Haemophilus pertussis - PMC

René H. M. Raeven, Naomi van Vlies, Merijn L. M. Salverda, Larissa van der Maas, Joost P. Uittenbogaard, Tim H. E. Bindels, Jolanda Rigters, Lisa M. Verhagen, Sabine Kruijer, Elly van Riet, Bernard Metz, Arno A. J. van der Ark

Vaccines (Basel) 2020 Sep; 8(3): 429. Published online 2020 Jul 30. doi: 10.3390/vaccines8030429

PMCID:: PMC7563335

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Improving specificity of Bordetella pertussis detection using a four target real-time PCR

Helena Martini, Liselot Detemmerman, Oriane Soetens, Erlangga Yusuf, Denis Piérard

PLoS One. 2017; 12(4): e0175587. Published online 2017 Apr 12. doi: 10.1371/journal.pone.0175587

PMCID:: PMC5389834

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Pertussis leukocytosis: mechanisms, clinical relevance and treatment

Nicholas H. Carbonetti

Pathog Dis. 2016 Oct 1; 74(7): ftw087. Published online 2016 Sep 7. doi: 10.1093/femspd/ftw087

PMCID:: PMC5761200

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The evolution of Bordetella pertussis has selected for mutations of acr that lead to sensitivity to hydrophobic molecules and fatty acids

Iain MacArthur, Thomas Belcher, Jerry D. King, Vasantha Ramasamy, Munirah Alhammadi, Andrew Preston

Emerg Microbes Infect. 2019; 8(1): 603–612. Published online 2019 Apr 10. doi: 10.1080/22221751.2019.1601502

PMCID:: PMC6461096

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Inactivation of the Mla system and outer-membrane phospholipase A results in disrupted outer-membrane lipid asymmetry and hypervesiculation in Bordetella pertussis

Eline F. de Jonge, Lana Vogrinec, Ria van Boxtel, Jan Tommassen

Curr Res Microb Sci. 2022; 3: 100172. Published online 2022 Nov 12. doi: 10.1016/j.crmicr.2022.100172

PMCID:: PMC9743053

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Biosynthesis of the Inner Core of Bordetella pertussis Lipopolysaccharides: Effect of Mutations on LPS Structure, Cell Division, and Toll-like Receptor 4 Activation

Jesús Pérez-Ortega, Ria van Boxtel, Michel Plisnier, Dominique Ingels, Nathalie Devos, Steven Sijmons, Jan Tommassen

Int J Mol Sci. 2023 Dec; 24(24): 17313. Published online 2023 Dec 9. doi: 10.3390/ijms242417313

PMCID:: PMC10743493

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Shortening the Lipid A Acyl Chains of Bordetella pertussis Enables Depletion of Lipopolysaccharide Endotoxic Activity

Jesús Arenas, Elder Pupo, Coen Phielix, Dionne David, Afshin Zariri, Alla Zamyatina, Jan Tommassen, Peter van der Ley

Vaccines (Basel) 2020 Dec; 8(4): 594. Published online 2020 Oct 9. doi: 10.3390/vaccines8040594

PMCID:: PMC7712016

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Pertussis: Microbiology, Disease, Treatment, and Prevention

Paul E. Kilgore, Abdulbaset M. Salim, Marcus J. Zervos, Heinz-Josef Schmitt

Clin Microbiol Rev. 2016 Jul; 29(3): 449–486. Published online 2016 Mar 30. doi: 10.1128/CMR.00083-15

PMCID:: PMC4861987

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The Fim and FhaB adhesins play a crucial role in nasal cavity infection and Bordetella pertussis transmission in a novel mouse catarrhal infection model

Jana Holubova, Ondrej Stanek, Attila Juhasz, Illiassou Hamidou Soumana, Peter Makovicky, Peter Sebo

PLoS Pathog. 2022 Apr; 18(4): e1010402. Published online 2022 Apr 8. doi: 10.1371/journal.ppat.1010402

PMCID:: PMC9020735

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Pertussis Toxin: A Key Component in Pertussis Vaccines?

Kelsey A. Gregg, Tod J. Merkel

Toxins (Basel) 2019 Oct; 11(10): 557. Published online 2019 Sep 21. doi: 10.3390/toxins11100557

PMCID:: PMC6832755

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Evolution of Bordetella pertussis over a 23-year period in France, 1996 to 2018

Valérie Bouchez, Sophie Guillot, Annie Landier, Nathalie Armatys, Soraya Matczak, the French pertussis microbiology study group, Julie Toubiana, Sylvain Brisse, French pertussis microbiology study group, French pertussis microbiology study group, Nathalie Brieu, Farida Hamdad, Marie Kempf, Hélène Pailhoriès, Cécile Jensen, Philippe Lehours, Jennifer Guiraud, Hervé Le Bars, Christophe Isnard, Nathalie Wilhelm, Alain Le Coustumier, Julien Delmas, Dominique De Briel, Laurent Souply, Saïd Aberrane,, Marie Coudé, Fabien Garnier, Ghislaine Descours, Hélène Jean-Pierre, Corentine Alauzet, Sophie-Anne Gibaud, Stéphane Bonacorsi, Lucien Brasme, Ludovic Lemée, Christelle Koebel, Philippe Lanotte, Stéphane Bland, Hélène Petitprez, Didier Raffenot, Marion Levast, Florence Doucet-Populaire, Nadège Bourgeois-Nicolaos, Christophe Burucoa, Florence Grattard, Stéphanie Marque-Juillet

Euro Surveill. 2021 Sep 16; 26(37): 2001213. doi: 10.2807/1560-7917.ES.2021.26.37.2001213

