scholarly journals Potable water and nosocomial Legionnaires' disease – check water from all rooms in which patient has stayed

1995 ◽  
Vol 114 (2) ◽  
pp. 267-276 ◽  
Author(s):  
T. J. Marrie ◽  
W. Johnson ◽  
S. Tyler ◽  
G. Bezanson ◽  
D. Haldane ◽  
...  

SummaryWe studied 7 patients with nosocomial Legionnaires' disease to determine the relationship between isolates ofLegionella pneumophilarecovered from potable water and those recovered from patients. Potable water was cultured from all rooms in which patients had stayed prior to the diagnosis of Legionnaires' disease. The 38 isolates ofL. pneumophila(31 environmental, 7 patient) were resolved into 9 distinct patterns by pulse-field gel electrophoresis (PFGE), 3 by plasmid content and 2 each with monoclonal antibodies and conventional agarose gel electrophoresis of small fragments of DNA.Using PFGE it was determined that 4 of the 7 patients were infected withL. pneumophilaidentical to an isolate recovered from the potable water supply in one of the rooms each had occupied prior to the diagnosis of Legionnaires' disease. Patients had resided in a mean of 3·57 rooms before a diagnosis of nosocomial Legionnaires' disease. We conclude that in the setting of contaminated potable water and nosocomial Legionnaires' disease water from all the rooms which the patient has occupied prior to this diagnosis should be cultured. PFGE of large DNA fragments discriminated best among the isolates ofL. pneumophila.

1980 ◽  
Vol 29 (3) ◽  
pp. 1092-1095
Author(s):  
G B Knudson ◽  
P Mikesell

Sixteen strains from the six serogroups of Legionella pneumophila were examined for the presence of extrachromosomal genetic elements by a modified cleared lysate procedure, dye-buoyant centrifugation, and agarose gel electrophoresis. Two strains, Atlanta-1 and Atlanta-2 from serogroup II, each contained a plasmid of cryptic function with a molecular weight of ca. 30 megadaltons.


1988 ◽  
Vol 60 (02) ◽  
pp. 133-136 ◽  
Author(s):  
R Schneppenheim ◽  
H Plendl ◽  
U Budde

SummaryA luminescence assay was adapted for detection of von Willebrand factor multimers subsequent to SDS-agarose gel electrophoresis and electroblotting onto nitrocellulose. The method is as fast as chromogenic detection methods and appears to be as sensitive as autoradiography without the disadvantages of the latter.


1987 ◽  
Vol 15 (16) ◽  
pp. 6749-6749 ◽  
Author(s):  
Michel Bellis ◽  
Michel Pagès ◽  
Gérard Roizès

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