A fast and reliable procedure for spore collection from anaerobic fungi: Application for RNA uptake and long-term storage of isolates

被引:29
作者
Calkins, Shelby [1 ]
Elledge, Nicole C. [1 ]
Hanafy, Radwa A. [1 ]
Elshahed, Mostafa S. [1 ]
Youssef, Noha [1 ]
机构
[1] Oklahoma State Univ, Dept Microbiol & Mol Genet, Stillwater, OK 74074 USA
基金
美国国家科学基金会;
关键词
Anaerobic fungi; Neocallimastigomycota; Spore collection; Long term preservation; BLASTOCLADIELLA-EMERSONII; BATRACHOCHYTRIUM-DENDROBATIDIS; NEOCALLIMASTIX-FRONTALIS; RUMEN FUNGUS; MEDIATED TRANSFORMATION; ASPERGILLUS-FUMIGATUS; ZOOSPORE GERMINATION; LIFE-CYCLE; GUT FUNGI; GENE;
D O I
10.1016/j.mimet.2016.05.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Anaerobic gut fungi (AGF) represent a basal fungal lineage (phylum Neocallimastigomycota) that resides in the rumen and alimentary tracts of herbivores. The AGF reproduce asexually, with a life cycle that involves flagellated zoospores released from zoosporangia followed by encystment, germination and the subsequent development of rhizomycelia. A fast and reliable approach for AGF spore collection is critical not only for developmental biology studies, but also for molecular biological (e.g. AMT-transformation and RNAi) approaches. Here, we developed and optimized a simple and reliable procedure for the collection of viable, competent, and developmentally synchronized AGF spores under strict anaerobic conditions. The approach involves growing AGF on agar medium in serum bottles under anaerobic conditions, and flooding the observed aerial growth to promote spore release from sporangia into the flooding suspension. The released spores are gently collected using a wide bore sterile needle. Process optimization resulted in the recovery of up to 7 x 10(9) spores per serum bottle. Further, the released spores exhibited synchronized development from flagellated spores to encysted spores and finally to germinating spores within 90 min from the onset of flooding. At the germinating spore stage, the obtained spores were competent, and readily uptook small interfering RNA (siRNA) oligonucleotides. Finally, using multiple monocentric and polycentric AGF isolates, we demonstrate that AGF grown on agar surface could retain viability for up to 16 weeks at 39 degrees C, and hence this solid surface growth procedure represents a simple, cryopreservative- and freezing temperature-free approach for AGF storage. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:206 / 213
页数:8
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