Evidence for infection in intervertebral disc degeneration: a systematic review.

PURPOSE: Back pain is a major problem worldwide and is linked to intervertebral disc degeneration and Modic change. Several studies report growth of bacteria following extraction of degenerate discs at spine surgery. A pathophysiological role for infection in back pain has been proposed.
METHOD: We conducted a PRISMA systematic review. MEDLINE, PubMed, Scopus and Web of Science were searched with the terms Modic change, intervertebral dis*, bacteria, microb*, and infect*. Date limits of 2001-2021 were set. Human studies investigating the role of bacteria in disc degeneration or Modic change in vertebrae were included.
RESULTS: Thirty-six articles from 34 research investigations relating to bacteria in human degenerate discs were found. Cutibacterium acnes was identified in pathological disc material. A 'candidate bacterium' approach has been repeatedly adopted which may have biased results to find species a priori, with disc microbial evidence heavily weighted to find C. acnes.
CONCLUSION: Evidence to date implicates C. acnes identified through culture, microscopy and sequencing, with some suggestion of diverse bacterial colonisation in the disc. This review found studies which used culture methods and conventional PCR for bacterial detection. Further agnostic investigation using newer methods should be undertaken.

Introduction: back pain and Modic change

Back pain, particularly low back pain (LBP) is now the world’s leading cause of morbidity [1]. A tiny proportion of LBP is caused by inflammatory disease or fracture. Most is mechanical LBP whose aetiology is complex and multifactorial with lumbar disc degeneration a significant contributor [2].

Modic change (MC) describes a lesion in the bone marrow of the vertebra adjacent to the endplate. While associated with disc degeneration [3], it is an independent risk factor for LBP [4] and often associated with poor LBP prognosis [2, 5]. MC is indicated by signal change on spine MRIs [6, 7], occurring in 43–81% of LBP patients [2, 8]. There is a genetic component: MC heritability estimates are 30% [9]. Three types of MC have been identified [6, 7]. Type 1 (MC1) is associated with bone marrow and endplate inflammation and oedema; fibrovascular granulation tissue forms and endplate fissure [10, 11]. In type 2 (MC2), healthy, red, haemopoietic bone marrow cells change to yellow, fatty marrow [11]. MC2 endplates show increased reactivity to bone and granulation tissue [10]. Type 3 (MC3), the rarest, indicates bone sclerosis MC is progressive; a cohort of lumbar disc herniation patients showed an increasing prevalence (9–29%) in MC1 over 14 months – whereas MC2 and MC3 did not increase [10].

Occult, or sub-clinical bacterial infection has been proposed to initiate and accelerate disc degeneration pathology. An infective aetiology has been proposed with several reviews linking microorganisms and disc degeneration [12, 13] or MC [2, 11, 14–17] though most investigations of infective disc degeneration are of small sample size and methods vary widely [16-19]. Two meta-analyses have implicated bacteria in disc pathophysiology. The pooled infection rate of nine studies was 36.2% [16] and of 12 studies 25.3% [18]; both analyses found Cutibacterium acnes (the bacterium formerly known as Propionibacterium acnes) the predominant disc resident.

C. acnes is a Gram-positive, facultative, aerotolerant anaerobe, non-spore-forming, rod bacterium [20, 21]. As a commensal, it colonises the skin, oral cavity, gastro-intestinal tract and genitourinary tract; it is, however, an opportunistic pathogen in skin, soft tissue and medical device implantation infections [20, 21]. Selective bacterial culture requires specific (plate or broth) growth media and environments, to which sample cells are added. Moreover, selective culture precludes the opportunity to isolate non-C. acnes bacteria. DNA based approaches, such as PCR for the 16S rRNA gene can be targeted to identify a single species or can be used more generically, with universal primers to capture a snapshot of all bacterial DNA present in a sample.

Rationale

This review aims to expand and investigate the occult infection in disc degeneration and MC. We aim to clarify if C. acnes is indeed the predominant species as previous work has implied and assess the utility of current laboratory and research practices in the detection and quantification of bacteria in disc material. Viral microorganisms have also been proposed to contribute to disc degeneration [22]; however, detailing viral or fungal pathogenesis is beyond the scope of this review.

Objectives

Studies of participants who underwent disc excision surgery with subsequent assessment of disc tissue for bacterial growth were included. We investigated whether discs adjacent to MC are at increased risk of bacterial proliferation. Only studies that explicitly stated removal and examination of discs from human participants were included. Cross-sectional and longitudinal observational studies were included.

Methods

A systematic review protocol was developed in accordance with PRISMA guidelines [23] but was not registered nor is accessible. Four electronic databases were searched: MEDLINE (Ovid), PubMed, Scopus (Ebesco) and Web of Science. The search was conducted on 02.03.21 and corroborated by two authors (IGS and PW). Articles to be included were agreed and a third author (FW) helped finalise decisions lacking consensus. Cited by and reference list searches of included articles were conducted, and a secondary search using Google Scholar was performed. Inclusion criteria specified original research articles published between 2001 and 2021 reporting both human spine disc surgery and the examination of disc bacteria in the context of occult infection. We excluded articles dealing with known infective aetiology (spondylodiscitis, post-operative infections). Exclusion criteria specified abstracts, case reports, editorials, letters, meta-analyses and reviews.

Results

A total of 495 articles were retrieved from four databases, 151 duplicates were removed. Title and abstract searching revealed 155 candidate papers, of these 120 were rejected after full text examination. The cited by search and Google Scholar search each contributed one new article. Figure 1 shows the PRISMA flow diagram and Figure 1 Supplementary (S1) details the search strategy and results. Thirty-six articles were included from 34 research studies; 27 reported finding bacteria in degenerate disc space, nine attributed bacterial findings to contamination. The results are shown in Table 1.

