期刊论文详细信息
BMC Microbiology
Typing of Ochrobactrum anthropi clinical isolates using automated repetitive extragenic palindromic-polymerase chain reaction DNA fingerprinting and matrix-assisted laser desorption/ionization–time-of-flight mass spectrometry
Alfredo Focà1  Maria Carla Liberto1  Giovanni Matera1  Maria Rosaria Catania2  Nadia Marascio1  Rossana Puccio1  Linda Rametti1  Giovanna Pulcrano2  Angela Quirino1 
[1] Institute of Microbiology, Department of Health Sciences, “Magna Graecia” University, Viale Europa, Catanzaro, Italy;Department of Molecular and Cellular Biology and Pathology L. Califano, Medicine School, University of Naples Federico II, Naples, Italy
关键词: Strain typing;    MALDI-TOF MS;    rep-PCR fingerprinting;    Ochrobactrum anthropi;   
Others  :  1141549
DOI  :  10.1186/1471-2180-14-74
 received in 2013-09-05, accepted in 2014-03-18,  发布年份 2014
PDF
【 摘 要 】

Background

Ochrobactrum anthropi (O. anthropi), is a non-fermenting gram-negative bacillus usually found in the environment. Nevertheless, during the past decade it has been identified as pathogenic to immunocompromised patients. In this study, we assessed the usefulness of the automated repetitive extragenic palindromic-polymerase chain reaction (rep-PCR-based DiversiLab™ system, bioMèrieux, France) and of matrix-assisted laser desorption/ionization-time-of-flight (MALDI-TOF MS) for typing of twentythree O. anthropi clinical isolates that we found over a four-months period (from April 2011 to August 2011) in bacteriemic patients admitted in the same operative unit of our hospital. Pulsed-field gel electrophoresis (PFGE), commonly accepted as the gold standard technique for typing, was also used. Analysis was carried out using the Pearson correlation coefficient to determine the distance matrice and the unweighted pair group method with arithmetic mean (UPGMA) to generate dendogram.

Results

Rep-PCR analysis identified four different patterns: three that clustered together with 97% or more pattern similarity, and one whose members showed < 95% pattern similarity. Interestingly, strains isolated later (from 11/06/2011 to 24/08/2011) displayed a pattern with 99% similarity. MALDI-TOF MS evaluation clustered the twentythree strains of O. anthropi into a single group containing four distinct subgroups, each comprising the majority of strains clustering below 5 distance levels, indicating a high similarity between the isolates.

Conclusions

Our results indicate that these isolates are clonally-related and the methods used afforded a valuable contribution to the epidemiology, prevention and control of the infections caused by this pathogen.

【 授权许可】

   
2014 Quirino et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150327075322837.pdf 1514KB PDF download
Figure 4. 39KB Image download
Figure 3. 115KB Image download
Figure 2. 52KB Image download
Figure 1. 169KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

