Detection of Streptococcus pyogenes virulence factors by multiplex PCR

Abstract

Streptococcus pyogenes (GAS) is a human pathogen that causes multiple infections worldwide. The pathogenic properties of GAS strains are often linked to the production of virulence factors such as toxins, proteases or DNases. Detection of virulence factors produced by GAS strains can be used to either determine pathogenic potential of the strain or as a rapid screening and typing method. We recently developed a method to detect simultaneously 20 GAS virulence factors (spd3, sdc, sdaB, sdaD, speB, spyCEP, scpA, mac, sic, speL, K, M, C, I, A, H, G, J, smeZ and ssa) in four low volume multiplex PCR reactions (Borek et al., 2011) and below we present a detailed protocol describing the method.

Keywords: :

• Streptococcus pyogenes
• multiplex PCR
• virulence factors
• Gram-positive pathogens
• PCR detection

Introduction

Streptococcus pyogenes (GAS) is a human pathogen that causes over 600 million of infections worldwide that result in over 500,000 deaths a year.¹ GAS causes mild infections of skin and mucosal surfaces, but is also able to cause severe, life threatening invasive diseases such as streptococcal toxic shock syndrome (STSS) or necrotizing fasciitis (NF).²

Severity of GAS infections depends on multiple bacterial and host factors. The pathogenic properties of GAS strains are often linked to the production of virulence factors such as toxins, proteases or DNases and toxins present in the particular GAS strain can be the predictor of its invasiveness.^3,4

Virulence factors are not equally distributed among S. pyogenes strains. Some of them are chromosomally encoded; others are related to the presence of mobile genetic elements. Profile of the virulence factors encoded by the particular strain is part of strain characteristics and their presence/absence can be used as diagnostic method and simple tool in clinical diagnosis.

So far, determination how S. pyogenes strains/isolates are related to each other has been rather expensive and time consuming task. To determine whether strains are related and what their pathogenic properties are, researchers and epidemiologists use usually restriction analysis of large chromosomal fragments—PFGE. PFGE is time-consuming, requires well trained personnel and the results are difficult to compare between laboratories. Other methods such as emm typing or MLST are based on the sequencing of one to several genes. Although, sequencing based methods are relatively easy to perform and easily comparable, cost of sequencing reactions can be too high for routine use. Because of these multiple disadvantages, new typing methods and schemes usually based on simple PCR reactions are proposed. A few years ago, multiplex PCR system that detects 11 superantigens has been described. The method is using SYBRGreen detection of small PCR products and requires real time PCR instrument with module for melting curve analysis.⁵

We recently developed a method that expands methods like those mentioned above, the set of four low volume multiplex PCR reactions detect simultaneously 20 GAS virulence factors, not only superantigens, (spd3, sdc, sdaB, sdaD, speB, spyCEP, scpA, mac, sic, speL, K, M, C, I, A, H, G, J, smeZ and ssa).⁶ The method has high resolution with Simpson’s index of diversity 0.943 (0.936–0.951) and can be used for both typing and detection of virulence factors.

Reagents

(1) Lysozyme stock 20 mg/ml (Sigma-Aldrich, L6876)

(2) Mutanolysin stock 10 U/μl (Sigma-Aldrich, M9901)

(3) RNase stock 10 mg/ml (Sigma-Aldrich, R5503)

(4) 1 mM stock of dNTP prepared from 100 mM stock solutions of individual dNTPs (Sigma-Aldrich, DNTP100)

(5) Taq polymerase (Fermentas, EP0402)

(6) 10× Taq buffer with (NH₄)₂SO₄ (Fermentas, B33)

(7) 25 mM MgCl₂ stock solution (Fermentas, R0971)

(8) Starters (see Table 1; Genomed, www.genomed.pl)