Fig. 1

PRISMA flow diagram for evidence for infection in intervertebral disc degeneration: a new systematic review including searches of databases and other sources

Adapted from: Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021;372:n71. https://doi.org/10.1136/bmj.n71

Table 1

Summary of studies included

Studies finding bacteria in disc material = 28	Participants	Bacteria identified	Lab techniques	Control group/control samples	Other measures	Results
(Agarwal, Golish et al. 2011)	52 single-level lumbar microdiscectomy patients No antibiotic use exclusion criteria noted	C. acnes Peptostreptococcus spp. S. aureus CoNS spp.	Routine bacterial culture Incubated for 5d under standard anaerobic conditions	No control or comparison group created & no control specimens taken	No host markers of infection assessed. Duration of LBP symptoms and prior surgeries (n = 11) recorded	10/52 (19%) patients had positive cultures: C. acnes (predominantly)
(Aghazadeh, Salehpour et al. 2017)	120 lumbar disc herniation patients (87 MC) Antibiotic use 1mth prior to surgery excluded	C. acnes CoNS Gram-negative bacilli Micrococcus Corynebacterium Neisseria spp.	Anaerobic & aerobic culture incubation glovebox each for 7d. Sub-culture and Gram-staining to identify C. acnes Specific C. acnes 16S rRNA PCR primers	No control or comparison group created. Paravertebral muscle (control) samples taken	No host markers of infection assessed. No pain scores assessed	60 patients including 42 MC had positive cultures. Predominantly C. acnes was found
(Albert, Lambert et al. 2013)	61 single-level lumbar disc herniation surgery patients Antibiotic use 14d prior to surgery excluded	C. acnes CoNS Gram-positive cocci Gram-negative rod Neisseria species	5 tissue samples collected from each patient. Columbia blood agar plates, aerobic & anaerobic incubation for 7d. Presumptive C. acnes 16S PCR rRNA priming & amplification	No control or comparison group created & no control specimens taken; longitudinal study with repeat measures	No host markers of infection assessed. FU MRIs conducted	28 patients with positive cultures, 80% of anaerobic bacterial positive culture patients developed new MC within ~ 1.5 years. Bacterial proliferation in disc increased risk of developing new MC
(Arndt, Charles et al. 2012)	83 lumbar disc replacement (degeneration) patients (32 MC1 & 25 MC2) No antibiotic use exclusion criteria noted	C. acnes CoNS S. aureus Enterobacter cloacae Enterobacter aerogenes Escherichia coli Micrococcus Corynebacterium minutissimum Corynebacterium coyleae Microbacterium Brevibacterium Rothia dentocariosum Enterococcus faecalis Streptococcus intermedius	Disc samples divided into three parts for analysis, 3 anaerobic media plate cultures 5d with supplementation. Peptone glucose yeast broth for 10d. Plates & broth screened daily for growth	No control or comparison group created & no control specimens	Additional histological examination showed host inflammatory cells in 33% of positive culture & 5% of negative culture specimens	40/83 had positive cultures. Males and MC2 higher rates of microbiological findings. Bacteria in almost half disc & predominantly in males. No correlation with MC1, positive cultures twice as prevalent in MC2 participants
(Bivona, Camacho et al. 2021)	96 anterior cervical discectomy fusion patients 165 discs Long-term antibiotic use excluded	C. acnes CoNS Staphylococcus spp. Stretococcus spp. Kocuria rhizophila	Aerobic & anaerobic 5d culturing. If growth; identified subcultures & Gram-staining, followed by MALDI-TOF MS	No control or comparison group created. Logus colli muscle (control) specimens taken	FU assessment of surgical success. No host markers of infection assessed. No pain scores assessed	Discs with positive control were excluded. 24/83 (29%) bacterial positive. Only study to report Kocuria rhizophila in disc material
(Capoor, Ruzicka et al. 2016)	290 lumbar disc herniation patients 290 (caudal to avoid statistical bias) discs Antibiotic use 1mth prior to surgery excluded	C. acnes CoNS Alpha-haemolytic streptococci	Two disc samples, one for culturing undertaken 2 h after acquisition (specimens not frozen). Anaerobic culturing 14d. Frozen sample PCR	‘Infective’ (≥ 1000 CFU/ml) C. acnes group compared with < 1000 CFU/ml or C. acnes negative. No control specimens	Pre-operative clinical data captured (straight leg tests, sensory & motor assessments). No host markers of infection assessed. No pain scores assessed	C. acnes identified in 115 (40%) of samples, at an ‘infective’ level in 39 (11%)
(Capoor, Ruzicka et al. 2017)	368 lumbar disc herniation patients 368 discs Antibiotic use 1mth prior to surgery excluded	C. acnes Staphylococcus saccharolyticus Staphylococcus epidermidus Staphylococci heamolyticus	Extended anaerobic culture. MALDI-TOF. C. acnes genotyping. C. acnes specific 16S probe for FISH & DNA dye for CLSM	‘Infective’ (≥ 1000 CFU/ml) C. acnes group compared with < 1000 CFU/ml or C. acnes negative. No control specimens	FISH/CLSM visualisation of host inflammatory cells & bacterial load assessed. No pain scores assessed	162/368 positive for bacterial growth; 119 were C. acnes. No predominance of any C. acnes phylotype. C. acnes seen ‘in situ’ within biofilm
(Chen, Wang et al. 2018)	32 cervical fusion patients (21 MC, 28 degenerative disc & 4 trauma patients) 66 discs Antibiotic use 1mth prior to surgery excluded	CoNS C. acnes Staphylococcus epidermidis Staphylococci haemolyticus Staphylococci capitis	Tryptone soy broth and 14 day sealed anaerobic bag incubation. Negative control samples (no tissue) also cultured. Gram-staining and PCR	Degenerate disc and trauma control groups. Sternocleidomastoid muscle specimens	FU assessment of surgical success. No host markers of infection assessed. No pain scores assessed. Disc herniations classified 1–4 severity, based on MRI	9 discs from 8 patients were 16S positive. Infection in degenerate cervical discs associated with younger age, and complete annulus tear but not MC
