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Artykuły w czasopismach na temat „Bordetella”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 7 lipca 2024

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1

Sebaihia, Mohammed, Andrew Preston, Duncan J. Maskell, Holly Kuzmiak, Terry D. Connell, Natalie D. King, Paul E. Orndorff, et al. "Comparison of the Genome Sequence of the Poultry Pathogen Bordetella avium with Those of B. bronchiseptica, B. pertussis, and B. parapertussis Reveals Extensive Diversity in Surface Structures Associated with Host Interaction." Journal of Bacteriology 188, no. 16 (August 15, 2006): 6002–15. http://dx.doi.org/10.1128/jb.01927-05.

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ABSTRACT Bordetella avium is a pathogen of poultry and is phylogenetically distinct from Bordetella bronchiseptica, Bordetella pertussis, and Bordetella parapertussis, which are other species in the Bordetella genus that infect mammals. In order to understand the evolutionary relatedness of Bordetella species and further the understanding of pathogenesis, we obtained the complete genome sequence of B. avium strain 197N, a pathogenic strain that has been extensively studied. With 3,732,255 base pairs of DNA and 3,417 predicted coding sequences, it has the smallest genome and gene complement of

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2

Allen, Andrew G., Tomoko Isobe, and Duncan J. Maskell. "Identification and Cloning of waaF (rfaF) from Bordetella pertussis and Use To Generate Mutants ofBordetella spp. with Deep Rough Lipopolysaccharide." Journal of Bacteriology 180, no. 1 (January 1, 1998): 35–40. http://dx.doi.org/10.1128/jb.180.1.35-40.1998.

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ABSTRACT A DNA locus from Bordetella pertussis capable of reconstituting lipopolysaccharide (LPS) O-antigen biosynthesis inSalmonella typhimurium SL3789 (rfaF511) has been isolated, by using selection with the antibiotic novobiocin. DNA within the locus encodes a protein with amino acid sequence similarity to heptosyltransferase II, encoded by waaF (previouslyrfaF) in other gram-negative bacteria. Mutation of this gene in B. pertussis, Bordetella parapertussis, and Bordetella bronchiseptica by allelic exchange generated bacteria with deep rough LPS phenotypes consistent with the proposed funct

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3

López-Boado, Yolanda S., Laura M. Cobb, and Rajendar Deora. "Bordetella bronchiseptica Flagellin Is a Proinflammatory Determinant for Airway Epithelial Cells." Infection and Immunity 73, no. 11 (November 2005): 7525–34. http://dx.doi.org/10.1128/iai.73.11.7525-7534.2005.

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ABSTRACT Motility is an important virulence phenotype for many bacteria, and flagellin, the monomeric component of flagella, is a potent proinflammatory factor. Of the three Bordetella species, Bordetella pertussis and Bordetella parapertussis are nonmotile human pathogens, while Bordetella bronchiseptica expresses flagellin and causes disease in animals and immunocompromised human hosts. The BvgAS two-component signal transduction system regulates phenotypic-phase transition (Bvg+, Bvg−, and Bvgi) in bordetellae. The Bvg− phase of B. bronchiseptica is characterized by the expression of flagel

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4

Parise, Gina, Meenu Mishra, Yoshikane Itoh, Tony Romeo, and Rajendar Deora. "Role of a Putative Polysaccharide Locus in Bordetella Biofilm Development." Journal of Bacteriology 189, no. 3 (November 17, 2006): 750–60. http://dx.doi.org/10.1128/jb.00953-06.

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ABSTRACT Bordetellae are gram-negative bacteria that colonize the respiratory tracts of animals and humans. We and others have recently shown that these bacteria are capable of living as sessile communities known as biofilms on a number of abiotic surfaces. During the biofilm mode of existence, bacteria produce one or more extracellular polymeric substances that function, in part, to hold the cells together and to a surface. There is little information on either the constituents of the biofilm matrix or the genetic basis of biofilm development by Bordetella spp. By utilizing immunoblot assays

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5

Sloan, Gina Parise, Cheraton F. Love, Neelima Sukumar, Meenu Mishra, and Rajendar Deora. "The Bordetella Bps Polysaccharide Is Critical for Biofilm Development in the Mouse Respiratory Tract." Journal of Bacteriology 189, no. 22 (June 22, 2007): 8270–76. http://dx.doi.org/10.1128/jb.00785-07.

