Screening for L-form bacteria
Disclosed herein are methods for screening clinical or biological samples to determine the presence of L-form bacteria within the sample. Methods include contacting a sample to a liquid growth medium and incubating the liquid growth medium at a temperature lower than 37 degrees C. The liquid growth medium is monitored for L-form bacterial growth. An amount of the liquid growth medium is transferred as an inoculant to a solid growth medium, and the solid growth medium is incubated under conditions that maintain a hydrated state of the inoculant to enable the L-form bacteria to efficiently interface with the solid growth medium and continue to grow.
1. A method for culturing of L-form bacteria within a sample, the method comprising:
(i) contacting a biological sample that has been treated to remove immune cell components to a first growth medium, wherein the first growth medium is a liquid, and wherein the first growth medium is a complex growth medium consisting of R2A media, chocolate blood, blood, Vogel Johnson media, Kligler's iron media, Columbia media, tryptic soy, Tinsdale media, Mueller-Hinton media, MacConkey media, brain-heart infusion (BHI) media, or lysogeny broth media;
(ii) incubating the first growth medium at a temperature above 20° C. and below 37° C., under conditions omitting rocking or shaking, to form an inoculant;
(iii) transferring a portion of the inoculant to a second growth medium, wherein the second growth medium is incorporated into a solid substrate;
(iv) immediately covering the inoculant on the solid substrate with an insert;
(v) incubating the solid substrate for less than thirty days under conditions that maintain a hydrated state of the inoculant on the sold substrate; and,
(vi) monitoring the solid substrate for the presence of bacterial colonies.
2. The method of claim 1 , wherein the biological sample is a blood sample, lymph fluid sample, mucous sample, cerebrospinal fluid sample, synovial fluid sample, or urine sample.
3. The method of claim 1 , wherein the treatment to remove immune cell components comprises filtration of the sample.
4. The method of claim 1 , wherein the method further comprises a step of monitoring the inoculant to detect the presence of L-form bacteria prior to transferring the portion of the inoculant to the second growth medium.
5. The method of claim 4 , wherein the monitoring comprises visual monitoring by microscopy.
6. The method of claim 1 , wherein the inoculant on the solid substrate is covered with an insert within seconds of the transfer.
7. The method of claim 6 , wherein the insert is a glass slide or a glass panel.
8. The method of claim 1 , wherein the second growth medium is selected from a complex growth medium, a defined growth medium, and a selective growth medium.
9. The method of claim 1 , wherein the solid substrate is incubated with the inoculant side facing down.
10. The method of claim 1 , wherein the solid substrate is incubated at a temperature between 30° C. and 40° C.
11. The method of claim 1 , wherein the solid substrate is incubated at a relative humidity of about 40% to 100%.
12. The method of claim 1 , further comprising the step of isolating one or more bacterial colonies.
13. The method of claim 12 , wherein the one or more bacterial colonies are identified, wherein the identifying comprises performing a polymerase chain reaction (PCR).
14. The method of claim 12 , wherein the one or more bacterial colonies are contacted with one or more antimicrobial compounds.
15. The method of claim 1 , wherein the sample has undergone comminuting prior to the treatment to remove immune cell components.
16. The method of claim 15 , wherein the comminuting is performed in a comminuting container containing comminuting media.
17. The method of claim 16 , wherein the comminuting media comprises beads, shards, particles, fragments, or filaments.
18. The method of claim 16 , wherein the comminuting media is formed out of glass, metal, plastic, ceramic, or any combination thereof.