Table 1. Starters for the detection of GAS virulence factors

Detected virulence factor	Primer sequence (forward)	Primer sequence (reverse)	Size of the PCR product (bp)
Mix 1
SpeL	CCTGAGCCGTGAAATTCCCA	ACACCAGAATTGTCGTTTGGT	657
SpeK	CCTTGTGTGTGTATCGCTTGC	TTGCTGTCCCCCATCAAACT	568
SpeM	ATCGCTCATCAAACTTTTCCT	CCTTGTGTGTGTATCGCTTGC	496
SpeC	GCCAATTTCGATTCTGCCGC	TGCAGGGTAAATTTTTCAACGACA	405
SmeZ	TTTCTCGTCCTGTGTTTGGA	TTCCAATCAAATGGGACGGAGAACA	246
SpeI	TTCATAGACGGCGTTCAACAA	TGAAATCTAGAGGAGCGGCCA	176
Mix 2
ssa	AAGAATACTCGTTGTAGCATGTGT	AATATTGCTCCAGGTGCGGG	678
SpeA	AGGTAGACTTCAATTTGGCTTGTGT	GGGTGACCCTGTTACTCACG	576
SpeH	TGAGATATAATTGTCGCTACTCACAT	CCTGAGCGGTTACTTTCGGT	480
SpeG	TGGAAGTCAATTAGCTTATGCAG	GCGAACAACCTCAGAGGGCAAA	384
SpeJ	TCCTTGTACTAGATGAGGTTGCAT	GGTGGGGTTACACCATCAGT	286
Mix 3
spd3	ATCGTCGTACTTGGCAAGGTT	GCCGCTTCTTCAAACTCTTCG	784
sdc	AAGCTTAGAAACTCTCTCGCCA	AGTTCCAGTAATAGCGTTTTTCCGT	600
sdaB	TATAGCGCATGCCGCCTTTT	TGATGGCGCAAGCAAGTACC	440
sdaD	TTTACGCTGAATCGGGCACT	GGCTCTGGTTTGCTTTCCCA	295
Mix 4
speB	AGACGGAAGAAGCCGTCAGA	TCAAAGCAGGTGCACGAAGC	952
spyCEP	GATCCGGCCCATCAAAGCAT	AGCTGCCACTGATGTTGGTG	786
scpA	GCTCGGTTACCTCACTTGTCC	CAATAGCAGCAAACAAGTCACC	622
Mac	TCTTGCCCTGTTGAAAGTGT	CGAGGTGGTATTTTTGACGCC	389
sic	TTACGTTGCTGATGGTGTATATGGT	TTTGATAGAGGGTTTTCAGCTGGC	150

(9) 1.5% SeaKemLE agarose (Lonza, 90004) in 1× TBE buffer

(10) 1× TBE electrophoresis buffer

Equipment

(1) Veriti or 9700 PCR by Life Technologies (formerly Applied Biosystems). Other PCR instruments were not tested.

(2) Gel electrophoresis Sub-Cell tank Model 192 (BioRad, 170-4509) with 26 well combs (BioRad, 170-4526)

Setup

Template

As a template for PCR reaction we use chromosomal DNA isolated using commercially available kits. S. pyogenes cells for DNA isolation are grown on half of the agar plate (Columbia with 5% sheep blood, BD, 221263; BioMerieux, 43 041).

(1) Scrape bacteria from the plate with the loop or swab.

(2) Re-suspend bacteria in 200 μl of TE buffer.

(3) Add 5 μl of RNase, 10 μl lysozyme and 2.5 μl of mutanolysin stocks.

(4) Incubate at 37°C for about 45 min.

(5) Follow with the standard chromosomal DNA isolation protocol.

(6) Dilute DNA to concentration ~10 ng/μl.

(7) Keep diluted template DNA at 4°C to avoid multiple freezing-thawing cycles.

Starters

Primer sequences were designed based on sequences of available S. pyogenes genomes. Amplicons sizes were designed so generated PCR products can be easily identified based on their size. We tested primer pairs individually so they are specific and yield only single PCR product. Primers for each PCR mix were tested in the multiplex PCR to test whether they behave the same way as individual primers.

(1) Mix equal volumes of individual 100 mM starters stock solutions into appropriate mixes, namely: “Mix 1,” “Mix 2,” “Mix 3” and “Mix 4.” Mixes 1 and 2 detect superantigens, Mix 3 detects DNases and Mix 4 detects proteases and sic gene. Primer sequences, composition of primer mixes and amplicon sizes within mixes are shown in Table 1.

(2) Aliquot primers pre-mixes into 50–100 μl portions. (Table 2, Problem 1).

Table 2. Problem handling

	Step	Problem	Possible reason	Solution
1	Reagents setup	We observed loss of PCR efficiency after multiple freezing-thawing cycles.	Primer degradation	To avoid degradation, aliquoted primer mixes should not be thawed more than 3–4 times. Small portions (50–100 μl) of primer mixes should be kept at -20°C.
2	Reaction setup	Uniformity	Reaction volume is small (5 μl). Preparation of single reaction that requires pipeting of volumes below 0.5 μl is very difficult.	We mix enough mastermix to fill whole 96 well plate and run multiple reactions at the same time.
3	Reaction setup	Uniformity	Pipetting errors caused by manual pipetting and small reaction volume.	We usually use an electronic pipette with the “dispense” mode.

Reaction setup

(1) All mixes, templates and reactions during setup should be kept on ice.

(2) Prepare diluted template DNA (concentration ~10 ng/μl). We preferably use 96 well format or 8/12 well strips to prepare templates. Using plate format noticeably speeds up the reaction setup. In majority of cases we run 96 well plate for each of four mixes and the same DNA template plate is used to setup all four plates.

(3) Mix together all reagents for PCR mastermixes according to Table 3. (Table 2, Problem 2).