(Coscia, Denys et al. 2016)	87 patients 169 discs (30 cervical herniation, 30 lumbar herniation, 30 lumbar discogenic pain, 30 scoliosis control discs & 45 trauma/ deformity control discs) No antibiotic use exclusion criteria noted	C. acnes CoNS	Traditional anaerobic culture & Gram-staining	5 comparison groups of discs created, importantly 2 non-degenerative control groups. No comparison specimens	WBC assessed & histological examination undertaken. No identification of microorganisms, host inflammation or infection with histology. MRI assessment of 27 patients (41 discs). # MC not published	Positive cultures found in 45% of discs, sub-clinical infection occurred at a much higher rate in herniation than control patients. No bacterial correlation with MC. Researchers did not separate bacteria from biofilm, perhaps explaining histology findings. Microbes cultured at higher rates in degenerate discs than control specimens
(Drago, Romano et al. 2020)	39 LBP surgery patients (16 MC2 & 23 MC-free) No antibiotic use exclusion criteria noted	C. acnes Bacillus spp. Lactobacillus spp. Staphylococcus hominis	Nucleus pulpous samples. Cultured & incubated 48 h/15d. Vitek 2 microbial identification	MC2 compared with MC-free patients. No comparison specimens	Full blood count, ESR, CRP & serum electrophoresis	6 (37.5%) MC2 samples and 1 (4.3%) MC-free sample cultured positive
(Fritzell, Bergström et al. 2004)	10 lumbar disc herniation patients w. large protrusions/extrusions No antibiotic use exclusion criteria noted	Bacillus cereus Citrobacter braaki Citrobacter freundii	16S rRNA PCR	No control or comparison group created & no control specimens	No host markers of infection assessed. Pain assessed pre-operatively & 6 weeks post	Small pilot study. 3 specimens from 2 patients were 16S positive
(Georgy, Vaida et al. 2018)	48 cervical surgery patients (13 MC1) No antibiotic use exclusion criteria noted	C. acnes	Aerobic and anaerobic culture plates (4 different agars) incubated for 7d	MC1 compared with other degenerative disc cases. No control specimens taken	No host markers of infection assessed. No pain scores assessed	54% MC1 and 20% MC1-free samples C. acnes positive C. acnes in degenerative disc material. MC1 discs affected at a higher rate
(Javanshir, Salehpour et al. 2017)	145 patients (25 cervical & 120 lumbar herniation) Antibiotic use 1mth prior to surgery excluded	C. acnes	Aerobic & anaerobic blood agar glove box, 7d incubation. Sub-culturing to CBA plates, 24 h incubation. Gram-staining all colonies with presumptive C. acnes rapid ID kit. Specific C. acnes 16S PCR primers	Compared C. acnes proliferation between cervical and lumbar herniation. No control specimens taken	No host markers of infection assessed. No pain scores assessed	55 (38%) C. acnes positive. No difference in bacterial positivity between cervical and lumbar disc samples. Sub-clinical disc infection not isolated to lumbar spine
(Najafi, Mahmoudi et al. 2020)	37 lumbar herniation with MC patients Antibiotic use 60d prior to surgery excluded	C. acnes	Culturing and PCR C. acnes specific primers	No control or comparison group created & no control specimens	VAS & disability scores taken prior to surgery. No host markers of infection assessed	23 (62%) bacteria positive, with no difference between disc protrusion, extrusion or budging. No association between VAS or disability scores and bacterial findings
(Ohrt-Nissen, Fritz et al. 2018)	65 (51 lumbar herniation (H) & 14 control (trauma surgery) patients (C)) Excluded if antibiotic used for 14d within 6mth of surgery	(H) C. acnes (H&C) Staphylococcus epidermidis (H&C) Staphylococcus capitis (H) Micrococcus luteus (H) Gemmiger formicilis (H) Kocuria dechangensis (C) Faecalibacterium prausnitzii (C) Staphylococcus aureus (C) Bacillus simplex	16S rRNA PCR and BLAST Bacterial aggregates and host inflammatory cells examined with FISH/CLSM	Control participants group. No control specimens taken	FISH/CLSM analysis, visualised host inflammatory cells. No pain assessments taken	16S rRNA detected in 16/51 cases & 7/14 controls. Bacterial aggregates & host inflammatory cells observed in bacterial positive cases only & not in control samples
(Rajasekaran, Tangavel et al. 2017)	22 patients (15 herniation, 5 degenerative & 2 non-degenerative). All disc from lumbar spine No antibiotic use exclusion criteria noted	73 bacterial proteins identified including 53 C. acnes & 17 S. epidermidis specific proteins	Dual 16S rRNA universal primer & proteomic analysis of host defence proteins	Non-degenerative control participants. Herniated and degenerated discs compared. No control specimens taken	Proteomics evaluation assessed host defence proteins. No pain assessments taken	Host defence signature responses to disc herniation and degeneration specific bacterial proteins identified in degenerate disc material. Host defence proteins suggestive of infection
(Rajasekaran, Soundararajan et al. 2020)	24 participants (8 MRI healthy, 8 disc degeneration & 8 disc herniation) No antibiotic use exclusion criteria noted	424 different microbial species. Highly abundant phyla: Proteobacteria, Parcubacteria, Firmicutes, Cyanobacteria & Actinobacteria	Genomic DNA extraction and universal amplification (V1-V9 16S rRNA primers) Proteins: Mass spectrometry analysis. Proteomics analysis	3 groups compared: healthy, degenerated and herniated discs. No control specimens taken	Proteomics evaluation assessed host defence proteins. No pain assessments taken	Microbiome signatures for healthy, degenerated and herniated discs
