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Mycobacterium avium ssp. Paratuberculosis and Crohn’s Disease—Time to Consider New Therapeutic Approaches?

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Submitted:

13 July 2023

Posted:

14 July 2023

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Abstract
Mycobacterium avium ssp paratuberculosis (MAP) is the causative agent of Johne’s disease (JD) in animals and a suspected cause of Crohn’s disease (CD) in humans. Crohn’s Disease is a progressive, detrimental granulomatous enteritis of which common therapies are targeted to suppressing certain components of the immune system. The efficacy of these treatments can be variable and temporary with no clear process of selection for the individual patient. However, diagnosis of MAP has been elusive in patients with Crohn’s Disease. In animals it can be detected by several different techniques, including bacterial cell culture, polymerase chain reaction (PCR), and immunological targets. To move to an understanding of the possible pathogenicity of MAP and the sup-posed cause of CD in humans, it is necessary to demonstrate the presence of cell wall deficient mycobacterial (CWDM) forms of MAP in blood and tissue cultures from patients with CD. From this, more tailored and accurate therapies can be implemented and be developed to eradicate this infectious organism from humans. Current anti-mycobacterial antibiotics have limited efficacy as MAP is subtly different from tuberculosis. Newer methods, such as vaccination and gut microbiome remediation will be essential as part of combination therapies.
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1. Introduction

