Isolation of the genome sequence strain Mycobacterium avium 104 from multiple patients over a 17-year period

被引:45
作者
Horan, KL
Freeman, R
Weigel, K
Semret, M
Pfaller, S
Covert, TC
van Soolingen, D
Leâo, SC
Behr, MA
Cangelosi, GA
机构
[1] Seattle Biomed Res Inst, Seattle, WA 98109 USA
[2] McGill Univ, Ctr Hlth, Montreal, PQ, Canada
[3] US EPA, Natl Exposure Res Lab, Cincinnati, OH USA
[4] Natl Inst Publ Hlth & Environm, NL-3720 BA Bilthoven, Netherlands
[5] Univ Sao Paulo, EPM, Dept Microbiol Immunol & Parasitol, UNIFESP,Escola Paulista Med, Sao Paulo, Brazil
关键词
D O I
10.1128/JCM.44.3.783-789.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genome sequence strain 104 of the opportunistic pathogen Mycobacterium avium was isolated from an adult AIDS patient in Southern California in 1983. Isolates of non-paratuberculosis M. avium from 207 other patients in Southern California and elsewhere were examined for genotypic identity to strain 104. This process was facilitated by the use of a novel two-step approach. In the first step, all 208 strains in the sample were subjected to a high-throughput, large sequence polymorphism (LSP)-based genotyping test, in which DNA from each strain was tested by PCR for the presence or absence of 4 hypervariable genomic regions. Nineteen isolates exhibited an LSP type that resembled that of strain 104. This subset of 19 isolates was then subjected to high-resolution repetitive sequence-based PCR typing, which identified 10 isolates within the subset that were genotypically identical to strain 104. These isolates came from 10 different patients at 5 clinical sites in the western United States, and they were isolated over a 17-year time span. Therefore, the sequenced genome of M. avium strain 104 has been associated with disease in multiple patients in the western United States. Although M. avium is known for its genetic plasticity, these observations also show that strains of the pathogen can be genotypically stable over extended time periods.
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页码:783 / 789
页数:7
相关论文
共 26 条
[1]   GENETIC DIVERSITY AMONG STRAINS OF MYCOBACTERIUM-AVIUM CAUSING MONOCLONAL AND POLYCLONAL BACTEREMIA IN PATIENTS WITH AIDS [J].
ARBEIT, RD ;
SLUTSKY, A ;
BARBER, TW ;
MASLOW, JN ;
NIEMCZYK, S ;
FALKINHAM, JO ;
OCONNOR, GT ;
VONREYN, CF .
JOURNAL OF INFECTIOUS DISEASES, 1993, 167 (06) :1384-1390
[2]   Comparison of large restriction fragments of Mycobacterium avium isolates recovered from AIDS and non-AIDS patients with those of isolates from potable water [J].
Aronson, T ;
Holtzman, A ;
Glover, N ;
Boian, M ;
Froman, S ;
Berlin, OGW ;
Hill, H ;
Stelma, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (04) :1008-1012
[3]  
Bauer J, 1999, J CLIN MICROBIOL, V37, P442
[4]   Molecular characterization of Mycobacterium tuberculosis isolates in a region of Brazil with a high incidence of tuberculosis [J].
Borsuk, S ;
Dellagostin, MM ;
Madeira, SD ;
Lima, C ;
Boffo, M ;
Mattos, I ;
da Silva, PEA ;
Dellagostin, OA .
MICROBES AND INFECTION, 2005, 7 (13) :1338-1344
[5]   Evaluation of a high-throughput repetitive-sequence-based PCR system for DNA fingerprinting of Mycobacterium tuberculosis and Mycobacterium avium complex strains [J].
Cangelosi, GA ;
Freeman, RJ ;
Lewis, KN ;
Livingston-Rosanoff, D ;
Shah, KS ;
Milan, SJ ;
Goldberg, SV .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (06) :2685-2693
[6]   Colony morphotypes on Congo red agar segregate along species and drug susceptibility lines in the Mycobacterium avium-intracellulare complex [J].
Cangelosi, GA ;
Palermo, CO ;
Laurent, JP ;
Hamlin, AM ;
Brabant, WH .
MICROBIOLOGY-UK, 1999, 145 :1317-1324
[7]   High-throughput method for detecting genomic-deletion polymorphisms [J].
de la Salmonière, YOLG ;
Kim, CC ;
Tsolaki, AG ;
Pym, AS ;
Siegrist, MS ;
Small, PM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (07) :2913-2918
[8]   Use of rapid genomic deletion typing to monitor a tuberculosis outbreak within an urban homeless population [J].
Freeman, R ;
Kato-Maeda, M ;
Hauge, KA ;
Horan, KL ;
Oren, E ;
Narita, M ;
Wallis, CK ;
Cave, D ;
Nolan, CM ;
Small, PM ;
Cangelosi, GA .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (11) :5550-5554
[9]  
Garriga X, 2000, INT J TUBERC LUNG D, V4, P463
[10]   Spoligotyping and Mycobacterium tuberculosis [J].
Gori, A ;
Bandera, A ;
Marchetti, G ;
Esposti, AD ;
Catozzi, L ;
Nardi, GP ;
Gazzola, L ;
Ferrario, G ;
van Embden, JDA ;
van Soolingen, D ;
Moroni, M ;
Franzetti, F .
EMERGING INFECTIOUS DISEASES, 2005, 11 (08) :1242-1248