Antibiotic susceptibility testing

Claim 1

A method for performing simultaneously a plurality of interrelated optical density tests, employing a sample tray having a multiplicity of wells in rectangular grid arrangement containing liquid samples, said wells having translucent bottoms, comprising: holding said tray accurately in a single predetermined stationary reading position without blocking off light paths through said wells, sending light from a light source through all said wells at approximately the same intensity to an array of light-intensity-detecting well-associated photocells, there being one photocell adjacent to each well, while simultaneously sending light directly from said light source to a reference detecting photocell without passing the light through a said sample, electronically sequentially transmitting the signals from all said photocells in a prescribed order, each signal corresponding to the intensity of light received by a said photocell, sequentially comparing the signal from each said well-associated photocell of said array with the simultaneous signal from said reference detecting photocell and developing a related signal therefrom for each well indicating a first adjusted value for each well, sequentially making an electronic comparison of each said related signal value with an electronically stored data reference value corresponding to a preliminary value for each well derived like said first adjusted value without interposing the sample between said light source and any of said well-associated photocells, and developing a resultant value from that comparison, sequentially comparing electronically said resultant values with one another for said interrelated optical density tests and with other stored values and determining a conclusion therefrom, and reading out the desired results thereby obained.

Claim 2

A method for performing simultaneously a plurality of interrelated optical density tests, employing a sample tray having a multiplicity of wells in rectangular grid arrangement containing liquid samples, said wells having translucent bottoms, comprising: holding said tray accurately in a single predetermined stationary reading position without blocking off light paths through said wells, sending light from a light source through all said wells at approximately the same intensity to an array of light-intensity-detecting well-associated photocells, there being one photocell adjacent to each well, while simultaneously sending light directly from said light source to a reference detecting photocell without passing the light through a said sample, electronically sequentially transmitting the signals from all said photocells in a prescribed order, each signal corresponding to the intensity of light received by a said photocell, sequentially comparing the signal from each said well-associated photocell of said array with the simultaneous signal from said reference detecting photocell and developing a related signal therefrom for each well indicating a first adjusted value for each well, sequentially making an electronic comparison of each said related signal value with an electronically stored data reference value corresponding to a preliminary value for each well derived like said first adjusted value without interposing the sample between said light source and any of said well-associated photocells, and developing a resultant value from that comparison, sequentially comparing electronically said resultant values with one another for said interrelated optical density tests and with other stored values and determining a conclusion therefrom, and reading out the desired results thereby obained.

Claim 6

A method for performing simultaneously a plurality of interrelated optical density tests, employing a sample tray having a multiplicity of wells in a rectangular grid, said wells having translucent bottoms, comprising: (a) sending light from a light source vertically at approximately the same intensity to an array of light-intensity-detecting well-associated photocells, there being one photocell corresponding to each well, (b) while simultaneously sending light directly from said light source to a reference detecting photocell, (c) electronically sequentially transmitting the signal from all said photocells in a prescribed order, each signal corresponding to the intensity of light received by a said photocell, (d) sequentially comparing the signal from each said photocell of said array with the simultaneous signal from said reference detecting photocell and developing a first related signal therefrom for each well-associated photocell, (e) storing said first related signal in a digital computer forming an integral part of the system, (f) holding the tray having its wells filled with liquid samples, accurately in a single predetermined reading position without blocking off light paths through said wells, (g) sending light from said light source vertically through all said filled wells at roughly the same intensity to the same said array of light-intensity-detecting well-associated photocells, there being one photocell for each well, (h) while simultaneously sending light directly from said light source to said reference detecting photocell without passing the light through a said sample, (i) electronically sequentially transmitting the signals for filled wells from all said photocells in a prescribed order, each signal corresponding to the intensity of light received by a said photocell, (j) sequentially comparing electronically, in the digital computer, the signal for the filled wells from each said photocell of said array with the signal from said reference detecting photocell and developing a second related signal therefrom for each well, (k) sequentially making an electronic comparison of each said second related signal value with the corresponding stored first related signal value for the same well, and developing a resultant value from that comparison, (l) sequentially comparing electronically said resultant values with one another for said interrelated optical density tests and with other stored values and determining a desired result from that comparison, and reading out the desired results thereby obtained.

