BioMed Central.......Gut Pathogens
Review ... Open Access ...
Mycobacterium avium subspecies paratuberculosis, Crohn's disease
and the Doomsday Scenario
Prof John Hermon-Taylor
Address: Division of Nutritional Sciences, Franklin-Wilkins Building, King's College London, 150 Stamford Street, London SE1 9NH, UK
Email: John Hermon-Taylor firstname.lastname@example.org
Published: 14 July 2009 Received: 9 July 2009
Gut Pathogens 2009, 1:15 doi:10.1186/1757-4749-1-15
Accepted: 14 July 2009.
This article is available from: http://www.gutpathogens.com/content/1/1/15
© 2009 Hermon-Taylor; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Johne's disease is chronic inflammation of the intestine caused by Mycobacterium avium subspecies paratuberculosis. Infection and disease are mainly in domestic livestock but can affect many species including primates. Johne's is a new disease which emerged at the turn of the 19th and 20th centuries and principally involved Europe and North America. It has since spread to former low incidence regions to become a global problem. Crohn's disease is a chronic inflammation of the intestine in humans which emerged in Europe and North America mid 20th century and increased to become a major healthcare problem. It has now spread to former low incidence regions.
Infected animals shed Mycobacterium avium subspecies paratuberculosis in milk and into the environment. Human populations are widely exposed. Outcomes maybe influenced by microbial phenotype. Exposure to extracellular forms of these pathogens may confer some natural protection; exposure to intracellular forms which have passaged through milk macrophages or environmental protists may pose a greater threat to humans particularly individuals with an inherited or acquired susceptibility.
Hot spots of human disease such as in Winnipeg which sits on rock at the junction of two rivers may result from local exposure to high levels of waterborne pathogens brought down from farmland. When appropriate methods are used most people with Crohn's disease are found to be infected. There are no data which demonstrate that these pathogens are harmless to humans. An overwhelming balance of probability and Public health risk favours the conclusion that Mycobacterium avium subspecies paratuberculosis is also pathogenic for people. A two tier cooperative pathogenic mechanism is proposed in Crohn's disease. Intracellular infection with the primary pathogen widely distributed throughout the gut causes an immune dysregulation and a specific chronic enteric neuropathy with loss of mucosal integrity. Segments of gross inflammatory disease result from the perturbed neuroimmune response to penetration into the gut wall of secondary pathogens from the lumen. These include both normal gut organisms and educated
members of the enteric microbiome such as more aggressive E. coli. More new diseases may arise from failure to apply a range of remedial measures to this longstanding zoonotic problem.
Review bacterium avium subspecies paratuberculosis (MAP). It is MAP and the emergence of Johne's and Crohn's diseases most common in ruminants but can affect many other.
Johne's disease (JD) is a systemic infection and chronic species including primates. It was first seen to emerge in inflammation of the intestine in animals caused by Myco-Europe and North America at the end of the 19th and
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Beginning of the 20th centuries. Crohn's disease (CD) in humans is a systemic disorder whose principal clinicopathological manifestation is also chronic inflammation of the intestine. It is also a new disease which was first seen to emerge in the same continents 40–50 years after JD and increased in frequency steadily until it has become a major healthcare problem. In some areas in the USA in recent years the incidence of CD has seemed to plateau around 7–8 per 105 population per year [1,2]. In Europe the incidence of CD in adults continues to grow [3-5]. Studies in Stockholm, Czech Republic, and Australia supported by data from Finland suggest that the incidence of CD in children in these areas in recent years has been rising in some cases as high as about 5 fold per decade [6-9]. These rapid changes in incidence rule out a primary genetic causation of CD. The data from recent genome wide scans which has identified 32 significant genomic loci related to susceptibility to CD are consistent with the involvement of intracellular bacterial pathogens including mycobacteria, in disease causation .
The rising incidence of CD reported from several former
low incidence countries in Asia shows that, as with JD, CD is spreading worldwide [11,12]. Recent work from New Zealand reported a high incidence of CD of 16.5 per 105 per year affecting the Canterbury region of South Island with Christchurch as its principal city . Mountains are to the northwest and rivers from them run across rich agricultural pastures and either side of Christchurch before entering the sea. A small river meanders through the city itself. Some of these features are reminiscent of the situation in Cardiff, South Wales UK where a high incidence of CD in city wards bordering the river Taff draining the upland pastures of the Brecons and running through the city was consistent with exposure of the local population to aerosols from the river .
