C. Jeppesen, MEDIA FOR AEROMONAS SPP, PLESIOMONAS-SHIGELLOIDES AND PSEUDOMONAS SPPFROM FOOD AND ENVIRONMENT, International journal of food microbiology, 26(1), 1995, pp. 25-41
Several media are proposed particularly for the detection of Aeromonas
spp. but also for Plesiomonas shigelloides and Pseudomonas spp. Some
are for general purposes and others specifically for the examination o
f clinical, environmental or food samples. All media are selective, du
e to antibiotics, bile salts, dyes and other selective agents, as well
as differential, primarily based on the ability of the microorganisms
to ferment/not ferment carbohydrates. As with all selective media, th
e recovery of stressed cells is sometimes prevented and the competing
flora is not always completely inhibited so that confirmatory tests ne
ed to be made on presumptive positive colonies. The choice of a specif
ic medium for isolation of Aeromonas spp. will always depend on the ty
pe of sample to be examined and whether the investigator needs qualita
tive detection or quantitative recovery. The best medium for quantitat
ive estimation of Aeromonas spp. from food and environmental samples s
eems to be starch ampicillin agar (SAA), though others might be recomm
ended. There is a need for a comparative study including Rippey Cabell
i agar (mA), ampicillin bile salts inositol xylose (MIX) agar, ampicil
lin dextrin agar (ADA), dextrin fuchsin sulphite agar (DFS) and starch
glutamate ampicillin penicillin C-glucose agar (SGAP-10C) in addition
to SAA. For routine analysis of environmental and food samples for P.
shigelloides, spread plating on inositol brilliant green bile salts (
IBB) and plesiomonas (PL) agars is recommended. For Pseudomonas spp.,
CFC agar permits quantitative recovery of both pigmented and non-pigme
nted strains from food and environmental samples, whilst at the same t
ime inhibiting most other organisms.