Volume 3, Number 4—December 1997
THEME ISSUE
Foodborne
Controlling Emerging Foodborne Microbial Hazards
Epidemiology and Detection as Options for Control of Viral and Parasitic Foodborne Disease
Table 3
Pathogen | Detection limit | Viability | Differentiation | Ref. |
---|---|---|---|---|
Flow Cytometry with Fluorescent Imaging and CCD | ||||
Cryptosporidium | NR | Yes, using differential fluorogenic vital dyes | NR | 58,59 |
DNA Hybridization | ||||
Giardia (16s-like rDNA) | 1cyst | NR | No | 60 |
Giardia (16s-like rDNA) | NR | NR | Yes-in situ hybridization with differential fluorescence G. lamblia; G. muris | 61 |
Polymerase Chain Reaction | ||||
Giardia (Giardin gene) | 1 cyst | Partial, using mRNA as target; Depends on inactivation method | NR | 62 |
Giardia (Giardin gene) | 1 cyst | NR | Yes-primer sequence G. duodenalis | 63 |
Cryptosporidium (Target not specified) | 20 oocysts | No | Yes-by hybridization C. parvum | 64 |
CCD = cooled charge couple device; NR = not reported
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