A conspicuously anomalous distribution in the incidence
of CD exists in North America either side of the Canadian border between Minnesota and Manitoba. In Minnesota to the south the well documented population-based incidence of CD in Olmsted County is 7.9 per 105/year  whereas in some areas of the city of Winnipeg little more than 400 miles to the north the incidence reaches a maximum 3.5 fold greater at 28.07 per 105/year . Winnipeg lies astride the junction of the Red River of the North running up from the south and the Assiniboine River coming in from the west. The city sits on bedrock which was once the floor of the immense prehistoric glacial lake Agassiz, with scant run-off in permeable sand and gravel aquifers . The 'hot spot' of CD in the city of Winnipeg we see now is probably due to local exposure of the human population to high levels of waterborne MAP brought down from the agricultural river catchments of the US Midwest, meeting those from the provinces of
Manitoba, Saskatchewan and Alberta. Waterborne MAP under these conditions would almost certainly include organisms which have adopted the intracellular phenotype having been taken up by abundant environmental protists .
Movement of people and pathogen
Migrant studies show that the incidence of CD in people moving from a low CD and JD incidence area to a high incidence area subsequently rises to that of the host population. The inverse situation is that in which MAP is introduced into an isolated community usually by importation of infected animals. This happened in Iceland in 1933 [reviewed in ]. After a latent period following introduction of the pathogen there were at intervals successive epidemics of JD in the island sheep, then in the cattle, then CD in the human population. From 1960 to a peak in 1992 the incidence of CD increased 18 fold. Thus in either case, if people move in amongst MAP or if MAP is moved in amongst people the result is the same namely a steep rise in the incidence of CD. The time interval between the emergence and rise of JD in animals and CD in humans in Iceland was again about 40–50 years. With the almost unlimited opportunity for MAP to spread and evolve in intensively farmed domestic livestock and associated contaminated environments over more than a half century, an evolving virulence and species adaptation of the pathogen would be reflected in the JD to CD interval becoming shorter. A recent example of this happening maybe the steep 4.5 fold increase in CD in the Czech Republic 1995–2007 following the rise in JD caused by the unimpeded importation of subclinically infected cattle from Western Europe after independence in 1990.
Natural Immunity to MAP from environmental and
occupational exposure Why don't dairy farmers and veterinarians exposed to MAP-infected animals get a much higher incidence of CD ?
Data from the US show that these occupations are in fact associated with a significantly reduced death rate from Inflammatory Bowel Disease . Children exposed to farm animals, particularly cattle, in early life also subsequently have a lower incidence of CD . Occupational exposure to MAP is associated with raised antibody levels to MAP lysates . An answer to the question consistent with these observations is that the extracellular classical ZN-positive phenotype of MAP excreted in trillions by heavily infected animals is not one to which humans are most susceptible. Exposure to this form of the organism may result in the acquisition of some natural immunity to disease. A good example of this happening as a result of purposeful exposure is the approximate 10 fold reduction in clinical Johne's disease achieved subsequently by vaccination of calves using conventional whole killed MAP vaccines with the organisms in this form . The well
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Described urban preponderance of CD may not be that
townsfolk have an increased susceptibility to CD, rather that country folk have some natural protection. Passage of MAP through bovine macrophages in milk and cheese or through environmental protists would result in a switch to an intracellular phenotype of MAP likely to have an enhanced virulence for humans [23,24].
MAP and the convergence of candidate pathogens With the new 21st century, a steadily increasing volume of parallel research has identified three principal sets of bacteria as candidates for the causation of the gross inflammatory disease of the intestine in CD. These are the community of normal gut flora , abnormal gut flora such as adherent invasive E. coli (AIEC) , and MAP. Because of the global advance of CD and the serious implications for Public Health as well as cumulative individual suffering, there is a need for researchers and clinicians in the field to recognise that the reliable evidence obtained from each of the three lines of inquiry is convergent and that there is actually no conflict between them.
From experimental as well as clinical evidence there is no doubt that bacteria from the normal intestinal microbial community can infect and inflame the gut wall and that they do so in CD. However, the spontaneous emergence and rise of CD in human populations across the globe due to an epidemic of normal gut flora, in the absence of another specific initiating cause, seems rather improbable. The enteric microbiome is a fertile environment for horizontal gene transfer .
Advancement of pathogenicity in bacteria may follow the acquisition and mutation of genes and changes in their regulation [28-30]. We already have examples of the pathological consequences of such adaptation in common gut bacteria such as E. coli which can be enteropathogenic, enterohaemorrhagic, enterotoxigenic, enteroaggregative and recently enteroadherent and invasive AIEC . Such adaptations usually arise due to the imposition of some external selection pressure. Recent evidence also suggests that common enteric bacteria like E. coli may display predictive behaviour .
