Voladri R K, Kernodle D S
Division of Infectious Diseases, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-2605, USA.
Antimicrob Agents Chemother. 1998 Dec;42(12):3163-8. doi: 10.1128/AAC.42.12.3163.
In contrast to most Staphylococcus aureus isolates in which the gene for staphylococcal beta-lactamase (blaZ) is plasmid borne, isolates typeable by group II bacteriophages frequently carry blaZ on the chromosome. Furthermore, the chromosomal gene encodes the type B variant of staphylococcal beta-lactamase for which the nucleotide and deduced amino acid sequences have not yet been reported. To better understand beta-lactamase production among phage group II staphylococci and the nature of the type B beta-lactamase, we determined the type and amount of enzyme produced by 24 phage group II isolates. Of these isolates, 1 did not produce beta-lactamase, 8 produced the type B enzyme, and 15 produced the type C enzyme. In all eight type B beta-lactamase-producing isolates, blaZ was located on the chromosome. This was in contrast to the type C beta-lactamase-producing isolates, in which blaZ was located on a 21-kb plasmid. The nucleotide sequence corresponding to the leader peptide and the N-terminal 85% of the mature exoenzyme form of type B S. aureus was determined. The deduced amino acid sequence revealed 3 residues in the leader peptide and 12 residues in the exoenzyme portion of the beta-lactamase that differ from the prototypic type A beta-lactamase sequence. These include the serine-to-asparagine change at residue 216 found in the kinetically similar type C enzyme, a threonine-to-lysine change at residue 128 close to the SDN loop (residues 130 to 132), and several substitutions not found in any of the other staphylococcal beta-lactamases. In summary, modern isolates of S. aureus typeable by group II phages produce type B or type C staphylococcal beta-lactamase. The type B gene resides on the chromosome and has a sequence that, when compared to the sequences of the other staphylococcal beta-lactamases, corresponds well with its kinetic properties.
与大多数金黄色葡萄球菌分离株不同,在这些分离株中葡萄球菌β-内酰胺酶(blaZ)基因是质粒携带的,而可通过II组噬菌体分型的分离株常常在染色体上携带blaZ。此外,染色体基因编码葡萄球菌β-内酰胺酶的B型变体,其核苷酸和推导的氨基酸序列尚未见报道。为了更好地了解II组噬菌体葡萄球菌中β-内酰胺酶的产生情况以及B型β-内酰胺酶的性质,我们测定了24株II组噬菌体分离株产生的酶的类型和数量。在这些分离株中,1株不产生β-内酰胺酶,8株产生B型酶,15株产生C型酶。在所有8株产生B型β-内酰胺酶的分离株中,blaZ位于染色体上。这与产生C型β-内酰胺酶的分离株相反,在这些分离株中blaZ位于一个21kb的质粒上。测定了与B型金黄色葡萄球菌成熟外切酶形式的前导肽和N端85%相对应的核苷酸序列。推导的氨基酸序列显示,β-内酰胺酶前导肽中有3个残基,外切酶部分有12个残基与原型A型β-内酰胺酶序列不同。这些包括在动力学上相似的C型酶中在第216位残基处丝氨酸到天冬酰胺的变化,靠近SDN环(第130至132位残基)的第128位残基处苏氨酸到赖氨酸的变化,以及在任何其他葡萄球菌β-内酰胺酶中均未发现的几个取代。总之,可通过II组噬菌体分型的现代金黄色葡萄球菌分离株产生B型或C型葡萄球菌β-内酰胺酶。B型基因位于染色体上,其序列与其他葡萄球菌β-内酰胺酶的序列相比,与其动力学性质相符。