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A qPCR assay for Bordetella pertussis cells that enumerates both live and dead bacteria

A qPCR assay for Bordetella pertussis cells that enumerates both live and dead bacteria
A qPCR assay for Bordetella pertussis cells that enumerates both live and dead bacteria
Bordetella pertussis is the causative agent of whooping cough, commonly referred to as pertussis. Although the incidence of pertussis was reduced through vaccination, during the last thirty years it has returned to high levels in a number of countries. This resurgence has been linked to the switch from the use of whole-cell to acellular vaccines. Protection afforded by acellular vaccines appears to be short-lived compared to that afforded by whole cell vaccines. In order to inform future vaccine improvement by identifying immune correlates of protection, a human challenge model of B. pertussis colonisation has been developed. Accurate measurement of colonisation status in this model has required development of a qPCR-based assay to enumerate B. pertussis in samples that distinguishes between viable and dead bacteria. Here we report the development of this assay and its performance in the quantification of B. pertussis from human challenge model samples. This assay has future utility in diagnostic labs and in research where a quantitative measure of both B. pertussis number and viability is required.
1932-6203
Ramkissoon, Stacy
8919acc7-f9af-4e23-b133-c80f0a890c40
Macarthur, Iain
2d0b23ed-ceab-45b8-8a8e-d2a91a40b1d9
Ibrahim, Muktar
15bab4d1-f800-4d51-9ac6-d7999bd2a5d2
De graaf, Hans
447e78ed-346f-45bb-9238-fce2118d5559
Read, Robert c.
b5caca7b-0063-438a-b703-7ecbb6fc2b51
Preston, Andrew
f8d06589-7c45-4286-9abd-fc805bff2039
Ho, Paulo lee
5ce39915-22c3-4390-9aef-552e78b047c9
Ramkissoon, Stacy
8919acc7-f9af-4e23-b133-c80f0a890c40
Macarthur, Iain
2d0b23ed-ceab-45b8-8a8e-d2a91a40b1d9
Ibrahim, Muktar
15bab4d1-f800-4d51-9ac6-d7999bd2a5d2
De graaf, Hans
447e78ed-346f-45bb-9238-fce2118d5559
Read, Robert c.
b5caca7b-0063-438a-b703-7ecbb6fc2b51
Preston, Andrew
f8d06589-7c45-4286-9abd-fc805bff2039
Ho, Paulo lee
5ce39915-22c3-4390-9aef-552e78b047c9

Ramkissoon, Stacy, Macarthur, Iain, Ibrahim, Muktar, De graaf, Hans, Read, Robert c. and Preston, Andrew , Ho, Paulo lee (ed.) (2020) A qPCR assay for Bordetella pertussis cells that enumerates both live and dead bacteria. PLoS ONE, 15 (4), [e0232334]. (doi:10.1371/journal.pone.0232334).

Record type: Article

Abstract

Bordetella pertussis is the causative agent of whooping cough, commonly referred to as pertussis. Although the incidence of pertussis was reduced through vaccination, during the last thirty years it has returned to high levels in a number of countries. This resurgence has been linked to the switch from the use of whole-cell to acellular vaccines. Protection afforded by acellular vaccines appears to be short-lived compared to that afforded by whole cell vaccines. In order to inform future vaccine improvement by identifying immune correlates of protection, a human challenge model of B. pertussis colonisation has been developed. Accurate measurement of colonisation status in this model has required development of a qPCR-based assay to enumerate B. pertussis in samples that distinguishes between viable and dead bacteria. Here we report the development of this assay and its performance in the quantification of B. pertussis from human challenge model samples. This assay has future utility in diagnostic labs and in research where a quantitative measure of both B. pertussis number and viability is required.

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e0232334 - Version of Record
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Published date: 30 April 2020

Identifiers

Local EPrints ID: 491206
URI: http://eprints.soton.ac.uk/id/eprint/491206
ISSN: 1932-6203
PURE UUID: 5707b9b1-5629-46fc-b8d1-2bf256f871d1
ORCID for Robert c. Read: ORCID iD orcid.org/0000-0002-4297-6728

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Date deposited: 17 Jun 2024 16:48
Last modified: 22 Jun 2024 01:45

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Contributors

Author: Stacy Ramkissoon
Author: Iain Macarthur
Author: Muktar Ibrahim
Author: Hans De graaf
Author: Robert c. Read ORCID iD
Author: Andrew Preston
Editor: Paulo lee Ho

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