The principal property of MAP which distinguishes it from all other candidate pathogens in the primary causation of CD is that it is an established multi-host chronic enteric pathogen. MAP has the proven specific ability to initiate and maintain chronic inflammation of the intestine of a range of different histopathological types in many species including primates. MAP infection in animals causes a local and systemic immune dysregulation. It is also specifically neuropathogenic especially for non-myelinated neurones and intestinal disease is accompanied by a chronic enteric neuropathy . Despite its broad pathogenicity, MAP infection can persist in animals for years.
Without necessarily progressing to clinical disease. Clinical disease in animals when it occurs is commonly of the pluribacillary type but paucimicrobial disease with the pathogens in a Ziehl Neelsen (ZN)-negative phenotype is well described.
The overall prevalence of MAP infection in US dairy herds is reported by a USDA survey to be 68.1% . A range of broadly similar data shows that MAP infection in farm animals is widespread in many areas of Western Europe and elsewhere. MAP contaminates and persists in water and the environment, is in dairy products, can survive milk pasteurisation, and is present in meat from infected animals. It is inevitable that human populations are widely exposed.
MAP in humans
MAP infection in humans is difficult to detect. The organisms are present in low abundance in a robust ZN-negative phenotype. They are intracellular and minimise their own immune recognition. They are extremely difficult to isolate and propagate in culture and are relatively resistant to chemical and enzymatic lysis. Reliable access to their DNA is only achieved during sample processing by combining exposure to stringent lysis buffers with an additional optimised mechanical disruption step. Freezing samples and tissue extracts especially at -20°C substantially reduces the PCR detection rate of their GC-rich DNA. The organisms have been cultured and detected in blood showing that, as in animals, the infection in humans is systemic [35-37]. At present, the benchmark diagnostic test for MAP infection in humans is nested PCR applied to single ~20 mg fresh endoscopic mucosal biopsies . When validated methodologies have been used most people with CD have been found to be infected with MAP . In simple words, most people with chronic inflammation of the intestine (of the CD type) are infected with a mycobacterium which is a proven specific cause of chronic inflammation of the intestine. There are no data which demonstrate that MAP are harmless to
humans. The overwhelming balance of probability and
public health risk favours the conclusion that MAP are
also pathogenic for people.
Inflammation in Crohn's disease caused by a two tier cooperative pathogenic mechanism MAP infects the gut widely in CD and is found both in the more normal looking intestine and the grossly inflamed and diseased segments of intestine . MAP antigens have appeared to dominate the immunological responses of intestinal CD4 T cell lines from patients with CD . Mannans released by MAP inhibit intracellular killing of
internalised bacteria .
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The MAP infection causes a primary microscopic inflammation accompanied by a specific immune dysregulation and enteric neuropathy . Mucosal integrity and other critical functions of the intestine are impaired. The visible segments of gross inflammatory disease result from the perturbed neuroimmune response to the secondary penetration into the gut wall of gut flora containing both normal intestinal bacteria and those which have undergone transformations leading to a more invasive phenotype like AIEC. It is important to note that genomic loci in the host conferring genetic susceptibility to Crohn's disease
have the potential to operate at the levels of both primary and secondary pathogens. The entry of food residues into the gut wall contributes an allergic component to the inflammatory mess. Although MAP has been found in intestinal granulomas in humans , the presence or absence of these and other features of the variable histopathological picture of CD are principally determined by the large scale response to the secondary co-pathogens including especially other granulomatous species like M. avium subspecies avium which are frequently recovered in culture from CD tissues . Thus the three lines of contemporary research inquiry come together in a two tiered co-operative pathogenic mechanism.
Imagine the collective human enteric microbiome in, say, a crowded Europe. A vast composite structure made up of millions of individual highly mobile microbial reservoirs variably interconnected in time and space and degree. A dynamic structure possessing an inherent self governing order and stability not easily displaced. Into this cellular system is progressively introduced a slowly growing specific mycobacterial pathogen which has acquired the genetic machinery necessary to cloak itself with a predicted fucosylated surface  so that it conforms with the familiar molecular environment particularly of the host's epithelial cells and mucosal compartment . It has come from the parallel universe of the collective enteric microbiome of human food animals and before that from the soil. It causes a microscopic inflammation and perturbs the microenvironment of the mucosa and gut wall. To survive and prosper it minimises its confrontation with the human immune system. It causes a variable immune dysregulation but it also inflames the fine structure and function of the enteric nervous system.
