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. 2018 Aug 22;18(1):89.
doi: 10.1186/s12866-018-1226-4.

The microbiota in the intestinal and respiratory tracts of naked mole-rats revealed by high-throughput sequencing

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The microbiota in the intestinal and respiratory tracts of naked mole-rats revealed by high-throughput sequencing

Wei Cong et al. BMC Microbiol. .

Abstract

Background: The naked mole-rat (NMR, Heterocephalus glaber) is being bred as a novel laboratory animal due to its unique biological characteristics, including longevity, cancer resistance, hypoxia tolerance, and pain insensitivity. It is expected that differences exist between the microbiota of wild NMRs and that of NMRs in an artificial environment. Overall, the effect of environment on changes in the NMR microbiota remains unknown. In an attempt to understand the microbiota composition of NMRs in captivity, variability in the microbiota of the intestinal and respiratory tracts of two groups of NMRs was assessed under two conditions.

Results: The results obtained by high-throughput sequencing revealed significant differences at the phylum, class, order, family and genus levels in the microbiota between the two groups of NMRs examined (first group in conventional environment, second group in barrier environment). For the trachea, 24 phyla and 533 genera and 26 phyla and 733 genera were identified for the first and second groups of animals. Regarding the cecum, 23 phyla and 385 genera and 25 phyla and 110 genera were identified in the microbiota of first and second groups of animals. There were no obvious differences between females and males or young and adult animals.

Conclusions: Our results suggest that the intestinal and respiratory tract NMR microbiota changed during captivity, which may be related to the transition to the breeding environment. Such changes in the microbiota of NMRs may have an effect on the original characteristics, which may be the direction of further research studies.

Keywords: Bacterial diversity; Cecum; Microbiota; Naked mole-rats; Trachea.

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Conflict of interest statement

Ethics approval and consent to participate

The animal experiments were reviewed and approved by the Institutional Animal Care and Use Committee of the Second Military Medical University.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
Rarefaction analysis of the different samples. a. Rarefaction curves comparing the number of reads with the number of OTUs based on DNA from the contents of (a) the trachea in the first 33 NMRs, b the trachea in the second 30 NMRs, c the cecum in the first 33 NMRs, and d the cecum in the second 30 NMRs
Fig. 2
Fig. 2
Cladogram of all 63 NMRs via LEfSe analysis. a Trachea; b cecum. Different colors represent different groups, and different color nodes in the branches represent the microbiota that plays an important role in the group. The yellow nodes represent a group of microbes that do not play an important role
Fig. 3
Fig. 3
Overall distribution of the bacterial population at the phylum level in the first and second groups of samples. a Trachea; b cecum
Fig. 4
Fig. 4
Bacterial diversity and evolutionary tree at the genus level. a Trachea; b cecum. Bacterial composition of the different communities. The relative read abundance of different bacterial phyla within the different communities. Sequences with a relative abundance lower than 1% were assigned as “others”
Fig. 5
Fig. 5
NMDS diagram of all samples. a Trachea samples R1-R63; b Cecum samples E1-E63

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