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VOLUM OMAGIAL - Facultatea de Ştiinţe ale Naturii şi Ştiinţe Agricole

VOLUM OMAGIAL - Facultatea de Ştiinţe ale Naturii şi Ştiinţe Agricole

VOLUM OMAGIAL - Facultatea de Ştiinţe ale Naturii şi Ştiinţe Agricole

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Aurelia Manuela Moldoveanu, Ioan Ar<strong>de</strong>lean / Ovidius University Annals, Biology-Ecology Series 14: 147-156 (2010)<br />

temperature variation (16º C, 23º C, 29º C) and<br />

registers a <strong>de</strong>crease of the quantity of inoculate from<br />

1.2 ∙10 8 cel/l to 1.2∙10 2 cel/l used with the increase of<br />

temperature, as well as an increased adhesion at high<br />

temperatures during the first hours from immersion.<br />

Experiments were realizes by Else [5] regarding<br />

the bacterial colonization of the hydrophile surface of<br />

metals (stainless steel, titanium and nickel) in<br />

variable conditions of temperature (30º C, 60º C and<br />

70º C) and humidity over a longer period of time<br />

(from a few days to 18 months). They observed an<br />

increase of adherent bacteria between 1.06∙10 2 cel/cm<br />

2 and 7.61 ∙10 2 cel/cm 2 at a temperature of 30º C on<br />

steel plates. They also observed a <strong>de</strong>crease of the<br />

number of bacteria from the first day for the plates<br />

exposed to high temperatures (60º C and 70º C),<br />

especially on those of nickel and steel.<br />

In what regards the role of the bacterial film in<br />

the mediation of invertebrate attachment and fouling<br />

formation, Lau et al. [35] realized experiments at<br />

different temperatures (16º C, 23º C and 30º C),<br />

noticing an increase in the number of bacteria from<br />

14.3∙10 3 cel/mm -2 at 16º C to 21.2∙10 3 cel/mm -2 at<br />

30º C. The experiments emphasized a more<br />

significant influence of the temperature on the<br />

biomass than on the bacterial <strong>de</strong>nsity.<br />

A number of experiments regarding the<br />

formation of biofilms in different conditions of<br />

temperature were realized by Di Bonaventura [36]<br />

together with other collaborators accomplish in 2007<br />

(4º C, 12º C, 22º C, 37º C) by Listeria<br />

monocytogenes on the hydrophile surface of glass,<br />

steel and the hydrophobe surface of polystyrene. The<br />

results emphasized a progressive increase on the<br />

surface at 4 ºC of 0.206, at 12 ºC BPI to 0.233 BPI,<br />

22º C to 0.366 BPI, in comparison to polystyrene and<br />

stainless steel. At 37º C the values are close to those<br />

from the three surfaces studied, but there is also<br />

greater species variability. Still, the most<br />

consi<strong>de</strong>rable growth of 1.275 was obtained on the<br />

hydrophobe surface of polystyrene.<br />

Bacterial <strong>de</strong>nsity registers an increase of the<br />

adherent bacteria with higher values for the biofilm<br />

formed in aquarium water kept at 18 ºC, compared to<br />

the one kept at 6 ºC. The values obtained are higher<br />

than those for seawater, which is due to the different<br />

physical and chemical properties of aquarium water<br />

and to the nutrients. Adherent marine bacteria attach<br />

151<br />

themselves to surfaces and form microcolonies in the<br />

first hour after immersion in the marine medium.<br />

They grow in size with the immersion period, data<br />

confirmed by [24].<br />

3.3 The formation of biofilms un<strong>de</strong>r the<br />

influence of salinity<br />

Variation of salinity was done in or<strong>de</strong>r to<br />

observe the influence of osmotic conditions on the<br />

process of bacterial adherence and the formation of<br />

the initial phases of biofilms. For the sli<strong>de</strong>s immersed<br />

in containers with seawater with 15g/l salinity, Figure<br />

3 displays an increase of bacterial <strong>de</strong>nsity to 12∙10 2<br />

cel/mm 2 one hour after immersion towards a<br />

doubling of this value to 25∙10 2 cel/mm 2 eight hours<br />

later.<br />

The sli<strong>de</strong>s were left over night for 12 hours and<br />

the following day there was a progressive increase of<br />

the cellular <strong>de</strong>nsity value of 49∙10 2 cel/mm 2 where<br />

there is a ten<strong>de</strong>ncy for a triple value towards 62∙10 2<br />

cel/mm 2 .<br />

In the case of containers with seawater with<br />

modified salinity (addition of osmosis water 10g/l),<br />

the bacterial <strong>de</strong>nsity increased to 4∙10 2 cel/mm 2 one<br />

hour after immersion to a double value of 8∙10 2<br />

cel/mm 2 after four hours and the progressive increase<br />

from 18 ∙10 2 cel/mm 2 after eight hours when there is<br />

a ten<strong>de</strong>ncy to triple the value of bacterial <strong>de</strong>nsity.<br />

After the 12 hour interval when the sli<strong>de</strong>s were left<br />

over night in containers, there is an increase of the<br />

cellular <strong>de</strong>nsity from 41∙10 2 cel/mm 2 24 hours after<br />

immersion to 54∙10 2 cel/mm 2 36 hours after<br />

immersion. The growth progression during the first<br />

12 hours in the case of the biofilms formed at a<br />

salinity of 15g/l is higher, with a value of 2.3 and<br />

displays a <strong>de</strong>crease after 24 hours to 1.1. In the case<br />

of the biofilms formed at a salinity of 10g/l, the<br />

growth progression is 2.4 during the first 12 hours<br />

and it <strong>de</strong>creases after 24 hours to 1.1. The difference<br />

between the two progressions is 2∙10 2 cel/mm 2 in the<br />

first 12 hours, it increases to 8∙10 2 cel/mm 2 24 hours<br />

after immersion and remains constant at this value<br />

until 36 hours.<br />

In the case of containers with seawater with<br />

modified salinity (addition of osmosis water 5g/l),<br />

Figure 4 displays an increase of bacterial <strong>de</strong>nsity<br />

from 2∙10 2 cel/mm 2 one hour after immersion to a

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