【 参考文献 】
  • [1]Soloaga R, Carrion N, Pidone J, Guelfand L, Margari A, Altieri R: Catheter-associated bacteremia caused by Ochrobactrum anthropi. Medicina (B Aires) 2009, 69(suppl.6):655-657.
  • [2]Nadjar D, Labia R, Cerceau C, Bizet C, Philippon A, Arlet G: Molecular characterization of chromosomal class C beta-lactamase and its regulatory gene in Ochrobactrum anthropi. Antimicrob Agents Chemother 2001, 45(suppl.8):2324-2330.
  • [3]Romano S, Aujoulat F, Jumas-Bilak E, Masnou A, Jeannot JL, Falsen E, Marchandin H, Teyssier C: Multilocus sequence typing supports the hypothesis that Ochrobactrum anthropi displays a human-associated subpopulation. BMC Microbiol 2009, 9:267. doi:10.1186/1471-2180-9-267 BioMed Central Full Text
  • [4]Daxboeck F, Zitta S, Assadian O, Krause R, Wenisch C, Kovarik J: Ochrobactrum anthropi bloodstream infection complicating hemodialysis. Am J Kidney Dis 2002, 40(suppl. 4):E17.
  • [5]Shrishrimal K: Recurrent: Ochrobactrum anthropi and Shewanella putrefaciens bloodstream infection complicating hemodialysis. Hemodial Int 2011. doi:10.1111/j.1542-4758.2011.00586.x
  • [6]Wi YM, Peck KR: Biliary sepsis caused by Ochrobactrum anthropi. Jpn J Infect Dis 2010, 63(suppl.6):444-446.
  • [7]Song S, Ahn JK, Lee GH, Park YG: An epidemic of chronic pseudophakic endophthalmitis due to Ochrobactrum anthropi: clinical findings and managements of nine consecutive cases. Ocul Immunol Inflamm 2007, 15(suppl.6):429-434.
  • [8]van Dijck P, Delmée M, Ezzedine H, Deplano A, Struelens MJ: Evaluation of pulsed-field gel electrophoresis and rep-PCR for the epidemiological analysis of Ochrobactrum anthropi strains. Eur J Clin Microbiol Infect Dis 1995, 14(suppl.12):1099-1102.
  • [9]Naik C, Kulkarni H, Darabi A, Bhanot N: Ochrobactrum anthropi: a rare cause of pneumonia. J Infect Chemother 2013, 19(1):162-5.
  • [10]Lebuhn M, Achouak W, Schloter M, Berge O, Meier H, Barakat M, Hartmann A, Heulin T: Taxonomic characterization of Ochrobactrum sp. Isolates from soil samples and wheat roots, and description of Ochrobactrum tritici sp. nov. and Ochrobactrum grignonense sp. nov. Int J Syst Evol Microbiol 2000, 50:2207-2223.
  • [11]Bathe S, Achouak W, Hartmann A, Heulin T, Schloter M, Lebuhn M: Genetic and phenotypic microdiversity of Ochrobactrum spp. FEMS Microbiol Ecol 2006, 56(suppl.2):272-280.
  • [12]Bizzini A, Jaton K, Romo D, Bille J, Prod’hom G, Greub G: MALDI-TOF Mass Spectrometry as an alternative to 16S rDna sequencing for identification of difficult to identify bacterial strains. J Clin Microbiol 2010. doi:10.1128/JCM.01463-10
  • [13]Treviño M, Navarro D, Barbeito G, García-Riestra C, Crespo C, Regueiro BJ: Molecular and epidemiological analysis of nosocomial carbapenem-resistant Klebsiella spp. using repetitive extragenic palindromic-polymerase chain reaction and matrix-assisted laser desorption/ionization-time of flight. Microb Drug Resist 2011, 17(3):433-442. doi:10.1089/mdr.2010.0182
  • [14]Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH, Swaminathan B: Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 1995, 33:2233-2239.
  • [15]Pulcrano G, Roscetto E, Iula VD, Panellis D, Rossano F, Catania MR: MALDI-TOF mass spectrometry and microsatellite markers to evaluate Candida parapsilosis transmission in neonatal intensive care units. Eur J Clin Microbiol Infect Dis 2012, 31:2919-2928.
  • [16]Appelbaum PC, Campbell DB: Pancreatic abscess associated with Achromobacter group Vd biovar 1. J Clin Microbiol 1980, 12:282-283.
  • [17]Cieslak TJ, Robb ML, Drabick CJ, Fischer GW: Catheter-associated sepsis caused by Ochrobactrum anthropi: report of a case and review of related nonfermentative bacteria. Clin Infect Dis 1992, 14(suppl.4):902-907.
  • [18]Treviño M, Navarro D, Barbeito G, Areses P, García-Riestra C, Regueiro BJ: Plasmid-mediated AMPc producing Proteus mirabilis in the Health Care Area of Santiago de Compostela: molecular and epidemiological analysis by rep-PCR and MALDI-TOF. Rev Esp Quimioter 2012, 25(2):122-8.
  • [19]Ligozzi M, Fontana R, Aldegheri M, Scalet G, Lo Cascio G: Comparative evaluation of an automated repetitive-sequence-based PCR instrument versus pulsed-field gel electrophoresis in the setting of a Serratia marcescens nosocomial infection outbreak. J Clin Microbiol 2010, 48(5):1690-5.
  文献评价指标  
  下载次数:58次 浏览次数:14次