Line probe assay for differentiation within Mycobacterium tuberculosis complex. Evaluation on clinical specimens and isolates including Mycobacterium pinnipedii

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Line probe assay for differentiation within Mycobacterium tuberculosis complex. Evaluation on clinical specimens and isolates including Mycobacterium pinnipedii. / Kjeldsen, Marianne Kirstine; Bek, Dorte; Rasmussen, Erik Michael; Priemé, Anders; Thomsen, Vibeke Østergaard.

I: Scandinavian Journal of Infectious Diseases, Bind 41, Nr. 9, 2009, s. 635-41.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Kjeldsen, MK, Bek, D, Rasmussen, EM, Priemé, A & Thomsen, VØ 2009, 'Line probe assay for differentiation within Mycobacterium tuberculosis complex. Evaluation on clinical specimens and isolates including Mycobacterium pinnipedii', Scandinavian Journal of Infectious Diseases, bind 41, nr. 9, s. 635-41. https://doi.org/10.1080/00365540903127425

APA

Kjeldsen, M. K., Bek, D., Rasmussen, E. M., Priemé, A., & Thomsen, V. Ø. (2009). Line probe assay for differentiation within Mycobacterium tuberculosis complex. Evaluation on clinical specimens and isolates including Mycobacterium pinnipedii. Scandinavian Journal of Infectious Diseases, 41(9), 635-41. https://doi.org/10.1080/00365540903127425

Vancouver

Kjeldsen MK, Bek D, Rasmussen EM, Priemé A, Thomsen VØ. Line probe assay for differentiation within Mycobacterium tuberculosis complex. Evaluation on clinical specimens and isolates including Mycobacterium pinnipedii. Scandinavian Journal of Infectious Diseases. 2009;41(9):635-41. https://doi.org/10.1080/00365540903127425

Author

Kjeldsen, Marianne Kirstine ; Bek, Dorte ; Rasmussen, Erik Michael ; Priemé, Anders ; Thomsen, Vibeke Østergaard. / Line probe assay for differentiation within Mycobacterium tuberculosis complex. Evaluation on clinical specimens and isolates including Mycobacterium pinnipedii. I: Scandinavian Journal of Infectious Diseases. 2009 ; Bind 41, Nr. 9. s. 635-41.

Bibtex

@article{5dc424a030df11df8ed1000ea68e967b,
title = "Line probe assay for differentiation within Mycobacterium tuberculosis complex. Evaluation on clinical specimens and isolates including Mycobacterium pinnipedii",
abstract = "A line probe assay (GenoType MTBC) was evaluated for species differentiation within the Mycobacterium tuberculosis complex (MTBC). We included 387 MTBC isolates, 43 IS6110 low-copy MTBC isolates, 28 clinical specimens with varying microscopy grade, and 30 isolates of non-tuberculous mycobacteria. The assay was 100% specific and identified all 387 isolates and 98% of all IS6110 low-copy strains in concordance with the gold standard. The 2% discrepancy was caused by 1 isolate showing a faint restriction fragment length polymorphism (RFLP) pattern. The assay could provide specifies identification in 13 of 19 (68%) microscopy-positive specimens and 0 of 9 microscopy-negative specimens. To our surprise, the probe for M. africanum subtype I reacted with M. pinnipedii. This cross-reaction has not previously been reported. The assay was rapid, easy to perform and directly applicable in highly smear-positive specimens. We predict that the assay will enable enhanced surveillance of species-specific treatment outcome, which may change treatment regimens.",
author = "Kjeldsen, {Marianne Kirstine} and Dorte Bek and Rasmussen, {Erik Michael} and Anders Priem{\'e} and Thomsen, {Vibeke {\O}stergaard}",
year = "2009",
doi = "10.1080/00365540903127425",
language = "English",
volume = "41",
pages = "635--41",
journal = "Infectious Diseases",
issn = "2374-4235",
publisher = "Taylor & Francis",
number = "9",

}

RIS

TY - JOUR

T1 - Line probe assay for differentiation within Mycobacterium tuberculosis complex. Evaluation on clinical specimens and isolates including Mycobacterium pinnipedii

AU - Kjeldsen, Marianne Kirstine

AU - Bek, Dorte

AU - Rasmussen, Erik Michael

AU - Priemé, Anders

AU - Thomsen, Vibeke Østergaard

PY - 2009

Y1 - 2009

N2 - A line probe assay (GenoType MTBC) was evaluated for species differentiation within the Mycobacterium tuberculosis complex (MTBC). We included 387 MTBC isolates, 43 IS6110 low-copy MTBC isolates, 28 clinical specimens with varying microscopy grade, and 30 isolates of non-tuberculous mycobacteria. The assay was 100% specific and identified all 387 isolates and 98% of all IS6110 low-copy strains in concordance with the gold standard. The 2% discrepancy was caused by 1 isolate showing a faint restriction fragment length polymorphism (RFLP) pattern. The assay could provide specifies identification in 13 of 19 (68%) microscopy-positive specimens and 0 of 9 microscopy-negative specimens. To our surprise, the probe for M. africanum subtype I reacted with M. pinnipedii. This cross-reaction has not previously been reported. The assay was rapid, easy to perform and directly applicable in highly smear-positive specimens. We predict that the assay will enable enhanced surveillance of species-specific treatment outcome, which may change treatment regimens.

AB - A line probe assay (GenoType MTBC) was evaluated for species differentiation within the Mycobacterium tuberculosis complex (MTBC). We included 387 MTBC isolates, 43 IS6110 low-copy MTBC isolates, 28 clinical specimens with varying microscopy grade, and 30 isolates of non-tuberculous mycobacteria. The assay was 100% specific and identified all 387 isolates and 98% of all IS6110 low-copy strains in concordance with the gold standard. The 2% discrepancy was caused by 1 isolate showing a faint restriction fragment length polymorphism (RFLP) pattern. The assay could provide specifies identification in 13 of 19 (68%) microscopy-positive specimens and 0 of 9 microscopy-negative specimens. To our surprise, the probe for M. africanum subtype I reacted with M. pinnipedii. This cross-reaction has not previously been reported. The assay was rapid, easy to perform and directly applicable in highly smear-positive specimens. We predict that the assay will enable enhanced surveillance of species-specific treatment outcome, which may change treatment regimens.

U2 - 10.1080/00365540903127425

DO - 10.1080/00365540903127425

M3 - Journal article

C2 - 20001279

VL - 41

SP - 635

EP - 641

JO - Infectious Diseases

JF - Infectious Diseases

SN - 2374-4235

IS - 9

ER -

ID: 18657332