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Résultats - Chapitre 3<br />

the optimal growth temperature: not shown). No mo<strong>de</strong>rately thermophilic or thermophilic<br />

Archaea were reported neither in this study; neither in the literature: except<br />

Methanothermococcus okinawensis that grows optimally at 60-65°C (Takaï et al., 2002), all<br />

the <strong>de</strong>scribed archaeal species originating from <strong>de</strong>ep-sea hydrothermal environments grow<br />

optimally in pure culture at or above 75°C. This suggests that most Archaea thriving in <strong>de</strong>epsea<br />

hydrothermal chimneys are hyperthermophilic.<br />

Members of Thermococcales at <strong>de</strong>ep-sea hydrothermal vents are wi<strong>de</strong>spread (Harmsen et<br />

al. 1997, Nercessian et al. 2003, Reysenbach et al. 2000, Takai et al. 2001), and members of<br />

the genus Thermococcus are some of the most numerous <strong>de</strong>scribed hyperthermophiles from<br />

<strong>de</strong>ep-sea vents. They have been isolated from sulfidic chimneys (Godfroy et al. 1996),<br />

sediments (Canganella et al. 1998), fluids (Grote, et al. 1999) and polychaete worms<br />

(Pledger & Baross 1991). Investigation of their natural distribution showed that a viable<br />

Thermococcus population was present in the surface layers of hydrothermal chimneys<br />

(Harmsen, et al. 1997, Schrenk, et al. 2003, Takai, et al. 2001). Interestingly, members of<br />

Thermococcales were not <strong>de</strong>tected in molecular diversity analyses of hydrothermal <strong>de</strong>posits,<br />

fluids or in situ colonizers <strong>de</strong>ployed at low temperatures (Alain, et al. 2004, Huber et al. 2002,<br />

Takai & Horikoshi 1999). However Thermococcus was <strong>de</strong>tected in in situ colonizers<br />

<strong>de</strong>ployed in thermophilic conditions (Corre 2000, Nercessian, et al. 2003, Reysenbach, et al.<br />

2000). These organisms should therefore be efficient surface colonizers. Furthermore,<br />

Thermococcus <strong>populations</strong> were observed early in the enrichment cultures performed in vials<br />

or bioreactor, at 60°C (this study) and 90°C (Postec, et al. 2005b). An early growth may<br />

confer on Thermococcus microorganisms a great ecological advantage to colonize a new<br />

hydrothermal environment. It may indicate that Thermococcus members are the primary<br />

heterotroph colonizers. This is consistent with the observations and hypothesis emitted by<br />

Nercessian et al. (2003), who showed that the proportion of Thermococcales-related<br />

phylotypes was higher from the shortest <strong>de</strong>ployments (4-7 days) of in situ collectors than in<br />

longer <strong>de</strong>ployments. Theses results differ from observations and hypothesis as reported by<br />

Reysenbach et al. (2000) suggesting that chemolithoautotrophs would be the first colonizers<br />

of vent surfaces and that thermophilic heterotrophs such Thermococcales would emerge<br />

after a sufficient organic carbon accumulation.<br />

Bacterial diversity<br />

All the sequences retrieved in our enrichment cultures were related to cultivated<br />

microorganisms originating from <strong>de</strong>ep-sea hydrothermal vents. Members of the genera<br />

Caminicella and Marinitoga were <strong>de</strong>tected in the enrichment cultures performed in vials and<br />

in the bioreactor, whatever the incubation time or the occurrence of subculturing, suggesting<br />

184

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