More than a hundred years go by. Both animal and
human total microbiomes swell with increasing population density. The mycobacterial pathogen acquires additional properties resulting in an evolution in its behaviour with an increase in pathogenicity and species range. Some normal inhabitants of the enteric microbiome adapt to the disturbed intestinal microenvironment and they too acquire characteristics which make them more invasive.
Chronic enteric disease emerges and spreads particularly in individuals with an inherited or acquired susceptibility. Humans responsible for controlling and managing these diseases, blind to what is really happening are distracted by detail and dismissive. The required remedial measures are not designed and applied and the problems get worse.
Left undisturbed, maybe the education in hostility already received by increasingly aggressive members of the former normal gut flora will progress to the point where they too can emerge from background to become primary independent pathogens in their own right. When they do so more new diseases will emerge.
Can anti-MAP treatment heal Crohn's disease?
The answer to this question supported by a correct interpretation of data both from open label studies [45-48] and the Australian controlled clinical trial is a qualified yes [49-51]. It can in some people with CD some of the time. When it does so in 'responders' receiving treatment with drug combinations including rifabutin and clarithromycin the clinical and pathological improvement can be dramatic and has been associated with the conversion of pre-treatment MAP positive tests in blood  and gut mucosa (my own unpublished observations) to negative.
Furthermore, some of the clinical benefit resulting from
treatment of CD with conventional 'immunosuppressive'
agents such as 6-mercaptopurine or methotrexate may
actually be a consequence of their demonstrable direct
anti-MAP action [53-55]. But MAP infections are difficult to eradicate. The organisms are generally resistant in vivo to drugs conventionally used in the treatment of tuberculosis.
Treatment is prone to all the problems of microbial
drug resistance and latency encountered in the management of chronic lung disease caused by other members of the M. Avium Complex. New clinical trials are needed of anti-MAP treatment in CD particularly of agents developed for the treatment of M. tuberculosis which are active against mycobacteria in the non-replicative state  and where the gene encoding the molecular target is shared by MAP. Rich clinical and commercial rewards are out there for those who do so successfully.
Recognition and acceptance of the true nature of the
expanding long term threat to human health posed by
widespread exposure to MAP, based upon a perceptive
understanding of the problem and the overwhelming balance of reliable scientific evidence, is a matter of urgency. The solutions lie in the identification and incremental introduction of a range of remedial measures which are both scientific and regulatory whose effective application on a global scale requires close international cooperation.
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MAP: Mycobacterium avium subspecies paratuberculosis; JD: Johne's disease; CD: Crohn's disease; AIEC: adherent Invasive E. coli; ZN: Ziehl Neelsen; US: United States of
America; USDA: US Department of Agriculture.
The author currently owns the patents to a virally vectored vaccine against Mycobacterium avium subspecies paratuberculosis intended as a treatment for MAP infection in humans.
I confirm that this is my work.
This article is based on an invited presentation at a meeting on 'Bacterial Triggers in the etiology of Crohn's disease' May 14–16 at Tišnov, Czech Republic under the auspices of the EU 6th Frame Programme integrated project PathogenCombat and organised by Prof. Karel Hruška and Prof. Ivo Pavlik to whom I express my thanks. I am grateful to Prof. Roger Pickup for
discussion on environmental issues. My research is funded by mostly donations from people suffering from Crohn's disease, their families and friends.
1. Loftus CG, Loftus EV Jr, Harmsen WS, Zinsmeister AR, Tremaine WJ, Melton LJ 3rd, Sandborn WJ: Update on the incidence and prevalence of Crohn's disease and ulcerative colitis in Olmsted County, Minnesota, 1940–2000. Inflamm Bowel Dis 2007, 13:254-61.
2. Herrinton LJ, Liu L, Lewis JD, Griffin PM, Allison J: Incidence and prevalence of inflammatory bowel disease in a Northern California managed care organization, 1996–2002. Am J Gastroenterol 2008, 103:1998-2006.
3. Molinié F, Gower-Rousseau C, Yzet T, Merle V, Grandbastien B, Marti R, Lerebours E, Dupas JL, Colombel JF, Salomez JL, Cortot A: Opposite evolution in incidence of Crohn's disease and ulcerative colitis in Northern France (1988–1999). Gut 2004,
4. Lapidus A: Crohn's disease in Stockholm County during 1990– 2001: an epidemiological update. World J Gastroenterol 2006, 12:75-81.