(Rollason, McDowell et al. 2013)	64 lumbar disc herniation patients Antibiotic use 14d prior to surgery excluded	C. acnes Predominance of phylotype strains II & III in disc material Presumptive C. acnes & Staphylococcus spp. identified S. aureus	Nucleus extracted from disc sample, disc dissected into five other parts. Aerobic & anaerobic incubation 7d Nucleotide sequencing of recA housekeeping gene to differentiate C. acnes phylotypes multiple disc samples analysed including separate nucleus analysis	No control or comparison group created & no control specimens	No host markers of infection assessed. No pain scores assessed	24 (38%) C. acnes growth 28% isolates type I A 9% isolates type I B 52% isolates type II 11% isolates type III C. acnes phylotypes in disc differ from those on the skin
(Salehpour, Aghazadeh et al. 2019)	120 single-level lumbar disc herniation patients Antibiotic use 1mth prior to surgery excluded	C. acnes	Blood agar plates, 7d aerobic & anaerobic glovebox. Sub-cultured & 24 h anaerobic incubation. Presumptive C. acnes rapid ID followed by 16S rRNA PCR	No control or comparison group created & no control specimens	No host markers of infection assessed. No pain scores assessed Study went on to examined C. acnes resistance to several different antibiotics	60 (50%) samples were positive for microorganisms study designed to assess C. acnes response to variety of antibiotic drugs
(Singh, Siddhlingeswara et al. 2020)	20 LBP MC patients No antibiotic use exclusion criteria noted	Identified 16S rRNA gene positive disc specimens	16S rRNA Universal eubacteria nested amplification protocol	No control or comparison group created & no control specimens	Measured or leucocytes, ESR and CRP taken. No pain scores assessed	18 (90%) samples demonstrated 16S rRNA gene presence
(Stirling, Worthington et al. 2001)	140 sciatica & LBP patients 36 discectomy (severe sciatica) No antibiotic use exclusion criteria noted	C. acnes CoNS Corynebacterium propinquum	Incubated & sub-cultured in broth for 2, 7 & 21d. Gram-staining for microorganisms. Measured C. acnes CFU in positive samples	Compared serology inflammatory markers in moderate and extreme sciatica patients. No control specimens taken	Serum IgG titres relative to lipid S antigen & CRP levels assessed. Undertook clinical assessment, no pain measures reported	19/36 (53%) positive cultures, 16/19 (84%) C. acnes identified in disc samples. First study to link sub-clinical infection with disc pathology. Higher rate of inflammatory serology associated with more severe sciatica and need for surgery
(Tang, Wang et al. 2018)	80 LBP discectomy patients (25 MC) Antibiotic use 1mth prior to surgery excluded	C. acnes CoNS	5 disc segments: 3 culture media plates & 2 enriched broth. Results read at 7 & 14d. If bacterial growth; universal primers & 16S rRNA PCR used for identification	MC compared with MC-free samples. Surrounding muscle & ligament samples taken	Measured severity of disc degeneration. VAS pain measure	23 samples positive (3 others excluded, suspicious for contamination). Higher rates of positive cultures in MC samples. No relationship between degeneration severity, nor VAS & bacterial infection
(Tang, Chen et al. 2019)	179 single-level lumbar disc herniation patients Antibiotic use 1mth prior to surgery excluded	C. acnes CoNS	3 culture media plates, 2 broth—aerobic & anaerobic culturing for 7 & 14d. Bacterial growth 16S rRNA PCR	Participants compared by age & grouped according to severity of disc degeneration. Surrounding muscle & ligament samples taken	Intervertebral disc height measured (degeneration severity). No pain measures reported	33 samples had positive bacterial growth (6 others excluded, suspicious for contamination). Higher infection rates in younger participants & in those with more degenerated discs
(Withanage, Pathirage et al. 2019)	101 lumbar disc herniation patients Antibiotic use 14d prior to surgery excluded	CoNS sup C.acnes Gemella morbilorum Staphylococci spp.	Enrichment broth & 3 aerobic media cultures followed by additional enrichment and incubation. 3 anaerobic media cultures for 2, 7 & 21d	Skin scapings & muscle biopsy control samples taken. No control or comparison group created	No host markers of infection assessed. No pain scores assessed	18 disc samples positive, 12 for aerobes (CoNS), 6 for anaerobes. First study to identify Gemella morbilorum in disc material. No control samples microbe positive
(Yuan, Zhou et al. 2017)	76 LBP and/or sciatica discectomy patients (70 herniation) 76 discs Antibiotic use 1mth prior to surgery excluded	C. acnes 3 unidentified species	Soy broth culture with serum anaerobic glovebox for 14d C. acnes specific primer & 16S rRNA PCR	Surrounding muscle tissue samples taken. No control or comparison group created	WBC counts taken, MRI signs of discitis assessed, other infection signs (fever/chills) assessed. No pain measures reported	23/76 samples showed anaerobic growth, 20 C. acnes, 4 of these samples were considered contaminated
(Yuan, Chen et al. 2018)	Sub-set from Yuan, Zhou et al. 2017 15 C. acnes positive & 15 C. acnes negative discs	NA	DNA extracted with boiling and bands visualised with UV photography	C. acnes positive samples matched with negative samples for cytokine analysis. Samples from Yuan 2017	Histological disc examination & cytokine quantified in disc tissue. Measures of TFN-a, IL-1b, IL-6, IL-8, MCP-1, MIP-1a, IP-10 & neutrophils	Visible bacteria present in 7 C. acnes positive and no C. acnes negative specimens. Little correlation between inflammatory markers and C. acnes positivity; only IL-8, MIP-1a & neutrophils significant
(Zhou, Chen et al. 2015)	46 LBP/sciatica patients (MC1 5, MC2 13) Antibiotic use 1mth prior to surgery excluded	C. acnes	Soy broth culture with serum incubated in anaerobic glovebox for 14d followed by 16S rRNA PCR with C. acnes specific primers	Samples with annular tear compared to those without. Surrounding muscle control specimens taken	Disc height measured. No host markers of infection assessed. No pain scores assessed	11 (23.9%) discs tested positive for 16S rRNA. Only discs with annular tears tested positive. No relationships between MC or sciatica & C. acnes in the disc found