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ABSTRACT Bordetellae are respiratory pathogens that infect both humans and animals. Bordetella bronchiseptica establishes asymptomatic and long-term to life-long infections of animal nasopharynges. While the human pathogen Bordetella pertussis is the etiological agent of the acute disease whooping cough in infants and young children, it is now being increasingly isolated from the nasopharynges of vaccinated adolescents and adults who sometimes show milder symptoms, such as prolonged cough illness. Although it has been shown that Bordetella can form biofilms in vitro, nothing is known about its

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6

Williams, Corinne L., Robert Haines, and Peggy A. Cotter. "Serendipitous Discovery of an Immunoglobulin-Binding Autotransporter in Bordetella Species." Infection and Immunity 76, no. 7 (April 21, 2008): 2966–77. http://dx.doi.org/10.1128/iai.00323-08.

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ABSTRACT We describe the serendipitous discovery of BatB, a classical-type Bordetella autotransporter (AT) protein with an ∼180-kDa passenger domain that remains noncovalently associated with the outer membrane. Like genes encoding all characterized protein virulence factors in Bordetella species, batB transcription is positively regulated by the master virulence regulatory system BvgAS. BatB is predicted to share similarity with immunoglobulin A (IgA) proteases, and we showed that BatB binds Ig in vitro. In vivo, a Bordetella bronchiseptica ΔbatB mutant was unable to overcome innate immune de

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7

Hegerle, N., A. S. Paris, D. Brun, G. Dore, E. Njamkepo, S. Guillot, and N. Guiso. "Evolution of French Bordetella pertussis and Bordetella parapertussis isolates: increase of Bordetellae not expressing pertactin." Clinical Microbiology and Infection 18, no. 9 (September 2012): E340—E346. http://dx.doi.org/10.1111/j.1469-0691.2012.03925.x.

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Cummings, C. A., M. M. Brinig, P. W. Lepp, S. van de Pas, and D. A. Relman. "Bordetella Species Are Distinguished by Patterns of Substantial Gene Loss and Host Adaptation." Journal of Bacteriology 186, no. 5 (March 1, 2004): 1484–92. http://dx.doi.org/10.1128/jb.186.5.1484-1492.2004.

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ABSTRACT Pathogens of the bacterial genus Bordetella cause respiratory disease in humans and animals. Although virulence and host specificity vary across the genus, the genetic determinants of this diversity remain unidentified. To identify genes that may underlie key phenotypic differences between these species and clarify their evolutionary relationships, we performed a comparative analysis of genome content in 42 Bordetella strains by hybridization of genomic DNA to a microarray representing the genomes of three Bordetella species and by subtractive hybridization. Here we show that B. pertu

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9

Spears, Patricia A., Louise M. Temple, David M. Miyamoto, Duncan J. Maskell, and Paul E. Orndorff. "Unexpected Similarities between Bordetella avium and Other Pathogenic Bordetellae." Infection and Immunity 71, no. 5 (May 2003): 2591–97. http://dx.doi.org/10.1128/iai.71.5.2591-2597.2003.

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ABSTRACT Bordetella avium causes an upper respiratory tract disease (bordetellosis) in avian species. Commercially raised turkeys are particularly susceptible. Like other pathogenic members of the genus Bordetella (B. pertussis and B. bronchiseptica) that infect mammals, B. avium binds preferentially to ciliated tracheal epithelial cells and produces similar signs of disease. These similarities prompted us to study bordetellosis in turkeys as a possible nonmammalian model for whooping cough, the exclusively human childhood disease caused by B. pertussis. One impediment to accepting such a host

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10

Marr, Nico, Alina Tirsoaga, Didier Blanot, Rachel Fernandez, and Martine Caroff. "Glucosamine Found as a Substituent of Both Phosphate Groups in Bordetella Lipid A Backbones: Role of a BvgAS-Activated ArnT Ortholog." Journal of Bacteriology 190, no. 12 (April 18, 2008): 4281–90. http://dx.doi.org/10.1128/jb.01875-07.

