Methods, systems, and devices for detecting and identifying microorganisms in microbiological culture samples

Patent metadata

Field	Value
Publication number	US-9874555-B2
Application number	US-201314391340-A
Country	US
Kind code	B2
Filing date	Mar 15, 2013
Priority date	Apr 12, 2012
Publication date	Jan 23, 2018
Grant date	Jan 23, 2018

Abstract

Provided herein are methods, systems, and devices for detecting and/or identifying one or more specific microorganisms in a culture sample. Indicator particles, such as surface enhanced Raman spectroscopy (SERS)-active nanoparticles, each having associated therewith one or more specific binding members having an affinity for the one or more microorganisms of interest, can form a complex with specific microorganisms in the culture sample. Further, agitating magnetic capture particles also having associated therewith one or more specific binding members having an affinity for the one or more microorganisms of interest can be used to capture the microorganism-indicator particle complex and concentrate the complex in a localized area of an assay vessel for subsequent detection and identification. The complex can be dispersed, pelleted, and redispersed so that the culture sample can be retested a number of times during incubation so as to allow for real-time monitoring of the culture sample.

First claim

The invention claimed is:

1. A method for detecting growth of one or more microorganisms in a sample, the method comprising:
(a) providing the sample suspected of containing the one or more microorganisms;
(b) disposing said sample in an assay vial, wherein said assay vial has disposed therein a culture medium capable of supporting microorganism growth to form a culture sample and a reagent comprising one or more indicator particles having associated therewith at least one specific binding member having an affinity for said one or more microorganisms; and one or more magnetic capture particles having associated therewith at least one specific binding member having an affinity for said one or more microorganisms, wherein the binding member associated with the indicator particles can be the same or different than the binding member associated with the magnetic capture particles;
(c) incubating the culture sample for a predetermined period of time to form a magnetic capture particle-microorganism-indicator particle complex if said one or more microorganisms are present in said sample, wherein incubating the culture sample promotes growth of said one or more microorganisms;
(d) agitating the assay vial;
(e) exposing said magnetic capture particle-microorganism-indicator particle complex to a magnetic field to induce said magnetic capture particle-microorganism-indicator particle complex to migrate to a localized area of said assay vial;
(f) optically interrogating said localized area of said assay vial to induce said capture particle-microorganism-indicator particle complex to produce a detectable signal indicating an amount of said one or more microorganisms in said sample;
(g) dispersing said magnetic capture particle-microorganism-indicator particle complex;
(h) repeating steps (c)-(g) one or more times; and
(i) determining whether said one or more microorganisms are present in said sample by comparing two or more of the detectable signals obtained in steps (c)-(h).

2. The method according to claim 1 , wherein steps (c)-(g) are repeated more than once, and wherein each repeating of steps (c)-(g) occurs in regular time intervals.

3. The method according to claim 1 , wherein steps (c) and (d) occur concurrently.

4. The method according to claim 1 , wherein step (e) forms a pellet comprising magnetic capture particle-microorganism-indicator particle complexes.

5. The method according to claim 4 , wherein the pellet is detectable using visual or optical means.

6. The method according to claim 1 , wherein the sample comprises a blood sample.

7. The method according to claim 1 , wherein the sample comprises a food sample.

8. The method according to claim 1 , wherein the sample comprises an environmental sample.

9. The method according to claim 1 , wherein the sample comprises an agricultural sample.

10. The method according to claim 1 , wherein disposing said sample in the assay vial comprises transferring a desired amount of said sample, along with optional culture media, from a vessel, wherein the vessel comprises: a container for receiving a culture sample therein, the container having an open end and a closed end; a lid configured to engage the open end of the container in a fluid-tight connection; a basket coupled to the lid and including at least one reservoir, the basket being disposed between the open end and the closed end of the container, the reservoir configured to hold a volume of the culture sample therein; and at least one needle assembly engaged with the lid, the needle assembly including a needle extending within the reservoir, wherein the needle is configured to selectively withdraw the culture sample contained in the reservoir, and wherein the needle is further configured to engage the assay vial for a biocontained transfer of the culture sample from the reservoir to the assay vial.

11. The method according to claim 1 , wherein disposing said sample in an assay vial comprises extracting the sample, along with culture media, in a biocontained fashion from a vessel in which the magnetic capture particles and indicator particles are not present.

Assignees

• Becton Dickinson Co
• Becton Dickinson Co

Inventors

• Weidemaier Kristin
• Campbell Robert L
• Carruthers Erin Gooch
• Curry Adam C
• Dolan Kevin G
• Liebmann-Vinson Andrea
• Woodley Wendy Dale
• Kuroda Melody M H
• Fallows Eric A
• Bartkowiak Miroslaw
• Danhof Scott N
• Kramer Gregory S
• Haubert Thomas D
• Marshall Michael L
• Prescott James A
• Somerville Randy J
• Ulrich M Scott
• Sebba David S

Classifications

• C12M23/38

  Caps; Covers; Plugs; Pouring means · CPC title

• G01N35/0098

  involving analyte bound to insoluble magnetic carrier, e.g. using magnetic separation (magnetic particles used in immunoassays G01N33/54326; magnetic separation in general B03C) · CPC title

• G01N33/56911 Primary

  Bacteria · CPC title

• B03C2201/26

  for use in medical or biological applications · CPC title

• B03C1/288

  disposed at the outer circumference of a recipient · CPC title