67%) of the isolates from septicaemia. β- haemolysin was expressed in 76 (72%) bovine, 11 (11%) carrier, and 8 (13%) septicaemia isolates. Significantly more bovine than human isolates expressed β-haemolysin and significantly fewer expressed α-haemolysin. Genotypically, the gene encoding α-haemolysin was detected in all isolates. A significant difference in the prevalence of the gene encoding β-haemolysin between the bovine (96%), human carrier (56%) and isolates from septicaemia (57%) was found. Of the bovine isolates, 75% of those carrying the gene encoding β- haemolysin expressed β-haemolysin phenotypically, whereas only 20% of the carrier isolates and 24% of the septicaemia isolates did so. No change in expression of haemolysins could be observed after subcultivation of bovine isolates in human blood and milk. After 5 to 10 subcultures in bovine blood and 1 to 4 in bovine milk, 9 of 10 human isolates originally phenotypically β-haemolysin negative initiated the expression of β-haemolysin. This study showed that a larger proportion of S. aureus of bovine origin carry the β- haemolysin gene compared to isolates from humans. Furthermore, a larger number of the isolates of bovine origin carrying the β-haemolysin gene express this gene phenotypically compared to isolates of human origin.
AB - The phenotypic expression of haemolysins and the presence of genes encoding α and β-haemolysin were determined in 105 Staphylococcus aureus isolates from bovine mastitis, 100 isolates from the nostrils of healthy humans, and 60 isolates from septicaemia in humans. Furthermore, the possible change in expression of haemolysins after subcultivation in human and bovine blood and milk was studied in selected isolates, α-haemolysin was expressed phenotypically in 39 (37%) of the bovine isolates, in 59 (59%) of the human carrier isolates, and in 40 (67%) of the isolates from septicaemia. β- haemolysin was expressed in 76 (72%) bovine, 11 (11%) carrier, and 8 (13%) septicaemia isolates. Significantly more bovine than human isolates expressed β-haemolysin and significantly fewer expressed α-haemolysin. Genotypically, the gene encoding α-haemolysin was detected in all isolates. A significant difference in the prevalence of the gene encoding β-haemolysin between the bovine (96%), human carrier (56%) and isolates from septicaemia (57%) was found. Of the bovine isolates, 75% of those carrying the gene encoding β- haemolysin expressed β-haemolysin phenotypically, whereas only 20% of the carrier isolates and 24% of the septicaemia isolates did so. No change in expression of haemolysins could be observed after subcultivation of bovine isolates in human blood and milk. After 5 to 10 subcultures in bovine blood and 1 to 4 in bovine milk, 9 of 10 human isolates originally phenotypically β-haemolysin negative initiated the expression of β-haemolysin. This study showed that a larger proportion of S. aureus of bovine origin carry the β- haemolysin gene compared to isolates from humans. Furthermore, a larger number of the isolates of bovine origin carrying the β-haemolysin gene express this gene phenotypically compared to isolates of human origin.
U2 - 10.1111/j.1699-0463.1999.tb01576.x
DO - 10.1111/j.1699-0463.1999.tb01576.x
M3 - Journal article
SN - 0903-4641
VL - 107
SP - 425
EP - 430
JO - APMIS
JF - APMIS
IS - 4
ER -