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ABSTRACT Endotoxins are amphipathic lipopolysaccharides (LPSs), major constituents of the outer membrane of gram-negative bacteria. They consist of a lipid region, covalently linked to a core oligosaccharide, to which may be linked a repetitive glycosidic chain carrying antigenic determinants. Most of the biological activities of endotoxins have been associated with the lipid moiety of the molecule: unique to gram-negative bacteria, LPS is a ligand of the mammalian TLR4-MD2-CD14 pathogen recognition receptor complex. Lipid A preparations are often heterogeneous with respect to both the numbers

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11

Diavatopoulos, D. A., C. A. Cummings, H. G. J. van der Heide, M. van Gent, S. Liew, D. A. Relman, and F. R. Mooi. "Characterization of a Highly Conserved Island in the Otherwise Divergent Bordetella holmesii and Bordetella pertussis Genomes." Journal of Bacteriology 188, no. 24 (October 13, 2006): 8385–94. http://dx.doi.org/10.1128/jb.01081-06.

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ABSTRACT The recently discovered pathogen Bordetella holmesii has been isolated from the airways and blood of diseased humans. Genetic events contributing to the emergence of B. holmesii are not understood, and its phylogenetic position among the bordetellae remains unclear. To address these questions, B. holmesii strains were analyzed by comparative genomic hybridization (CGH) to a Bordetella pertussis microarray and by multilocus sequence typing. Both methods indicated substantial sequence divergence between B. pertussis and B. holmesii. However, CGH identified a putative pathogenicity islan

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12

Pishko, Elizabeth J., David J. Betting, Christina S. Hutter, and Eric T. Harvill. "Bordetella pertussis Acquires Resistance to Complement-Mediated Killing In Vivo." Infection and Immunity 71, no. 9 (September 2003): 4936–42. http://dx.doi.org/10.1128/iai.71.9.4936-4942.2003.

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ABSTRACT In order to initially colonize a host, bacteria must avoid various components of the innate immune system, one of which is complement. The genus Bordetella includes three closely related species that differ in their ability to resist complement-mediated killing. Bordetella parapertussis and Bordetella bronchiseptica resist killing in naïve serum, a characteristic that may aid in efficient respiratory tract colonization and has been attributed to expression of O antigen. Bordetella pertussis lacks O antigen and is sensitive to naïve serum in vitro, yet it also efficiently colonizes t

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13

Guiso, N. "Bordetella." EMC - Biologie médicale 2, no. 3 (January 2007): 1–5. http://dx.doi.org/10.1016/s2211-9698(07)71378-x.

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Srigley, Jocelyn A., David M. Goldfarb, and Jeffrey M. Pernica. "Bordetella Species Other than Bordetella pertussis." Clinical Microbiology Newsletter 37, no. 8 (April 2015): 61–65. http://dx.doi.org/10.1016/j.clinmicnews.2015.03.004.

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Heininger, Ulrich, Peggy A. Cotter, Howard W. Fescemyer, Guillermo Martinez de Tejada, Ming H. Yuk, Jeff F. Miller, and Eric T. Harvill. "Comparative Phenotypic Analysis of the Bordetella parapertussis Isolate Chosen for Genomic Sequencing." Infection and Immunity 70, no. 7 (July 2002): 3777–84. http://dx.doi.org/10.1128/iai.70.7.3777-3784.2002.

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ABSTRACT The genomes of three closely related bordetellae are currently being sequenced, thus providing an opportunity for comparative genomic approaches driven by an understanding of the comparative biology of these three bacteria. Although the other strains being sequenced are well studied, the strain of Bordetella parapertussis chosen for sequencing is a recent human clinical isolate (strain 12822) that has yet to be characterized in detail. This investigation reports the first phenotypic characterization of this strain, which will likely become the prototype for this species in comparison

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16

Harvill, Eric T., Andrew Preston, Peggy A. Cotter, Andrew G. Allen, Duncan J. Maskell, and Jeff F. Miller. "Multiple Roles for BordetellaLipopolysaccharide Molecules during Respiratory Tract Infection." Infection and Immunity 68, no. 12 (December 1, 2000): 6720–28. http://dx.doi.org/10.1128/iai.68.12.6720-6728.2000.

