Bellais S, Poirel L, Leotard S, Naas T, Nordmann P
Service de Bactériologie-Virologie, Hôpital de Bicêtre, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine Paris-Sud, 94275 Le Kremlin-Bicêtre Cedex, France.
Antimicrob Agents Chemother. 2000 Nov;44(11):3028-34. doi: 10.1128/AAC.44.11.3028-3034.2000.
The class B carbapenem-hydrolyzing beta-lactamase IND-1 has been characterized for Chryseobacterium indologenes strain 001. With internal primers for the bla gene for IND-1 (bla(IND-1)) and an internal bla(IND-1) probe, PCR amplifications failed, while hybridization results were positive when DNA from another C. indologenes isolate, strain CIP101026, was used as a template. Thus, a bla(IND)-related gene was cloned from this C. indologenes reference strain. Sequencing of the insert of a recombinant plasmid conferring resistance to carbapenems revealed an open reading frame with a G + C content of 39.9% and coding for a 243-amino-acid preprotein named IND-2. IND-2 shared 80% amino acid identity with IND-1 and had a similar broad-spectrum resistance profile, including resistance to carbapenems. It was classified in functional subgroup 3a of class B carbapenem-hydrolyzing beta-lactamases. IND-1 and IND-2, despite their genetic diversity, possessed similar kinetic parameters, except that ceftazidime was hydrolyzed less by IND-2. To obtain the entire bla(IND)-related gene sequences of eight other C. indologenes isolates, PCR was performed using internal and external primers, followed by inverse PCR techniques. The likely chromosome-mediated metallo-beta-lactamases of the 10 C. indologenes isolates were divided into several groups and subgroups. IND-1, IND-2, IND-2a, IND-3, and IND-4 shared 77 to 99% amino acid identity.
已对吲哚金黄杆菌001菌株的B类碳青霉烯水解β-内酰胺酶IND-1进行了特性分析。使用IND-1的bla基因(bla(IND-1))内部引物和bla(IND-1)内部探针进行PCR扩增失败,而以另一株吲哚金黄杆菌分离株CIP101026的DNA为模板时杂交结果为阳性。因此,从该吲哚金黄杆菌参考菌株中克隆了一个与bla(IND)相关的基因。对赋予碳青霉烯抗性的重组质粒插入片段进行测序,发现一个开放阅读框,其G + C含量为39.9%,编码一种名为IND-2的243个氨基酸的前体蛋白。IND-2与IND-1具有80%的氨基酸同一性,并且具有相似的广谱抗性谱,包括对碳青霉烯的抗性。它被归类为B类碳青霉烯水解β-内酰胺酶功能亚组3a。IND-1和IND-2尽管存在遗传多样性,但具有相似的动力学参数,只是头孢他啶被IND-2水解的程度较低。为了获得其他8株吲哚金黄杆菌分离株的完整bla(IND)相关基因序列,使用内部和外部引物进行PCR,随后采用反向PCR技术。这10株吲哚金黄杆菌分离株可能的染色体介导金属β-内酰胺酶被分为几个组和亚组。IND-1、IND-2、IND-2a、IND-3和IND-4具有77%至99%的氨基酸同一性。