A novel TaqMan qPCR assay for rapid detection and quantification of pro-inflammatory microalgae Prototheca spp. in milk samples
Language English Country Great Britain, England Media print
Document type Journal Article
Grant support
MZE-RO0518
Ministry of Agriculture
QK1910092
National Agency for Agricultural Research
PubMed
33515018
DOI
10.1093/mmy/myaa120
PII: 6123940
Knihovny.cz E-resources
- Keywords
- limit of detection, Prototheca bovis, milk, real-time PCR,
- MeSH
- DNA chemistry isolation & purification MeSH
- Farms MeSH
- Cloning, Molecular MeSH
- Real-Time Polymerase Chain Reaction methods MeSH
- Limit of Detection MeSH
- Environmental Microbiology MeSH
- Dairying MeSH
- Milk microbiology MeSH
- Multiplex Polymerase Chain Reaction methods MeSH
- Plasmids genetics MeSH
- Prototheca genetics growth & development isolation & purification MeSH
- Sensitivity and Specificity MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- DNA MeSH
Animal or human protothecosis belongs to rather rare, endemic, pro-inflammatory infections. It is caused by achlorophyllous algae of the genus Prototheca. Especially, P. bovis (formerly P. zopfii genotype 2) is often inflected as a non-bacterial causative agent of dairy cattle mastitis. In this study, we present a multiplex real-time PCR (qPCR) system for rapid and exact Prototheca spp. detection and quantification. Limit of detection, diagnostic sensitivity, and specificity were determined. For the first time, specific sequences of AccD (encoding acetyl CoA reductase) for P. bovis, cox1 (encoding cytochrome C oxidase subunit 1) for P. wickerhamii, cytB (encoding cytochrome B) for P. blashkeae and atp6 (encoding transporting ATPase F0 subunit 6) for P. ciferrii (formerly P. zopfii genotype 1) were used for species identification and quantification together with 28S rRNA sequence detecting genus Prototheca. The developed qPCR assay was applied to 55 individual cow milk samples from a herd suspected of protothecosis, 41 bulk milk samples from different Czech farms, 16 boxed milk samples purchased in supermarkets and 21 environmental samples originating from a farm suspected of protothecosis. Our work thus offers the possibility to diagnose protothecosis in the samples, where bacterial mastitis is the most commonly presumed and thereby assisting adequate corrective measures to be taken.
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