Membrane Damaging Toxins from Coagulase-Negative Staphylococcus Are Associated with Self-Reported Temporomandibular Disorder (TMD) in Patients with Chronic Fatigue Syndrome J Chronic Fatigue Syndrome, Vol: 12 Issue: 3, Cover Date: 2004, Publication Date: 2005, Copyright Date: 2004, Page: 25 - 43 Authors: Lee N. Metcalf, BSc; Neil R. McGregor, MDSc, PhD; Timothy K. Roberts, PhD Affiliations: Lee N. Metcalf BSc, Bioanalytical Research Group, Department of Biological Sciences, University of New Castle, Callaghan, NSW 2308, Australia Neil R. McGregor MDSc PhD, Jaw and Oro-facial Pain Research Unit, Centre for Oral Health Research, Bio21 Molecular Science and Biotechnology Institute, University of Sydney, University of Melbourne, Parkville, VIC, 3012, Australia, binrm@bigpond.com Timothy K. Roberts PhD, Bioanalytical Research Group, Department of Biological Sciences, University of Newcastle, Callaghan, NSW 2308, Australia Address correspondence to: Dr. Neil R. McGregor, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 2 Park Street, Parkville, Victoria 3012, Australia (E-mail: binrm@bigpond.com ). The authors would like to thank, Henry L. Butt, PhD, R. Hugh Dunstan, PhD, and Professor Iven J. Klineberg, PhD for their contributions to the manuscript and the development of the study design and comments. Also the Gideon Lang Foundation, the Judith Mason CFS Research Grant and the Lower Hunter CFS/ME Fundraising Association for their financial support and members of the Hunter Valley branches of the ME/CFS society of NSW for their support and encouragement. Available online at http://www.haworthpress.com/web/JCFS Aim: To assess whether there is any association between membrane damaging toxin production by Staphylococcus spp. and self-reported TMD symptom expression in a group of patients selected to have CFS. Methods: Thirty-three defined Chronic Fatigue Syndrome (CFS) patients and 33 age and sex-matched controls were assessed to evaluate the relationship between carriage of membrane damaging toxin producing staphylococcus, CFS and temporomandibular dysfunction (TMD) symptoms. Results: The CFS patients had an increased prevalence of face pain (Odds Ratio = 21.0, 95% CL 4.2-106, P < .001) and temporomandibular joint (TMJ) clicking/locking (OR = 5.7, 95% CL 1.423.5, P < .007), and the coagulase-negative staphylococcus maximum% Beta-toxin haemolysis per patient. Both multivariate and univariate analyses revealed an association between the membrane damaging delta-toxin producing CoNS (MDT-CoNS) species per subject and face pain prevalence and intensity within both the CFS patients and the control subjects. No association was found between CoNS toxin production and TMJ clicking/locking. Importantly, alpha and beta-toxin production by CoNS was associated with patient reporting of arthritis. Conclusions: These data confirm the original observations of the association between MDTCoNS and facial muscle pain (Butt et al, 1998; McGregor et al, 2003). These data also suggest that MDT-CoNS associated facial muscle pain expression represents a distinct clinical entity, which has an increased prevalence in CFS patients. Keywords: Staphylococcal toxins, staphylococcal haemolysins, bacterial toxins, pain aetiology, myofascial pain syndrome, chronic fatigue syndrome, TMD pain © 2004 by The Haworth Press, Inc. All rights reserved.