Suquet Marc, Labbé Catherine, Puyo Sophie, Mingant Christian, Quittet Benjamin, Boulais Myrina, Queau Isabelle, Ratiskol Dominique, Diss Blandine, Haffray Pierrick
Ifremer, UMR 6539, PFOM Department, Station Expérimentale d'Argenton, Argenton, France.
INRA, UR 1037, LPGP, Rennes, France.
PLoS One. 2014 Apr 2;9(4):e93486. doi: 10.1371/journal.pone.0093486. eCollection 2014.
This study is the first demonstration of successful post-thawing development to reproduction stage of diploid cryopreserved larvae in an aquatic invertebrate. Survival, growth and reproductive performances were studied in juvenile and adult Pacific oysters grown from cryopreserved embryos. Cryopreservation was performed at three early stages: trochophore (13±2 hours post fertilization: hpf), early D-larvae (24±2 hpf) and late D-larvae (43±2 hpf). From the beginning (88 days) at the end of the ongrowing phase (195 days), no mortality was recorded and mean body weights did not differ between the thawed oysters and the control. At the end of the growing-out phase (982 days), survival of the oysters cryopreserved at 13±2 hpf and at 43±2 hpf was significantly higher (P<0.001) than those of the control (non cryopreserved larvae). Only the batches cryopreserved at 24±2 hpf showed lower survival than the control. Reproductive integrity of the mature oysters, formely cryopreserved at 13±2 hpf and 24±2 hpf, was estimated by the sperm movement and the larval development of their offspring in 13 crosses gamete pools (five males and five females in each pool). In all but two crosses out of 13 tested (P<0.001), development rates of the offspring were not significantly different between frozen and unfrozen parents. In all, the growth and reproductive performances of oysters formerly cryopreserved at larval stages are close to those of controls. Furthermore, these performances did not differ between the three initial larval stages of cryopreservation. The utility of larvae cryopreservation is discussed and compared with the cryopreservation of gametes as a technique for selection programs and shellfish cryobanking.
本研究首次证明了水生无脊椎动物二倍体冷冻保存幼虫在解冻后成功发育至繁殖阶段。对由冷冻保存胚胎培育出的幼年和成年太平洋牡蛎的存活、生长和繁殖性能进行了研究。在三个早期阶段进行了冷冻保存:担轮幼虫期(受精后13±2小时:hpf)、早期D形幼虫期(24±2 hpf)和晚期D形幼虫期(43±2 hpf)。从开始阶段(88天)到生长阶段结束(195天),未记录到死亡情况,解冻后的牡蛎与对照组的平均体重无差异。在养成阶段结束时(982天),在13±2 hpf和43±2 hpf冷冻保存的牡蛎的存活率显著高于对照组(未冷冻保存的幼虫)(P<0.001)。只有在24±2 hpf冷冻保存的批次显示出比对照组更低的存活率。通过精子活力及其后代在13个杂交配子池(每个池中有五只雄性和五只雌性)中的幼虫发育情况,评估了先前在13±2 hpf和24±2 hpf冷冻保存的成熟牡蛎的生殖完整性。在13次测试中的11次杂交中(P<0.001),冷冻和未冷冻亲本的后代发育率没有显著差异。总体而言,先前在幼虫阶段冷冻保存的牡蛎的生长和繁殖性能与对照组接近。此外,在冷冻保存的三个初始幼虫阶段之间,这些性能没有差异。讨论了幼虫冷冻保存的实用性,并将其与配子冷冻保存作为一种选择计划和贝类冷冻保存技术进行了比较。