Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
1.
Antimicrob Agents Chemother ; 59(10): 6026-31, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26195516

ABSTRACT

Antibiotic resistance in Ureaplasma urealyticum/Ureaplasma parvum and Mycoplasma hominis is an issue of increasing importance. However, data regarding the susceptibility and, more importantly, the clonality of these organisms are limited. We analyzed 140 genital samples obtained in Bern, Switzerland, in 2014. Identification and antimicrobial susceptibility tests were performed by using the Mycoplasma IST 2 kit and sequencing of 16S rRNA genes. MICs for ciprofloxacin and azithromycin were obtained in broth microdilution assays. Clonality was analyzed with PCR-based subtyping and multilocus sequence typing (MLST), whereas quinolone resistance and macrolide resistance were studied by sequencing gyrA, gyrB, parC, and parE genes, as well as 23S rRNA genes and genes encoding L4/L22 ribosomal proteins. A total of 103 samples were confirmed as positive for U. urealyticum/U. parvum, whereas 21 were positive for both U. urealyticum/U. parvum and M. hominis. According to the IST 2 kit, the rates of nonsusceptibility were highest for ciprofloxacin (19.4%) and ofloxacin (9.7%), whereas low rates were observed for clarithromycin (4.9%), erythromycin (1.9%), and azithromycin (1%). However, inconsistent results between microdilution and IST 2 kit assays were recorded. Various sequence types (STs) observed previously in China (ST1, ST2, ST4, ST9, ST22, and ST47), as well as eight novel lineages, were detected. Only some quinolone-resistant isolates had amino acid substitutions in ParC (Ser83Leu in U. parvum of serovar 6) and ParE (Val417Thr in U. parvum of serovar 1 and the novel Thr417Val substitution in U. urealyticum). Isolates with mutations in 23S rRNA or substitutions in L4/L22 were not detected. This is the first study analyzing the susceptibility of U. urealyticum/U. parvum isolates in Switzerland and the clonality outside China. Resistance rates were low compared to those in other countries. We hypothesize that some hyperepidemic STs spread worldwide via sexual intercourse. Large combined microbiological and clinical studies should address this important issue.


Subject(s)
Genotype , Mycoplasma hominis/genetics , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 23S/genetics , Ureaplasma urealyticum/genetics , Ureaplasma/genetics , Adult , Anti-Bacterial Agents/pharmacology , Drug Resistance, Multiple, Bacterial , Erythromycin/pharmacology , Female , Genitalia, Female/microbiology , Genitalia, Male/microbiology , Humans , Male , Microbial Sensitivity Tests , Middle Aged , Multilocus Sequence Typing , Mycoplasma Infections/drug therapy , Mycoplasma Infections/microbiology , Mycoplasma hominis/classification , Mycoplasma hominis/drug effects , Mycoplasma hominis/isolation & purification , Ofloxacin/pharmacology , Polymerase Chain Reaction , Quinolones/pharmacology , Ribosomal Proteins/genetics , Switzerland , Ureaplasma/classification , Ureaplasma/drug effects , Ureaplasma/isolation & purification , Ureaplasma Infections/drug therapy , Ureaplasma Infections/microbiology , Ureaplasma urealyticum/classification , Ureaplasma urealyticum/drug effects , Ureaplasma urealyticum/isolation & purification
3.
Ecohealth ; 12(1): 164-73, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25297819

ABSTRACT

The geographic distributions of Ixodes scapularis (black-legged tick) and the bacterium Borrelia burgdorferi (the causative agent of Lyme disease) are expanding in the USA. To assess the role of migratory songbirds in the spread of this tick and pathogen, we captured passerines in central Illinois during the fall of 2012. We compared forested sites in regions where I. scapularis populations were either previously or not yet established. Ticks were removed from birds and blood samples were taken from select avian species. Ticks were identified by morphology and molecular techniques were used to detect B. burgdorferi and other tick-borne pathogens in ticks and avian blood samples. Ixodes spp. were detected on 10 of 196 migrants (5.1%), with I. scapularis larvae found on 2 individuals. Borrelia burgdorferi sensu stricto was detected in the blood of 9 of 29 birds sampled (31%), yet only 1 infected bird was infested by ticks. The ticks were mostly Haemaphysalis leporispalustris and I. dentatus larvae, and none tested positive for B. burgdorferi. Infestation of birds by Ixodes spp. differed significantly by region, while B. burgdorferi infection did not. These data suggest that migratory birds may play a larger role in the dispersal of B. burgdorferi than previously realized.


Subject(s)
Animal Migration , Borrelia burgdorferi/physiology , Ixodes/physiology , Songbirds/microbiology , Animals , Bird Diseases/microbiology , Bird Diseases/parasitology , Disease Vectors , Lyme Disease/epidemiology , Lyme Disease/transmission , Midwestern United States/epidemiology , Population Surveillance , Seasons , Songbirds/parasitology
SELECTION OF CITATIONS
SEARCH DETAIL