45 lumbar spine surgery patients (24 MC1, 8MC2)

77 discs

Excluded if antibiotic used for 15d within 3 m of surgery

C. avidum

Streptococcus spp.

44 lumbar herniation patients (7 MC1, 4 MC2)

64 degenerative lumbar spine disease patients (64 MC)

80 discs

30 LBP or sciatica lumbar excision patients

120 discs

54 lumbar disc herniation patients

Antibiotic use history recorded – not excluded

Anaerobic streptococci

Actinomyces sup

Streptococcus spp.

Lactococus lactis

Burkholderiales

22 lumbar disc herniation patients (2 MC1, 6 MC2)

30 discs

812 participants (550 disc & paraspinal samples, 191 disc only, 46 sham; paraspinal only & 25 control; trauma patients)

Acinetobacter

Candida

Corybacterium

Cutibacterium (C. acnes) Staphylococcus

313 participants (303 MC1, 58 MC2)

385 discs

S. epidermidis

Saccharopolyspora hirsuta

Studies finding bacteria in disc material

Stirling’s work first identified raised IgG antibodies in 43/140 (31%) patients with sciatica or LBP. Severely affected patients underwent microdiscectomy, and bacteria was detected in 19/36 (53%) samples [24]. C. acnes 16/19 (83%), coagulase-negative staphylococci (CoNS) 2/19 (11%) and Corynebacterium propinquum 1/19 (5%) were cultured [24]. A high proportion of positive serology tests were from patients with microorganism positive disc samples [24]. Fritzell and colleagues found 2/10 (20%) degenerate disc samples tested positive for Bacillus cereus, Citrobacter braakii and C. freundii, and asserted these were ‘true findings’ based on their strict collection methodology [25]. Similarly, C. acnes (7/52, 13.5%), Peptostreptococcus spp. (1/52, 2%), Staphylococcus aureus (1/52, 2%) and CoNS (1/52, 2%) were cultured from lumbar herniation microdiscectomy specimens [26]. Yuan and colleagues (2017) found C. acnes with culture and selective PCR in 16/76 (21%) discs, having discarded four positive disc samples with a corresponding positive muscle control sample [27]. Histological examination confirmed rod-shaped bacteria in half the PCR positive samples and no randomly selected PCR negative samples [27].

Contamination may be distinguished from infection by bacterial quantification—counting colony forming units (CFU). Proposing ≥ 1000 CFU/ml indicates active infection, C. acnes (115/290), CoNS (31/290) and alpha-haemolytic streptococci were isolated after disc herniation material homogenisation and qPCR amplification [28]. Bacteria were identified in 45% of samples; 11% positive for C. acnes ≥ 1000 CFU/ml [28]. Adding to the cohort and improving methodology by incorporating mass spectrometry, a second study found C. acnes ≥ 1000 CFU/ml in 10% of 368 patients’ samples [29]. Staphylococcus, Streptococcus and Corynebacterium ≥ 1000 CFU/ml were detected in 13 samples [29]. Another analysis of herniated disc samples, with a lower ‘infective’ CFU criteria reported C. acnes 24/64 (38%), CoNS 5/65 (8%) and Gram-negative diplococci 1/64 colonisation of 1–150 CFU per sample [30]. Another investigation reported a predominance of CoNS in 7/66 (11%) and C. acnes in 2/66 (3%) cervical disc samples using anaerobic culturing and PCR [31]. Withanage and colleagues (2019) cultured CoNS, C. acnes and Gemella morbillorum in 18/101 (18%) lumbar herniation samples [32].

Salehpour and co-workers found bacteria in 60/120 (50%) lumbar herniation discs; positive samples were screened for C. acnes with a kit and PCR. C. acnes accounted for 77% cases of bacterial growth and researchers went on to investigate C. acnes sensitivity to antibiotics [33]. Recently, 96 cervical degeneration patients were recruited and 55% of all disc samples grew positive cultures [34]. Disc samples with a corresponding bacterial positive muscle biopsy were eliminated from analysis, leaving 17/96 (18%) of participants with a positive disc sample and a ‘clean’ control sample. Predominantly C. acnes along with CoNS, Staphylococcus spp., Streptococcus spp. and one example of Kocuria rhizophila was cultured in disc specimens [34].

