establishing and maintaining sf1ep cell stocks for treponema pallidum cultivation

<meta charset="utf8"></head><body>使用哺乳动物细胞共培养物对 梅毒螺旋 体进行可扩展的体外培养

Treponema pallidum is a species of spiral-shaped bacteria (called spirochetes) that causes syphilis and related infections in humans and other primates. Syphilis is a serious disease with long-term effects on infected individuals, and it is estimated that over 8 million new cases of syphilis occur worldwide each year1. T. pallidum has been subdivided into three subspecies based on the diseases they cause in humans as well as minor genetic differences: subspecies pallidum (which causes the sexually transmitted disease syphilis), subspecies pertenue (yaws), and subspecies endemicum (causing bejel or endemic syphilis)2,3. T. pallidum subsp. pertenue also causes infections in baboons, chimpanzees, and other primates. A closely related organism called Treponema paraluiscuniculi (also called Treponema paraluisleporidarum) causes an infection in rabbits and hares4,5. All of these bacteria are very closely related, with greater than 98% DNA sequence identity at the genome level6,7,8. They each have a single, small circular chromosome about 1.14 million base pairs (Mb) in size. The members of this T. pallidum group are found only in association with their mammalian hosts; as such, they are obligate pathogens that are dependent on their host species for survival and growth9,10.
Attempts to culture T. pallidum in vitro began shortly after its identification by Schaudinn and Hoffman in 190511,12. However, these efforts failed to lead to consistent, reproducible growth of the organism. As a result, T. pallidum research studies required propagation of the organism through the experimental infection of laboratory animals, most commonly the rabbit13,14. In 1981, Fieldsteel et al.15 introduced a tissue culture system that promoted the multiplication of T. pallidum strains for a period of up to 2 weeks. This system involved co-culture of T. pallidum with Sf1Ep cottontail rabbit epithelial cells in a modified tissue culture medium (T. pallidum Culture Medium 1, TpCM-1) based on Eagle&#39;s Minimum Essential Medium (MEM) and 20% fetal bovine serum (FBS). Other culture conditions required were incubation at 34 &#176;C in an atmosphere containing 1.5% O2 and 5% CO29,16. In this system, T. pallidum attaches to the Sf1Ep cells and multiplies when in close association with the mammalian cell surface. Despite many subculture attempts and other modifications, the Fieldsteel et al. system failed to promote continuous in vitro growth.
In 2018, our laboratory reported that the use of a modified medium called TpCM-2 (in which Eagle&#39;s MEM was replaced with a more complex tissue culture medium, CMRL 1066) provided T. pallidum the required nutrients to permit consistent long-term culture17. To date, this modification has led to a consistent, continuous culture of at least 5 strains of T. pallidum subsp. pallidum (Nichols, SS14, Mexico A, UW231B, and UW249B) and one strain of T. pallidum subsp. endemicum (Bosnia A)18,19. As an example, the Nichols strain has now been cultured continuously in vitro for over 6 years. Thus far, attempts to culture yaws isolates (T. pallidum subsp. pertenue) or T. paraluiscuniculiin vitro have been unsuccessful18. The TpCM-2 system still requires the presence of Sf1Ep cells, low oxygen concentrations, and incubation at 34 &#176;C, making the system more complex than most bacterial culture techniques. However, this modified T. pallidum culture system has been useful for further defining the bacterium&#39;s growth requirements18, determining minimal inhibitory concentrations (MICs) of antimicrobial compounds and peptides20,21,22,23,24,25, propagating new strains from patient tissue aspirates26, isolating clonal populations of the organism27, characterizing the tprK antigenic variation system27,28, examining gene expression29, and performing mutational analysis30,31,32.
Here, we describe the current methods for cultivating T. pallidum in vitro. We hope this information will help facilitate the more widespread application of this in vitro culture technique to the improved diagnosis, treatment, and prevention of syphilis and related treponemal infections.

