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Volume 19, Number 8—August 2013
Books and Media

PCR Detection of Microbial Pathogens

Cite This Article

Mark WilksEditor
Humana Press, New York, New York, USA, 2012
ISBN-10: 1603273522
ISBN-13: 978:1603273527
Pages: 328; Price: US $84.00

This book covers general challenges of introducing primarily noncommercial PCRs and specific procedures into the laboratory, including sample treatment, extraction protocols, quality and quality assurance, and internal and external laboratory processes. The chapters on specific pathogens illustrate principles that could be applied in many diagnostic laboratories.

The editor’s preface to this book is helpful in framing approaches to PCR pathogen detection methods. The focus is primarily on detection of bacterial pathogens, with the exception of Pneumocystis spp., and the case is made for using less expensive noncommercial strategies that enable more flexibility and customization. The book addresses the many parameters of nucleic acid preparation, buffer choice, primer construction, inhibition, cycling parameters, detection, and statistical analysis.

The ≈300 pages of text are divided in 21 chapters, of which the first 3 cover concepts of importance to all clinical laboratories using PCRs. The third chapter, which covers quality and quality assurance, is particularly comprehensive in its treatment of internal and external laboratory process and PCR controls. This chapter covers a variety of concepts, from Westguard rules for investigations of systematic and other errors, to proficiency testing, and includes many useful tables. Of importance to clinical laboratories and epidemiologic investigations alike, the authors make an essential point that up to 75% of errors in the testing process can be attributed to improper sample collection and transport of specimens, areas that often get less attention than assay quality control. The fourth chapter covers preanalytical and extraction protocols specifically for molecular detection of pathogens in whole blood, which is a particularly challenging specimen.

The remaining chapters cover a mixture of mostly real-time and some conventional PCRs targeting specific pathogens (sometimes by multiplex approaches), and 1 chapter describes a loop-mediated isothermal amplification method for detection of Campylobacter spp. The pathogens and techniques covered represent a good survey of approaches and vendor equipment choices. The quality of the chapters in this book varies widely, and some repetitive information is included. Overall, this book would be of interest to those involved in PCR principles and laboratory quality control. It contains examples of successful noncommercial diagnostic PCRs. If your pathogen(s) of interest are covered, it is an added bonus.

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Deborah F. TalkingtonComments to Author 

Author affiliation: Centers for Disease Control and Prevention, Atlanta, Georgia, USA

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Cite This Article

DOI: 10.3201/eid1908.130528

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Table of Contents – Volume 19, Number 8—August 2013

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Please use the form below to submit correspondence to the authors or contact them at the following address:

Deborah F. Talkington, Centers for Disease Control and Prevention, 1600 Clifton Rd NE, Mailstop C03, Atlanta, GA 30033, USA

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Page created: June 27, 2013
Page updated: June 27, 2013
Page reviewed: June 27, 2013
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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