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Methodenartikel

An Assay to Determine Polymicrobial Biofilm Initiation on Virus-Infected Cells

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8 juli 2025

In dit artikel

Samenvatting

Source: Plotkin, B. J. et al., Determination of Biofilm Initiation on Virus-infected Cells by Bacteria and Fungi. J. Vis. Exp. (2016)

This video illustrates the initiation of polymicrobial biofilm formation on virus-infected cells by bacteria and fungi. Herpes simplex virus infection impedes bacterial attachment to the cells, preventing bacterial-fungal co-localization. In contrast, uninfected cells display bacterial-fungal co-localization and initiation of biofilm formation.

Protocol

1. HSV Strains and Handling

NOTE: Recombinant non-spreading HSV-1(KOS) gL86 and HSV-2 (KOS) 333gJ- with beta-galactosidase reporter activity is used for the assay.

  1. Use virus from a single lot and store at -80 °C at a 1:1 ratio of Dulbecco's modified Eagle's medium (DMEM) with 20% fetal bovine serum (FBS) and skim milk until use. Before viral lot storage, determine virus concentration by o-nitrophenyl-β-D-galactopyranoside (ONPG) and 5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside (X-Gal) assay.
  2. Determine virus viability and multiplicity of infection (MOI) by X-Gal staining for each experimental assay run using reporter virus entry assay, as previously described (Figure 1).
  3. Dilute virus (Opt-MEM) to desired MOI. Fix monolayers (paraformaldehyde; 0.5 ml/well) before staining. Place virus viability controls in a separate microtiter plate in parallel with polymicrobial assay plates.

2. HeLa 299 Cell Handling

  1. Grow at 37 °C, 5% CO2 in DMEM with 4.5 g/L glucose, 10% heat-inactivated fetal bovine serum (FBS), gentamicin (50 µg/ml) and L-glutamine. Passage cells at 80% confluence with Trypsin solution (ethylenediaminetetraacetic acid, 0.53 M EDTA; 0.05% Trypsin; 5 ml/flask).

3. C. albicans Handling

NOTE: C. albicans obtained from a clinical laboratory source is stored at -80 °C in Remmel skim milk 2x medium.

  1. Culture frozen stock onto Sabouraud Dextrose Medium (37 °C). After 24 hr subculture the C. albicans onto Fungisel medium (37 °C; 48 hr) for use.
  2. Generate germ tube (GT) forms (pick representative colonies; 3 ml FBS; 3 hr; 37 °C; absorbance600 (Abs600), 0.3). After incubation, wash GT (Hanks' Balanced Salt Solution, HBSS; 2x; 4,000 x g). Add washed GT to warmed HBSS (37 °C; 0.32 Abs600). GT forms should be 99% of cells observed as determined by hemocytometer count.
  3. Make yeast form (YF) stock suspensions by picking representative Fungisel colonies (HBSS, 3 ml; 0.32 Abs600). Count the number of YF forms/ml microscopically using a hemocytometer. YF forms should be 99% of cells observed as determined by hemocytometer count.
  4. Make working fungal stock (250 µl of GT or YF stock in 25 ml HBSS; 37 °C; 105 colony forming unit, (CFU/ml)

4. S. aureus Handling

  1. Store S. aureus American Type Culture Collection, ATCC 25923 (-80 °C; Remmel skim milk 2x). Culture onto sheep blood agar (5%; 37 °C; 24 hr). Pick representative colonies and transfer to mannitol salts medium within 2 days for stock (37 °C; 18 hr).
  2. Make S. aureus stock suspension (3 ml HBSS; 1.32 Abs600 ;108 CFU/ml)
    1. Make working S. aureus stock (100 µl of the stock in 25 ml HBSS; 105 CFU/ml).