5. Vind I, Riis L, Jess T, Knudsen E, Pedersen N, Elkjaer M, Bak Andersen I, Wewer V, Nørregaard P, Moesgaard F, Bendtsen F, Munkholm P, DCCD study group: Increasing incidences of inflammatory bowel disease and decreasing surgery rates in Copenhagen City and County, 2003–2005: a population-based study from the Danish Crohn colitis database. Am J Gastroenterol 2006, 101:1274-82.
6. Hildebrand H, Finkel Y, Grahnquist L, Lindholm J, Ekbom A, Askling J: Changing pattern of paediatric inflammatory bowel disease in northern Stockholm 1990–2001. Gut 2003, 52:1432-4.
7. Pozler O, Maly J, Bonova O, Dedek P, Frühauf P, Havlickova A, Janatova T, Jimramovsky F, Klimova L, Klusacek D, Kocourkova D, Kolek A, Kotalova R, Marx D, Nevoral J, Petro R, Petru O, Plasilova I, Seidl Z, Sekyrova I, Semendak N, Schreierova I, Stanek J, Sykora J, Sulakova A, Toukalkova L, Travnickova R, Volf V, Zahradnicek L, Zenisková I: Incidence of Crohn disease in the Czech Republic in the years 1990 to 2001 and assessment of pediatric population with inflammatory bowel disease. J Pediatr Gastroenterol Nutr 2006, 42:186-9.
8. Phavichitr N, Cameron DJ, Catto-Smith AG: Increasing incidence of Crohn's disease in Victorian children. J Gastroenterol Hepatol 2003, 18:329-32.
9. Turunen P, Kolho KL, Auvinen A, Iltanen S, Huhtala H, Ashorn M: Incidence of inflammatory bowel disease in Finnish children, 1987–2003. Inflamm Bowel Dis 2006, 12:677-83.
10. Barrett JC, Hansoul S, Nicolae DL, Cho JH, Duerr RH, Rioux JD, Brant SR, Silverberg MS, Taylor KD, Barmada MM, Bitton A, Dassopoulos T, Datta LW, Green T, Griffiths AM, Kistner EO, Murtha MT, Regueiro MD, Rotter JI, Schumm LP, Steinhart AH, Targan SR, Xavier RJ, NIDDK IBD Genetics Consortium, Libioulle C, Sandor C, Lathrop M, Belaiche J, Dewit O, Gut I, Heath S, Laukens D, Mni M, Rutgeerts P, Van Gossum A, Zelenika D, Franchimont D, Hugot JP, de Vos M, Vermeire S, Louis E, Belgian-French IBD Consortium, Wellcome Trust Case Control Consortium, Cardon LR, Anderson CA, Drummond H, Nimmo E, Ahmad T, Prescott NJ, Onnie CM, Fisher SA, Marchini J, Ghori J, Bumpstead S, Gwilliam R, Tremelling M, Deloukas P, Mansfield J, Jewell D, Satsangi J, Mathew CG, Parkes M, Georges M, Daly MJ: Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nat Genet 2008, 40:955-62.
11. Thia KT, Loftus EV Jr, Sandborn WJ, Yang SK: An update on the epidemiology of inflammatory bowel disease in Asia. Am J Gastroenterol 2008, 103:3167-82.
12. Leong RW, Lau JY, Sung JJ: The epidemiology and phenotype of Crohn's disease in the Chinese population. Inflamm Bowel Dis 2004, 10:646-51.
13. Gearry RB, Richardson A, Frampton CM, Collett JA, Burt MJ, Chapman BA, Barclay ML: High incidence of Crohn's disease in Canterbury, New Zealand: results of an epidemiologic study. Inflamm Bowel Dis 2006, 12:936-43.
14. Pickup RW, Rhodes G, Arnott S, Sidi-Boumedine K, Bull TJ, Weight-man A, Hurley M, Hermon-Taylor J: Mycobacterium avium subsp. paratuberculosis in the catchment area and water of the River Taff in South Wales, United Kingdom, and its potential relationship to clustering of Crohn's disease cases in the city of Cardiff. Appl Environ Microbiol 2005, 71:2130-9.
15. Green C, Elliott L, Beaudoin C, Bernstein CN: A population-based ecologic study of inflammatory bowel disease: searching for etiologic clues. Am J Epidemiol 2006, 164:615-623.
