Human intervertebral discs harbour a unique microbiome and dysbiosis determines health and disease
Background To document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs (IVD). Methods Genomic DNA from 24 lumbar IVDs [8—MRI normal discs (ND) from brain dead yet alive organ donors, 8—disc herniation (DH), 8—disc degeneration...
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Published in: | European spine journal Vol. 29; no. 7; pp. 1621 - 1640 |
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Abstract | Background
To document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs (IVD).
Methods
Genomic DNA from 24 lumbar IVDs [8—MRI normal discs (ND) from brain dead yet alive organ donors, 8—disc herniation (DH), 8—disc degeneration (DD)] was subjected to 16SrRNA sequencing for profiling the diversity of human disc microbiome in health and disease. The disc microbiome was further compared to established human gut and skin microbiomes.
Results
All healthy MRI normal discs from brain dead yet alive organ donors also had a rich bacterial presence. A total of 424 different species (355-ND, 346-DD, and 322-DH) were detected, with 42.75% OTUs being classified at kingdom level, 44% at the phylum level, 22.62% at genus level, and 5.5% at species level. Varying biodiversity and abundance between healthy and diseased discs were documented with protective bacteria being abundant in normal discs, and putative pathogens abundant in DD and DH.
Propionibacterium acnes
had a similar but lower abundance to other pathogens in all three groups ND (3.07%), DD (3.88%), DH (1.56%). Fifty-eight bacteria were common between gut and IVD microbiomes, 29 between skin and IVD microbiomes, and six common to gut/skin/IVD.
Conclusion
Our study challenges the hitherto concept of sterility in healthy IVD and documented a microbiome even in MRI normal healthy discs. The varying abundance of bacteria between ND, DD, and DH documents ‘dysbiosis’ as a possible etiology of DD. Many known pathogens were identified in greater abundance than
Propionibacterium acnes,
and there was evidence for the presence of the gut/skin/spine microbiome axis. |
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AbstractList | BACKGROUNDTo document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs (IVD). METHODSGenomic DNA from 24 lumbar IVDs [8-MRI normal discs (ND) from brain dead yet alive organ donors, 8-disc herniation (DH), 8-disc degeneration (DD)] was subjected to 16SrRNA sequencing for profiling the diversity of human disc microbiome in health and disease. The disc microbiome was further compared to established human gut and skin microbiomes. RESULTSAll healthy MRI normal discs from brain dead yet alive organ donors also had a rich bacterial presence. A total of 424 different species (355-ND, 346-DD, and 322-DH) were detected, with 42.75% OTUs being classified at kingdom level, 44% at the phylum level, 22.62% at genus level, and 5.5% at species level. Varying biodiversity and abundance between healthy and diseased discs were documented with protective bacteria being abundant in normal discs, and putative pathogens abundant in DD and DH. Propionibacterium acnes had a similar but lower abundance to other pathogens in all three groups ND (3.07%), DD (3.88%), DH (1.56%). Fifty-eight bacteria were common between gut and IVD microbiomes, 29 between skin and IVD microbiomes, and six common to gut/skin/IVD. CONCLUSIONOur study challenges the hitherto concept of sterility in healthy IVD and documented a microbiome even in MRI normal healthy discs. The varying abundance of bacteria between ND, DD, and DH documents 'dysbiosis' as a possible etiology of DD. Many known pathogens were identified in greater abundance than Propionibacterium acnes, and there was evidence for the presence of the gut/skin/spine microbiome axis. To document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs (IVD). Genomic DNA from 24 lumbar IVDs [8-MRI normal discs (ND) from brain dead yet alive organ donors, 8-disc herniation (DH), 8-disc degeneration (DD)] was subjected to 16SrRNA sequencing for profiling the diversity of human disc microbiome in health and disease. The disc microbiome was further compared to established human gut and skin microbiomes. All healthy MRI normal discs from brain dead yet alive organ donors also had a rich bacterial presence. A total of 424 different species (355-ND, 346-DD, and 322-DH) were detected, with 42.75% OTUs being classified at kingdom level, 44% at the phylum level, 22.62% at genus level, and 5.5% at species level. Varying biodiversity and abundance between healthy and diseased discs were documented with protective bacteria being abundant in normal discs, and putative pathogens abundant in DD and DH. Propionibacterium acnes had a similar but lower abundance to other pathogens in all three groups ND (3.07%), DD (3.88%), DH (1.56%). Fifty-eight bacteria were common between gut and IVD microbiomes, 29 between skin and IVD microbiomes, and six common to