2018
DOI: 10.1016/j.cca.2018.01.030
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Promising alternatives for one-tier testing of Lyme borreliosis

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Cited by 7 publications
(8 citation statements)
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“…The direct test involves microscopic analysis, cultivation of Borrelia for 12 weeks in Barbour-Stoenner-Kelly medium and DNA sequences by PCR 11. The histopathological examination of the mitral valve obtained during the surgery from a patient with a confirmed diagnosis of Lyme endocarditis shows fibrin deposit and inflammatory infiltrate, and the presence of spirochetes 11. The indirect method is based on serological diagnosis, based on the detection of IgG and IgM antibodies.…”
Section: Discussionmentioning
confidence: 99%
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“…The direct test involves microscopic analysis, cultivation of Borrelia for 12 weeks in Barbour-Stoenner-Kelly medium and DNA sequences by PCR 11. The histopathological examination of the mitral valve obtained during the surgery from a patient with a confirmed diagnosis of Lyme endocarditis shows fibrin deposit and inflammatory infiltrate, and the presence of spirochetes 11. The indirect method is based on serological diagnosis, based on the detection of IgG and IgM antibodies.…”
Section: Discussionmentioning
confidence: 99%
“…The indirect method is based on serological diagnosis, based on the detection of IgG and IgM antibodies. In humans, it takes 2–6 weeks after the vector bite for the body to produce such antibodies 11…”
Section: Discussionmentioning
confidence: 99%
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“…Seroreactivity after successful treatment of Lyme borreliosis may persist for years [ 8 , 10 ]. Another diagnostic challenge is the possibility of false positive test results, possibly caused by cross-reactivity with other spirochaetal or bacterial antigens, as well as viral antigens, autoantigens [ 50 52 ]. Because using whole-cell lysates in ELISA is hindered by a greater possibility of cross-reactivity with other pathogenic bacteria, it is recommended that laboratories use at least a second generation ELISA test based on a recombinant antigen, which decreases the likelihood of cross-reactivity.…”
Section: Diagnostic Considerationsmentioning
confidence: 99%
“…Nucleic Acid Amplification Testing (NAAT), these methods remain inadequate due to the low concentration and transient presence of Bb in the blood. Culturing Bb is also not practical due the slow growth of the bacteria, as well as the need for specialized growth media [9][10][11] . Therefore, current testing methods work indirectly by detecting specific antibodies produced by the body's immune response to the infection.…”
Section: Introductionmentioning
confidence: 99%