A taxonomic study of Chryseobacterium species in meat
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De Beer, Hanli
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University of the Free State
Abstract
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English: Microbial diversity in a food complicates the prediction or measurement of the
effect of specific micro-organisms on a perishable food commodity stored under
different conditions. Gram-negative yellow-pigmented colonies belonging to the
Flavobacteriaceae family are often present when total numbers on food samples
are investigated. Changes in the taxonomy of flavobacteria since its inception in
1923 have, however, complicated the identification of these bacteria. Many
organisms previously regarded as Flavobacterium have been found to belong to
several new genera in the family Flavobacteriaceae. With the introduction of a
chemotaxonomic approach and molecular techniques such as rRNA sequencing, it
is now possible to refine the differentiation between closely related genera.
Chromosomal DNA characteristics further enhance accurate differentiation
between various species. This study used a polyphasic taxonomic approach that
included a combination of phenotypic and genotypic testing methods in order to
characterise and classify Gram-negative yellow-pigmented strains isolated from
raw chicken, red meat and fish.
During this study 129 Gram-negative yellow-pigmented pure cultures were isolated
from raw chicken, red meat and fish samples. Protein fingerprint profiles and long
chain fatty acid analyses revealed that the majority of organisms belonged to the
genus Chryseobacterium. The 16S rRNA sequence and DNA-DNA hybridisation
methods were used to give the relationship between test strains and the reference
strains of various species in the genus. Several isolated strains from the chicken,
red meat and fish could be equated with C. balustinum (2), C. defluvii (16), C.
scophthalmum (4) or C. gleum (2) strains. A few strains (9) did not show any
affiliation with any reference strain. Two new Chryseobacterium species, however,
have been proposed from the findings of this study namely Chryseobacterium
vrystaatense sp.nov.,which is comprised of the type strain R-23566 (= LMG
22846T) and 36 strains isolated from raw chicken samples. Strains showed strong
DNase- and also urease and lecithinase activity but were not capable of starch
and tyrosine hydrolysis. The mol % G + C of R-23566 was 37.6 %. The second
new species, Chryseobacterium piscium sp. nov., comprised four strains which
were obtained from marine fish, with R-23621 as the type strain. The G + C mol
% was 33.6 %. This group was psychrotrophic in that they grew within 24 hours at
4 °C but very poorly at 32 °C.
In order to establish the source of potential Chryseobacterium contamination,
different areas and processing stages in the chicken abattoir were sampled.
Chryseobacterium species contributed to 8.3 % of the total bacterial count on
whole birds in this study. It was evident that the washing processes lowered the
total counts on carcasses. A significant increase in the total bacterial counts, as
well as total Chryseobacterium counts was reported and Chryseobacterium
species were found to represent between 20 and 25 % of the total population after
portioning procedures during this study. Live chickens as source of
Chryseobacterium contamination should be investigated in future.