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Mycoplasmal
Infections in Blood from Patients with CFS, Fibromyalgia Syndrome or Gulf
War Illness
Joerg
Haier, M.D., Ph.D., Marwan Nasralla, Ph.D. and Garth L. Nicolson, Ph.D.
The
Institute for Molecular Medicine
15162 Triton Lane
Huntington Beach, CA 92649-1041, USA

Background: Mycoplasmal infections are associated with several
acute and chronic illnesses. Since we previously found that about one-half
of Gulf War Illness (GWI) patients had mycoplasmal infections, such as
M. fermentans, patients with Chronic Fatigue Syndrome (CFS) and/or Fibromyalgia
Syndrome (FMS) were examined for mycoplasmal infections in blood leukocytes.

Patients: Blood samples from 203 patients (148 female, 55 male)
diagnosed with CFS or FMS were investigated for Mycoplasma spp. and M.
fermentans infections using forensic Polymerase Chain Reaction. Clinical
characteristics of CFS/FMS patients and GWI patients were similar. In
particular, major signs and symptoms, such as chronic fatigue, joint/muscle
pain, depression, paraesthesia, cognitive and vision problems were found
in all of these diagnoses.
PCR
Amplification: Genus-specific primers for mycoplasma were selected
from 16S mRNA sequences. The universal probes GPO 1 and MGSO were used
for the detection of mycoplasmas and the UNI- probe was used as an internal
probe for confirmation with cDNA hybridization. Specific primers for M.
fermentans (SB1: forward probe, SB2: reverse probe, SB3: internal probe)
were selected from the tuf gene sequence.

Using the genus-specific primers positive PCR results were obtained if
the PCR product was 717 base pair in size (or 850 bp for M. fermentans-specific
primers). The results were confirmed by cDNA hybridization with the specific
internal 32P-labeled probe. In the healthy control group (n=32) no PCR
product was obtained, and hybridization signals were not observed. The
Mycoplasma spp. sequence was amplified from the peripheral blood of 144
patients (71.4 %). No specific PCR product could be detected in the 57
negative patients (28.6 %) and a significant difference (p < 0.001)
was found between patients and healthy controls (0/32). Moreover, the
incidence rate was similar in female and male patients. The incidence
(41.5%) of M.fermentans infection was significantly higher than in healthy
controls (p < 0.001).

Systemic mycoplasmal infections can be considered important in causing
morbidity in CFS/FMS. These infections can be treated with multiple cycles
of the following antibiotics: doxycycline, ciprofloxacin, azithromycin
or clarithromycin.
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