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ABSTRACT Bordetella pertussis, Bordetella parapertussis, and Bordetella bronchiseptica are closely related subspecies that cause respiratory tract infections in humans and other mammals and express many similar virulence factors. Their lipopolysaccharide (LPS) molecules differ, containing either a complex trisaccharide (B. pertussis), a trisaccharide plus an O-antigen-like repeat (B. bronchiseptica), or an altered trisaccharide plus an O-antigen-like repeat (B. parapertussis). Deletion of the wlb locus results in the loss of membrane-distal polysaccharide domains in the three subspecies of bor

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17

Pittet, Laure F., Stéphane Emonet, Jacques Schrenzel, Claire-Anne Siegrist, and Klara M. Posfay-Barbe. "Bordetella holmesii: an under-recognised Bordetella species." Lancet Infectious Diseases 14, no. 6 (June 2014): 510–19. http://dx.doi.org/10.1016/s1473-3099(14)70021-0.

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Hoegh, Silje V., Charlotte N. Agergaard, Marianne N. Skov, and Michael Kemp. "False-Positive Diagnostics of Bordetella Pertussis using IS481 PCR is Limited in Danish Patients." Open Microbiology Journal 13, no. 1 (February 28, 2019): 51–54. http://dx.doi.org/10.2174/1874285801913010051.

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Background: Bordetella pertussis is routinely detected using real-time PCR based on the multicopy insertion sequence IS481, which is not specific for Bordetella pertussis. Objective: The aim of this retrospective study was to evaluate the proportion of other Bordetella species misidentified as Bordetella pertussis using IS481-targeted real-time PCR. Methods: Clinical specimens from 228 Danish patients (median age 15 years, 0 to 90 years old) formerly identified as positive for Bordetella pertussis (IS481+) by routine PCR in 2011-2015, were subjected to real-time PCR targeting the insertion seq

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19

Gerlach, Gabriele, Simone Janzen, Dagmar Beier, and Roy Gross. "Functional characterization of the BvgAS two-component system of Bordetella holmesii." Microbiology 150, no. 11 (November 1, 2004): 3715–29. http://dx.doi.org/10.1099/mic.0.27432-0.

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The BvgAS two-component system is the master regulator of virulence gene expression in the mammalian pathogens Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica. This paper reports the partial cloning and characterization of the bvgAS loci of the ‘new’ Bordetella species Bordetella holmesii, Bordetella trematum and Bordetella hinzii, which are increasingly recognized as opportunistic pathogens in humans. It is demonstrated that the cytoplasmic signalling domains of the BvgS histidine kinases of B. pertussis and B. holmesii are functionally interchangeable, while sign

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Ucieklak, Karolina, Sabina Koj, and Tomasz Niedziela. "Conserved Structural Features of Core Oligosaccharides among the Lipopolysaccharides of Respiratory Pathogens from the Genus Bordetella Analyzed Exclusively by NMR Spectroscopy." International Journal of Molecular Sciences 22, no. 3 (January 21, 2021): 1029. http://dx.doi.org/10.3390/ijms22031029.

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Bacterial pathogens expose on the cell surface a variety of complex carbohydrate molecules. Gram-negative bacteria produce lipopolysaccharides, which are the main components of the outer membrane of bacterial envelopes and play a major role in host–pathogen interactions. B. pertussis, B. parapertussis, B. bronchiseptica, and B. holmesii, are mammalian respiratory pathogens, having substantial economic impact on human health and agriculture. B. pertussis is responsible for whooping cough (pertussis) and B. holmesii is the second pertussis etiological factor, but the current anti-pertussis vacci

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21

Burns, Valorie C., Elizabeth J. Pishko, Andrew Preston, Duncan J. Maskell, and Eric T. Harvill. "Role of Bordetella O Antigen in Respiratory Tract Infection." Infection and Immunity 71, no. 1 (January 2003): 86–94. http://dx.doi.org/10.1128/iai.71.1.86-94.2003.

