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1.
J Clin Microbiol ; 48(10): 3813-6, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20686077

ABSTRACT

Five Mycobacterium tuberculosis isolates were obtained from three body sites from a Dutch patient. The isolates displayed a single genotype by 24-locus MIRU-VNTR typing (except for a single locus not amplified from one isolate) but were differentiated by small variations in IS6110 fingerprints, spoligotypes, 6 hypervariable MIRU-VNTR loci, and/or DiversiLab profiles, revealing patterns of microevolution in a clonal infection.


Subject(s)
Bacterial Typing Techniques , DNA Fingerprinting , Evolution, Molecular , Mycobacterium tuberculosis/classification , Mycobacterium tuberculosis/genetics , Tuberculosis/microbiology , Cluster Analysis , DNA Transposable Elements , DNA, Bacterial/genetics , Female , Genotype , Humans , Middle Aged , Mycobacterium tuberculosis/isolation & purification , Netherlands
2.
Int J Syst Evol Microbiol ; 59(Pt 5): 1049-53, 2009 May.
Article in English | MEDLINE | ID: mdl-19406791

ABSTRACT

A non-chromogenic, slowly growing Mycobacterium strain was isolated from a maxillary sinus lavage from a symptomatic patient in Riyadh, Saudi Arabia. It was initially identified as a member of the Mycobacterium tuberculosis complex by a commercial line-probe assay. Its 16S rRNA, hsp65 and rpoB gene and 16S-23S internal transcribed spacer sequences were unique; phylogenetic analysis based on the 16S rRNA gene sequence groups this organism close to Mycobacterium szulgai and Mycobacterium malmoense. Its unique biochemical properties and mycolic acid profile support separate species status. We propose the name Mycobacterium riyadhense sp. nov. to accommodate this strain. The type strain is NLA000201958(T) (=CIP 109808(T) =DSM 45176(T)).


Subject(s)
Diagnostic Errors , Maxillary Sinus/microbiology , Maxillary Sinusitis , Mycobacterium tuberculosis/isolation & purification , Mycobacterium/classification , Reagent Kits, Diagnostic , Adult , Bacterial Proteins/genetics , DNA, Bacterial/analysis , DNA, Bacterial/genetics , DNA, Ribosomal Spacer/genetics , Genes, rRNA , Humans , Male , Maxillary Sinusitis/diagnosis , Maxillary Sinusitis/microbiology , Molecular Probe Techniques , Molecular Sequence Data , Mycobacterium/genetics , Mycobacterium/isolation & purification , Mycobacterium/physiology , Mycobacterium Infections/diagnosis , Mycobacterium Infections/microbiology , Mycobacterium tuberculosis/classification , Mycobacterium tuberculosis/genetics , Mycolic Acids/analysis , Phylogeny , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 23S/genetics , Saudi Arabia , Sequence Analysis, DNA , Species Specificity , Therapeutic Irrigation , Tuberculosis/diagnosis , Tuberculosis/microbiology , Young Adult
3.
J Clin Microbiol ; 45(8): 2467-73, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17507515

ABSTRACT

This study constitutes a first attempt to describe the genetic population structure and drug resistance of the tubercle bacilli circulating in Saudi Arabia. A total of 1,505 clinical isolates of M. tuberculosis, isolated between 2002 and 2005 from seven regions of Saudi Arabia, were studied. The sample studied showed a male-to-female sex ratio of 1.27, with half of the cases among foreign-born individuals and 47% within the 21- to 40-year-old age group; a total resistance rate of 19.7%; and multiple drug resistance of 4.5%. Upon spoligotyping, a total of 387 individual patterns were obtained (clustering rate, 86.4%; 182 clusters containing between 2 and 130 isolates per cluster). A total of 94% of the strains matched the spoligotype patterns in an international database. Nearly 81% of the isolates in this study belonged to established phylogeographic clades: Central Asian (CAS), 22.5%; ill-defined T clade, 19.5%; East African-Indian (EAI), 13.5%; Haarlem, 7.5%; Latin American-Mediterranean, 7.2%; Beijing, 4.4%; Manu, 2.7%; X, 0.9%; and Bovis, 0.9%. Two clonal complexes with unique spoligotyping signatures (octal codes 703777707770371 and 467777377413771) specific to Saudi Arabia were identified. These belonged to the CAS and EAI clades, respectively, as confirmed upon secondary typing using mycobacterial interspersed repetitive units (MIRUs). The results obtained underline the predominance of historic clones of principal genetic group 1, which are responsible for roughly 45% of all tuberculosis cases in Saudi Arabia. The high rate of clustering observed might be an indication of rapid ongoing transmission within certain communities and/or subpopulations in Saudi Arabia; nonetheless, spoligotyping is known to overestimate clustering, and only a systematic second-line typing, such as MIRUs, coupled with a better tuberculosis registry and epidemiological investigations would allow us to know the exact rate of ongoing transmission and associated risk factors in Saudi Arabia.


Subject(s)
Bacterial Typing Techniques , DNA, Bacterial/genetics , Mycobacterium tuberculosis/classification , Mycobacterium tuberculosis/isolation & purification , Tuberculosis/microbiology , Adolescent , Adult , Aged , Aged, 80 and over , Antitubercular Agents/pharmacology , Child , Child, Preschool , Cluster Analysis , Drug Resistance, Multiple, Bacterial , Female , Genotype , Humans , Infant , Interspersed Repetitive Sequences/genetics , Male , Middle Aged , Molecular Epidemiology , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/genetics , Saudi Arabia/epidemiology , Tuberculosis/epidemiology
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