Molecular Characterization of a Respiratory Syncytial Virus Outbreak in a Hematology Unit in Heidelberg, Germany

被引:38
作者
Geis, Steffen [1 ]
Prifert, Christiane [2 ]
Weissbrich, Benedikt [2 ]
Lehners, Nicola [3 ]
Egerer, Gerlinde [3 ]
Eisenbach, Christoph [4 ]
Buchholz, Udo [5 ]
Aichinger, Elisabeth [6 ,7 ]
Dreger, Peter [3 ]
Neben, Kai [3 ]
Burkhardt, Ulrich [1 ]
Ho, Anthony D. [3 ]
Kraeusslich, Hans-Georg [1 ]
Heeg, Klaus [8 ]
Schnitzler, Paul [1 ]
机构
[1] Heidelberg Univ, Dept Infect Dis Virol, Heidelberg, Germany
[2] Univ Wurzburg, Inst Virol & Immunobiol, Wurzburg, Germany
[3] Heidelberg Univ, Dept Internal Med 5, Heidelberg, Germany
[4] Heidelberg Univ, Dept Internal Med 4, D-69115 Heidelberg, Germany
[5] Robert Koch Inst, Dept Infect Dis Epidemiol, Berlin, Germany
[6] Robert Koch Inst, Postgrad Training Programme Appl Epidemiol, Berlin, Germany
[7] Baden Wuerttemberg State Hlth Off, Stuttgart, Germany
[8] Heidelberg Univ, Dept Infect Dis Med Microbiol & Hyg, Heidelberg, Germany
关键词
CELL TRANSPLANTATION RECIPIENTS; GROUP-A; SUBGROUP-A; NOSOCOMIAL OUTBREAK; G-PROTEIN; INFECTION; PNEUMONIA; DIVERSITY; DISEASES; STRAINS;
D O I
10.1128/JCM.02151-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In 2011 and 2012, a large outbreak of respiratory syncytial virus (RSV) infections affecting 57 laboratory-confirmed patients occurred in an adult hematology unit in Heidelberg, Germany. During the outbreak investigation, we performed molecular genotyping of RSV strains to differentiate between single versus multiple introductions of the virus into the unit. Furthermore, we assessed the time of viral shedding of consecutive samples from the patients in order to better understand the possible impact of prolonged shedding for outbreak control management. We used subtype-specific reverse transcription-PCR on nasopharyngeal and bronchoalveolar specimens for routine diagnostics and for measuring the viral shedding period. Samples of 47 RSV-infected patients involved in the outbreak were genotyped by sequence analysis and compared to samples from RSV-infected hospitalized children representing the timing of the annual RSV epidemic in the community. Molecular investigation of the virus strains from clinical samples revealed a unique cluster with identical nucleotide sequences of RSV type A (RSV A outbreak strain) for 41 patients, while 3 patients were infected with different RSV A (nonoutbreak) strains and three other patients with RSV type B. Outbreak strains were identified in samples from November 2011 until January 2012, while nonoutbreak strains were from samples coinciding with the community epidemic in February and March 2012. Median duration of viral shedding time was 24.5 days (range, 1 to 168 days) with no difference between outbreak and nonoutbreak strains (P = 0.45). Our investigation suggests a single introduction of the RSV A outbreak strain into the unit that spread among the immunocompromised patients. Prolonged viral shedding may have contributed to nosocomial transmission and should be taken into account in the infection control management of RSV outbreaks in settings with heavily immunosuppressed patients.
引用
收藏
页码:155 / 162
页数:8
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