<meta charset="utf8"></head><body>作者聚焦：推进梅毒研究 — 梅毒螺旋 体培养和基因工程的创新

梅毒螺旋体（梅毒螺旋体）的体外培养程序

Much of our research is directed at gaining a better understanding of T.pallidum metabolism. Understanding its growth requirements will facilitate so many aspects of syphilis research. Understanding of the T.pallidum physiology, structure, host immunity, antimicrobial susceptibility, and perhaps ultimately, could lead to new methods of syphilis control.One of our biggest challenges is the presence of mammalian cells in the culture system. If we can determine what nutrients the cells are providing, we can remove them from the system and it would simplify it. That would allow us to have no contaminated mammalian cell DNA or protein, which would make the experimental analysis easier.For over 100 years after its initial isolation, T.pallidum was propagated through infection of rabbits. The in vitro culture system allows you to avoid the use of animals and is more cost effective. It also allows for techniques such as genetic engineering that would not be possible in the animal model.The availability of an in vitro culture method has already greatly expanded the number of groups studying Treponema pallidum. It has also led to advances such as the first mutagenesis of the organism, as well as high throughput screening of antibiotics for those useful in treating syphilis. In vitro culture has paved the way for the detailed analysis of T.pallidum growth requirements, gene function, and immune targets.These questions are difficult, if not impossible, to address effectively using just the rabbit model. We hope that these approaches will help improve the diagnosis, treatment, and prevention of syphilis. In addition to our efforts to improve the in vitro cultivation system, we will focus on genetic manipulation of T.pallidum through transposon mutagenesis.We hope to do a large scale functional screen to identify genes important in T.pallidum pathogenesis.

建立和维护用于 梅毒螺旋体 培养的 Sf1Ep 细胞储备

establishing-maintaining-sf1ep-cell-stocks-for-treponema-pallidum

Research

JoVE Journal

Immunology and Infection

Establishing and Maintaining Sf1Ep Cell Stocks for Treponema pallidum Cultivation

73 次观看. 首先，将新鲜制备的预热 Sf1Ep 细胞培养基和解冻的 Sf1Ep 细胞放入工作平台上的冷冻瓶中。向冻存管中加入 1 mL Sf1Ep 细胞培养基，并轻轻混匀。将混合物转移至含有 5 mL Sf1Ep 细胞培养基的无菌 15 mL 锥形离心管中，并轻轻混合。将细胞悬液以 100 G 离心 7 分钟，弃去上清液，然后将沉淀重悬于 15 mL 新鲜 Sf1Ep 细胞培养基中。将细胞悬液转移到 T75 组?...

视频: 建立和维护用于 梅毒螺旋体 培养的 Sf1Ep 细胞储备

Procedures for In Vitro Cultivation of Treponema pallidum, the Syphilis Spirochete

For over a century, Treponema pallidum subsp. pallidum, the spiral-shaped bacterium that causes syphilis, could only be propagated by inoculation and harvest of the organisms from rabbit testes. In 2018, we described a method to continuously cultivate T. pallidumin vitro. This system utilizes co-culture with rabbit epithelial cells (Sf1Ep cells) in a serum-containing tissue culture medium called TpCM-2. The T. pallidum doubling time in culture is similar to that estimated to occur during natural infection (about 33-45 h). The organism can be cultured continuously with a standard passage time of 1 week in a low oxygen (1.5%) environment at 34 &#176;C. This article contains the protocols for culturing T. pallidum, methods for growing and maintaining the required tissue culture cells, and the technique for generating isogenic strains by limiting dilution. The ability to grow T. pallidum in vitro provides new experimental avenues to study and understand this enigmatic organism.

This protocol describes in vitro cultivation of the syphilis pathogen Treponema pallidum subsp. pallidum in co-culture with mammalian cells. The method is scalable; it can be used to produce large quantities of T. pallidum and to generate clonal cultures.

For over a century, Treponema pallidum subsp. pallidum, the spiral-shaped bacterium that causes syphilis, could only be propagated by inoculation and ...

科研

免疫与感染

To begin, place freshly prepared prewarm Sf1Ep cell medium and thawed Sf1Ep cells in a cryo vial on a working platform. Add one milliliter of Sf1Ep cell medium to the cryo vial, and mix gently. Transfer the mixture to a sterile 15-milliliter conical centrifuge tube containing five milliliters of Sf1Ep cell medium, and gently mix.Centrifuge the cell suspension at 100 G for seven minutes and discard the supernatant before resuspending the pellet in 15 milliliters of fresh Sf1Ep cell medium. Transfer the cell suspension to a T75 tissue culture flask and place it in a standard humidified tissue culture incubator for one week. After incubation, aspirate the medium from the flask and rinse the cell layer with five milliliters of sterile PBS.After aspirating the PBS, add 2.5 milliliters of trypsin-EDTA to the flask and seal the cap. Incubate the flask at 37 degrees Celsius for five minutes. Tap the flask gently to dislodge the cells and observe under an inverted microscope to confirm the dispersal of the cells.Add five milliliters of Sf1Ep growth medium and rock the flask to mix with the trypsin-EDTA. Transfer the cell suspension to a conical tube and quantitate the cells using a hemocytometer or automated cell counter. To freeze Sf1Ep cells, spin the cells at 100 G for seven minutes and resuspend the pellet in Sf1Ep medium supplemented with 10%DMSO.Distribute one milliliter of cell suspension to each cryo vial and freeze overnight at minus 70 to minus 80 degrees Celsius.

