Microbiological diagnosis and molecular typing of Legionella strains during an outbreak of legionellosis in Southern Germany

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• 作者：Andreas Essig^a ; Heike von Baum^a ; Theodor Gonser^b ; Georg Haerter^c ; ¹ ; Christian Lü ; ck^d ; ^{Christian.Lueck@Uniklinikum-Dresden.de" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Legionnaire's disease ; Outbreak ; Cooling tower ; Legionella pneumophila ; Molecular typing ; Pneumonia
• 刊名：International Journal of Medical Microbiology
• 出版年：2016
• 出版时间：February 2016
• 年：2016
• 卷：306
• 期：2
• 页码：109-114
• 全文大小：223 K

文摘

An explosive outbreak of Legionnaires’ disease with 64 reported cases occurred in Ulm/Neu-Ulm in the South of Germany in December 2009/January 2010 caused by Legionella (L.) pneumophila serogroup 1, monoclonal (mAb) subtype Knoxville, sequence type (ST) 62. Here we present the clinical microbiological results from 51 patients who were diagnosed at the University hospital of Ulm, the results of the environmental investigations and of molecular typing of patients and environmental strains. All 50 patients from whom urine specimens were available were positive for L. pneumophila antigen when an enzyme-linked immunosorbent assay (EIA) was used following concentration of those urine samples that tested initially negative. The sensitivity of the BinaxNow rapid immunographic assay (ICA), after 15 min reading and after 60 min reading were 70% and 84%, respectively. Direct typing confirmed the monoclonal subtype Knoxville in 5 out of 8 concentrated urine samples. Real time PCR testing of respiratory tract specimens for L. pneumophila was positive in 15 out of 25 (60%) patients. Direct nested sequence based typing (nSBT) in some of these samples allowed partial confirmation of ST62. L. pneumophila serogroup 1, monoclonal subtype Knoxville ST62, defined as the epidemic strain was isolated from 8 out of 31 outbreak patients (26%) and from one cooling tower confirming it as the most likely source of the outbreak. While rapid detection of Legionella antigenuria was crucial for the recognition and management of the outbreak, culture and molecular typing of the strains from patients and environmental specimens was the clue for the rapid identification of the source of infection.