Briñas Laura, Zarazaga Myriam, Sáenz Yolanda, Ruiz-Larrea Fernanda, Torres Carmen
Area de Bioquímica y Biología Molecular, Universidad de La Rioja, 26006 Logroño, Spain.
Antimicrob Agents Chemother. 2002 Oct;46(10):3156-63. doi: 10.1128/AAC.46.10.3156-3163.2002.
TEM-, SHV-, and OXA-type beta-lactamases were studied by PCR with 124 ampicillin-resistant (AMP(r)) Escherichia coli isolates recovered from foods of animal origin (n = 20) and feces of humans (n = 49) and healthy animals (n = 55). PCR showed that 103 isolates were positive for TEM and negative for SHV and OXA. Three E. coli isolates showed a positive reaction for OXA, and one showed a positive reaction for SHV. The remaining 17 E. coli isolates were negative for the three enzymes by PCR. Fifty-seven of the 103 bla(TEM) amplicons were sequenced. Different molecular variants of bla(TEM-1) were found in 52 isolates: bla(TEM-1a) (n = 9), bla(TEM-1b) (n = 36), bla(TEM-1c) (n = 6), and bla(TEM-1f) (n = 1). Four inhibitor-resistant TEM (IRT) beta-lactamase-encoding genes were also detected: bla(TEM-30c) (IRT-2), bla(TEM-34b) (IRT-6), bla(TEM-40b) (IRT-11), and bla(TEM-51a) (IRT-15). A new bla(TEM) gene, named bla(TEM-95b), which showed a mutation in amino acid 145 (P-->A) was detected. It was found in a food isolate of chicken origin (AMP(r), amoxicillin-clavulanic acid susceptible). The promoter region in 24 bla(TEM) amplicons was analyzed, and the weak P3 promoter was found in 23 of them (bla(TEM-1) in 20 amplicons and bla(TEM-51a), bla(TEM-30c), and bla(TEM-95b) in 1 amplicon each). The strong Pa/Pb promoter was found only in the bla(TEM-34b) gene. No extended-spectrum beta-lactamases were detected. Mutations at position -42 or -32 in the ampC gene promoter were demonstrated in 4 of 10 E. coli isolates for which the cefoxitin MIC was >/=16 micro g/ml. Different variants of bla(TEM-1) and IRT bla(TEM) genes were found among the AMP(r) E. coli isolates from foods and the feces of humans and healthy animals, and a new gene, bla(TEM-95b) (P3), was detected.
采用聚合酶链反应(PCR)对124株从动物源性食品(n = 20)、人类粪便(n = 49)和健康动物粪便(n = 55)中分离得到的耐氨苄西林(AMP(r))大肠埃希菌进行TEM型、SHV型和OXA型β-内酰胺酶研究。PCR结果显示,103株分离株TEM呈阳性,SHV和OXA呈阴性。3株大肠埃希菌分离株OXA呈阳性反应,1株SHV呈阳性反应。其余17株大肠埃希菌分离株PCR检测这三种酶均为阴性。对103个bla(TEM)扩增子中的57个进行了测序。在52株分离株中发现了bla(TEM-1)的不同分子变体:bla(TEM-1a)(n = 9)、bla(TEM-1b)(n = 36)、bla(TEM-1c)(n = 6)和bla(TEM-1f)(n = 1)。还检测到4个耐抑制剂TEM(IRT)β-内酰胺酶编码基因:bla(TEM-30c)(IRT-2)、bla(TEM-34b)(IRT-6)、bla(TEM-40b)(IRT-11)和bla(TEM-51a)(IRT-15)。检测到一个新的bla(TEM)基因,命名为bla(TEM-95b),该基因在第145位氨基酸发生突变(P→A)。它存在于一株鸡肉来源的食品分离株中(AMP(r),对阿莫西林-克拉维酸敏感)。分析了24个bla(TEM)扩增子的启动子区域,其中23个发现了弱P3启动子(20个扩增子中的bla(TEM-1)以及各1个扩增子中的bla(TEM-51a)、bla(TEM-30c)和bla(TEM-95b))。仅在bla(TEM-34b)基因中发现了强Pa/Pb启动子。未检测到超广谱β-内酰胺酶。在10株头孢西丁最低抑菌浓度(MIC)≥16 μg/ml的大肠埃希菌分离株中,有4株在ampC基因启动子的-42或-3位发生了突变。在来自食品以及人类和健康动物粪便的耐AMP(r)大肠埃希菌分离株中发现了bla(TEM-1)和IRT bla(TEM)基因的不同变体,并检测到一个新基因bla(TEM-95b)(P3)。