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ABSTRACT Lipopolysaccharide (LPS), as the major surface molecule of gram-negative bacteria, interacts with the host in complex ways, both inducing and protecting against aspects of inflammatory and adaptive immunity. The membrane-distal repeated carbohydrate structure of LPS, the O antigen, can prevent antibody functions and may vary as a mechanism of immune evasion. Genes of the wbm locus are required for the assembly of O antigen on the animal pathogen Bordetella bronchiseptica and the human pathogen B. parapertussis. However, the important human pathogen B. pertussis lacks these genes and a

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22

Carbonetti, Nicholas H. "Bordetella pertussis." Current Opinion in Infectious Diseases 29, no. 3 (June 2016): 287–94. http://dx.doi.org/10.1097/qco.0000000000000264.

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Parkhill, Julian, Mohammed Sebaihia, Andrew Preston, Lee D. Murphy, Nicholas Thomson, David E. Harris, Matthew T. G. Holden, et al. "Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica." Nature Genetics 35, no. 1 (August 10, 2003): 32–40. http://dx.doi.org/10.1038/ng1227.

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Locht, Camille, Nicholas H. Carbonetti, James D. Cherry, F. Heath Damron, Kathryn M. Edwards, Rachel Fernandez, Eric T. Harvill, et al. "Highlights of the 12th International Bordetella Symposium." Clinical Infectious Diseases 71, no. 9 (May 28, 2020): 2521–26. http://dx.doi.org/10.1093/cid/ciaa651.

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Abstract To commemorate the 100th anniversary of the Nobel prize being awarded to Jules Bordet, the discoverer of Bordetella pertussis, the 12th International Bordetella Symposium was held from 9 to 12 April 2019 at the Université Libre de Bruxelles, where Jules Bordet studied and was Professor of Microbiology. The symposium attracted more than 300 Bordetella experts from 34 countries. They discussed the latest epidemiologic data and clinical aspects of pertussis, Bordetella biology and pathogenesis, immunology and vaccine development, and genomics and evolution. Advanced technological and met

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Julio, Steven M., and Peggy A. Cotter. "Characterization of the Filamentous Hemagglutinin-Like Protein FhaS in Bordetella bronchiseptica." Infection and Immunity 73, no. 8 (August 2005): 4960–71. http://dx.doi.org/10.1128/iai.73.8.4960-4971.2005.

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ABSTRACT Filamentous hemagglutinin (FHA) is a large (>200 kDa), rod-shaped protein expressed by bordetellae that is both surface-associated and secreted. FHA mediates bacterial adherence to epithelial cells and macrophages in vitro and is absolutely required for tracheal colonization in vivo. The recently sequenced Bordetella bronchiseptica genome revealed the presence of a gene, fhaS, that is nearly identical to fhaB, the FHA structural gene. We show that although fhaS expression requires the BvgAS virulence control system, it is maximal only under a subset of conditions in which BvgAS is

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Mortensen, J. E., A. Brumbach, and T. R. Shryock. "Antimicrobial susceptibility of Bordetella avium and Bordetella bronchiseptica isolates." Antimicrobial Agents and Chemotherapy 33, no. 5 (May 1, 1989): 771–72. http://dx.doi.org/10.1128/aac.33.5.771.

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Khelef, N., B. Danve, M. J. Quentin-Millet, and N. Guiso. "Bordetella pertussis and Bordetella parapertussis: two immunologically distinct species." Infection and Immunity 61, no. 2 (1993): 486–90. http://dx.doi.org/10.1128/iai.61.2.486-490.1993.

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Boursaux-Eude, Caroline, and Nicole Guiso. "Polymorphism of Repeated Regions of Pertactin in Bordetella pertussis, Bordetella parapertussis, andBordetella bronchiseptica." Infection and Immunity 68, no. 8 (August 1, 2000): 4815–17. http://dx.doi.org/10.1128/iai.68.8.4815-4817.2000.

