西班牙特内里费岛(加那利群岛)和纳瓦拉(伊比利亚半岛)叶状地衣群落中的绿藻菌(Watanabeales, Trebouxiophyceae)与lecanoralean霉菌结成伙伴

William B. Sanders, Asunción de los Ríos, Sergio Pérez-Ortega
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引用次数: 0

摘要

虽然人们已经对叶状地衣形成真菌的多样性进行了深入探讨,但对其藻类共生体的关注相对较少。我们研究了西班牙大陆和加那利群岛两个外热带叶状地衣群落中的雷卡诺地衣Bacidina(Ramalinaceae)、Byssoloma、Fellhanera和Tapellaria(Pilocarpaceae)以及石墨藻Gyalectidium(Gomphillaceae)的单细胞绿色藻类共生体。我们利用 TEM 技术检查了苔藓中藻类共生体的类焦磷酸,并从整个苔藓以及从其中一些地衣中分离出来的培养物中获得了一些藻类 nrSSU 和 rbcL 序列。拟肾上腺素结构和分子序列数据支持将 Chloroidium(Watanabeales, Trebouxiophyceae)认定为两个群落中 Byssoloma subdiscordans 和 Fellhanera bouteillei(Pilocarpaceae) 苔藓的藻类寄生体。同样,Bacidina apiahica(拉玛琳科)和 Tapellaria epiphylla(黄皮科)也似乎与 Chloroidium 合作,因为它们存在相同的类肾炎素类型,尽管我们只能从后者的一个培养分离物中获得噬菌体序列。这些结果与之前从佛罗里达州南部叶状地衣群落中获得的结果形成了鲜明对比,后者只发现了 Heveochlorella(Jaagichlorella)菌株作为叶状地衣中 Pilocarpaceae 和 Gomphillaceae 的噬菌体。另一方面,我们在与 Gyalectidium setiferum 和 G. minus 相关联的噬菌体中观察到的类肾上腺素与 Heveochlorella(Jaagichlorella)的类肾上腺素一致。然而,可能由于附生藻类的存在,从 G. minus 获得的藻体序列数据质量较差,因此无法从更多角度观察类肾炎素结构。尽管如此,在热核超微结构上的明显差异可以让我们在 TEM 中将绿藻和小球藻的藻体区分开来。我们的研究结果表明,在西班牙的叶状群落中,单细胞绿色藻类共生体的多样性比以前在其他地区观察到的要高,这表明进一步研究这些群落中的共生体配对可能会揭示出独特而多样的藻类共生体偏好模式。
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Chloroidium phycobionts (Watanabeales, Trebouxiophyceae) partner with lecanoralean mycobionts in foliicolous lichen communities of Tenerife (Canary Islands) and Navarra (Iberian Peninsula), Spain

While the diversity of foliicolous lichen-forming fungi has been explored in substantial depth, relatively little attention has been paid to their algal symbionts. We studied the unicellular green phycobionts of the lecanoralean lichens Bacidina (Ramalinaceae), Byssoloma, Fellhanera and Tapellaria (Pilocarpaceae) and graphidalean Gyalectidium (Gomphillaceae) from two extratropical foliicolous communities in continental Spain and the Canary Islands. We examined the pyrenoids of algal symbionts within thalli using TEM, and obtained several algal nrSSU and rbcL sequences from whole thalli, and also from cultures isolated from some of these lichens. Pyrenoid structure and molecular sequence data provided support for recognizing Chloroidium (Watanabeales, Trebouxiophyceae) as phycobiont in thalli of Byssoloma subdiscordans and Fellhanera bouteillei (Pilocarpaceae) in both communities. Bacidina apiahica (Ramalinaceae) and Tapellaria epiphylla (Pilocarpaceae) likewise appeared to partner with Chloroidium based on the presence of the same pyrenoid type, although we were able to obtain a phycobiont sequence only from a culture isolate of the latter. These results contrast with those obtained previously from a foliicolous lichen community in southern Florida, which revealed only strains of Heveochlorella (Jaagichlorella) as phycobiont of foliicolous Pilocarpaceae and Gomphillaceae. On the other hand, the pyrenoid we observed in the phycobionts associated with Gyalectidium setiferum and G. minus corresponded to that of Heveochlorella (Jaagichlorella). However, the poor quality of the phycobiont sequence data obtained from G. minus, probably due to the presence of epibiontic algae, could not provide additional perspective on the pyrenoid structure observations. Nonetheless, clear differences in pyrenoid ultrastructure can allow Chloroidium and Heveochlorella phycobionts to be distinguished from each other in TEM. Our results indicate a greater diversity of unicellular green-algal symbionts in foliicolous communities from Spain than previously observed in other geographical areas, and suggest that further studies focused on symbiont pairing in these communities might reveal distinctive and varied patterns of phycobiont preference.

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