The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Evidence of cellulose metabolism by the giant panda gut microbiome
Open accessAbstract
The giant panda genome codes for all necessary enzymes associated with a carnivorous digestive system but lacks genes for enzymes needed to digest cellulose, the principal component of their bamboo diet. It has been posited that this iconic species must therefore possess microbial symbionts capable of metabolizing cellulose, but these symbionts have remained undetected. Here we examined 5,522 prokaryotic ribosomal RNA gene sequences in wild and captive giant panda fecal samples. We found lower species richness of the panda microbiome than of mammalian microbiomes for herbivores and nonherbivorous carnivores. We detected 13 operational taxonomic units closely related to Clostridium groups I and XIVa, both of which contain taxa known to digest cellulose. Seven of these 13 operational taxonomic units were unique to pandas compared with other mammals. Metagenomic analysis using ∼37-Mbp contig sequences from gut microbes recovered putative genes coding two cellulose-digesting enzymes and one hemicellulose-digesting enzyme, cellulase, β-glucosidase, and xylan 1,4-β-xylosidase, in Clostridium group I. Comparing glycoside hydrolase profiles of pandas with those of herbivores and omnivores, we found a moderate abundance of oligosaccharide-degrading enzymes for pandas (36%), close to that for humans (37%), and the lowest abundance of cellulases and endohemicellulases (2%), which may reflect low digestibility of cellulose and hemicellulose in the panda's unique bamboo diet. The presence of putative cellulose-digesting microbes, in combination with adaptations related to feeding, physiology, and morphology, show that giant pandas have evolved a number of traits to overcome the anatomical and physiological challenge of digesting a diet high in fibrous matter.
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Cites
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
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A human gut microbial gene catalogue established by metagenomic sequencing
MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624
Evolution of mammals and their gut microbes
Ley, R. E., Hamady, M., Lozupone, C., Turnbaugh, P. J., Ramey, R. R., Bircher, J. S., Schlegel, M. L., Tucker, T. A., Schrenzel, M. D., Knight, R., et al. (2008) · Science · doi:10.1126/science.1155725 · Cited by 3,747
De novo assembly of human genomes with massively parallel short read sequencing
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“The de novo assembly (22) for Illumina Genome Analyzer sequence data resulted in a set of ∼37 Mbp (SI Appendix, Table S4).”
MethodThe Pfam protein families database
Finn, R. D., Mistry, J., Tate, J., Coggill, P., Heger, A., Pollington, J. E., Gavin, O. L., Gunasekaran, P., Ceric, G., Forslund, K., et al. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkp985 · Cited by 2,694
The sequence and de novo assembly of the giant panda genome
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Cited by
Functional diversity within the simple gut microbiota of the honey bee
Engel, P., Martinson, V. G., & Moran, N. A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1202970109 · Cited by 874
Metadata
- Authors
- Zhu, L., Wu, Q., Dai, J., Zhang, S., & Wei, F.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2011-10-17
- Volume
- 108
- Issue
- 43
- Pages
- 17714-17719
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2136720095
- Cited by
- 508
- References
- 6
- FWCI
- 8.35
- Type
- journal article
- Language
- en
- Open access
- bronze
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