Evidence map›Paper›PMID 22865061›Full record

ArticleApplied and environmental microbiology2012

Genotyping of present-day and historical Geobacillus species isolates from milk powders by high-resolution melt analysis of multiple variable-number tandem-repeat loci.

R Brent Seale, Rajat Dhakal, Kanika Chauhan, Heather M Craven, Hilton C Deeth, Christopher J Pillidge, Ian B Powell, Mark S Turner

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Article in Applied and environmental microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

R Brent SealeSchool of Agriculture and Food Sciences, The University of Queensland, St. Lucia Campus, Brisbane, Queensland, Australia. r.seale@uq.edu.au
Rajat Dhakal
Kanika Chauhan
Heather M Craven
Hilton C Deeth
Christopher J Pillidge
Ian B Powell
Mark S Turner

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spores of thermophilic Geobacillus species are a common contaminant of milk powder worldwide due to their ability to form biofilms within processing plants. Genotyping methods can provide information regarding the source and monitoring of contamination. A new genotyping method was developed based on multilocus variable-number tandem-repeat (VNTR) analysis (MLVA) in conjunction with high-resolution melt analysis (MLV-HRMA) and compared to the currently used method, randomized amplified polymorphic DNA PCR (RAPD-PCR). Four VNTR loci were identified and used to genotype 46 Geobacillus isolates obtained from retailed powder and samples from 2 different milk powder processing plants. These 46 isolates were differentiated into 16 different groups using MLV-HRMA (D = 0.89). In contrast, only 13 RAPD-PCR genotypes were identified among the 46 isolates (D = 0.79). This new method was then used to analyze 35 isolates obtained from powders with high spore counts (>10(4) spores · g(-1)) from a single processing plant together with 27 historical isolates obtained from powder samples processed in the same region of Australia 17 years ago. Results showed that three genotypes can coexist in a single processing run, while the same genotypes observed 17 years ago are present today. While certain genotypes could be responsible for powders with high spore counts, there was no correlation to specific genotypes being present in powder plants and retailed samples. In conclusion, the MLV-HRMA method is useful for genotyping Geobacillus spp. to provide insight into the prevalence and persistence of certain genotypes within milk powder processing plants.

Indexed as

Food HandlingMinisatellite RepeatsAnimalsAustraliaCluster AnalysisGenotypeGeobacillusMilkMolecular TypingRandom Amplified Polymorphic DNA TechniqueTransition Temperature

Identifiers

PMID22865061
PMCPMC3457474

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