The combination of CRISPR-MVLST and PFGE provides increased discriminatory power for differentiating human clinical isolates of Salmonella enterica subsp. enterica serovar Enteritidis

Food Microbiology

Volumn 34, Issue 1, 2013, Pages 164-173

  Shariat, Nikki ^a   DiMarzio, Michael J ^a   Yin, Shuang ^a   Dettinger, Lisa ^b   Sandt, Carol H ^b   Lute, James R ^b   Barrangou, Rodolphe ^a,c   Dudley, Edward G ^a  

^a PENNSYLVANIA STATE UNIVERSITY   (United States)

^b PENNSYLVANIA DEPARTMENT OF HEALTH   (United States)

^c DuPont Nutrition and Health   (United States)

Author keywords

CRISPR MVLST; Molecular subtyping; Salmonella Enteritidis

Indexed keywords

ARTICLE; BACTERIUM IDENTIFICATION; CLASSIFICATION; EVALUATION; FECES; GENETICS; HUMAN; INVERTED REPEAT; ISOLATION AND PURIFICATION; METHODOLOGY; MICROBIOLOGY; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PHYLOGENY; POLYMERASE CHAIN REACTION; PULSED FIELD GEL ELECTROPHORESIS; SALMONELLA ENTERITIDIS; SALMONELLOSIS; URINE;

BACTERIAL TYPING TECHNIQUES; ELECTROPHORESIS, GEL, PULSED-FIELD; FECES; HUMANS; INVERTED REPEAT SEQUENCES; MOLECULAR SEQUENCE DATA; PHYLOGENY; POLYMERASE CHAIN REACTION; SALMONELLA ENTERITIDIS; SALMONELLA INFECTIONS; URINE;

BACTERIA (MICROORGANISMS); SALMONELLA ENTERICA; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SALMONELLA ENTERITIDIS;

EID: 84872243390     PISSN: 07400020     EISSN: 10959998     Source Type: Journal    
DOI: 10.1016/j.fm.2012.11.012     Document Type: Article

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