Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0023241 (Legionella)
 6,990 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Species identification of Legionella in routine laboratory testing is hampered by the lack of highly discriminatory phenotypic tests. Amplification polymorphism of the intergenic 16S-23S spacer regions (ISR) has been previously developed for identification of species within the Legionellaceae [Hookey, J.V., Birtles, R.J. & Saunders, N.A. (1995). J Clin Microbiol 33, 2377-2381], but it did not provide enough resolution to distinguish all members of the bluish-white autofluorescent species and the red autofluorescent group of the Legionellaceae. By choosing new primers that target regions 4 (positions 1521-1541 of Escherichia coli 16S rRNA gene) and 6 (positions 114-132 of E.coli 23S rRNA gene) within the rDNA operon close to the 16S-23S intergenic spacer, 34 profiles were determined among the 79 type and reference strains representing 42 species that were tested. Analysis of the RFLP generated after Hinfl restriction digestion of the PCR products further improved the method, allowing complete discrimination among the species and subspecies of Legionella tested. Twenty-three well-identified strains from unrelated origins belonging to seven species gave amplification patterns identical to that of their type strain. The technique was also tested on 80 field isolates that could not be unequivocally assigned to groups by phenotypic methods. Seventy-two per cent (58/80) of these isolates had a profile identical to that of a type strain, while 27% (22/80) may correspond to new taxa since their ISR-PCR profiles did not match any of the known profiles.
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PMID:Species identification of Legionella via intergenic 16S-23S ribosomal spacer PCR analysis. 973 26

The Mediterranean seaside resort of Le Grau du Roi includes 40 hectares of landscaped areas spray irrigated with river water supplied through a separate network. Wastewater collected from several municipalities is treated in an activated sludge wastewater treatment plant (WWTP) and polished in waste stabilization ponds (WSPs). Planned substitution of treated wastewater for river water is hindered by spray irrigation prohibition within a 100 m distance from houses and recreational areas. WWTP and WSP effluents were monitored for pathogens with a particular attention to Legionella in Spring and Summer 2006. Helminth eggs, salmonellae and enteroviruses were never detected neither in WWTP effluent nor in the ponds. Legionella spp content was slightly higher or of the order of magnitude of river water contents. Regarding Legionella pneumophila contents, WSP effluent did not significantly differ from the river water. E.coli and enterococci contents in WSP effluents complied with the "excellent quality" criteria of the European Directive for coastal bathing waters. Therefore, substituting WSP effluents to river water is unlikely to alter health risks related to spray irrigation and, in this case, the buffer zone required by the French water reuse guidelines appears being short of support.
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PMID:Water reuse for urban landscape irrigation: aspersion and health related regulations. 1840 Nov 52