Table 3. Reaction setup

Reagent	Mix 1 per reaction	Mix 1 mastermix per 96 well plate (×110)	Mix 2 and 4 per reaction	Mix 2 and 4 mastermix per 96 well plate (×110)	Mix 3 per reaction	Mix 3 mastermix per 96 well plate (×110)
100 μM Primers mix	0.6 μl	66 μl	0.5 μl	55 μl	0.4 μl	44 μl
10× Taq polymerase buffer with (NH4)2SO4	0.5 μl	55 μl	0.5 μl	55 μl	0.5 μl	55 μl
25 mM MgCl2	0.5 μl	55 μl	0.5 μl	55 μl	0.5 μl	55 μl
1 mM dNTP	0.5 μl	55 μl	0.5 μl	55 μl	0.5 μl	55 μl
10× diluted chromosomal DNA template	2.8 μl	—	2.9 μl	—	3.0 μl	—
Taq polymerase	0.1 μl (0.5 U)	11 μl	0.1 μl (0.5 U)	11 μl	0.1 μl (0.5 U)	11 μl

(4) Dispense 2.2 μl (mastermix 1), 2.1 μl (mastermix 2 and 4) or 2.0 μl (mastermix 3) of the prepared mastermix to each well of the reaction plate or PCR tubes. Dispense mastermixes on the side of the tube/well. (Table 2, Problem 3).

(5) Using multichannel 0.5–10 μl pipette, add 2.8 μl of DNA template to wells/plates with mastermix 1, 2.9 μl to wells/plates with mastermixes 2 and 4, 3.0 μl to wells/plates with mastermix 3.

(6) Close tubes or seal the plate.

(7) Mix well and spin for 15 sec (tubes) or 1 min at 2500 rpm (plates).

(8) Place plate/tubes in a thermocycler and run program 1 or 2.

Equipment setup

The equipment does not need any special setup. We usually store pre-programmed PCR programs listed in Table 4.

Table 4. PCR program setup

	Program 1 (Mix 1, 2 and 3)		Program 2 (Mix 4)
	Temperature	Time	Temperature	Time
Initial denaturation	95°C	3 min	95°C	3 min
Denaturation	95°C	15 sec	95°C	15 sec
Annealing	60°C	20 sec	52.5°C	45 sec
Elongation	72°C	2 min	72°C	3 min
Final elongation	72°C	7 min	72°C	7 min

Procedure

(1) PCR amplification

Amplification reactions are performed for 40 cycles using two different programs. Reactions with primer mixes 1–3 are amplified using program 1 and reactions with mix 4 are amplified using program 2.

(2) Gel electrophoresis

We analyze products of multiplex PCR reactions by electrophoresis in 1.5% (wt/vol) SeaKemLE agarose gel in TBE buffer, with addition ethidium bromide. Separation is performed with current 160 mV for about 100 min. Gels are photographed under UV light.

(3) Gel analysis

As a result of each multiplex reaction a set of multiple bands of various sizes can be observed (Fig. 1). Each PCR product corresponds with detected virulence factor. We usually note the absence/presence of a band as a 0 or 1 in a string of digits. As a result of four multiplex reactions we generate a string of 20 digits. Digitizing the results makes them easy to compare between strains. For example, during analysis of products generated with Mix1 code 000011 denotes that we did not detect genes speL, speK, speM and speC but detected products smeZ and speI. Example of the whole analysis can be seen on Figure 1 where marked strains would have codes 01011000010001111110 and 00011010010101011111.

Figure 1. Detection of S. pyogenes virulence factors in four multiplex PCR reactions.

Timing

The whole procedure can be performed during a single day, including DNA isolation.

(1) DNA isolation: ~90 min

(2) Reaction setup: ~15 min for 96 well plate, but only using multichannel pipettes and pre-dispensed template masterplate

(3) PCR amplification: Program 1, ~2 h 15 min; Program 2, ~4 h

(4) Gel electrophoresis: ~100 min

Anticipated Results

As a result of each multiplex reaction a set of multiple bands of various sizes can be observed. Presence of certain band denotes the presence of the particular gene. The generated strings of 20 digits can be used as a marker of each strain and be further used for strain clustering and the construction of phylogenetic trees. Categorization of strains based on the virulence factors correlates with emm typing and superantigens profile is a good predictor of emm type.⁶

Primers from Mix 4 and sdaB primers from Mix 3 detect chromosomal genes that are present in virtually all GAS strain and they can serve as positive controls for PCR amplification. In our laboratory, we typed over 1,000 GAS strains and only in two cases we were unable to detect speB for unknown reasons. Products that correspond with sic gene are detected only in M1 serotype strains. Usually with M77 serotype strains we do not detect any genes from Mix2 and in some cases M81 strains do not yield any products after amplification with primers from Mix1. It is caused by lack of particular virulence factors in M77 and M81 strains, not by fault PCR amplification.

The method can be used when rapid strain comparison is required; it is fast and simple when compared with standard PFGE. The method is also inexpensive because it uses small reaction volumes (5 μl) and cost of reagents is markedly low.

The use of virulence factor detection can be used as an extension of any S. pyogenes typing and detection scheme. However if the researchers want to mix our primers with primers they use routinely, we recommend testing each individual primer pair they want to add to their typing scheme, whether it performs well in a mix. For laboratories that use method that detect 11 superantigens described by Lingtes,⁵ we recommend use of Mix3 and Mix4 separately, as described in our manuscript to extend sensitivity and specificity of their detection.

Acknowledgments

The work was financed by the grant from National Center for Science (NCN) number NN401 536140.