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» LymeNet Flash » Questions and Discussion » Medical Questions » Seronegative Strain of Lyme Disease in SouthEast

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Author Topic: Seronegative Strain of Lyme Disease in SouthEast
Sarah
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Now this artcile *always* gets me- who's to say that MANY other states aren't like this>? This is one reason you can have lyme and test negative- because the test strain is nothing like yours!!!
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Seronegative Strain of Lyme Disease in SouthEast
SouthEast Appears to Have a Unique Type of Lyme Disease
Nov. 2, 1999

The Southeast appears to have its own version of the tick-borne ailment Lyme disease that is not detectable by most standard tests, according to Georgia researchers.

Extensive laboratory testing of 23 adults with the characteristic bull's eye rash showed that 70 percent were not infected with the spirochete known to cause Lyme disease, according to the study published in the November issue of Archives of Dermatology.

Thirty percent of patients did test positive for the spirochete, but on closer analysis, even in those patients, the spirochete B called Borrelia burgdorferi B had a different protein composition than that causing Lyme disease in New England and the Midwest, said Dr. Michael Felz, family medicine physician at the Medical College of Georgia and principal investigator on the study.

"There is some kind of tick-transmitted illness here that acts like Lyme disease but only fits the laboratory pattern 30 percent of the time, at least when you apply a test that was designed for New England and the Midwest where Lyme disease is more common," Dr. Felz said. "In other words, we may need a whole new testing system for this illness in the Southeast."

MCG collaborated with Georgia Southern University in Statesboro and the Centers for Disease Control and Prevention in Fort Collins, Colo., on the CDC-funded study.

The three-year study included Georgians and South Carolinians who lived within 200 miles of Augusta and came to the MCG Family Practice Center to see Dr. Felz after developing enlarging red rashes, 2 to 8 inches in diameter. Approximately 90 percent were certain they had been bitten by a tick.

Before each patient began the standard therapy of a three-week oral regimen of the antibiotic doxycycline hyclate, photographs, biopsies and blood samples were taken for a complete series of tests. Tests included the sophisticated polymerase chain reaction assay for spirochete DNA in biopsy samples; the PCR was positive in five of 23 cases.

"These data say yes, there is some Lyme disease here that meets the criteria of current national lab testing standards. Yet the majority of cases B seven out of 10 B are something different," Dr. Felz said. "The tick species transmitting this illness seems to be different and may be transmitting an organism that is very different.

"Lyme disease in the southeastern United States seems to be due to genetically variant strains of the spirochete Borrelia burgdorferi," Dr. Felz said. "These strains probably have a different DNA backbone and cause different clinical symptoms and signs than is the case in other parts of the country."

Dr. Felz, who has studied ticks and the diseases they carry for nine years, says this study is the "most scientifically rigorous analysis" of Lyme disease ever in the southeastern United States.

Lyme disease typically begins with an enlarging, red circular rash and can cause flulike symptoms of malaise, headache, fever and muscle soreness. Left untreated, it also can lead to more serious secondary problems including arthritis, nerve palsy, meningitis and heart arrhythmias.

Researchers found no evidence that the disease progressed to the second stage in any of the study patients, leading them to believe that the Lyme disease organism in the Southeast may be a less virulent strain and/or more responsive to antibiotic therapy.

Dr. Felz's collaborators at MCG on the study include Dr. Francis W. Chandler Jr., director of Immunopathology and Histopathology Laboratories, and Dr. Daniel W. Rahn, rheumatologist and Lyme disease expert who is vice dean for clinical affairs in the School of Medicine. Other collaborators include Dr. James H. Oliver Jr., Institute of Arthopodology and Parasitology at Georgia Southern University, and Dr. Martin E. Schriefer, CDC in Fort Collins.


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bobdavis
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Even if it was the same strain of lyme as is found in Lyme CT, they would still test negative up to 60% of the time. My daughter has "classic lyme". She had the rash at a bite site, then on her belly, then congestive heart failure, etc, she was REAL sick. She was bit in NY and tests negative. I was bit in Virginia, after 23 years I can still work. The rash did not show up for a couple of weeks, then it shows up every month or so for 23 years. When someone said I might have lyme, I advised him he was wrong because "I am not that sick". So I know there are varying strains also my symptoms are more GI oriented.
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RoadRunner
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Hi sarah great info!!!!

Beep Beep


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Deb_Shea
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Sarah-great posts-I am always amazed what you manage to get on this board!
I agree Bob and also I think that lyme "works" differently in different people...deb

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t-bone
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Awesome post! Kind of scary, though. I wonder how many different strains there are in the US that we don't know about and can't test for?

------------------
t-bone


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Tincup
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tbone...