Modic change

Eight articles found higher rates of positive bacterial samples came from MC patients than participants without MC. For example, 54% of patients with MC1 were positive for the presence of C. acnes compared to 20% of patients without MC1, in a study of 48 cervical biopsy samples [35]. Four studies combined samples from MC1 and MC2 patients; Aghazadeh and colleagues (2017) reported 80% of MC samples were C. acnes positive while only 14% of MC-free samples were positive [36]. Yuan and co-workers (2018) found 12/15 (80%) of C. acnes positive cultures were from MC participants; however, the small sample size of this study made drawing statistically based conclusions difficult [37]. Tang and colleagues (2018) reported 26/80 (33%) herniation samples were positive for bacteria using PCR. One positive sample excluded from subsequent analysis which showed 15/25 (60%) patients with disc bacteria had MC [38].

Disc bacteria was recorded in recent studies of MC patients (type unspecified) [39, 40]. Singh and co-workers (2020) reported 90% of 20 LBP; MC participants’ samples were positive for 16S rRNA gene with PCR. This investigation found evidence of inflammation associated with MC; participants had raised levels of leucocytes, ESR and CRP [39]. Najafi and colleagues (2020) found a high rate of C. acnes prevalence via culturing in 23/37 (62%) samples from LBP patients [40].

Two studies reported occult infection in MC2 adjacent discs. Arndt and co-workers (2012) did not find differences when MC1 and MC2 were pooled and compared to MC-free samples; however, MC2 specimens alone showed greater bacterial positivity than other samples [41]. Drago and colleagues (2020) concluded MC2 may be associated with occult infection when samples from 6/16 (37.5%) MC2 patients and only 1/23 (4%) MC-free control returned positive bacterial cultures [42].

One longitudinal study has demonstrated bacterial proliferation precedes MC1 development. In 28/61 (46%), herniation surgery patients positive for microorganisms, 80% developed new MC1 in the subsequent 12–24 months [43]. 44% of negative culture patients developed MC1 giving an OR of 5.6 (95% CI 1.51–21.95) for new MC1 given a positive anaerobic microbe culture [43]. Four articles did not find bacterial abundance differed between MC and MC-free degenerate discs [31, 44–46].

Disc herniation and infection

The most included studies used homogeneous groups of disc herniation participants (i.e. all with herniated discs). Four studies compared and reported increased abundance and/or species differences in herniated over non-herniated discs [44, 46–48]. Coscia and co-workers (2016) found positive bacterial cultures in 76/145 (45%) of excised disc material, but notably, 32/61 (52%) herniation patients versus 19/77 (25%) controls samples were positive for C. acnes (45%), CoNS (40%) and various species (4%) [46]. Two studies included patients with herniated and non-herniated discs but did not report and bacterial abundance differences [25, 37].

Two studies reported a positive relationship between herniation severity and C. acnes proliferation. Zhou and colleagues (2015) found 10/28 (36%) discs supported C. acnes proliferation when the protective annular was torn [45]. Only 1/18 (6%) untorn disc did, however, this specimen was removed from the analysis as its corresponding muscle control sample was also culture positive [45]. Chen and co-workers (2018) found more positive cultures in more damaged discs that were extruded or sequestered than those budging or protruded [31]. Yet Najafi and colleagues (2020) found no bacterial differences between disc pathologies of extrusion, protrusion or bulging [40].

Patient subgroup infection

Eight studies identified patient subgroups other than those with MC or herniation as susceptible to occult infection. Two studies reported greater bacterial growth in men than women [28, 41] while one reported higher rates of infection in disc samples from women [34]. Two research groups reported higher rates of disc infection in younger participants [28, 29, 38, 49], Yet Najafi and co-workers (2020) found specimens from older patients with MC were more likely to be C. acnes positive [40]. Two studies reported increased proliferation of microorganisms differed at spinal levels. Greater C. acnes abundance at L4–L5 than other lumbar discs was reported in herniation patients [41] and greater C. acnes colonisation in C6–C7 and L4–L5 than other spinal levels was also found [50]. Most articles did not report bacterial differences in sex, age or spinal level subgroups.

Disc colonisation by multiple microbes

Of 27 positive studies, five reported finding several species depicting a bacterial ecosystem. Utilising a pre-operative biopsy approach to decease contamination, 40/83 (48%) lumbar disc samples returned positive cultures for C. acnes (35%), CoNS (31%), Staphylococcus aureus (6%), three species of Gram-negative bacilli (6%), Micrococcus spp. (6%), Corynebacterium spp. (6%) and single examples of five other species using only routine culturing [41]. Another study found C. acnes (38%), CoNS (6%), Gram-negative bacilli (2.5%) Micrococcus spp. (4%), Corynebacterium spp. (3.5%) and Neisseria spp. (2.5%) in 60/120 (50%) herniation samples using Gram-staining culturing and 16S rRNA gene PCR [36]. Ohrt-Nissen and colleagues (2018) listed BLAST scores following genome sequencing and recorded eight species in herniation and six in non-degenerative samples [44]. Using microscopy, they saw host inflammatory cell activation only in degenerate disc samples, not in control samples [44].

Using the agnostic techniques of proteomics and 16S rRNA gene analysis, Rajasekaran’s study of 22 herniation samples demonstrated many more bacterial proteins than either degenerate or discs from participants with a healthy spine [47]. A total of 2061 bacterial proteins were identified, only 178 of these shared between the three disc groups [47]. In a subsequent study using culture-independent 16S rRNA gene sequencing [48] 424 species were reported, including five dominant taxa with abundance ranges from 13 to 16% [48]. Microbiota signatures for both disc degeneration and herniation were characterized as shifts in composition and diversity away from the disc microbiome of a healthy spine [48]. C. acnes was found in similar proportions in all disc groups and was not the most dominant bacteria with relative abundance ranging from 1.5 to 3% [48].