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ABSTRACT Pertactin is an outer membrane protein expressed byBordetella pertussis, Bordetella parapertussis, and Bordetella bronchiseptica that induces protective immunity to Bordetella infections. The immunodominant and immunoprotective epitopes of pertactin include two repeated regions, I and II. Comparison of these two repeated regions showed that B. parapertussis pertactin is invariant, whereas B. pertussis pertactin varies mostly in region I and B. bronchiseptica pertactin varies in both repeated regions I and II, but mostly in region II. These differences may result from specific characte

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Vandamme, Peter A., Charlotte Peeters, Margo Cnockaert, Elisabeth Inganäs, Enevold Falsen, Edward R. B. Moore, Olga C. Nunes, Célia M. Manaia, Theodore Spilker, and John J. LiPuma. "Bordetella bronchialis sp. nov., Bordetella flabilis sp. nov. and Bordetella sputigena sp. nov., isolated from human respiratory specimens, and reclassification of Achromobacter sediminum Zhang et al. 2014 as Verticia sediminum gen. nov., comb. nov." International Journal of Systematic and Evolutionary Microbiology 65, Pt_10 (October 1, 2015): 3674–82. http://dx.doi.org/10.1099/ijsem.0.000473.

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The phenotypic and genotypic characteristics of four Bordetella hinzii-like strains from human respiratory specimens and representing nrdA gene sequence based genogroups 3, 14 and 15 were examined. In a 16S rRNA gene sequence based phylogenetic tree, the four strains consistently formed a single coherent lineage but their assignment to the genus Bordetella was equivocal. The respiratory quinone, polar lipid and fatty acid profiles generally conformed to those of species of the genus Bordetella and were characterized by the presence of ubiquinone 8, of phosphatidylethanolamine, phosphatidylglyc

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Stenzel, T., D. Pestka, B. Tykałowski, M. Śmiałek, A. Koncicki, and A. Bancerz-Kisiel. "Detection of Bordetella avium by TaqMan real-time PCR in tracheal swabs from wildlife birds." Polish Journal of Veterinary Sciences 20, no. 1 (March 28, 2017): 31–36. http://dx.doi.org/10.1515/pjvs-2017-0005.

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Abstract Bordetella avium, the causing agent of bordetellosis, a highly contagious infection of the respiratory tract in young poultry, causes significant losses in poultry farming throughout the world. Wildlife birds can be a reservoir of various pathogens that infect farm animals. For this reason the studies were conducted to estimate the prevalence of Bordetella avium in wildlife birds in Poland. Tracheal swab samples were collected from 650 birds representing 27 species. The bacterial DNA was isolated directly from the swabs and screened for Bordetella avium by TaqMan real-time PCR. The as

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Teimurazov, M. G., O. V. Tazina, A. A. Abaimova, M. E. Platonov, T. B. Manin, A. V. Ruzina, and S. V. Pankratov. "Bordetella avium and Bordetella hinzii isolated from chickens from different farms in the Russian Federation." "Veterinary Medicine" Journal 26, no. 07 (July 2023): 11–16. http://dx.doi.org/10.30896/0042-4846.2023.26.7.11-16.

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Daniels, Heather L., and Camille Sabella. "Bordetella pertussis (Pertussis)." Pediatrics in Review 39, no. 5 (May 2018): 247–57. http://dx.doi.org/10.1542/pir.2017-0229.

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Schwanz, Thomas. "Erregerlexikon: Bordetella pertussis." Krankenhaushygiene up2date 17, no. 02 (June 2022): 141–56. http://dx.doi.org/10.1055/a-1745-7799.

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Lawson, R. A. "Bordetella bronchiseptica pneumonia." Thorax 49, no. 12 (December 1, 1994): 1278. http://dx.doi.org/10.1136/thx.49.12.1278-b.

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Wallihan, Rebecca, Rangaraj Selvarangan, Mario Marcon, Katalin Koranyi, Kevin Spicer, and Mary Anne Jackson. "Bordetella parapertussis Bacteremia." Pediatric Infectious Disease Journal 32, no. 7 (July 2013): 796–98. http://dx.doi.org/10.1097/inf.0b013e31828d2ca4.

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Papasian, C. J., N. J. Downs, R. L. Talley, D. J. Romberger, and G. R. Hodges. "Bordetella bronchiseptica bronchitis." Journal of Clinical Microbiology 25, no. 3 (1987): 575–77. http://dx.doi.org/10.1128/jcm.25.3.575-577.1987.

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Couturier, Amy P., and Karen Dahl. "Bordetella Holmesii Endocarditis." Pediatric Infectious Disease Journal 33, no. 6 (June 2014): 661–64. http://dx.doi.org/10.1097/inf.0000000000000234.

