Molecular Epidemiology of Nontypeable Haemophilus influenzae Causing Community-Acquired Pneumonia in Adults

被引:35
作者
Puig, Carmen [1 ,2 ,3 ,4 ]
Calatayud, Laura [1 ,2 ,3 ]
Marti, Sara [1 ,2 ,3 ]
Tubau, Fe [1 ,2 ]
Garcia-Vidal, Carolina [5 ,6 ]
Carratala, Jordi [5 ,6 ]
Linares, Josefina [1 ,2 ,3 ,4 ]
Ardanuy, Carmen [1 ,2 ,3 ]
机构
[1] Hosp Univ Bellvitge, Dept Microbiol, Barcelona, Spain
[2] ISCIII, CIBER Enfermedades Resp CIBERes, Madrid, Spain
[3] IDIBELL, Epidemiol Bacterial Infect Grp, Barcelona, Spain
[4] Univ Barcelona, Dept Pathol & Expt Therapeut, Barcelona, Spain
[5] Hosp Univ Bellvitge, Dept Infect Dis, Barcelona, Spain
[6] ISCIII, Spanish Network Res Infect Dis REIPI, Madrid, Spain
关键词
PENICILLIN-BINDING PROTEIN-3; AMPICILLIN RESISTANCE GENES; AMINO-ACID SUBSTITUTIONS; BETA-LACTAM RESISTANCE; ANTIMICROBIAL SUSCEPTIBILITY; ANTIBIOTIC-RESISTANCE; INFECTIONS; DIVERSITY; PATHOGENS; STRAINS;
D O I
10.1371/journal.pone.0082515
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nontypeable Haemophilus influenzae (NTHi) is an opportunistic pathogen which causes a variety of respiratory infections. The objectives of the study were to determine its antimicrobial susceptibility, to characterize the beta-lactam resistance, and to establish a genetic characterization of NTHi isolates. Ninety-five NTHi isolates were analyzed by pulsed field gel electrophoresis (PFGE) and multi locus sequence typing (MLST). Antimicrobial susceptibility was determined by microdilution, and the ftsI gene (encoding penicillin-binding protein 3, PBP3) was PCR amplified and sequenced. Thirty (31.6%) isolates were non-susceptible to ampicillin (MIC >= 2 mg/L), with 10 of them producing beta-lactamase type TEM-1 as a resistance mechanism. After ftsI sequencing, 39 (41.1%) isolates showed amino acid substitutions in PBP3, with Asn526 -> R Lys being the most common (69.2%). Eighty-four patients were successfully treated with amoxicillin/clavulanic acid, ceftriaxone and levofloxacin. Eight patients died due either to aspiration or complication of their comorbidities. In conclusion, NTHi causing CAP in adults shows high genetic diversity and is associated with a high rate of reduced susceptibility to ampicillin due to alterations in PBP3. The analysis of treatment and outcomes demonstrated that NTHi strains with mutations in the ftsI gene could be successfully treated with ceftriaxone or fluoroquinolones.
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