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1.
Int J Microbiol ; 2012: 218791, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22287969

RESUMO

Members of the Gram-negative genus Legionella are typically found in freshwater environments, with the exception of L. longbeachae, which is present in composts and potting mixes. When contaminated aerosols are inhaled, legionellosis may result, typically as either the more serious pneumonia Legionnaires' disease or the less severe flu-like illness Pontiac fever. It is presumed that all species of the genus Legionella are capable of causing disease in humans. As a followup to a prior clinical study of legionellosis in rural Thailand, indigenous soil samples were collected proximal to cases' homes and workplaces and tested for the presence of legionellae by culture. We obtained 115 isolates from 22/39 soil samples and used sequence-based methods to identify 12 known species of Legionella represented by 87 isolates.

2.
BMC Infect Dis ; 11: 157, 2011 Jun 02.
Artigo em Inglês | MEDLINE | ID: mdl-21635754

RESUMO

BACKGROUND: Compared to the civilian population, military trainees are often at increased risk for respiratory infections. We investigated an outbreak of radiologically-confirmed pneumonia that was recognized after 2 fatal cases of serotype 7F pneumococcal meningitis were reported in a 303-person military trainee company (Alpha Company). METHODS: We reviewed surveillance data on pneumonia and febrile respiratory illness at the training facility; conducted chart reviews for cases of radiologically-confirmed pneumonia; and administered surveys and collected nasopharyngeal swabs from trainees in the outbreak battalion (Alpha and Hotel Companies), associated training staff, and trainees newly joining the battalion. RESULTS: Among Alpha and Hotel Company trainees, the average weekly attack rates of radiologically-confirmed pneumonia were 1.4% and 1.2% (most other companies at FLW: 0-0.4%). The pneumococcal carriage rate among all Alpha Company trainees was 15% with a predominance of serotypes 7F and 3. Chlamydia pneumoniae was identified from 31% of specimens collected from Alpha Company trainees with respiratory symptoms. CONCLUSION: Although the etiology of the outbreak remains unclear, the identification of both S. pneumoniae and C. pneumoniae among trainees suggests that both pathogens may have contributed either independently or as cofactors to the observed increased incidence of pneumonia in the outbreak battalion and should be considered as possible etiologies in outbreaks of pneumonia in the military population.


Assuntos
Infecções por Chlamydia/microbiologia , Chlamydophila pneumoniae/isolamento & purificação , Meningite Pneumocócica/epidemiologia , Militares/estatística & dados numéricos , Pneumonia Bacteriana/microbiologia , Streptococcus pneumoniae/isolamento & purificação , Adolescente , Adulto , Infecções por Chlamydia/epidemiologia , Chlamydophila pneumoniae/genética , Chlamydophila pneumoniae/fisiologia , Estudos Transversais , Surtos de Doenças , Feminino , Humanos , Masculino , Meningite Pneumocócica/microbiologia , Meningite Pneumocócica/mortalidade , Pessoa de Meia-Idade , Pneumonia Bacteriana/epidemiologia , Streptococcus pneumoniae/genética , Streptococcus pneumoniae/fisiologia , Estados Unidos/epidemiologia , Adulto Jovem
3.
Diagn Microbiol Infect Dis ; 70(1): 1-9, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21397428

RESUMO

A multiplex real-time PCR assay for the detection of Mycoplasma pneumoniae (MP181), Chlamydia (Chlamydophila) pneumoniae (CP-Arg), Legionella spp. (Pan-Leg), and the human RNase P (RNase P) gene was developed for rapid testing of atypical bacterial respiratory pathogens in clinical specimens. This method uses 4 distinct hydrolysis probes to detect 3 leading causes of community-acquired pneumonia. The assay was evaluated for specificity and sensitivity by testing against 35 related organisms, a dilution series of each specific target and 197 clinical specimens. Specificity testing demonstrated no cross-reactivity. A comparison to previously validated singleplex real-time PCR assays for each agent was also performed. The analytical sensitivity for specific pathogen targets in both the singleplex and multiplex was identical (50 fg), while efficiencies ranged from 82% to 97% for the singleplex assays and from 90% to 100% for the multiplex assay. The clinical sensitivity of the multiplex assay was improved for the Pan-Leg and CP-Arg targets when compared to the singleplex. The MP181 assay displayed equivalent performance. This multiplex assay provides an overall improvement in the diagnostic capability for these agents by demonstrating a sensitive, high-throughput and rapid method. This procedure may allow for a practical and efficient means to test respiratory clinical specimens for atypical pneumonia agents in health care settings and facilitate an appropriate public health response to outbreaks.


Assuntos
Infecções por Chlamydia/diagnóstico , Chlamydophila pneumoniae/isolamento & purificação , Legionella/isolamento & purificação , Legionelose/diagnóstico , Infecções por Mycoplasma/diagnóstico , Mycoplasma pneumoniae/isolamento & purificação , Reação em Cadeia da Polimerase/métodos , Técnicas Bacteriológicas/métodos , Infecções por Chlamydia/microbiologia , Chlamydophila pneumoniae/genética , Infecções Comunitárias Adquiridas/diagnóstico , Infecções Comunitárias Adquiridas/microbiologia , Humanos , Legionella/genética , Legionelose/microbiologia , Infecções por Mycoplasma/microbiologia , Mycoplasma pneumoniae/genética , Sondas de Oligonucleotídeos/genética , Reação em Cadeia da Polimerase/normas , Ribonuclease P/genética , Sensibilidade e Especificidade
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