I had one tonight! Very good! Here is a strain list and info. Very good site.
http://www.pasteur.fr/recherche/borrelia/Borreliaspecies.html

Borrelia burgdorferi sensu lato strains


A larva of the Tick Ixodes scapularis ()
Strain lists brought to you by
Dani�le Postic &
Guy Baranton

The strains marked with an * have all been classified in our laboratory using restriction
fragment length polymorphism of rrf (5S) rrl (23S) intergenic spacer amplicons (). For
more information on Borrelia strains see the

Strains listed alpha-numerically

Strains listed by species
sensu stricto
(was Group 20047)
(was Group VS461)
(was Group F63B)
(was Group 21123, also known as Group 21038)
(were known as Groups VS116 and M19)
(was known as Group PotiB2)
(were known as Group DN 127)
References describing new species:
B. burgdorferi
Johnson, R. C., G. P. Schmid, F. W. Hyde, A. G. Steigerwalt and D. J. Brenner.
(1984)
Borrelia burgdorferi sp. nov.: etiological agent of Lyme disease.
Int. J. System. Bacteriol. 34: 496-497.
B. garinii
Baranton, G., D. Postic, I. Saint Girons, P. Boerlin, J. C. Piffaretti, M. Assous and
P. A. D. Grimont. (1992)
Delineation of Borrelia burgdorferi sensu stricto, Borrelia garinii sp. nov. and
group VS461 associated with Lyme borreliosis.
.
B. afzelii
Canica, M. M., F. Nato, L. du Merle, J. C. Mazie, G. Baranton and D. Postic.
(1993)
Monoclonal antibodies for identification of Borrelia afzelii sp. nov. associated
with late cutaneous manifestations of Lyme Borreliosis.
Scand. J. Infect. Dis. 25: 441-448.
B. japonica
Kawabata, H., T. Masuzawa and Y. Yanagihara. (1993).
Genomic analysis of Borrelia japonica sp nov isolated from Ixodes ovatus in
Japan.
.
Postic, D., J. Belfaiza, E. Isogai, I. Saint Girons, P. A. D. Grimont and G.
Baranton. (1993).
A new genomic species in Borrelia burgdorferi sensu lato isolated from Japanese
ticks.
Research in Microbiology. 144: 467-473.
B. andersonii
Marconi, R. T., D. Liveris and I. Schwartz. (1995).
Identification of novel insertion elements, restriction fragment length
polymorphism patterns, and discontinuous 23S rRNA in Lyme Disease
Spirochetes: Phylogenetic analyses of rRNA genes and their intergenic spacers in
Borrelia japonica sp. nov.and genomic group 21038 (Borrelia andersonii sp.
nov.) isolates.
J. Clin. Microbiol. 33: 2427-2434.
Assous, M. V., D. Postic, G. Paul, P. N�vot and G. Baranton. (1994).
Individualisation of two new genomic groups among American Borrelia
burgdorferi sensu lato strains.
FEMS Microbiol Lett. 121: 93-98.
Postic, D., M. V. Assous, P. A. D. Grimont and G. Baranton. (1994).
Diversity of Borrelia burgdorferi sensu lato evidenced by restriction fragment
length polymorphism of rrf (5S) rrl (23S) intergenic spacer amplicons.
.
Borrelia valaisiana
Wang,G., A.P.Van Dam, A. Le Fleche, D. Postic, O. Peter, G. Baranton, R. De
Boer, L. Spanjaard, and J. Dankert. (1997).
Genetic and phenotypic analysis of Borrelia valaisiana sp. nov. (Borrelia
genomic groups VS116 and M19).
Int. J. Syst. Bacteriol. 47: 926-932.
Postic, D., M. V. Assous, P. A. D. Grimont and G. Baranton. (1994).
Diversity of Borrelia burgdorferi sensu lato evidenced by restriction fragment
length polymorphism of rrf (5S) rrl (23S) intergenic spacer amplicons.
. Postic, D., M. V. Assous, P. A. D. Grimont and G. Baranton. (1994).
Diversity of Borrelia burgdorferi sensu lato evidenced by restriction fragment
length polymorphism of rrf (5S) rrl (23S) intergenic spacer amplicons.
.
Group DN127
Assous, M. V., D. Postic, G. Paul, P. N�vot and G. Baranton. (1994).
Individualisation of two new genomic groups among American Borrelia
burgdorferi sensu lato strains.
FEMS Microbiol Lett. 121: 93-98.
Postic, D., M. V. Assous, P. A. D. Grimont and G. Baranton. (1994).
Diversity of Borrelia burgdorferi sensu lato evidenced by restriction fragment
length polymorphism of rrf (5S) rrl (23S) intergenic spacer amplicons.
.
Borrelia bissettii
Postic, D., Marti Ras N., Lane R.S., Hendson M., and G. Baranton. (1998)
Expanded diversity among Californian Borrelia isolates and description of
Borrelia bissettii sp. nov. (formerly Borrelia group DN127)
J. Clin. Microbiol. 36: 3497-3504.

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