Calkins Shelby, Elledge Nicole C, Hanafy Radwa A, Elshahed Mostafa S, Youssef Noha
Department of Microbiology and Molecular Genetics, Oklahoma State University, Stillwater, OK 74074, United States.
Department of Microbiology and Molecular Genetics, Oklahoma State University, Stillwater, OK 74074, United States.
J Microbiol Methods. 2016 Aug;127:206-213. doi: 10.1016/j.mimet.2016.05.019. Epub 2016 Jun 8.
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 7×10(9) spores per serum bottle. Further, the released spores exhibited synchronized development from flagellated spores to encysted spores and finally to germinating spores within 90min 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 16weeks at 39°C, and hence this solid surface growth procedure represents a simple, cryopreservative- and freezing temperature-free approach for AGF storage.
厌氧肠道真菌(AGF)代表了一个基部真菌谱系(新美鞭菌门),存在于食草动物的瘤胃和消化道中。AGF进行无性繁殖,其生命周期包括从游动孢子囊释放出有鞭毛的游动孢子,随后是包囊形成、萌发以及随后的根状菌丝体发育。一种快速可靠的AGF孢子收集方法不仅对发育生物学研究至关重要,而且对分子生物学方法(如AMT转化和RNA干扰)也很关键。在这里,我们开发并优化了一种简单可靠的程序,用于在严格厌氧条件下收集有活力、有能力且发育同步的AGF孢子。该方法包括在厌氧条件下于血清瓶中的琼脂培养基上培养AGF,并用水淹没观察到的气生菌丝,以促进孢子从孢子囊释放到淹没悬浮液中。使用宽口径无菌针头轻轻收集释放的孢子。经过工艺优化后,每个血清瓶可回收多达7×10⁹个孢子。此外,从淹没开始90分钟内,释放的孢子表现出从有鞭毛的孢子到包囊化孢子,最终到萌发孢子的同步发育。在萌发孢子阶段,获得的孢子具有活性,并且易于摄取小干扰RNA(siRNA)寡核苷酸。最后,使用多个单中心和多中心AGF分离株,我们证明在琼脂表面生长的AGF在39°C下可保持活力长达16周,因此这种固体表面生长程序代表了一种简单的、无需冷冻保存和特定冷冻温度的AGF保存方法。