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1.
Clin Infect Dis ; 69(11): 2003-2010, 2019 11 13.
Article in English | MEDLINE | ID: mdl-30753345

ABSTRACT

BACKGROUND: Mycobacterium canettii forms part of the Mycobacterium tuberculosis complex. Mycobacterium canettii infections are mainly described in the Horn of Africa. The permanent presence of French soldiers in Djibouti raises the question of the risk of being infected with M. canettii. Here, we describe M. canettii infections among French military and their families between 1998 and 2015. METHODS: This retrospective study relied on 3 sources of data: the reference center for mycobacteria in the Biology Department at Percy Military Hospital in Paris, the French Military Center for Epidemiology and Public Health, and the scientific literature. After an exhaustive census of the strains, we studied the epidemiological data on 20 cases among French soldiers and their families. RESULTS: Twenty cases of M. canettii infections are reported, including 5 unpublished cases. Adenitis predominates (n = 15), especially in the cervico facial area and among children; 1 case was observed 1 month after dental care in Djibouti. The pulmonary forms were less frequent (n = 6), and 3 atypical forms are described. All patients had stayed in Djibouti. CONCLUSIONS: Cases of M. canettii infection among the French military consisted mainly of adenitis; disseminated forms were possible with immunodeficiency. Their evolution under specific treatments was comparable to that of tuberculosis. The presumed origin of the infection seemed to be environmental, possibly a water reservoir, and not due to human-to-human contagion.


Subject(s)
Mycobacterium Infections/diagnosis , Mycobacterium Infections/microbiology , Mycobacterium/pathogenicity , Adolescent , Adult , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Military Personnel/statistics & numerical data , Retrospective Studies , Tuberculosis/microbiology , Young Adult
2.
Infect Genet Evol ; 33: 233-41, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25965840

ABSTRACT

Propionibacterium acnes plays a central role in the pathogenesis of acne and is responsible for severe opportunistic infections. Numerous typing schemes have been developed that allow the identification of phylotypes, but they are often insufficient to differentiate subtypes. To better understand the genetic diversity of this species and to perform epidemiological analyses, high throughput discriminant genotyping techniques are needed. Here we describe the development of a multiple locus variable number of tandem repeats (VNTR) analysis (MLVA) method. Thirteen VNTRs were identified in the genome of P. acnes and were used to genotype a collection of clinical isolates. In addition, publically available sequencing data for 102 genomes were analyzed in silico, providing an MLVA genotype. The clustering of MLVA data was in perfect congruence with whole genome based clustering. Analysis of the clustered regularly interspaced short palindromic repeat (CRISPR) element uncovered new spacers, a supplementary source of genotypic information. The present MLVA13 scheme and associated internet database represents a first line genotyping assay to investigate large number of isolates. Particular strains may then be submitted to full genome sequencing in order to better analyze their pathogenic potential.


Subject(s)
Minisatellite Repeats , Multilocus Sequence Typing , Propionibacterium acnes/classification , Propionibacterium acnes/genetics , Cluster Analysis , Clustered Regularly Interspaced Short Palindromic Repeats , Genes, Bacterial , Gram-Positive Bacterial Infections/microbiology , Humans , Molecular Typing , Propionibacterium acnes/isolation & purification , Sequence Analysis, DNA
3.
Emerg Infect Dis ; 20(1): 21-8, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24520560

ABSTRACT

"Mycobacterium canettii," an opportunistic human pathogen living in an unknown environmental reservoir, is the progenitor species from which Mycobacterium tuberculosis emerged. Since its discovery in 1969, most of the ≈70 known M. canettii strains were isolated in the Republic of Djibouti, frequently from expatriate children and adults. We show here, by whole-genome sequencing, that most strains collected from February 2010 through March 2013, and associated with 2 outbreaks of lymph node tuberculosis in children, belong to a unique epidemic clone within M. canettii. Evolution of this clone, which has been recovered regularly since 1983, may mimic the birth of M. tuberculosis. Thus, recognizing this organism and identifying its reservoir are clinically important.


Subject(s)
Mycobacterium/classification , Tuberculosis, Lymph Node/epidemiology , Tuberculosis, Lymph Node/microbiology , Adolescent , Adult , Biosynthetic Pathways , Child , Child, Preschool , Cluster Analysis , Clustered Regularly Interspaced Short Palindromic Repeats , Djibouti/epidemiology , Female , Genome, Bacterial , Humans , Infant , Male , Middle Aged , Mycobacterium/genetics , Mycobacterium/metabolism , Phylogeny , Polymorphism, Single Nucleotide , Vitamin B 12/biosynthesis , Young Adult
4.
PLoS One ; 7(12): e52841, 2012.
Article in English | MEDLINE | ID: mdl-23300794

ABSTRACT

Molecular and phylogeographic studies have led to the definition within the Mycobacterium tuberculosis complex (MTBC) of a number of geotypes and ecotypes showing a preferential geographic location or host preference. The MTBC is thought to have emerged in Africa, most likely the Horn of Africa, and to have spread worldwide with human migrations. Under this assumption, there is a possibility that unknown deep branching lineages are present in this region. We genotyped by spoligotyping and multiple locus variable number of tandem repeats (VNTR) analysis (MLVA) 435 MTBC isolates recovered from patients. Four hundred and eleven isolates were collected in the Republic of Djibouti over a 12 year period, with the other 24 isolates originating from neighbouring countries. All major M. tuberculosis lineages were identified, with only two M. africanum and one M. bovis isolates. Upon comparison with typing data of worldwide origin we observed that several isolates showed clustering characteristics compatible with new deep branching. Whole genome sequencing (WGS) of seven isolates and comparison with available WGS data from 38 genomes distributed in the different lineages confirms the identification of ancestral nodes for several clades and most importantly of one new lineage, here referred to as lineage 7. Investigation of specific deletions confirms the novelty of this lineage, and analysis of its precise phylogenetic position indicates that the other three superlineages constituting the MTBC emerged independently but within a relatively short timeframe from the Horn of Africa. The availability of such strains compared to the predominant lineages and sharing very ancient ancestry will open new avenues for identifying some of the genetic factors responsible for the success of the modern lineages. Additional deep branching lineages may be readily and efficiently identified by large-scale MLVA screening of isolates from sub-Saharan African countries followed by WGS analysis of a few selected isolates.


Subject(s)
Mycobacterium tuberculosis/genetics , Tuberculosis/microbiology , Animals , Cluster Analysis , Djibouti , Genes, Bacterial , Genotype , Humans , Kenya , Minisatellite Repeats , Models, Genetic , Multilocus Sequence Typing , Mutation , Mycobacterium tuberculosis/isolation & purification , Phylogeny , Phylogeography , Polymorphism, Single Nucleotide , Somalia , Sudan
5.
Diagn Microbiol Infect Dis ; 70(1): 154-6, 2011 May.
Article in English | MEDLINE | ID: mdl-21397427

ABSTRACT

Successful control of tuberculosis relies on the rapid detection of Mycobacterium tuberculosis. Few chromatographic lateral flow assays for the discrimination of the M. tuberculosis complex were developed from culture media. We compared the values of 2 assays to assess their place in diagnosis of tuberculosis. We conclude of their efficiency and relevance to supplant the conventional methods.


Subject(s)
Clinical Laboratory Techniques/methods , Reagent Kits, Diagnostic , Tuberculosis/diagnosis , Humans , Immunoassay/methods , Mycobacterium tuberculosis/isolation & purification
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