In Vitro Cultivation of Treponema pallidum in Co-Culture with Sf1Ep Cells

To begin, place the trypsinized Sf1Ep cell culture and a 6-well plate on a working platform. Add the appropriate number of Sf1Ep cells and Sf1Ep medium to each well of a 6-well plate. Incubate the plates at 37 degrees Celsius with 5%carbon dioxide overnight.Combine the components of TpCM-2 in a sterile container, adding dithiothreitol as a dry powder last. Gently mix and filter sterilize the medium using a 0.22 micrometer filter unit. Pre-equilibrate the medium in an anaerobic jar evacuate the chamber using house vacuum and refill with a 95%nitrogen and 5%carbon dioxide mixture three times.Then refill with 1.5%oxygen, 5%carbon dioxide and balance nitrogen gas mixture. Quickly transfer the medium to a tri-gas incubator, set up at 34 degrees Celsius and incubate overnight. After overnight incubation, remove the medium from the Sf1Ep culture and rinse the cells with a small volume of the pre-equilibrated TpCM-2.After removing the rinse, add an appropriate amount of TpCM-2 and equilibrate the plate in 1.5%oxygen, 5%carbon dioxide, and balance nitrogen atmosphere at 34 degrees Celsius for three to four hours. Remove the existing T.pallidum culture from the low oxygen incubator and examine the Sf1Ep cell layer in each well. After recording the cell density and appearance, pipette the medium from each well into a sterile 15 milliliter conical tube.Rinse each well with 0.35 milliliters of prewarmed trypsin-EDTA and add the rinse to the 15 milliliter tube. Add another 0.35 milliliters of trypsin-EDTA to each well and incubate for five minutes at 37 degrees Celsius to remove Sf1Ep cells from the plate and T.pallidum from Sf1Ep cell. After detachment, combine the dissociated T.pallidum and Sf1Ep cells with the reserve medium collected in the 15 milliliter conical tube and record the total volume retrieved for calculation of the yield per culture.Inoculate the previously prepared plate of Sf1Ep cells with a set volume of the harvested T.pallidum. After exchanging the atmosphere in the plate, incubate at 34 degrees Celsius within the brewer jar or in a tri-gas incubator. After inoculation, use a helper counting chamber to enumerate T.pallidum under dark-field microscopy.Add 50%glycerol to a final concentration of 10%to the T.pallidum culture and disperse the glycerol through gentle pipetting or inversion. Distribute the preparation in one to two milliliters aliquots into screw capped freezer vials, and immediately place the vials in a 80 degrees Celsius freezer or a liquid nitrogen freezer. Prepare and pre equilibrate two 96-well plates with 1000 Sf1Ep cells and 200 microliters of TpCM-2 per well and incubate overnight in a tissue culture incubator.The next day, replace Sf1Ep medium with TpCM-2 as described previously. After quantitation, dilute T.pallidum in TpCM-2 to produce two preparations with concentrations of 10 and 40 cells per milliliter. Inoculate 50 microliters per well of the 10 T.pallidum per milliliter preparation into one of the prepared 96 ell plates.In the two control wells in each plate, inoculate the 2 x 10 to the power of three T.pallidum per milliliter dilution. Equilibrate the plates with the low oxygen gas mixture and incubate them in a brewer jar or tri-gas incubator at 34 degrees Celsius. On the seventh day, remove half of the medium and replace it with fresh equilibrated TpCM-2.Once positive wells are identified by dark-field microscopy, trypsinize the positive wells and transfer the cell suspension to the previously prepared 24-well plates for further expansion. T.pallidum typically retain over 90%motility and multiply logarithmically with a doubling time of 33 to 45 hours for approximately seven days before entering the stationary phase. Over the course of one week, the spirochetes underwent approximately four to five doublings.

建立和维护用于 梅毒螺旋体 培养的 Sf1Ep 细胞储备

建立和维护用于梅毒螺旋体培养的 Sf1Ep 细胞储备