Mycobacterium species are gram-positive, catalase-positive, aerobic, and occasionally microaerophilic non-spore-forming acid-fast bacilli. They may adopt an infectious life cycle[1] in animals, while the animal response may include an immunological life cycle[2]. Members of the Mycobacterium genus are oligotrophs that evolve to survive in challenging environments. Some members of the genus are able to utilise methanol or carbon monoxide as carbon sources.[3] Culture media for the growth of mycobacteria rely on low nutrient content and are formulated for the growth of bacillary strains of mycobacteria with intact cell walls. Members of the Mycobacterium genus, in common with other bacteria, proceed through four stages of growth; the lag phase, the log (growth) phase, the decline phase, and the death phase. Each growth phase is a response to alterations in atmosphere and nutrients. Mycobacteria, both in culture media and in the host, can remain viable after the decline phase by entering a state variously called latency, dormancy, or non-replicating persistence (NRP). This adaptation enables the life cycle of the Mycobacterium species to reset to the lag phase when a favourable atmosphere and nutrients are encountered.
Bacterial life within a closed culture system is archetypal and most mycobacteria can survive for long periods by adopting reversible quiescent metabolic states that reflect the external environment. There is little known about this aspect of the mycobacterial life cycle, which may involve NRP and the loss of the cell wall. NRP may be a result of the pressures of antimicrobial therapy, adverse environmental conditions or lack of nutrients and oxygen. NRP can be reversed in vivo when favourable conditions for growth eventuate.[4]
CWDM represent part of the life cycle of Mycobacterium species. In the latent phase of mycobacterial infection, the microorganism may cease to grow, and enter a cell wall deficient state if nutrients are unavailable and atmospheric conditions are suboptimal. There have been few studies on the fundamental processes that drive mycobacterial latency. In-vitro observations indicate that the CWDM state occurs naturally in old fluid cultures of mycobacteria, and can be artificially induced through chemical stripping of the cell wall, or by long-term incubation of mycobacteria in low nutrient media.[5,6,7]
Development of growth media for previously uncultured organisms[8] is very difficult, and requires patience and innovations.[9] The detection and cultivation of cell wall deficient mycobacteria (CWDM) in blood and tissues is possible using both old and newly developed techniques.[9,10] The ZN stain can be used for monitoring the growth of CWDM in culture[11,12] if alterations to the ZN stain method are made.
Mycobacterial colonisation of blood has been reported in inflammatory bowel disease and in healthy controls using molecular detection methods[13,14,15], including PCR. However, visual confirmation of the existence of CWDM has mostly been lacking, with the exception of electron microscopy of CWDM isolates cultured from tissue collected from patients with Crohn’s disease.[16]
Turbidity measurements using mycobacterial culture media such as Middlebrooks 7H9 broth are unsuitable for short term growth monitoring of CWDM, as they contain precipitants. In the absence of methods to detect CWDM, PCR is used as a surrogate test to detect mycobacteria in specimens from patients with IBD, in place of culture. PCR does not differentiate between viable and non-viable mycobacteria, without modifications to the PCR protocols.[17,18] PCR has been used to detect mycobacterial DNA in patients with CD disease as well as in healthy human controls.[19] Some other inflammatory diseases may also involve CWDM in stealth form, or as “non-replicating persister” (NRP) forms.[20,21]
The cultivation of CWDM forms from human hosts by the authors has proven to be extremely difficult, but is achievable. In lieu of viable isolates of CWDM from human sources, other researchers have instead simulated CWDM though the chemical deconstruction of acid-fast bacilli[22,23] (AFB). Artificially manufactured CWDM differ from those found in nature, as others have observed.[24] The cell wall deficient state may be a defence against bacteriophage attacks.[25]
MTBC are ontogenetic[26,27], and this trait may be inherited by CWDM. Naturally occurring CWDM produce biofilm, and their inner membranes have been exposed to host antibodies targeting mycobacterial virulence factors.[27] Formation of antigen-antibody complexes[28] will also alter the exposed mycobacterial bacterial inner membrane.
Mycobacterium species are a diverse group of organisms that range from non-pathogenic, to opportunistically pathogenic, to obligately pathogenic. Obligate pathogens such as MTBC are invariably pathogenic in humans. Members of Mycobacterium avium complex (MAC) are opportunistic pathogens, and may cause disease in immunocompromised hosts but are able to transiently colonise healthy subjects without causing diseases.
Non-tuberculous mycobacteria (NTM) are not routinely isolated in clinical laboratories, neither in the bacillary form, nor as CWDM. Partly because they are not actively sought, and partly because they are extremely difficult to isolate using common culture methods. Although they are ubiquitous in the environment, they are seldom seen as laboratory contaminants. There are a wide range of conditions for optimal growth of different members of the Mycobacterium genus, meaning that only a narrow range of NTM are detected in the laboratory. Diagnosis of tuberculosis is a high priority, given its global disease burden, so laboratory methods are optimised to detect MTBC acid fast bacilli(AFB).[29,30] These methods are slightly different between the two groups.
The clinical significance of a single isolation of NTM is difficult to establish unless it is an obligate pathogen. Isolates of MAC usually require serial isolations from culture to confirm a pathogenic role, because of widespread presence in the environment, including the water supply of domestic homes[31] and hospitals. Hence semi-quantitation is used to differentiate transient acquisition from opportunistic infection. Enumeration of organisms present in samples may suggest a pathogenic role in a subject, as higher numbers of organisms may relate to infection, rather than carriage.[32] The ZN stain of a sample may indicate there are high numbers of acid-fast organisms (AFO) present[32]. Growth on solid media enables numbers of organisms to be estimated.
Quantitation of bacteria is also a useful measure of therapeutic response, both in vitro through antimycobacterial susceptibility testing and in vivo, to monitor a reduction of the number of organisms as well as the viability of the cells over time. In the healthy subject, low numbers of NTM may be present without consequences. This may present difficulties in interpretation, unless transient carriage can be differentiated from infection, through specimen monitoring and clinical evaluation. If culture of CWDM is available then the PCR result will be complementary and confirmatory.

