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Lisa Quigley

Researcher at Teagasc

Publications -  10
Citations -  1490

Lisa Quigley is an academic researcher from Teagasc. The author has contributed to research in topics: Raw milk & Lactobacillus. The author has an hindex of 9, co-authored 10 publications receiving 1226 citations. Previous affiliations of Lisa Quigley include University College Cork.

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The complex microbiota of raw milk

TL;DR: There is concern that the presence of antibiotic residues in milk leads to the development of resistance, particularly among pathogenic bacteria, and the approaches, both culture-dependent and culture-independent, which can be taken to investigate the microbial composition of milk are compared.
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High-throughput sequencing for detection of subpopulations of bacteria not previously associated with artisanal cheeses.

TL;DR: High-throughput sequencing was employed to reveal the highly diverse bacterial populations present in 62 Irish artisanal cheeses and, in some cases, associated cheese rinds and revealed the presence of several genera not previously associated with cheese, including Faecalibacterium, Prevotella, and Helcococcus.
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Molecular approaches to analysing the microbial composition of raw milk and raw milk cheese.

TL;DR: The benefits associated with culture-independent methods are highlighted, which include enhanced sensitivity, rapidity and the detection of microorganisms not previously associated with such products.
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The microbial content of raw and pasteurized cow milk as determined by molecular approaches

TL;DR: Assessment of the microbial population of milk from a selection of commercial milk producers, pre- and postpasteurization reveals the presence of a previously unrecognized and diverse bacterial population in unpasteurized cow milk, and identifies several bacterial genera for the first time.
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A comparison of methods used to extract bacterial DNA from raw milk and raw milk cheese

TL;DR: Seven different methods which have been designed or modified to extract total DNA from raw milk and raw milk cheese with a view to its subsequent use for the PCR of bacterial DNA are compared.