Nj. Ashbolt et al., THE IDENTIFICATION AND HUMAN HEALTH SIGNIFICANCE OF ENVIRONMENTAL AEROMONADS, Water science and technology, 31(5-6), 1995, pp. 263-269
Citations number
27
Categorie Soggetti
Water Resources","Environmental Sciences","Engineering, Civil
Aeromonads readily grow in waters, particularly if nutrified to concen
trations in excess of total coliforms. Strains of aeromonads can cause
gastroenteritis and tissue necrosis. Several suspected virulence fact
ors, such as haemolysins, cytotoxins and enterotoxins may be involved
in their pathogenesis. Amongst the thirteen recognised hybridisation g
roups of Aeromonas, only five species were identified by eight phenoty
pic characteristics from 339 strains isolated from marine, fresh river
or storm waters or from tertiary and sewage/primary effluents. The ma
jority of strains (50%) showed atypical phenotypes, and 24% of 208 ran
domly selected strains were not identified as aeromonads with a genus
specific 16S rDNA-targeted PCR. Most discrepancies occurred with A. sc
hubertii phenotypes, none of which were identified as aeromonads by PC
R, Marine waters contained the largest proportion of atypical phenotyp
es (45/67) of which 60%, compared to <20% for other water sources, wer
e not identified as aeromonads by PCR. A. hydrophila was generally the
predominant species identified (93/339), although A. caviae was more
prevalent in tertiary treated sewage effluents. Freshwaters contained
the largest proportion of aeromonads with haemolysin and/or enterotoxi
n activity, whereas cytotoxin activity was more prevalent from stormwa
ter isolates. Freshwater strains of A. veronii biotype sobria and A. h
ydrophila appeared to be the most toxigenic. Furthermore, river sites
downstream of sewage effluent release contained more aeromonads than s
ites immediately upstream of the discharge. Hence, there was a clear p
ositive correlation between freshwater eutrophication and the presence
of potentially virulent aeromonads, the majority of which were A. hyd
rophila and A. veronii which can most rapidly and accurately be identi
fied by PCR.