نتایج جستجو برای: bordetella species

تعداد نتایج: 551491  

Journal: :Enfermedades infecciosas y microbiologia clinica 2011
M Luisa Mateos Gustavo Gabilondo Teresa Hellín Jesús Chacón

1. Lutvik LI. Infections in asplenic patients. En: Mandell GL, Bennett JE, Dolin R, editores. Principles and Practice of Infectious Diseases. 6th ed. Philadelphia: Elsevier Churchill Livingstone; 2005. p. 3524–32. 2. Steinberg MH. Management of sickle cell disease. N Engl J Med. 1999;340:1021–30. 3. Weyant RS, Hollis DG, Weaver RE, Amin MFM, Steigerwalt AG, O’Connor SP, et al. Bordetella holmes...

2014
Laure F. Pittet Stéphane Emonet Patrice François Eve-Julie Bonetti Jacques Schrenzel Melanie Hug Martin Altwegg Claire-Anne Siegrist Klara M. Posfay-Barbe

Bordetella holmesii, an emerging pathogen, can be misidentified as Bordetella pertussis by routine polymerase chain reaction (PCR). In some reports, up to 29% of the patients diagnosed with pertussis have in fact B. holmesii infection and invasive, non-respiratory B. holmesii infections have been reported worldwide. This misdiagnosis undermines the knowledge of pertussis' epidemiology, and may ...

Journal: :Microbiology 1995
B Beall G N Sanden

The bfeA (Bordetella ferric enterobactin) receptor gene was cloned from a Bordetella pertussis chromosomal library by using a screen in Escherichia coli to detect iron-repressed genes encoding exported proteins translationally fused to the E. coli phoA gene. The bfeA gene encoded a protein with a molecular mass of approximately 80 kDa and about 50% amino acid sequence identity to both the fepA-...

Journal: :Journal of clinical microbiology 2015
Margaret M Williams Thomas H Taylor David M Warshauer Monte D Martin Ann M Valley M Lucia Tondella

Real-time PCR (rt-PCR) is an important diagnostic tool for the identification of Bordetella pertussis, Bordetella holmesii, and Bordetella parapertussis. Most U.S. public health laboratories (USPHLs) target IS481, present in 218 to 238 copies in the B. pertussis genome and 32 to 65 copies in B. holmesii. The CDC developed a multitarget PCR assay to differentiate B. pertussis, B. holmesii, and B...

2012
Jun Kurushima Asaomi Kuwae Akio Abe

Bordetella bronchiseptica is closely related with B. pertussis and B. parapertussis, the causative agents of whooping cough. These pathogenic species share a number of virulence genes, including the gene locus for the type III secretion system (T3SS) that delivers effector proteins. To identify unknown type III effectors in Bordetella, secreted proteins in the bacterial culture supernatants of ...

Journal: :Journal of clinical microbiology 2011
Kathleen M Tatti Kansas N Sparks Kathryn O Boney Maria Lucia Tondella

A novel multitarget real-time PCR (RT-PCR) assay for the rapid identification of Bordetella pertussis, B. parapertussis, and B. holmesii was developed using multicopy insertion sequences (ISs) in combination with the pertussis toxin subunit S1 (ptxS1) singleplex assay. The RT-PCR targets for the multiplex assay include IS481, commonly found in B. pertussis and B. holmesii; IS1001 of B. parapert...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2000
J M Vincent J D Cherry W F Nauschuetz A Lipton C M Ono C N Costello L K Sakaguchi G Hsue L A Jackson R Tachdjian P A Cotter J A Gornbein

A serological study was undertaken to investigate infections in active-duty United States soldiers with illnesses characterized by prolonged, afebrile, nonproductive coughs. Fifty-four soldiers were enrolled with such illness of >/=2 weeks' duration (case patients) along with 55 well soldiers (control subjects). Serum samples were tested for IgG and IgA antibody to 3 Bordetella pertussis antige...

Journal: :FEMS microbiology letters 2008
Anders Omsland Katrina M Miranda Richard L Friedman Scott Boitano

Bordetella bronchiseptica can establish prolonged airway infection consistent with a highly developed ability to evade mammalian host immune responses. Upon initial interaction with the host upper respiratory tract mucosa, B. bronchiseptica are subjected to antimicrobial reactive nitrogen species (RNS) and reactive oxygen species (ROS), effector molecules of the innate immune system. However, t...

Journal: :Journal of clinical microbiology 2006
Kazunari Kamachi Hiromi Toyoizumi-Ajisaka Kohei Toda Sann Chan Soeung Svay Sarath Ya Nareth Yoshinobu Horiuchi Kazunobu Kojima Motohide Takahashi Yoshichika Arakawa

We developed a loop-mediated isothermal amplification (LAMP) method to detect Bordetella pertussis infection. This LAMP assay detected B. pertussis with high sensitivity, but not other Bordetella species. Among nasopharyngeal swab samples from subjects with suspected pertussis, LAMP results showed a high level of agreement with results of conventional PCR. This method is a rapid, sensitive, and...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2013
Loren Rodgers Stacey W Martin Amanda Cohn Jeremy Budd Mario Marcon Andrew Terranella Sema Mandal Douglas Salamon Amy Leber Maria-Lucia Tondella Kathleen Tatti Kevin Spicer Allen Emanuel Elizabeth Koch Londell McGlone Lucia Pawloski Mysheika Lemaile-Williams Naomi Tucker Radhika Iyer Thomas A Clark Mary Diorio

BACKGROUND During 9 May 2010-7 May 2011, an outbreak of pertussis-like illness (incidence, 80 cases per 100 000 persons) occurred in Franklin County, Ohio. The majority of cases were identified by IS481-directed polymerase chain reaction (PCR), which does not differentiate among Bordetella species. We sought to determine outbreak etiology and epidemiologic characteristics. METHODS We obtained...

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