Visualising CWDM in culture

Since the discovery of the ZN stain in 1883, the stain methodology has undergone modifications to optimise the laboratory detection of MTBC.
Laboratory staining methods are often selected that are convenient, cost effective and technically expedient. The acid-alcohol decolouriser used in most laboratories selects for MTBC and is preferred because it is a “clean” stain and results in a slide without excess carbol-fuchsin (CF) residue. In turn this results in unambiguous reporting of acid-alcohol fast bacilli, strongly indicative of tuberculosis.
The formula of the CF stain used in the ZN stain to visualise CWDM is integral to detection. (Table 1) Concentrations of basic fuchsin vary greatly in recipes for CF. Laboratories making their own CF often use 1% basic fuchsin. This may be sub-optimal for CWDM. The authors recommend the following recipe for the detection of CWDM.
Table 1. Formula for preparing Carbol Fuchsin Stain.
Table 1. Formula for preparing Carbol Fuchsin Stain.
Basic Fuchsin 24 gm (CARL ROTH GmbH &Co (C.I 42510)
Ethanol 95% 120 ml
Distilled Water 800 ml
Phenol 48 ml

2. Materials and Methods

2.1. ZIEHL-NEELSEN STAIN FOR CWDM

Step 1. Carbol fuchsin stain: 1). Dissolve basic fuchsin in the alcohol and add the water slowly while shaking. 2). Add Phenol. Filter.
Step 2. ZN decolouriser: 20% H2SO4 in distilled water.
Step 3. Counterstain: Loeffler’s methylene blue; 10ml glacial acetic acid; 1 litre Distilled Water; 2.5gm methylene blue; Filter.

2.2. Method for Staining

1. Flood the slide with carbol fuchsin. Gentle heat may be applied to the slide. Leave for 8-10 minutes.
2. Rinse off the carbol fuchsin with water.
3.Decolourise for two minutes using the acid decolouriser with a wash between. ie, 1 minute of the decolouriser, wash, add more decolouriser, then wash off again. Alternatively, the decolouriser can be applied until clearance of carbol fuchsin can be seen.
4. Cover slide with methylene blue counterstain for 2 minutes; wash off, dry the slide without blotting.

2.3. Microscope Slides

Positively-charged slides enable the retention of blood-containing culture material on the slide during the staining process.

2.4. Sample collection

Blood samples should be collected in tubes containing sodium citrate as the anticoagulant. EDTA should not be used as the anticoagulant as it is bactericidal[33] and inhibits biofilm formation.

2.5. Detection of CWDM

To confirm methodology and detection of CWDM, the following experiment can be performed using the BD BACTEC™ MGIT™ mycobacterial growth indicator tube (MGIT).
1)
To a MGIT tube supplemented with OADC and PANTA, add enough sterile filtered sucrose solution in water to arrive at a final concentration in the MGIT of 1% sucrose. If MAC is suspected, add mycobactin J. (Allied Monitor Inc., Fayette, MO) according to manufacturer’s instructions.
2)
The buffy coat from a human subject is harvested after centrifugation of the sodium citrated blood sample for 10 minutes at 3000 RPM. Some consideration should be given to separate culture of the erythrocyte component.[34]
3)
Inoculate the MGIT tube with buffy coat and incubate for 30 days at 370c, with a primary reading of the culture deposit at 8 days, using the above ZN stain method.
Note: The MGIT tube is optimised for the culture of MTBC in the AFB form, not for CWDM culture.

