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Buckner, A. M.

Publications and source records attributed to Buckner, A. M..

2 recordsLinked to original sources

Genetic profiling via a novel PCR-RFLP method enabled identification of four genera of anaerobic gut fungi isolated from nyala, giraffe, and zebra hosts

Herbivore gut microbiomes may contain a diversity of anaerobic gut fungi (AGF, phylum Neocallimastigomycota), important for fibre degradation. To perform functional studies and elucidate niches of different AGF species, representative fungal isolates must be obtained into axenic culture, which is a resource-intensive process. Here we leverage the integration of morphological and functional assessments of AGF isolates with a newly developed PCR-RFLP strategy, to distinguish and identify isolates of interest from faecal samples from zoo-housed animals. In silico prediction of PCR-RFLP profiles of cultured genera, followed by experimental validation, confirmed that LSU-based PCR-RFLP with AluI and Hyp188I digestion was effective in identification of fungi of distinct genera. Together our workflow resulted in isolation of a so far uncultured Piromyces (NY08) species and Neocallimastix cameroonii from nyala samples, as well as Feramyces austinii from giraffe and Khoyollomyces ramosus from zebra. Amplicon sequencing confirmed that these species dominated AGF communities in their hosts, likely benefiting isolation success, and we identified enrichment conditions which also affected cultivability. The workflow developed here aids efficient AGF isolations, which are instrumental in expanding opportunities for functional studies that provide insight into the physiology and ecology of these fungi and help realise applications in white and green biotechnology. One sentence summaryA validated PCR-RFLP strategy, developed based on genetic diversity data from Neocallimastigomycota, enables efficient identification of isolates of these anaerobic gut fungi from environmental samples, as demonstrated via targeted enrichment of anaerobic gut fungi common in faeces of giraffe, zebra and nyala, resulting in isolation of species of genera Feramyces, Neocallimastix, Khoyollomyces, and a novel Piromyces/NY08 species.

microbiology↗

Determining the culturability of the bovine rumen bacterial and archaeal microbiota

Ruminants play an important part in global food security, but also emit methane which contributes to global warming. Microbes in the rumen strongly influence the energy retention efficiency from the hosts plant-based diet and produce methane as a by-product. While thousands of novel microbial genomes have been assembled from metagenome sequence data, their culturability is ill-defined. Here different media were used to isolate microbes from rumen fluid. 34 genera were grown, and the majority belonged to the phylum Bacillota (75.28% {+/-} 6.34), Bacteroidota (19.99% {+/-} 4.85), Pseudomonadota (2.46% {+/-} 2.01), and Actinomycetota (2.09% {+/-} 1.07). The most abundant genera were Selenomonas (28.08% {+/-} 11.71), Streptococcus (22.67% {+/-} 6.06), Prevotella (18.71% {+/-} 4.02), and unclassified Lachnospiraceae (11.50% {+/-} 2.54). When comparing the mean relative abundance of these genera between media, 31 were significantly enriched on at least one medium. The composition of the source rumen fluid was vastly different to those cultured. Bacteroidota (52.53% {+/-} 5.10) predominated, with by Bacillota (41.00% {+/-} 3.96), the archaeal Euryarchaeota (5.12% {+/-} 1.94), Pseudomonadota (1.22% {+/-} 0.78), and Actinomycetota (0.12% {+/-} 0.08) comprising the rest. The most abundant genera were Prevotella (29.13% {+/-} 4.16), Butyrivibrio (18.21% {+/-} 2.08), Succiniclasticum (15.57% {+/-} 5.03), unclassified Bacteroidetes (13.91% {+/-} 1.67), and unclassified Prevotellaceae (9.50% {+/-} 2.01). These data further emphasise the importance of using defined media to selectively enrich for different microbial taxa. This is essential to understand the complex workings of the rumen microbes to enhance digestion efficiency and reduce the loss of energy as methane.

microbiology↗