Literature DB >> 22933596

Cryopreservation of Mycobacterium tuberculosis complex cells.

Zhiquan Shu1, Kris M Weigel, Scott D Soelberg, Annie Lakey, Gerard A Cangelosi, Kyong-Hoon Lee, Jae-Hyun Chung, Dayong Gao.   

Abstract

Successful long-term preservation of Mycobacterium tuberculosis cells is important for sample transport, research, biobanking, and the development of new drugs, vaccines, biomarkers, and diagnostics. In this report, Mycobacterium bovis bacillus Calmette-Guérin and M. tuberculosis H37Ra were used as models of M. tuberculosis complex strains to study cryopreservation of M. tuberculosis complex cells in diverse sample matrices at different cooling rates. Cells were cryopreserved in diverse sample matrices, namely, phosphate-buffered saline (PBS), Middlebrook 7H9 medium with or without added glycerol, and human sputum. The efficacy of cryopreservation was quantified by microbiological culture and microscopy with BacLight LIVE/DEAD staining. In all sample matrices examined, the microbiological culture results showed that the cooling rate was the most critical factor influencing cell viability. Slow cooling (a few degrees Celsius per minute) resulted in much higher M. tuberculosis complex recovery rates than rapid cooling (direct immersion in liquid nitrogen) (P < 0.05). Among the three defined cryopreservation media (PBS, 7H9, and 7H9 plus glycerol), there was no significant differential effect on viability (P = 0.06 to 0.87). Preincubation of thawed M. tuberculosis complex cells in 7H9 broth for 20 h before culture on solid Middlebrook 7H10 plates did not help the recovery of the cells from cryoinjury (P = 0.14 to 0.71). The BacLight LIVE/DEAD staining kit, based on Syto 9 and propidium iodide (PI), was also applied to assess cell envelope integrity after cryopreservation. Using the kit, similar percentages of "live" cells with intact envelopes were observed for samples cryopreserved under different conditions, which was inconsistent with the microbiological culture results. This implies that suboptimal cryopreservation might not cause severe damage to the cell wall and/or membrane but instead cause intracellular injury, which leads to the loss of cell viability.

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Year:  2012        PMID: 22933596      PMCID: PMC3486236          DOI: 10.1128/JCM.00896-12

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  22 in total

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Journal:  Cytometry A       Date:  2004-10       Impact factor: 4.355

2.  Cryopreservation of human lymphocytes for assessment of lymphocyte subsets and natural killer cytotoxicity.

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Journal:  J Immunol Methods       Date:  1986-06-24       Impact factor: 2.303

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Journal:  Biopreserv Biobank       Date:  2009-06       Impact factor: 2.300

Review 4.  The role of intracellular freezing in the death of cells cooled at supraoptimal rates.

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Journal:  Cryobiology       Date:  1977-06       Impact factor: 2.487

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Journal:  Am J Physiol       Date:  1984-09

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Authors:  S J Duthie; L Pirie; A McE Jenkinson; S Narayanan
Journal:  Mutagenesis       Date:  2002-05       Impact factor: 3.000

8.  Reduced detection by Ziehl-Neelsen method of acid-fast bacilli in sputum samples preserved in cetylpyridinium chloride solution.

Authors:  N Selvakumar; S Sudhamathi; M Duraipandian; T R Frieden; P R Narayanan
Journal:  Int J Tuberc Lung Dis       Date:  2004-02       Impact factor: 2.373

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Journal:  Appl Microbiol       Date:  1972-09

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Authors:  S Y Wang; M L Hsu; C H Tzeng; H C Hsu; C K Ho
Journal:  Cryobiology       Date:  1998-08       Impact factor: 2.487

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  8 in total

1.  Evaluation of the Xpert MTB/RIF Ultra Assay for Direct Detection of Mycobacterium tuberculosis Complex in Smear-Negative Extrapulmonary Samples.

Authors:  Daniel Perez-Risco; David Rodriguez-Temporal; Ivan Valledor-Sanchez; Fernando Alcaide
Journal:  J Clin Microbiol       Date:  2018-08-27       Impact factor: 5.948

Review 2.  Dead or alive: molecular assessment of microbial viability.

Authors:  Gerard A Cangelosi; John S Meschke
Journal:  Appl Environ Microbiol       Date:  2014-07-18       Impact factor: 4.792

3.  Survival of Bacterial and Parasitic Pathogens from Zebrafish (Danio rerio) After Cryopreservation and Thawing.

Authors:  Lauren J Norris; Virginia Watral; Michael L Kent
Journal:  Zebrafish       Date:  2018-01-25       Impact factor: 1.985

4.  Biosecurity and Health Monitoring at the Zebrafish International Resource Center.

Authors:  Katrina N Murray; Zoltán M Varga; Michael L Kent
Journal:  Zebrafish       Date:  2016-03-31       Impact factor: 1.985

5.  A Rapid Method for Quantifying Viable Mycobacterium avium subsp. paratuberculosis in Cellular Infection Assays.

Authors:  Hannah B Pooley; Kumudika de Silva; Auriol C Purdie; Douglas J Begg; Richard J Whittington; Karren M Plain
Journal:  Appl Environ Microbiol       Date:  2016-08-30       Impact factor: 4.792

6.  Biosynthetic enhancement of the detection of bacteria by the polymerase chain reaction.

Authors:  Julie S Do; Kris M Weigel; John S Meschke; Gerard A Cangelosi
Journal:  PLoS One       Date:  2014-01-17       Impact factor: 3.240

7.  Phenotypically Adapted Mycobacterium tuberculosis Populations from Sputum Are Tolerant to First-Line Drugs.

Authors:  Obolbek Turapov; Benjamin D O'Connor; Asel A Sarybaeva; Caroline Williams; Hemu Patel; Abdullaat S Kadyrov; Akpay S Sarybaev; Gerrit Woltmann; Michael R Barer; Galina V Mukamolova
Journal:  Antimicrob Agents Chemother       Date:  2016-03-25       Impact factor: 5.191

8.  Characterization of Drug-Resistant Lipid-Dependent Differentially Detectable Mycobacterium tuberculosis.

Authors:  Annelies W Mesman; Seung-Hun Baek; Chuan-Chin Huang; Young-Mi Kim; Sang-Nae Cho; Thomas R Ioerger; Nadia N Barreda; Roger Calderon; Christopher M Sassetti; Megan B Murray
Journal:  J Clin Med       Date:  2021-07-23       Impact factor: 4.241

  8 in total

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