3. Results

Using additional supplementation and the above ZN stain it is possible to semi-quantitate CWDM to obtain an approximation of numbers of CWDM present in a sample after 30 days incubation. During incubation of the buffy coat in the MGIT tube, the CWDM undergo initial rapid growth, followed by NRP. (Personal data) Nucleases may also be produced extracellularly in the initial growth phase.[35,36]
CWDM are readily visible under x 1000 oil immersion as ZN positive spheres. Sizes of CWDM vary from very small to larger than a white blood cell. (WBC) Figure 1, Figure 2 and Figure 3.
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Figure 1. ZN stain. Blue object is a WBC. The large red object is a CWDM (x1000 magnification under oil immersion).
Figure 1. ZN stain. Blue object is a WBC. The large red object is a CWDM (x1000 magnification under oil immersion).
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Figure 2. ZN stain. Blood culture from a subject with CD showing pleomorphic forms (x1000 magnification under oil immersion).
Figure 2. ZN stain. Blood culture from a subject with CD showing pleomorphic forms (x1000 magnification under oil immersion).
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Nearly all healthy subjects carry small numbers of intracellular CWDM, possibly to aid immune recognition of mycobacteria (personal data). This has been termed ‘trained immunity. Some IBD patients carry large numbers of CWDM in peripheral blood that can be cultivated using more extensive protocols than are covered in this preliminary report.
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Figure 3. ZN stain Supplemented MGIT tube 370c incubation for 30 days. Patient diagnosed with refractory Crohn’s disease. Note the variation in size and some evidence of bilateral division (x1000 magnification under oil immersion).
Figure 3. ZN stain Supplemented MGIT tube 370c incubation for 30 days. Patient diagnosed with refractory Crohn’s disease. Note the variation in size and some evidence of bilateral division (x1000 magnification under oil immersion).
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3.1. Fluid culture media for CWDM.

As we found with the ZN stain, there is no single culture medium that can be considered standard for cultivation of CWDM.
Bacterial culture is necessary for confirmation of the ZN stain result and for the subsequent antimycobacterial susceptibility tests and molecular studies. Other researchers have shown little difference in the performance of supplemented 7H9 medium and MGIT tubes, when used in non-automated manual procedures.[37,38] In-house fluid media has advantages as an experimental vehicle in the development of CWDM culture media, including the ability to supplement the media with specific nutrients, and monitoring for variations in replication times of isolates in response to additives. The authors believe that because of the numerous variables, (nutrients, osmolarity, atmosphere etc) that in-house bespoke fluid media is cost-effective and sufficiently flexible for further development of media for CWDM, until such time that consensus is reached and commercially manufactured CWDM is available.
CWDM are incapable of growth in 7H9 base medium except when that medium has additional supplements. For the practical purposes of media development, 7H9 medium can be used as a base medium, provided supplementation (i.e., OADC, amino acids, vitamins etc) is possible. Cost can also be a factor in innovation however. Development of media for CWDM requires a large degree of trial and error.
Experiments using 7H9 fluid media as the base are necessary to identify supplementary constituents that may either stimulate or inhibit growth of CWDM. We have observed that CWDM cultivation media must be able to compensate for the effect of nutrient flux on the CWDM. (Titration of media may also be helpful to establish performance limits.)
The rudimentary membrane structure of CWDM may render them susceptible to osmotic and atmospheric changes. The adjustments in constituents of fluid media that must be undertaken to arrive at a “goldilocks zone” to support ongoing growth are further complicated by apparent strain diversity, nutrient requirements, and inhibitory factors. The structure of CWDM is often fragile and isolates may progress through a series of growth changes depending on the strain of CWDM and the duration of incubation. This effort is however, necessary to be able to cultivate the CWDM for susceptibility studies and molecular analysis.[9]
Middlebrooks 7H9 medium is a low nutrient, defined medium, and is widely used for isolation of MTBC from a variety of sample types. The use of low nutrient mycobacterial culture medium is based on the restricted availability of nutrients for MTBC in vivo in the host.[39] In vivo the nutrient requirements of MTBC may differ depending on the stage of the disease, and this also applies to CWDM in general.
NTM may require more complex nutrients, amino acids and vitamins (i.e., mycobactin J) to grow in vitro. The effects of nutrient flux may impact more on CWDM, which have only the inner semipermeable membrane to modulate intracellular nutrient availability. Resuscitation promotion factors (RPF) may improve growth considerably. RPF have been associated with the reversion of the CWDM to bacillary forms and may have a role in acceleration or inhibition of growth.[40]

