Pulsed‐field gel electrophoretic identification of Salmonella enterica serovar Typhimurium live vaccine strain Zoosaloral H

Letters in Applied Microbiology

Volumn 19, Issue 6, 1994, Pages 469-472

  Schwarz, S ^a   Liebisch, Babett ^a  

^a INSTITUTE FOR EPIDEMIOLOGY AND PATHOGEN DIAGNOSTICS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

SALMONELLA; VACCINES;

GEL ELECTROPHORESIS ANALYSIS; LIVE VACCINES; OBSERVATION PERIOD; PULSED FIELD GEL ELECTROPHORESIS; PULSED FIELDS; RESTRICTION ENZYMES; SALMONELLA ENTERICA; SALMONELLA ENTERICA SEROVAR TYPHIMURIUM; SEROVARS; VACCINE STRAINS;

ELECTROPHORESIS;

RESTRICTION ENDONUCLEASE; VACCINE;

ARTICLE; BACTERIUM IDENTIFICATION; CONTROLLED STUDY; NONHUMAN; PULSED FIELD GEL ELECTROPHORESIS; SALMONELLA ENTERICA;

ANIMALIA; BACTERIA (MICROORGANISMS); SALMONELLA ENTERICA; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHIMURIUM; TYPHIMURIUM;

EID: 0028080341     PISSN: 02668254     EISSN: 1472765X     Source Type: Journal    
DOI: 10.1111/j.1472-765X.1994.tb00984.x     Document Type: Article

References (9)

1. A physical map of the Salmonella typhimurium LT2 genome made by using XbaI analysis
2. The XbaI‐BlnI‐CeuI genomic cleavage map of Salmonella paratyphi B
3. Heteroduplex analysis of Salmonella virulence plasmids and their prevalence in isolates of defined sources
4. Clonal lines of Salmonella enterica serotype Enteritidis documented by IS200‐, ribo‐, pulsed‐field gel electrophoresis and RFLP typing
5. DNA finger‐printing by pulsed‐field gel electrophoresis is more effective than ribotyping in distinguishing among methicillin‐resistant Staphylococcus aureus isolates
6. Pulsed‐field gel electrophoresis for epidemiological studies of Campylobacter hyointestinalis isolates
7. Use of ribotyping, IS200 typing and plasmid analysis for the identification of Salmonella enterica subsp. enterica serovar Typhimurium vaccine strain Zoosaloral H and its differentiation from wild type strains of the same serovar
8. Dissection of the Salmonella typhimurium genome by use of a Tn5 derivative carrying rare restriction sites