5. Candida and S. aureus Suspensions

  1. Make mixed C. albicans and S. aureus suspension (250 µl YF or GT stock and 100 µl S. aureus stock in 25 ml HBSS).

6. Polymicrobial Biofilm Assay

  1. Seed 96 well plates with 200 µl of 2 x 105 HeLa cells/ml (85% confluence level). Rock plates (30 - 45 min; 37 °C) before incubation (37 °C; 5% CO2 incubator; 18 hr). Wash monolayers (1x; Opt-MEM) then seed with HSV (HSV-1 (KOS) gL86 or HSV-2 (KOS) 33 gJ- in 100 µl Opt-MEM ; MOI 50 and 10). Incubate plates (3 hr; 37 °C; 5% CO2). Use only one viral strain per day.
  2. Wash infected monolayers (1x; phosphate-buffered saline (PBS) with Mg+2 and Ca+2; 100 µl). Replace PBS with warm HBSS leaving 25 µl in each well.
    1. Add YF, GT and/or S. aureus working suspensions (100 µl; target to cell ratio =5:1; n=16) as indicated in Table 1. Incubate plates (static; 30 min; 37 °C; 5% CO2).
  3. After incubation, aspirate one column at a time immediately refilling with 300 µl PBS with Mg+2 and Ca+2. Repeat this step twice then add radio-immunoprecipitation assay lysis buffer (RIPA; filter sterilized; 200 µl of a 1:50 dilution).
  4. Rapidly triturate the HeLa cell lysate then place 50 µl onto mannitol salts (MS) and/or Fungisel (F) media (Figure 2). Spread the lysate using a glass rod bent at a 90° angle. Incubate the plates (18 hr at 37 °C). Manually count the number of colonies per plate. Controls consist of S. aureus and/or C. albicans adherence to HSV-uninfected HeLa cells.

Experimental setup table for microbiological growth analysis, tubes labeled A-H, columns 1-12.

Table 1. General Template Determination of Microbial Adherence in Polymicrobial Interactions. GT= Candida albicans germ tube phenotype; YF= C. albicans yeast form phenotype; MSSA= methicillin-sensitive Staphylococcus aureus; MS= mannitol salts medium; F= Fungisel medium.

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Resultaten

Virus infection assay; blue-stained cells; microscope image; varying MOI; cellular infection study.
Figure 1. X-gal Staining Pictures of Dosage Dependent HSV-1 Infection in HeLa Cells. HeLa cells infected with HSV-1 at various MOI and X-Gal stained. (A) HeLa cells in well of 96 well plate with X-Gal stained mock-infected HeLa cell cont...

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Openbaarmakingen

No conflicts of interest declared.

Materialen

Lijst van materialen gebruikt in dit artikel
NaamBedrijfCatalogusnummerOpmerkingen
C.albicans
BBL Sabouraud DextroseBD211584
Fungisel AgarDot Scientific7205A
S.aureus
Mannitol Salt AgarTroy Biologicals7143B
Sheep blood agarTroy Biologicals221239
Hela cells
1xDMEM (Dubelcco's Modified Eagle Medium, with 4.5 g/L glucose and L-glutamine, without sodium pyruvateCorning10-017-CM
Gentamicin 50mg/mlSigma139750µg/ml final concentration in the complete DMEM
Trypsin EDTA (0.05% Trypsin, 0.53M EDTA)Solution 1XCorning25-052-CI
Fetal Bovine SerumAtlanta BiologicalsS1115010% final concentration in the complete DMEM
Other medium and reagents
ONPGThermo Scientific34055
Ultra-Pure X galInvitrogen15520-018
1x HBSS (Hanks' Balanced Salt Solution)Corning20-021-CV
1XPBSDot Scientific30042-500
RIPA LysisLife Technologies89901
Supplies
96-Well platesEvergreen Scientific222-8030-01F
Culture tubes 100x13Thomas Scientific9187L61

Tags

Herpes simplexvirusbacteri le fungale colocalisatieheparansulfaatcolony formation assaycellysebuffermicrobi le adhesieHeLa cellenRIPA lysebuffer