16. Province of Manitoba Department of Natural Resources, Water Resources Branch. Aquifer maps of southern Manitoba; map 2: Sand and Gravel Aquifers
17. Mura M, Bull TJ, Evans H, Sidi-Boumedine K, McMinn L, Rhodes G, Pickup R, Hermon-Taylor J: Replication and long-term persistence of bovine and human strains of Mycobacterium avium subsp. paratuberculosis within Acanthamoeba polyphaga. Appl Environ Microbiol 2006, 72:854-9.
18. Hermon-Taylor J, El-Zaatari FAK: The Mycobacterium avium subspecies paratuberculosis problem and its relation to the causation of Crohn disease. In Pathogenic Mycobacteria in Water: a guide to Public Health Consequences, Monitoring and Management Edited by: Pedley S, Bartram J, Rees G, Dufour A, Cotruvo JA. London: IWA Publishing; 2004:74-94.
19. Cucino C, Sonnenberg A: Occupational mortality from inflammatory bowel disease in the United States 1991–1996. Am J Gastroenterol 2001, 96:1101-5.
20. Radon K, Windstetter D, Poluda AL, Mueller B, von Mutius E, Koletzko S, Chronische Autoimmunerkrankungen und Kontakt zu Tieren (Chronic Autoimmune Disease and Animal Contact) Study Group: Contact with farm animals in early life and juvenile inflammatory bowel disease: a case-control study. Pediatrics 2007, 120:354-61.
21. Chiodini RJ, Thayer WR, Coutu JA: Presence of Mycobacterium paratuberculosis antibodies in animal healthcare workers. In Proceedings of the Fifth International Colloquium on Paratuberculosis 1996 Edited by: Chiodini RJ, Hines ME, Collins MT. Rehoboth MA: International Association of Paratuberculosis; 1996:324-8.
22. Rosseels V, Huygen K: Vaccination against paratuberculosis. Expert Rev Vaccines 2008, 7:817-32.
23. Cirillo JD, Falkow S, Tompkins LS, Bermudez LE: Interaction of Mycobacterium avium with environmental amoebae enhances virulence. Infect Immun 1997, 65:3759-67.
24. Patel D, Danelishvili L, Yamazaki Y, Alonso M, Paustian ML, Bannantine JP, Meunier-Goddik L, Bermudez LE: The ability of Mycobacterium avium subsp. paratuberculosis to enter bovine
epithelial cells is influenced by preexposure to a hyperosmolar environment and intracellular passage in bovine mammary epithelial cells. Infect Immun 2006, 74:2849-55.
Page 5 of 6...(page number not for citation purposes).
Gut Pathogens 2009, 1:15
25. Macfarlane GT, Blackett KL, Nakayama T, Steed H, Macfarlane S: The gut microbiota in inflammatory bowel disease. Curr Pharm Des 2009, 15:1528-36.
26. Martinez-Medina M, Aldeguer X, Lopez-Siles M, González-Huix F, López-Oliu C, Dahbi G, Blanco JE, Blanco J, Garcia-Gil LJ, Darfeuille-Michaud A: Molecular diversity of Escherichia coli in the human gut: new ecological evidence supporting the role of adherent-invasive E. coli (AIEC) in Crohn's disease. Inflamm Bowel Dis 2009, 15:872-82.
27. Kurokawa K, Itoh T, Kuwahara T, Oshima K, Toh H, Toyoda A, Takami H, Morita H, Sharma VK, Srivastava TP, Taylor TD, Noguchi H, Mori H, Ogura Y, Ehrlich DS, Itoh K, Takagi T, Sakaki Y, Hayashi T, Hattori M: Comparative metagenomics revealed commonly enriched gene sets in human gut microbiomes. DNA
Res 2007, 14:169-81.
28. Ahmed N, Dobrindt U, Hacker J, Hasnain SE: Genomic fluidity and pathogenic bacteria: applications in diagnostics, epidemiology and intervention. Nat Rev Microbiol 2008, 6:387-94.
29. Perfeito L, Fernandes L, Mota C, Gordo I: Adaptive mutations in bacteria: high rate and small effects. Science 2007, 317:813-5.
30. Osborne SE, Walthers D, Tomljenovic AM, Mulder DT, Silphaduang U, Duong N, Lowden MJ, Wickham ME, Waller RF, Kenney LJ, Coombes BK: Pathogenic adaptation of intracellular bacteria by rewiring a cis-regulatory input function. Proc Natl Acad Sci USA 2009, 106:3982-7.
31. Darfeuille-Michaud A, Neut C, Barnich N, Lederman E, Di Martino P, Desreumaux P, Gambiez L, Joly B, Cortot A, Colombel JF: Presence of adherent Escherichia coli strains in ileal mucosa of patients with Crohn's disease. Gastroenterology 1998, 115:1405-13.