Claim 7

A method for performing simultaneously a plurality of interrelated optical density tests, employing a sample tray having a multiplicity of wells in a rectangular grid, said wells having translucent bottoms, comprising: (a) sending light from a light source vertically at approximately the same intensity to an array of light-intensity-detecting well-associated photocells, there being one photocell corresponding to each well, (b) while simultaneously sending light directly from said light source to a reference detecting photocell, (c) electronically sequentially transmitting the signal from all said photocells in a prescribed order, each signal corresponding to the intensity of light received by a said photocell, (d) sequentially comparing the signal from each said photocell of said array with the simultaneous signal from said reference detecting photocell and developing a first related signal therefrom for each well-associated photocell, (e) storing said first related signal in a digital computer forming an integral part of the system, (f) holding the tray having its wells filled with liquid samples, accurately in a single predetermined reading position without blocking off light paths through said wells, (g) sending light from said light source vertically through all said filled wells at roughly the same intensity to the same said array of light-intensity-detecting well-associated photocells, there being one photocell for each well, (h) while simultaneously sending light directly from said light source to said reference detecting photocell without passing the light through a said sample, (i) electronically sequentially transmitting the signals for filled wells from all said photocells in a prescribed order, each signal corresponding to the intensity of light received by a said photocell, (j) sequentially comparing electronically, in the digital computer, the signal for the filled wells from each said photocell of said array with the signal from said reference detecting photocell and developing a second related signal therefrom for each well, (k) sequentially making an electronic comparison of each said second related signal value with the corresponding stored first related signal value for the same well, and developing a resultant value from that comparison, (l) sequentially comparing electronically said resultant values with one another for said interrelated optical density tests and with other stored values and determining a desired result from that comparison, and reading out the desired results thereby obtained.

Claim 8

A method for determining susceptibility of a bacteria culture to various antimicrobic drugs and of determining the minimum inhibitory concentration of the bacteria culture to those drugs to which it is susceptible, utilizing a plurality of interrelated optical density tests, comprising: providing a microtube tray having a rectangular grid array of many light-transmissive wells, and a series of photodetectors, including a photodetector associated with each said well and a reference photodetector not associated with a tray well, each photodetector being adapted to provide a signal corresponding to the sensed light intensity, initially calibrating the photodetectors by passing light from a source of generally uniform intensity to the photodetectors and electronically sequencing the photodetectors to read a signal from each photodetector, comparing in a onboard computer the values of the signals obtained for each well-associated photodetector sequentially with the value of the reference signal obtained simultaneously for the reference photodetector, and providing an initial calibration value for each well-associated photodetector which is a function of the well photodetector signal and the reference signal, and with the computer, storing and retaining the calibration value for each wel-associated photodetector, placing in the wells a plurality of different antimicrobic drugs, each drug being included in a series of wells in serially diluted known concentration of the bacteria, and placing the wells adjacent to the well-associated photodetectors, following a period for bacterial growth, passing light of generally uniform intensity simultaneously through each well and to the reference photodetector and reading the intensity of the transmitted light with the photodetectors by electronically sequencing the photodetectors to read an after-culture signal from each, comparing in the computer the value of each after-culture signal obtained from the well-associated photodetectors sequentially with the value of the after-culture signal obtained substantially simultaneously from the reference photodetector and providing an after-culture value for each well-associated photodetector which is a function of the after-culture well photodetector signal and the after-culture reference signal, comparing in the computer, for each well, the after-culture value with the initial calibration value and providing a comparison signal for each well which allows for variations in the intensity of the light directed from the source onto the different wells and for variations in the sensitivities of the photocells, automatically and sequentially comparing in the computer the comparison signal values with one another and with a limit comparison signal value which represents a cutoff between inhibition and growth, correlating in the computer the comparisons with stored data identifying the antimicrobic drug and concentration in each well, and obtaining therefrom an indication of which antimicrobic drugs inhibit growth of the bacteria, automatically selecting with the computer the minimum inhibitory concentration of each inhibitory drug by selecting the minimum concentration of each drug which produced a comparison signal value on the inhibition side of the limit comparison signal value, and automatically displaying in situ the minimum inhibitory concentration for each inhibitory drug, and, for each drug that does not inhibit growth, displaying that the bacteria is resistant to that drug.

