Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Optimization of a Phage Amplification Assay To Permit Accurate Enumeration of Viable Mycobacterium avium subsp. paratuberculosis Cells

25 Apr 2009

Abstract excerpt

A commercially available phage amplification assay, FASTPlaqueTB (Biotec Laboratories, Ipswich, United Kingdom), when used according to the manufacturer's instructions, does not permit accurate enumeration of Mycobacterium avium subsp. paratuberculosis. The aim of this study was to optimize the phage amplification assay conditions to permit accurate quantification of viable M. avium subsp. paratuberculosis cells....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Infectious Diseases and Mycology
Share to Mycobacterium research and diagnosis
Share to Tuberculosis Research and Epidemiology

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19395561
DOI: 10.1128/aem.00294-09

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Optimization of a Phage Amplification Assay To Permit Accurate Enumeration of Viable Mycobacterium avium subsp. paratuberculosis CellsPMID 19395561Read ↗

Bacteriophage-Based Methods for Detection of Viable Mycobacterium avium subsp. paratuberculosis and Their Potential for Diagnosis of Johne's DiseaseSemantic proximity Read ↗

Development of a New, Combined Rapid Method Using Phage and PCR for Detection and Identification of Viable <i>Mycobacterium paratuberculosis</i> Bacteria within 48 HoursSemantic proximity Read ↗

A novel one-day phage-based test for rapid detection and enumeration of viable Mycobacterium avium subsp. paratuberculosis in cows’ milkSemantic proximity Read ↗

Phage infection, transfection and transformation of Mycobacterium avium complex and Mycobacterium paratuberculosisSemantic proximity Read ↗

Phage Amplification Assay for Detection of Mycobacterial Infection: A ReviewSemantic proximity Read ↗

Use of a phage-based assay for phenotypic detection of mycobacteria directly from sputum.Semantic proximity Read ↗

Development of a rapid phage-based method for the detection of viable Mycobacterium avium subsp. paratuberculosis in blood within 48 hSemantic proximity Read ↗

Development of an F57 Sequence-Based Real-Time PCR Assay for Detection ofMycobacterium aviumsubsp.paratuberculosisin MilkSemantic proximity Read ↗

Evaluation of quantitative polymerase chain reaction assays targeting Mycobacterium avium, M. intracellulare, and M. avium subspecies paratuberculosis in drinking water biofilmsSemantic proximity Read ↗

Comparative evaluation of the MGITTM and BACTEC culture systems for the recovery of Mycobacterium avium subsp. paratuberculosis from milkSemantic proximity Read ↗

Mycobacterium Avium subsp. paratuberculosis isolates induce in vitro granuloma formation and show successful survival phenotype, common anti-inflammatory and antiapoptotic responses within ovine macrophages regardless of genotype or host of origin.Semantic proximity Read ↗

The development and use of Actiphage <sup>®</sup> to detect viable mycobacteria from bovine tuberculosis and Johne’s disease‐infected animalsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.