32. Tagkopoulos I, Liu YC, Tavazoie S: Predictive behaviour within microbial genetic networks. Science 2008, 320:1313-7.
33. Scanu AM, Bull TJ, Cannas S, Sanderson JD, Sechi LA, Dettori G, Zanetti S, Hermon-Taylor J: Mycobacterium avium subspecies paratuberculosis infection in cases of irritable bowel syndrome and comparison with Crohn's disease and Johne's disease: common neural and immune pathogenicities. J Clin Microbiol 2007, 45:3883-90.
34. Johne's Disease on U.S. Dairies, 1991–2007 (info sheet, 4p, 4/ 08) [http://nahms.aphis.usda.gov]
35. Naser SA, Ghobrial G, Romero C, Valentine JF: Culture of Mycobacterium avium subspecies paratuberculosis from the blood of patients with Crohn's disease. Lancet 2004, 364:1039-44.
36. Bentley RW, Keenan JI, Gearry RB, Kennedy MA, Barclay ML, Roberts RL: Incidence of Mycobacterium avium subspecies paratuberculosis in a population-based cohort of patients with Crohn's disease and control subjects. Am J Gastroenterol 2008, 103:1168-72.
37. Kirkwood CD, Wagner J, Boniface K, Vaughan J, Michalski WP, Catto-Smith AG, Cameron DJ, Bishop RF: Mycobacterium avium subspecies paratuberculosis in children with early-onset Crohn's disease. Inflamm Bowel Dis 2009 in press.
38. Bull TJ, McMinn EJ, Sidi-Boumedine K, Skull A, Durkin D, Neild P, Rhodes G, Pickup R, Hermon-Taylor J: Detection and verification of Mycobacterium avium subsp.paratuberculosis in fresh ileocolonic mucosal biopsy specimens from individuals with and without Crohn's disease. J Clin Microbiol 2003, 41:2915-23.
39. Feller M, Huwiler K, Stephan R, Altpeter E, Shang A, Furrer H, Pfyffer GE, Jemmi T, Baumgartner A, Egger M:Mycobacterium avium subspecies paratuberculosis and Crohn's disease: a systematic review and meta-analysis. Lancet Infect Dis 2007, 7:607-13.
40. Olsen I, Tollefsen S, Aagaard C, Reitan LJ, Bannantine JP, Andersen P, Sollid LM, Lundin KE: Isolation of Mycobacterium avium subspecies paratuberculosis reactive CD4 T cells from intestinal biopsies of Crohn's disease patients. PLoS One 2009,
41. Mpofu CM, Campbell BJ, Subramanian S, Marshall-Clarke S, Hart CA, Cross A, Roberts CL, McGoldrick A, Edwards SW, Rhodes JM: Microbial mannan inhibits bacterial killing by macrophages: a possible pathogenic mechanism for Crohn's disease. Gastroenterology 2007, 133:1487-98.
42. Ryan P, Aarons S, Bennett MW, Lee G, O'Sullivan GC, O'Connell J, Shanahan F: Mycobacterium paratuberculosis detected by nested PCR in intestinal granulomas isolated by LCM in cases of Crohn's disease. Methods Mol Biol 2002, 193:205-11.
43. Sheridan JM, Bull TJ, Hermon-Taylor J: Use of bioinformatics to predict a function for the GS element in Mycobacterium
avium subspecies paratuberculosis. J Mol Microbiol Biotechnol 2003, 5:57-66.
44. Coyne MJ, Reinap B, Lee MM, Comstock LE: Human symbionts use a host-like pathway for surface fucosylation. Science 2005, 307:1778-81.
45. Gui GP, Thomas PR, Tizard ML, Lake J, Sanderson JD, Hermon-Taylor J: Two-year-outcomes analysis of Crohn's disease treated with rifabutin and macrolide antibiotics. J Antimicrob Chemother 1997, 39:393-400.
46. Borody TJ, Leis S, Warren EF, Surace R: Treatment of severe Crohn's disease using antimycobacterial triple therapy – approaching a cure? Dig Liver Dis 2002, 34:29-38.
47. Shafran I, Kugler L, El-Zaatari FA, Naser SA, Sandoval J: Open clinical trial of rifabutin and clarithromycin therapy in Crohn's disease. Dig Liver Dis 2002, 34:22-8.
48. Borody TJ, Bilkey S, Wettstein AR, Leis S, Pang G, Tye S: Anti-mycobacterial therapy in Crohn's disease heals mucosa with longitudinal scars. Dig Liver Dis 2007, 39:438-44.