PMCID:: PMC8447829

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The History of Pertussis Toxin

Camille Locht, Rudy Antoine

Toxins (Basel) 2021 Sep; 13(9): 623. Published online 2021 Sep 5. doi: 10.3390/toxins13090623

PMCID:: PMC8472871

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Reinvestigating the Coughing Rat Model of Pertussis To Understand Bordetella pertussis Pathogenesis

Jesse M. Hall, Jason Kang, Sophia M. Kenney, Ting Y. Wong, Graham J. Bitzer, Claire O. Kelly, Caleb A. Kisamore, Dylan T. Boehm, Megan A. DeJong, M. Allison Wolf, Emel Sen-Kilic, Alexander M. Horspool, Justin R. Bevere, Mariette Barbier, F. Heath Damron

Infect Immun. 2021 Dec; 89(12): e00304-21. Prepublished online 2021 Jun 14. Published online 2021 Nov 16. doi: 10.1128/IAI.00304-21

PMCID:: PMC8594615

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A comprehensive resource for Bordetella genomic epidemiology and biodiversity studies

Sébastien Bridel, Valérie Bouchez, Bryan Brancotte, Sofia Hauck, Nathalie Armatys, Annie Landier, Estelle Mühle, Sophie Guillot, Julie Toubiana, Martin C. J. Maiden, Keith A. Jolley, Sylvain Brisse

Nat Commun. 2022; 13: 3807. Published online 2022 Jul 1. doi: 10.1038/s41467-022-31517-8

PMCID:: PMC9249784

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Isolate-Based Surveillance of Bordetella pertussis, Austria, 2018–2020

Adriana Cabal, Daniela Schmid, Markus Hell, Ali Chakeri, Elisabeth Mustafa-Korninger, Alexandra Wojna, Anna Stöger, Johannes Möst, Eva Leitner, Patrick Hyden, Thomas Rattei, Adele Habington, Ursula Wiedermann, Franz Allerberger, Werner Ruppitsch

Emerg Infect Dis. 2021 Mar; 27(3): 862–871. doi: 10.3201/eid2703.202314

PMCID:: PMC7920692

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Substrate specificity of the pyrophosphohydrolase LpxH determines the asymmetry of Bordetella pertussis lipid A

Jesús Arenas, Elder Pupo, Eline de Jonge, Jesús Pérez-Ortega, Joerg Schaarschmidt, Peter van der Ley, Jan Tommassen

J Biol Chem. 2019 May 17; 294(20): 7982–7989. Published online 2019 Mar 29. doi: 10.1074/jbc.RA118.004680

PMCID:: PMC6527161

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A pangenome approach-based loop-mediated isothermal amplification assay for the specific and early detection of Bordetella pertussis

Eduardo Juscamayta-López, Faviola Valdivia, María Pía Soto, Brenda Nureña, Helen Horna

Sci Rep. 2023; 13: 4356. Published online 2023 Mar 16. doi: 10.1038/s41598-023-29773-9

PMCID:: PMC10018623

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PMC Images search for Haemophilus pertussis

Figure 1

Trial flowchart. Stage 1. DTaP, diptheria, tetanus, acellular pertussis; DTwP, diptheria, tetanus, whole-cell pertussis; Hib, Haemophilus influenzae type b; HepB, hepatitis B; IPV, inactivated poliovirus vaccine; NIP, National immunisation program; OFC, oral food challenge; SPT, skin prick testing.

OPTIMUM study protocol: an adaptive randomised controlled trial of a mixed whole-cell/acellular pertussis vaccine schedule

BMJ Open. 2020;10(12):e042838.
Figure 2

Trial flowchart. Stage 2. DTaP, diptheria, tetanus, acellular pertussis; DTwP, diptheria, tetanus, whole-cell pertussis; Hib, Haemophilus influenzae type b; HepB, hepatitis B; IPV, inactivated poliovirus vaccine; NIP, National immunisation program; OFC, oral food challenge; SPT, skin prick testing.

OPTIMUM study protocol: an adaptive randomised controlled trial of a mixed whole-cell/acellular pertussis vaccine schedule

BMJ Open. 2020;10(12):e042838.
FIG. 2

Amplification of DNA from B. pertussis and other species appearing in the human respiratory tract with primers PIp1 and PIp2. Lane 1, Moraxella catarrhalis; lane 2, Escherichia coli; lane 3, Haemophilus influenzae; lane 4, Haemophilus parainfluenzae; lane 5, B. pertussis; lane 6, negative control; lane 7, Klebsiella pneumoniae; lane 8, Legionella pneumophila; lane 9, Pseudomonas aeruginosa; lane 10, Staphylococcus aureus; lane 11, coagulase-negative staphylococci; lane 12, Streptococcus pneumoniae; lane 13, Streptococcus pyogenes.

Evaluation of PCR for Diagnosis of Bordetella pertussis and Bordetella parapertussis Infections

J Clin Microbiol. 1998 Mar;36(3):679-683.
Figure 3

Microbial findings in 64 cases with complete sampling and the proportion of coinfections. S. pneumoniae, Streptococcus pneumoniae; H. influenzae, Haemophilus influenzae; B. pertussis, Bordetella pertussis; C. pneumoniae, Chlamydophila pneumoniae; M. pneumoniae, Mycoplasma pneumoniae; M. catarrhalis, Moraxella catarrhalis; H. parainfluenzae, Haemophilus parainfluenzae.

Etiology of community-acquired pneumonia and diagnostic yields of microbiological methods: a 3-year prospective study in Norway

BMC Infect Dis. 2015;15:64.