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Ducours, M., P. Rispal, M. P. Danjean, Y. Imbert, E. Dupont, E. M. Traissac, and S. Grosleron. "Bordetella bronchiseptica infection." Médecine et Maladies Infectieuses 47, no. 7 (November 2017): 453–58. http://dx.doi.org/10.1016/j.medmal.2017.05.012.

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Cullinane, L. C., M. R. Alley, R. B. Marshall, and B. W. Manktelow. "Bordetella parapertussisfrom lambs." New Zealand Veterinary Journal 35, no. 10 (October 1987): 175. http://dx.doi.org/10.1080/00480169.1987.35433.

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Mäkinen, Johanna, Jussi Mertsola, Frits R. Mooi, Shirley Van Amersfoorth, Heikki Arvilommi, Matti K. Viljanen, and Qiushui He. "Bordetella pertussisIsolates, Finland." Emerging Infectious Diseases 11, no. 1 (January 2005): 183–84. http://dx.doi.org/10.3201/eid1101.040632.

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Fry, Norman K., John Duncan, Henry Malnick, Marina Warner, Andrew J. Smith, Margaret S. Jackson, and Ashraf Ayoub. "Bordetella petriiClinical Isolate." Emerging Infectious Diseases 11, no. 7 (July 2005): 1131–33. http://dx.doi.org/10.3201/eid1107.050046.

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Scott-Garrard, Maya M., Yu-Wei Chiang, and Frederic David. "Comparative onset of immunity of oral and intranasal vaccines against challenge with Bordetella bronchiseptica." Veterinary Record Open 5, no. 1 (August 2018): e000285. http://dx.doi.org/10.1136/vetreco-2018-000285.

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Three groups of approximately eight-week-old beagles were vaccinated once with 1 ml of placebo vaccine (oral, n=9), 1 ml of Recombitek® Oral Bordetella (oral, n=10) or 1 ml Nobivac® Intra-Trac3 (intranasal, 0.5 ml/nostril, n=10). Seven days after vaccination, the three groups were challenged with virulent Bordetella bronchiseptica via aerosolisation. Eight of nine dogs in the placebo group and no dogs in the Recombitek® Oral Bordetella or Nobivac® Intra-Trac3 vaccine groups developed spontaneous cough of two or more consecutive days (disease case definition). Dogs in the Recombitek® Oral Borde

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Kawai, Hirokazu, Tatsuo Aoyama, Yuji Murase, Chieko Tamura, and Atsushi Imaizump. "A Causal Relationship between Bordetella pertussis and Bordetella parapertussis Infections." Scandinavian Journal of Infectious Diseases 28, no. 4 (January 1996): 377–81. http://dx.doi.org/10.3109/00365549609037923.

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Chenal-Francisque, Viviane, Valérie Caro, Caroline Boursaux-Eude, and Nicole Guiso. "Genomic analysis of the adenylate cyclase-hemolysin C-terminal region of Bordetella pertussis, Bordetella parapertussisand Bordetella bronchiseptica." Research in Microbiology 160, no. 5 (June 2009): 330–36. http://dx.doi.org/10.1016/j.resmic.2009.03.006.

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Kumar, Sandeep, Bhoj R. Singh, Monika Bhardwaj, and Vidya Singh. "Occurrence ofBordetellaInfection in Pigs in Northern India." International Journal of Microbiology 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/238575.

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Bordetella bronchisepticainfection causing atrophic rhinitis in pigs is reported from almost all countries. In the present study, occurrence ofBordetellainfection in apparently healthy pigs was determined in 392 pigs sampled to collect 358 serum samples and 316 nasal swabs from Northern India by conventional bacterioscopy, detection of antigen with multiplex polymerase chain reaction (mPCR), and detection of antibodies with microagglutination test (MAT) and enzyme linked immune-sorbent assay (ELISA).Bordetella bronchisepticacould be isolated from six (1.92%) nasal swabs. Although isolates vari

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Halperin, Scott, Alicja Kasina, and Margaret Swift. "Prolonged survival of Bordetella pertussis in a simple buffer after nasopharyngeal secretion aspiration." Canadian Journal of Microbiology 38, no. 11 (November 1, 1992): 1210–13. http://dx.doi.org/10.1139/m92-200.

