Molecular characterization and antimicrobial susceptibility patterns of Clostridium difficile strains isolated from hospitals in south-east Scotland

被引:49
作者
Mutlu, Esvet
Wroe, Allison J.
Sanchez-Hurtado, Karla
Brazier, Jon S.
Poxton, Ian R.
机构
[1] Univ Edinburgh, Coll Med & Vet Med, Ctr Infect Dis, Edinburgh EH16 4SB, Midlothian, Scotland
[2] Univ Wales Hosp, NPHS Microbiol Cardiff, Anaerobe Ref Lab, Cardiff CF4 4XW, S Glam, Wales
关键词
D O I
10.1099/jmm.0.47176-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Clostridium difficile isolates (n= 149) collected in south-east Scotland between August and October 2005 were typed by four different methods and their susceptibility to seven different antibiotics was determined. The aims were to define the types of strain occurring in this region and to determine whether there were any clonal relationships among them with respect to genotype and antibiotic resistance pattern. Ribotyping revealed that 001 was the most common type (n= 113, 75.8 %), followed by ribotype 106 (12 isolates, 8.1 %). The majority of the isolates (96.6 %, n = 144) were of toxinotype 0, with two toxinotype V isolates and single isolates of toxinotypes I, IV and XIII. PCR and restriction analysis of the NC gene from 147 isolates gave two restriction patterns: 145 of pattern VII and two of pattern I. Binary toxin genes were detected in only three isolates: two isolates of ribotype 126, toxinotype V, and one isolate of ribotype 023, toxinotype IV. S-types showed more variation, with 64.5 % (n = 40) of the common S-type (4939) and 21 % (n= 13) of S-type 4741, with six other S-types (one to three isolates each). All ribotype 001 isolates were of the same S-type (4939), with three isolates of other ribotypes being this S-type. No resistance was found to metroniclazole or vancomycin, with resistance to tetracycline only found in 4.3 % of the isolates. A high proportion of isolates were resistant to clindamycin (62.9 %), moxifloxacin, ceftriaxone (both 87.1 %) and erythromycin (94.8 %). Resistance to three antibiotics (erythromycin, clindamycin and ceftriaxone) was seen in 66 isolates, with erythromycin, ceftriaxone and moxifloxacin resistance seen in 96 isolates. Resistance to all four of these antibiotics was found in 62 isolates and resistance to five (the above plus tetracycline) in one isolate: a ribotype 001, toxinotype 0 strain. Whilst ribotype 001 was the most commonly encountered type, there was no evidence of clonal relationships when all other typing and antibiotic resistance patterns were taken into account.
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页码:921 / 929
页数:9
相关论文
共 47 条
[1]   Resistance to moxifloxacin in toxigenic Clostridium difficile isolates is associated with mutations in gyrA [J].
Ackermann, G ;
Tang, YJ ;
Kueper, R ;
Heisig, P ;
Rodloff, AC ;
Silva, J ;
Cohen, SH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (08) :2348-2353
[2]   Prevalence and association of macrolide-lincosamide- streptogramin B (MLSB) resistance with resistance to moxifloxacin in Clostridium difficile [J].
Ackermann, G ;
Degner, A ;
Cohen, SH ;
Silva, J ;
Rodloff, AC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (03) :599-603
[3]   Toxigenic status of Clostridium difficile in a large Spanish teaching hospital [J].
Alonso, R ;
Martín, A ;
Peláez, T ;
Marín, M ;
Rodríguez-Creixéms, M ;
Bouza, E .
JOURNAL OF MEDICAL MICROBIOLOGY, 2005, 54 (02) :159-162
[4]  
[Anonymous], MACKIE MCCARTNEY PRA
[5]   Antimicrobial susceptibility pattern of Clostridium difficile and its relation to PCR ribotypes in a Swedish University Hospital [J].
Aspevall, O ;
Lundberg, A ;
Burman, LG ;
Åkerlund, T ;
Svenungsson, B .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (05) :1890-1892
[6]   Clinical features of Clostridium difficile-associated diarrhoea due to binary toxin (actin-specific ADP-ribosyltransferase)-producing strains [J].
Barbut, F ;
Decré, D ;
Lalande, V ;
Burghoffer, A ;
Noussair, L ;
Gigandon, A ;
Espinasse, F ;
Raskine, L ;
Robert, J ;
Mangeol, A ;
Branger, C ;
Petit, JC .
JOURNAL OF MEDICAL MICROBIOLOGY, 2005, 54 (02) :181-185
[7]   Comparison of PCR-ribotyping, arbitrarily primed PCR, and pulsed-field gel electrophoresis for typing Clostridium difficile [J].
Bidet, P ;
Lalande, V ;
Salauze, B ;
Burghoffer, B ;
Avesani, V ;
Delmée, M ;
Rossier, A ;
Barbut, F ;
Petit, JC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2484-2487
[8]   Reduced susceptibility of Clostridium difficile to metronidazole [J].
Brazier, JS ;
Fawley, W ;
Freeman, J ;
Wilcox, MH .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 48 (05) :741-742
[9]   Typing of Clostridium difficile [J].
Brazier, JS .
CLINICAL MICROBIOLOGY AND INFECTION, 2001, 7 (08) :428-431
[10]   Comparison of PCR-based approaches to molecular epidemiologic analysis of Clostridium difficile [J].
Collier, MC ;
Stock, F ;
DeGirolami, PC ;
Samore, MH ;
Cartwright, CP .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (05) :1153-1157