Evidence map›Paper›PMID 28601089›Full record

ArticleBiological research2017

Rapid culture-based detection of living mycobacteria using microchannel electrical impedance spectroscopy (m-EIS).

Roli Kargupta, Sachidevi Puttaswamy, Aiden J Lee, Timothy E Butler, Zhongyu Li, Sounak Chakraborty, Shramik Sengupta

Abstract read
In one paragraph

Article in Biological research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Roli KarguptaDepartment of Bioengineering, University of Missouri, 252 Agricultural Engineering Building, 1406 E. Rollins Street, Columbia, MO, 65211, USA.
Sachidevi PuttaswamyDepartment of Bioengineering, University of Missouri, 252 Agricultural Engineering Building, 1406 E. Rollins Street, Columbia, MO, 65211, USA.
Aiden J LeeDepartment of Bioengineering, University of Missouri, 252 Agricultural Engineering Building, 1406 E. Rollins Street, Columbia, MO, 65211, USA.
Timothy E ButlerDepartment of Bioengineering, University of Missouri, 252 Agricultural Engineering Building, 1406 E. Rollins Street, Columbia, MO, 65211, USA.
Zhongyu LiDepartment of Statistics, University of Missouri, Columbia, MO, USA.
Sounak ChakrabortyDepartment of Bioengineering, University of Missouri, 252 Agricultural Engineering Building, 1406 E. Rollins Street, Columbia, MO, 65211, USA.
Shramik SenguptaDepartment of Bioengineering, University of Missouri, 252 Agricultural Engineering Building, 1406 E. Rollins Street, Columbia, MO, 65211, USA. senguptas@missouri.edu.

Funding

Electrical System for Rapidly Detecting Viable Bacteria in Blood CultureR44AI096572 · NIAID · TECHSHOT, INC. · PI BOLAND, EUGENE DAVID · 2014 to 2016
$2.9M
NIAID NIH HHS R44 AI096572
6 · The paper itself

Abstract

backgroundMultiple techniques exist for detecting Mycobacteria, each having its own advantages and drawbacks. Among them, automated culture-based systems like the BACTEC-MGIT™ are popular because they are inexpensive, reliable and highly accurate. However, they have a relatively long "time-to-detection" (TTD). Hence, a method that retains the reliability and low-cost of the MGIT system, while reducing TTD would be highly desirable.

methodsLiving bacterial cells possess a membrane potential, on account of which they store charge when subjected to an AC-field. This charge storage (bulk capacitance) can be estimated using impedance measurements at multiple frequencies. An increase in the number of living cells during culture is reflected in an increase in bulk capacitance, and this forms the basis of our detection. M. bovis BCG and M. smegmatis suspensions with differing initial loads are cultured in MGIT media supplemented with OADC and Middlebrook 7H9 media respectively, electrical "scans" taken at regular intervals and the bulk capacitance estimated from the scans. Bulk capacitance estimates at later time-points are statistically compared to the suspension's baseline value. A statistically significant increase is assumed to indicate the presence of proliferating mycobacteria.

resultsOur TTDs were 60 and 36 h for M. bovis BCG and 20 and 9 h for M. smegmatis with initial loads of 1000 CFU/ml and 100,000 CFU/ml respectively. The corresponding TTDs for the commercial BACTEC MGIT 960 system were 131 and 84.6 h for M. bovis BCG and 41.7 and 12 h for M smegmatis, respectively.

conclusionOur culture-based detection method using multi-frequency impedance measurements is capable of detecting mycobacteria faster than current commercial systems.

Indexed as

Dielectric SpectroscopyBacteriological TechniquesCulture MediaHumansMycobacteriumReproducibility of ResultsTime FactorsCulture MediaBD Bactec MGIT 960Electrical impedance spectroscopyM. bovis BCGM. smegmatisMycobacteriaTuberculosis

Identifiers

PMID28601089
PMCPMC5466763

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.