Evidence of contamination

Nine reports attributing bacterial colonisation in disc samples to contamination were found. Ben-Galim and colleagues (2006) cultured multiple samples from 30 LBP patients and found two patients returned four positive CoNS specimens: 4/120 (4%) [51]. Another study involving lumbar herniation patients cultured C. acnes in 2/54 (4%) discs, in 10/54 (19%) muscle tissue control and in negative air control samples [52]. Li and colleagues (2016) recruited 22 herniation patients contributing 30 discs specimens, CoNS and Staphylococcus epidermidis were cultured from three and one samples, respectively [53]. Another investigation of 44 herniation specimens analysed with a high-quality next generation PCR assay did not detect evidence of the bacterial 16S rRNA gene in samples [54].

C. acnes was detected in 7/45 (16%) disc specimens with culturing and PCR, however, 24% of posterior surgical approach samples were associated with positive culture, whereas only 9% of anterior approach samples were [55]. In this study, there were no disc bacterial differences between MC and MC-free patients [55]. Fritzell and colleagues (2019) later study also found no relationship between disc bacterial findings and MC in 2/40 (5%) LBP patients. Bacterial cultures from muscle tissues samples from LBP and control groups returned 30% and 20%, respectively [56]. Using a video assisted minimal skin contact anterior surgical approach, Rigal and co-workers (2016) found 6/313 (2%) disc biopsies from MC patients grew positive bacterial cultures [57]. There was no relationship between bacterial findings and outcomes a year following surgery [57]. The largest disc infection investigation to date collected samples from 812 participants. Contamination (muscle) control samples along with disc samples were taken from disc degenerative (case) and non-degenerative (control) participants [58]. Significantly higher rates of bacteria were cultured from control group samples of muscle and disc (48%) than degenerate disc samples (17%) [58]. Prior surgeries and multilevel surgeries were associated with higher rates of bacterial growth [58]. There was no difference in disc bacterial prevalence between case and control groups, MC or vertebral level treated [58]. Recently, 1/64 MC samples verified C. acnes growth from disc material, no patients had any signs of infection [59]. Researchers concluded that infection and C. acnes disc penetration must be rare if extant [59].

Discussion

Articles in this review link occult infection and disc degeneration, finding evidence of bacteria, mainly C. acnes, using selective microbial culture and targeted PCR. Targeted culturing predominated with only six studies using universal PCR or genome-wide sequencing techniques [38, 39, 47, 48, 55, 56]. A causal role for bacteria in disc degeneration or MC is not clear, and all but two studies were cross sectional. Causality was suggested by Albert and colleagues (2013) in their longitudinal study which showed discs with bacteria increased the likelihood to develop MC1 in adjacent vertebrae [43], though Rigal and co-workers (2016) saw no influence of their few positive bacterial cases on outcome [57].

MC1 adjacent discs have been proffered as inflammatory and most vulnerable to occult infection [14]; however, only study showed MC1 was associated with increased rates of disc bacterial growth [35]. MC specimens have been reported more infective than MC-free specimens [36-39] as have MC2 samples [41, 42]. Increased immune activation in MC2 compared with MC-free samples has also been found, however, without examination of disc bacteria [60]. MC type is not static, MC1 can progress to MC2, or recover and a significant percentage of MC radiography report mixed types, most commonly a mix of MC1 and MC2 [61]. Thus, MC types are semi-fluid, we therefore cannot dismiss the possibility that MC2 also represents vulnerability to infection, inflammation and advanced disc degeneration.

A mechanistic explanation for occult infection has been proposed: harbouring C. acnes in disc tissue corresponded with annular tears, with intact discs not returning positive PCR tests [45].

Chen and colleagues (2018) found more positive cultures in more damaged discs that were extruded or sequestered than those budging or protruded [31]. It is interesting that Ahmed-Yahia and colleagues (2019) concluded high rates of contamination due to surgical approach [55] Samples from participants were assigned to either Group 1 ALIF or disc prothesis (herniation not specified) or Group 2 TLIF for herniated discs. The second group’s higher rate of bacteria positive samples drew the conclusion TLIF was a more contaminating approach—when there may have been disc pathology differences between the two groups.

It is possible that C. acnes accesses the nucleus pulpous via disruption to the annulus fibrosus. In rats, MC1-like changes, increased 16S rRNA gene expression and immune activation occurred with injection of C. acnes isolates to the disc [62]. In vitro, MC adjacent disc cells had an increased inflammatory response to C. acnes compared with healthy disc cells [63]. If these findings mirror interactions in the human spine, damaged discs and bacteria may culminate in a synergistic degenerative sequela, producing local inflammation and therefore more pain. Of course, C. acnes may not be the only bacterial species that causes inflammation and degeneration when artificially introduced to a disc.

While this review found evidence to support occult infection in degenerate discs, particularly C. acnes—it remains unclear the extent to which bacteria reside in the disc space. Wedderkopp and colleages (2009) sampled MC lesions and found only two samples cultured positive for bacteria; however, these two patients were treated with antibiotics which brought one temporarily pain relief [64]. This finding does hint at bacterial involvement in degeneration and pain; however, other research efforts administering antibiotics for back pain have met with varying successes. No antibiotic studies have assessed disc bacterial prevalence, and hence are excluded from this review [65-67]. A recent, interesting review by Gilligan and colleagues (2021) summarises eight antibiotic trials for LBP [68]. These authors conclude a LBP sub-type (likely patients with MC1, wishing to avoid surgery) may be amenable to antibiotic therapy [68]. To enter the bone or disc space antibiotic regimes are necessarily protracted and responsible antibiotic stewardship calls for such treatments to be approached with prudence.