Claim 9

A method for determining susceptibility of a bacteria culture to various antimicrobic drugs and of determining the minimum inhibitory concentration of the bacteria culture to those drugs to which it is susceptible, utilizing a plurality of interrelated optical density tests, comprising: providing a microtube tray having a rectangular grid array of many light-transmissive wells, and a series of photodetectors, including a photodetector associated with each said well and a reference photodetector not associated with a tray well, each photodetector being adapted to provide a signal corresponding to the sensed light intensity, initially calibrating the photodetectors by passing light from a source of generally uniform intensity to the photodetectors and electronically sequencing the photodetectors to read a signal from each photodetector, comparing in a onboard computer the values of the signals obtained for each well-associated photodetector sequentially with the value of the reference signal obtained simultaneously for the reference photodetector, and providing an initial calibration value for each well-associated photodetector which is a function of the well photodetector signal and the reference signal, and with the computer, storing and retaining the calibration value for each wel-associated photodetector, placing in the wells a plurality of different antimicrobic drugs, each drug being included in a series of wells in serially diluted known concentration of the bacteria, and placing the wells adjacent to the well-associated photodetectors, following a period for bacterial growth, passing light of generally uniform intensity simultaneously through each well and to the reference photodetector and reading the intensity of the transmitted light with the photodetectors by electronically sequencing the photodetectors to read an after-culture signal from each, comparing in the computer the value of each after-culture signal obtained from the well-associated photodetectors sequentially with the value of the after-culture signal obtained substantially simultaneously from the reference photodetector and providing an after-culture value for each well-associated photodetector which is a function of the after-culture well photodetector signal and the after-culture reference signal, comparing in the computer, for each well, the after-culture value with the initial calibration value and providing a comparison signal for each well which allows for variations in the intensity of the light directed from the source onto the different wells and for variations in the sensitivities of the photocells, automatically and sequentially comparing in the computer the comparison signal values with one another and with a limit comparison signal value which represents a cutoff between inhibition and growth, correlating in the computer the comparisons with stored data identifying the antimicrobic drug and concentration in each well, and obtaining therefrom an indication of which antimicrobic drugs inhibit growth of the bacteria, automatically selecting with the computer the minimum inhibitory concentration of each inhibitory drug by selecting the minimum concentration of each drug which produced a comparison signal value on the inhibition side of the limit comparison signal value, and automatically displaying in situ the minimum inhibitory concentration for each inhibitory drug, and, for each drug that does not inhibit growth, displaying that the bacteria is resistant to that drug.

Claim 18

A method of identifying microorganisms, comprising: placing a series of different reagents in a large number of wells arranged in a rectangular grid in a light-transmissive sample tray held stationary throughout the method, establishing a known uniform concentration of a culture of the microorganism and placing the uniform concentration in equal volumes in the wells, following a predetermined period for bacterial growth, passing light from a light source in substantially equal intensity through all said wells and through a color filter and collimator, according to the opacity value for each well, initiating an automatic sequence while the tray is held stationary of (a) automatically sensing the intensity of the collimated light transmitted through each well by photodetector means adjacent to the wells and filter and opposite the light source, (b) automatically and electronically sequentially comparing, in a computer, the opacity values for each well with an opacity for light from the same source not passing through any well but passing through the filter, and generating a signal from such comparison, (c) automatically and sequentially comparing that signal with a value corresponding to inhibited reaction for each well, (d) automatically and sequentially comparing the opacity values from different tests to obtain probability values for various suspected organisms, (e) automatically and sequentially comparing these probability values with computer-stored information about the suspected organisms, and (f) automatically and sequentially printing the names of the most probable organism and the computer probability values for each.

Claim 19

A method of identifying microorganisms, comprising: placing a series of different reagents in a large number of wells arranged in a rectangular grid in a light-transmissive sample tray held stationary throughout the method, establishing a known uniform concentration of a culture of the microorganism and placing the uniform concentration in equal volumes in the wells, following a predetermined period for bacterial growth, passing light from a light source in substantially equal intensity through all said wells and through a color filter and collimator, according to the opacity value for each well, initiating an automatic sequence while the tray is held stationary of (a) automatically sensing the intensity of the collimated light transmitted through each well by photodetector means adjacent to the wells and filter and opposite the light source, (b) automatically and electronically sequentially comparing, in a computer, the opacity values for each well with an opacity for light from the same source not passing through any well but passing through the filter, and generating a signal from such comparison, (c) automatically and sequentially comparing that signal with a value corresponding to inhibited reaction for each well, (d) automatically and sequentially comparing the opacity values from different tests to obtain probability values for various suspected organisms, (e) automatically and sequentially comparing these probability values with computer-stored information about the suspected organisms, and (f) automatically and sequentially printing the names of the most probable organism and the computer probability values for each.