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A simple method for recovery of Bordetella pertussis is described using phosphate-buffered saline containing a casein hydrolysate for transporting secretions collected by nasopharyngeal aspirate. Bordetella pertussis was reisolated from 92% of clinical specimens held at 4 °C for 1 week and from all specimens held at −20 °C. This method will facilitate the centralization of laboratory facilities for the diagnosis of pertussis. Key words: Bordetella pertussis, specimen transport, nasopharyngeal secretions.

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Chow, Siu-Kei, Sophie Arbefeville, Bobby L. Boyanton, Emily M. Dault, James Dunn, Patricia Ferrieri, Wallace Greene, et al. "Multicenter Performance Evaluation of the Simplexa Bordetella Direct Kit in Nasopharyngeal Swab Specimens." Journal of Clinical Microbiology 59, no. 1 (October 14, 2020): e01041-20. http://dx.doi.org/10.1128/jcm.01041-20.

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ABSTRACTDetection of Bordetella pertussis and Bordetella parapertussis using molecular methods is sensitive and specific with a short turnaround time compared to other diagnostic methods. In this multicenter study, we compared the performance of the Simplexa Bordetella Direct kit to those of other molecular assays in detecting and differentiating B. pertussis and B. parapertussis in nasopharyngeal swab specimens. The limits of detection (LODs) were 150 CFU/ml or 3 fg/μl of DNA for B. pertussis and 1,500 CFU/ml or 10 fg/μl of DNA for B. parapertussis. A total of 1,103 fresh and residual frozen

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Reissinger, Annette, Jason A. Skinner, and Ming H. Yuk. "Downregulation of Mitogen-Activated Protein Kinases by the Bordetella bronchiseptica Type III Secretion System Leads to Attenuated Nonclassical Macrophage Activation." Infection and Immunity 73, no. 1 (January 2005): 308–16. http://dx.doi.org/10.1128/iai.73.1.308-316.2005.

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ABSTRACT Bordetella bronchiseptica utilizes a type III secretion system (TTSS) to establish a persistent infection of the murine respiratory tract. Previous studies have shown that the Bordetella TTSS mediated cytotoxicity in different cell types, inhibition of NF-κB in epithelial cells, and differentiation of dendritic cells into a semimature state. Here we demonstrate modulation of mitogen-activated protein kinase (MAPK) signaling pathways and altered cytokine production in macrophages and dendritic cells by the Bordetella TTSS. In macrophages, the MAPKs ERK and p38 were downregulated. This

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SACCO, R. E., K. B. REGISTER, and G. E. NORDHOLM. "Restriction enzyme analysis and ribotyping distinguish Bordetella avium and Bordetella hinzii isolates." Epidemiology and Infection 124, no. 1 (February 2000): 83–90. http://dx.doi.org/10.1017/s0950268899003337.

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Fifty-seven bacterial isolates previously identified as Bordetella avium or B. hinzii were characterized by restriction enzyme analysis (REA) and/or ribotyping. Twenty restriction endonucleases were evaluated for REA. Digestion of chromosomal DNA from the 42 B. avium and 15 B. hinzii isolates with Hinf I produced 8 and 7 distinct fingerprint profiles, respectively. Digestion with DdeI further discriminated these Bordetella species and produced 12 fingerprint profiles for B. avium and 4 profiles of B. hinzii. In addition, B. avium isolates were clearly distinguishable from B. hinzii isolates by

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I. O., Enyi,, Hart, A. I., and Siminialayi, I. M. "Effect of Cardisoma guanhumi (land crab) extract on liver function and liver histology of Swiss mice infected with Bordetella pertussis." International Journal of Contemporary Research and Review 11, no. 01 (January 23, 2020): 20201–11. http://dx.doi.org/10.15520/ijcrr.v11i01.781.

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Pertussis also known as whooping cough is an acute human respiratory tract disease caused by Bordetella pertussis that is known to be associated with liver pathology. The aim of this study was to investigate the effects of Bordetella pertussis infection on the liver function and histology of Swiss mice and to evaluate the mitigating effects of Cardisoma guanhumi extract on these changes in comparison to erythromycin treatment. The animals were divided into five groups: group 1 was normal control; group 2 was infected with Bordetella pertussis without treatment (negative control); groups 3 and

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