This review highlights the heterogeneity of microbial discovery, identification and sequencing techniques that have biased many reports in this field. Qualifying and quantifying bacteria uniquely associated with disc degeneration and MC is currently incomplete and a primary step in understanding if antibiotic treatment is suitable for LBP. As a handful of studies indicate; bacteria may reside in the healthy disc space [44, 47, 48], an additional reason to proceed with caution. Agnostic examination of disc samples as standard practice will give a better understanding of the commensal and/or pathogenic nature of degenerate disc bacteria. This is needed before antibiotics can reasonably be considered for back pain treatment. While selective and acute bias to identify bacteria in disc specimens persists, such advances are impossible. Bias in this field is underscored by several studies finding a high prevalence of bacteria yet low numbers of species [27, 35, 38, 45, 46, 50]. Immediately storing samples in culture medium [40] for example, selects against most other bacteria, making accurate determination of the whole range of species impossible.

Rao and colleagues (2020) scrupulously collected samples from (control) participants with non-degenerate discs, as well as multiple control specimens from surrounding disc anatomy. Yet no more advanced bacterial identification than microbial culture was undertaken in samples from 812 participants, the largest study of its kind [58]. C. acnes specific culturing may explain why discs removed from patients with previous and more extensive surgery had higher rates of positive bacterial culture [58]. Moderately high rates of positive bacterial samples were obtained from discs (17%), (comparable with other studies reporting disc bacteria; see Table 1.), yet almost half muscle control specimens were positive for bacteria [58]. No bacterial differences were found between case degenerate and control discs [58]. In contrast, Coscia and co-workers (2016) showed lower bacterial abundance in non-degenerative disc samples; perhaps curiously, also only using culture identification [46].

Alamin and colleagues (2017) reported a sterile disc environment, despite using a high-quality next generation PCR assay [54]. These results could be due to insufficient DNA extraction from disc samples, a fair possibility as their validation cohort amplicon sequencing worked on cultured samples and found similar pathogenic bacteria from disc material as previous reports [54].

A small number of studies reported an ecosystem of bacteria in degenerate discs [36, 41, 44, 47, 48]. Ohrt-Nissen and co-workers (2018) found a similar diversity of species in healthy and degenerate disc samples. Only finding host inflammatory cell activation in degenerate disc material adds credence to the notion that disc degeneration results from bacterial imbalance rather than from the presence of bacteria themselves [44]. Perhaps not surprisingly, more exploratory technologies found greater diversity of bacterial species. Rajasekaran’s group used proteomics to identify 73 bacterial specific proteins along with upregulation of defence proteins, a host immune counter to bacterial infection [47]. Bacterial proteins unique to degenerate, herniated and healthy discs were found as well as overlaps between disc groups [47]. These data led them to conclude a presence of commensal, albeit low level, human disc bacteria. Support for this idea gained further traction with a second project which used a metagenomic approach to find 424 different species, support for the existence of disc microbiota and a disc microbiome [48]. Higher alpha-diversity and differences in beta-diversity were found in healthy discs compared with degenerated or herniated samples [48]. This paper begs replication—and if this is forthcoming may provide a guide towards future possible LBP treatments.

If bacteria do sequester into the disc space another challenge posed to successful identification is the tendency of bacteria to cluster and grow unevenly distributed within a protective biofilm [14]. Viewing and quantifying bacteria within biofilm may accurately assess colonisation. Two studies used fluorescence in situ hybridization (FISH) staining and viewed samples with specialised confocal laser scanning microscopy (CLSM) [29, 44]. These technologies enable quantifying bacterial biofilm sequestration and growth along with producing high-resolution, three-dimensional pictures of a bacterium in situ [12]. Use of FISH/CLSM permits tissue assessment of uncontaminated samples. Well-established biofilm formation is impossible from the brief skin contact that may occur during spine surgery. FISH/CLSM could offer an important contribution to verifying bacterial colonisation within degenerate disc material.

Limitations

It is clear why controversy continues to surround the question of occult infection and bacteria in the degenerate disc space. Most protocols kept samples free of contamination, although removing a totally ‘sterile’ disc is difficult if not impossible, thus contamination poses an ongoing challenge. Acquiring healthy human disc specimens is difficult; thus, a rare control group in these investigations. Only two longitudinal examinations were relevant [43, 57], yet knowing what becomes of patients with high bacterial loads in degenerate discs will help determine the pathogenic (or not) nature of such microbes. Only 12 studies used surrounding tissue as negative control samples, routine collection of these samples will help future research clarify the extent of sample contamination. FISH/CLSM is a time-consuming procedure, covering only a fraction of a tissue biopsy [44], specialised equipment and skills are required and only ~ 15% of researchers use it [12]. Nonetheless, proponents have made multiple calls to include FISH/CLSM as standard for disc material analysis [12, 14, 29, 44].

Conclusion

Evidence in this systematic review implicates C. acnes as a bacterial resident in degenerate disc tissue, identified through culture, PCR and microscopy. Some evidence suggests a broad diversity of microbes within the disc. Most laboratory techniques were biased towards identifying C. acnes. The field will benefit from new genomic methods which identify bacteria by their genetic material and may be known as well as unknown (i.e. not yet catalogued). The inclusion of omics analyses and advanced histological techniques are not widely used yet to determine sub-clinical infection within the degenerate disc will strengthen such research.

Key Messages

Contamination is not an adequate explanation for positive bacterial findings in degenerate disc material.

Culturing bias towards finding C. acnes has overwhelmed research examining occult infection in degenerate discs.

Agnostic, exploratory disc bacteria assessment may best inform any occult infection and disc degeneration links.

Insufficient evidence exists to suggest changes to current clinical treatment.

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 17 KB)