Evaluation of an immunomagnetic separation assay in combination with cultivation to improve Legionella pneumophila serogroup 1 recovery from environmental samples

被引:17
作者
Allegra, S. [1 ]
Girardot, F. [1 ]
Grattard, F. [1 ]
Berthelot, P. [1 ]
Helbig, J. H. [2 ]
Pozzetto, B. [1 ]
Riffard, S. [1 ]
机构
[1] Univ St Etienne, Grp Immunite Muqueuses & Agents Pathogenes, EA 3064, Fac Med,Univ Lyon, F-42023 St Etienne 02, France
[2] Tech Univ Dresden, Inst Med Microbiol & Hyg, Fac Med, Dresden, Germany
关键词
culture; environmental samples; immunomagnetic separation; Legionella; monoclonal antibody; ESCHERICHIA-COLI O157-H7; CRYPTOSPORIDIUM-PARVUM OOCYSTS; SOLID-PHASE CYTOMETRY; HOT-WATER SYSTEMS; RAPID DETECTION; FLOW-CYTOMETRY; MONOCLONAL-ANTIBODIES; TIME PCR; QUANTITATIVE DETECTION; MYCOBACTERIUM-AVIUM;
D O I
10.1111/j.1365-2672.2011.04955.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: Legionella isolation from environmental samples is often difficult because of the presence of heterotrophic-associated bacteria that frequently overgrow when using standard culture (ISO 11731, 1998; NF T90-431, 2003) methods. To improve Legionella pneumophila recovery from complex water samples (water from cooling towers, biofilms), we evaluated an immunomagnetic separation (IMS) assay using a monoclonal antibody raised against the lipopolysaccharide of Leg. pneumophila sg1 in combination with culture. Methods and Results: This study was conducted on 51 environmental specimens. The comparison between IMS-culture and standard culture (ISO 11731, 1998; NF T90-431, 2003) methods was made using ISO 17994, 2004 criteria for establishing equivalence between microbiological methods based on the upper and lower (X-H and X-L) values of the relative difference (95% confidence limit) and D as maximum acceptable deviation (value of the confidence limit). Conclusions: We found that the average performance of IMS culture was higher than the reference method. Significance and Impact of the Study: Thus, this IMS-culture assay is particularly well adapted to the detection of Leg. pneumophila sg1 in environmental samples with high levels of interfering microflora.
引用
收藏
页码:952 / 961
页数:10
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