Vaš brskalnik ne omogoča JavaScript!
JavaScript je nujen za pravilno delovanje teh spletnih strani. Omogočite JavaScript ali pa uporabite sodobnejši brskalnik.
Nacionalni portal odprte znanosti
Odprta znanost
DiKUL
slv
|
eng
Iskanje
Brskanje
Novo v RUL
Kaj je RUL
V številkah
Pomoč
Prijava
A loop-mediated isothermal amplification (LAMP) assay for the rapid detection of Enterococcus spp. in water
ID
Martzy, Roland
(
Avtor
),
ID
Kolm, Claudia
(
Avtor
),
ID
Brunner, Kurt
(
Avtor
),
ID
Mach, Robert L.
(
Avtor
),
ID
Krska, Rudolf
(
Avtor
),
ID
Šinkovec, Hana
(
Avtor
),
ID
Sommer, Regina
(
Avtor
),
ID
Farnleitner, Andreas H.
(
Avtor
),
ID
Reischer, Georg H.
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(686,33 KB)
MD5: 877C429ED158ABE3D647F39901A1A9AC
URL - Izvorni URL, za dostop obiščite
https://www.sciencedirect.com/science/article/pii/S0043135417303603
Galerija slik
Izvleček
Faecal pollution of water and the resulting potential presence of human enteric pathogens is a predominant threat to public health. Microbiological water quality can be assessed by the detection of standard faecal indicator bacteria (SFIB) such as E. coli or certain Enterococcus species. In recent years, isothermal amplification methods have become a useful alternative to polymerase chain reaction (PCR), allowing molecular diagnostics with simple or no instrumentation. In this study, a novel screening method for the molecular detection of Enterococcus spp. by loop-mediated isothermal amplification (LAMP) is described. A set of six specific LAMP primers was designed to amplify a diagnostic fragment of the Enterococcus 23S rRNA gene, which is present in several enterococcal species targeted by quantitative PCR (qPCR), which is the standard technique recommended by the US Environmental Protection Agency. Sensitivity and specificity tests were performed using a set of 30 Enterococcus and non-target bacterial reference strains. It is shown that LAMP is equally sensitive and even more specific than the qPCR assay. A dilution series of Enterococcus faecalis DNA revealed that the LAMP method can reliably detect 130 DNA target copies per reaction within 45 min. Additionally, enterococci isolated from Austrian surface waterbodies, as well as a set of DNA extracts from environmental waters, were tested. Contingency analysis demonstrated a highly significant correlation between the results of the developed LAMP assay and the reference qPCR method. Furthermore, a simple staining procedure with a fluorescence dye demonstrated the identification of amplified products by eye. In conclusion, this method is an important component for the efficient screening and testing of water samples in low-resource settings lacking sophisticated laboratory equipment and highly trained personnel, requiring only a simple heating block.
Jezik:
Angleški jezik
Ključne besede:
Enterococcus spp.
,
faecal indicator bacteria
,
loop-mediated isothermal amplification
,
microbiological water quality
,
low-resource methods
,
molecular diagnostics
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
BF - Biotehniška fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2017
Št. strani:
Str. 62-69
Številčenje:
Vol. 122
PID:
20.500.12556/RUL-153147
UDK:
61
ISSN pri članku:
1879-2448
DOI:
10.1016/j.watres.2017.05.023
COBISS.SI-ID:
178110723
Datum objave v RUL:
19.12.2023
Število ogledov:
902
Število prenosov:
45
Metapodatki:
Citiraj gradivo
Navadno besedilo
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Kopiraj citat
Objavi na:
Gradivo je del revije
Naslov:
Water Research
Založnik:
Pergamon
ISSN:
1879-2448
COBISS.SI-ID:
23055365
Podobna dela
Podobna dela v RUL:
Podobna dela v drugih slovenskih zbirkah:
Nazaj