49. Selby W, Pavli P, Crotty B, Florin T, Radford-Smith G, Gibson P, Mitchell B, Connell W, Read R, Merrett M, Ee H, Hetzel D, Antibiotics in Crohn's Disease Study Group: Two-year combination antibiotic therapy with clarithromycin, rifabutin, and clofazimine for Crohn's disease. Gastroenterology 2007, 132:2313-9.
50. Behr MA, Hanley J: Antimycobacterial therapy for Crohn's disease: a reanalysis. Lancet Infect Dis 2008, 8:344.
51. Behr MA, Kapur V: The evidence for Mycobacterium paratuberculosis in Crohn's disease. Curr Opin Gastroenterol 2008, 24:17-21.
52. Chamberlin W, Ghobrial G, Chehtane M, Naser SA: Successful treatment of a Crohn's disease patient infected with bacteremic Mycobacterium paratuberculosis. Am J Gastroenterol 2007, 102:689-91.
53. Greenstein RJ, Su L, Haroutunian V, Shahidi A, Brown ST: On the action of methotrexate and 6-mercaptopurine on M. avium subspecies paratuberculosis. PLoS One 2007, 2(1):e161.
54. Greenstein RJ, Su L, Shahidi A, Brown ST: On the action of 5amino-salicylic acid and sulfapyridine on M. avium including subspecies paratuberculosis. PLoS One 2007, 2(6):e516.
55. Shin SJ, Collins MT: Thiopurine drugs azathioprine and 6-mercaptopurine inhibit Mycobacterium paratuberculosis growth in vitro. Antimicrob Agents Chemother 2008, 52:418-26.
56. Bryk R, Gold B, Venugopal A, Singh J, Samy R, Pupek K, Cao H, Popescu C, Gurney M, Hotha S, Cherian J, Rhee K, Ly L, Converse PJ, Ehrt S, Vandal O, Jiang X, Schneider J, Lin G, Nathan C: Selective killing of nonreplicating mycobacteria. Cell Host Microbe 2008, 3:137-45.
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Prof John Hermon Taylor August 2009.
TCCC.UK Supports The Scientific Work Of Prof John Hermon Taylor, Raising Awareness & Funds Across The World. We Have Been Behind Him For Over 13 Years Now, Of His 17 Years or More Of This Excellent Scientific Work, And We Will Never Give Up On Him, And Neither Should You.
*** If You Really Want To Help Us To Help You or Your Partner, Your Family Member or Your Good Friend, Please Donate To Our Cause. This Is At The Critical Last Stage Now, It Will Mean So Much To All Those Suffering This Horrendous Illness & Change Their Lives For The Better For Ever, Giving Them Back Their Quality Of Life, That Some Of Us Take For Granted.
PLEASE HELP US To HELP OTHERS.
Professor John Hermon-Taylor,
Division of Nutritional Sciences,
School of Biomedical and Health Sciences,
Franklin-Wilkins Building, Kings College London,
Stamford Street, London, SE1 9NH. United Kingdom.
UK Tel No : 0207 848 4552.
Tel : + 44 (0) 207 848 4552.
The New DNA Crohns Vaccine fund at King's is coded MEN 3936. Donor cheques ( with very sincere thanks from me ) should be made payable to : -
"King's College London"
with MEN 3936 written on the back. THANKYOU.
Funds / Donations can be sent DIRECT to : -
Prof JHT @ Kings College London (address as above)
Please mark your mail "TCCC.UK" (as origin )
Please make your donation cheques payable to : -
" Kings College London "
Please put on rear of cheque : -
Crohns Vaccine A/c No : MEN 3936.
Very Many Thanks.
Tim @ TCCC.UK.
13TH JULY 2009.
** The New DNA Crohns Anti-Map Vaccine - Update 13th July 2009.
The New DNA Crohns Vaccine as expected and as always, is a long haul, but we should have everything in place to try to get the investment in place for this autumn 2009. It's £1.5 million for the manufacture of both the vaccine components, but we are going to start with a trial of MVA.HAV + MVA.HAV.
The manufacture and regulatory approval of this initial trial should be much easier. The manufacture cost of this MVA.HAV is going to be a more manageable £460,000..the first trial will cost probably double that at £ 920.000.
Prof John Hermon Taylor at Kings College Hospital, London.
Prof John Hermon Taylor.
** The Prof JHT flew out to the USA in July 2009 & Left This Update With me.