gut/skin/IVD. Our study challenges the hitherto concept of sterility in healthy IVD and documented a microbiome even in MRI normal healthy discs. The varying abundance of bacteria between ND, DD, and DH documents 'dysbiosis' as a possible etiology of DD. Many known pathogens were identified in greater abundance than Propionibacterium acnes, and there was evidence for the presence of the gut/skin/spine microbiome axis. Background To document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs (IVD). Methods Genomic DNA from 24 lumbar IVDs [8—MRI normal discs (ND) from brain dead yet alive organ donors, 8—disc herniation (DH), 8—disc degeneration (DD)] was subjected to 16SrRNA sequencing for profiling the diversity of human disc microbiome in health and disease. The disc microbiome was further compared to established human gut and skin microbiomes. Results All healthy MRI normal discs from brain dead yet alive organ donors also had a rich bacterial presence. A total of 424 different species (355-ND, 346-DD, and 322-DH) were detected, with 42.75% OTUs being classified at kingdom level, 44% at the phylum level, 22.62% at genus level, and 5.5% at species level. Varying biodiversity and abundance between healthy and diseased discs were documented with protective bacteria being abundant in normal discs, and putative pathogens abundant in DD and DH. Propionibacterium acnes had a similar but lower abundance to other pathogens in all three groups ND (3.07%), DD (3.88%), DH (1.56%). Fifty-eight bacteria were common between gut and IVD microbiomes, 29 between skin and IVD microbiomes, and six common to gut/skin/IVD. Conclusion Our study challenges the hitherto concept of sterility in healthy IVD and documented a microbiome even in MRI normal healthy discs. The varying abundance of bacteria between ND, DD, and DH documents ‘dysbiosis’ as a possible etiology of DD. Many known pathogens were identified in greater abundance than Propionibacterium acnes, and there was evidence for the presence of the gut/skin/spine microbiome axis. |
Author | Matchado, Monica Steffi Soundararajan, Dilip Chand Raja Sri Vijay Anand, K. S. Dharmalingam, K. Kanna, Rishi Mugesh Muthurajan, Raveendran Shetty, Ajoy Prasad Rajasekaran, Shanmuganathan Tangavel, Chitraa Nayagam, Sharon Miracle |
Author_xml | – sequence: 1 givenname: Shanmuganathan orcidid: 0000-0001-6043-006X surname: Rajasekaran fullname: Rajasekaran, Shanmuganathan email: rajasekaran.orth@gmail.com organization: Department of Spine Surgery, Ganga Hospital – sequence: 2 givenname: Dilip Chand Raja surname: Soundararajan fullname: Soundararajan, Dilip Chand Raja organization: Department of Spine Surgery, Ganga Hospital – sequence: 3 givenname: Chitraa surname: Tangavel fullname: Tangavel, Chitraa organization: Ganga Research Centre – sequence: 4 givenname: Raveendran surname: Muthurajan fullname: Muthurajan, Raveendran organization: Department of Plant Biotechnology, Tamil Nadu Agricultural University – sequence: 5 givenname: K. S. surname: Sri Vijay Anand fullname: Sri Vijay Anand, K. S. organization: Department of Spine Surgery, Ganga Hospital – sequence: 6 givenname: Monica Steffi surname: Matchado fullname: Matchado, Monica Steffi organization: Ganga Research Centre – sequence: 7 givenname: Sharon Miracle surname: Nayagam fullname: Nayagam, Sharon Miracle organization: Ganga Research Centre – sequence: 8 givenname: Ajoy Prasad surname: Shetty fullname: Shetty, Ajoy Prasad organization: Department of Spine Surgery, Ganga Hospital – sequence: 9 givenname: Rishi Mugesh surname: Kanna fullname: Kanna, Rishi Mugesh organization: Department of Spine Surgery, Ganga Hospital – sequence: 10 givenname: K. surname: Dharmalingam fullname: Dharmalingam, K. organization: Aravind Medical Research Foundation |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32409889$$D View this record in MEDLINE/PubMed |
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Keywords | Inflammaging Sub-clinical infection Dysbiosis Disc degeneration Microbiome |
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To document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs (IVD).
Methods... To document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs (IVD). Genomic DNA from... BackgroundTo document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs... BACKGROUNDTo document the role of sub-clinical infections in disc disorders and investigate the existence of microbiome in intervertebral discs (IVD).... |
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SubjectTerms | Abundance Bacteria Biodiversity Dysbacteriosis Etiology Intervertebral discs Magnetic resonance imaging Medicine Medicine & Public Health Microbiomes Neurodegeneration Neurosurgery Organ donors Original Article Pathogens Propionibacterium acnes Skin Spine (lumbar) Sterility Surgical Orthopedics |
Title | Human intervertebral discs harbour a unique microbiome and dysbiosis determines health and disease |
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