3.2. Solid culture media for CWDM

Solid culture media such as Lowenstein Jensen (LJ), Middlebrook7H10, and Middlebrook 7H11 are commonly used for isolation of mycobacteria, with a global preference for LJ medium, because of ease of manufacture and cost effectiveness. There is no general agreement on a single solid medium.[41] The selection of media is a mixture of prior experience, personal whims and established laboratory procedures. Supplements can be a major expense for some laboratories, particularly as the revival and growth of CWDM is still somewhat stochastic. Fluid media usually promote mycobacterial growth better than solid media, but solid media is more useful for quantitation. PCR is a poor substitute for growth on solid media. Sheep blood agar (SBA) has been used for cultivation of MTBC on solid agar where it was found to perform better than other standard media, such as Lowenstein Jensen media (LJ).[42,43]
Mycobacterium avium grew better on SBA than on LJ when colonies were counted. SBA may be a higher nutrient medium than LJ. It may also be possible that addition of egg yolk to LJ inhibits growth of CWDM. This suggests that more concentrated, or more specifically formulated nutrient media can be used to advantage. Markova et al. reported isolation of CWDM on semi solid agar medium.[44] Other cell wall deficient bacteria can be grown on conventional laboratory semi-solid and solid media.[45,46,47]
The authors have not yet had unalloyed success with solid media to grow CWDM, but biphasic media may hold some promise.

4. Discussion

There are over 190 members of the Mycobacterium genus. Members of MAC, which proportionally represent a small number of the total, exhibit significant variances in growth requirements. CWDM similarly show diverse growth requirements in fluid supplemented 7H9 media. There have been few reports of the detection of CWDM in the literature. Coccoid forms of mycobacteria have been reported and are associated with environmental stress[5]. There have been numerous reports supporting or rejecting microbial involvement of CWDM in chronic inflammatory illnesses. Few of these reports have centred on the microbial attributes of CWDM to establish and drive inflammation. This can only be achieved when the pathogen is able to be studied.
Visualisation of CWDM in blood samples from humans is possible using the MGIT tube. Small changes in the Ziehl-Neelsen staining procedure are necessary to allow for differences of NTM. The MGIT tube is useful for initial isolation, but not for replication over a longer period. Extended incubation in CWDM growth media is necessary to collect sufficient DNA from CWDM for whole genome sequencing and prospective employment of MALTI-TOF for identification of isolates. Additionally, susceptibility testing requires that isolates are in the log phase of growth.
Microscopic detection is necessary before growth media for CWDM can be designed and assessed for performance. The ability to cultivate CWDM in broth media means that more specific studies on the molecular genome of isolates may be undertaken, and specific antimycobacterial therapies designed. These steps are important to better understand the involvement (if any) of CWDM in chronic disease states and in latent tuberculosis.
Antimicrobial combination therapy is presently required to be administered for extended periods, from months to years, without supporting laboratory susceptibility data. It is feasible, but untested, that once therapy is removed, the CWDM will reset to a log phase of growth. Future treatments may also require biofilm disrupters, repurposed antimicrobial compounds, and modern vaccine therapy to maintain remission and possibly achieve cures. The possibility that MAP and CD are intimately associated, raises the almost fantastic idea of the defeat of CD through the One Health concept of infection control, targeted at what is possibly a zoonotic disease.[48]

Author Contributions

JA Conceptualization, methodology, validation, formal analysis, investigation, resources, data curation, writing—original draft preparation, visualization, supervision, project administration, DA formal analysis, investigation, resources, visualization, All authors have read and agreed to the published version of the manuscript. GA Conceptualization, validation, formal analysis, investigation, data curation, writing—original draft preparation, visualization, supervision, project administration.

Funding

This research received no external funding.

Institutional Review Board Statement

Not relevant for this study.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Not applicable.

Conflicts of Interest

JA has filed patents in the field of staining and growth of MAP/mycobacteria. DA and GA have no conflict of interest.

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