Environmentally Responsible Bioengineering for Spore Surface Expression of Helicobacter pylori Antigen

The development of genetic technologies and bioengineering are creating an increasing number of genetically engineered microorganisms with new traits for diverse industrial applications such as vaccines, drugs and pollutant degraders. However, the destiny of genetically engineered bacterial spores released into the environment as long-life organisms has remained a big environmental challenge. In this study, an environmentally responsible and sustainable gene technology solution based on the concept of thymine starvation is successfully applied for cloning and expression of a Helicobacter pylori antigen on Bacillus subtilis spore surface. As an example, a recombinant Bacillus subtilis strain A1.13 has been created from a gene fusion of the corresponding N-terminal fragment of spore coat protein CotB in B. subtilis and the entire urease subunit A (UreA) in H. pylori and the fusion showed a high stability of spore surface expression. The outcomes can open the door for developing highly safe spore vectored vaccines against this kind of pathogen and contributing to reduced potential risks of genetically engineered microorganisms released in the environment.


INTRODUCTION
The creation of genetically engineered microbes (GEMs), which are made by bioengineering a more robust protein into microorganisms for improved features of interest, is thought to be a more cost-effective and safe way to improve the environment and finally human health.Bioengineered microorganisms are more powerful than naturally occurring ones and may be either faster degraders to contaminants in the environment, or next-generation vaccines, probiotics, enzyme producers, which have been produced in the industry and health sectors. 1 However, the most challenging environmental issue is the ultimate fate of GEMs, especially bioengineered long-life spores, once released in the environment because these spores can live indefinitely in soil and harsh environmental conditions. 2,3t has been suggested by an innovative approach that spores under thymine starvation could be germination-deficient and die. 2 The concept of death without thymine has been introduced for B. subtilis, the most popular industrial microbe. 4Based on the existence of two genes thyA and thyB discovered to encode for thymidylate synthase enzymes, 5 recombinant spores of this bacterium have been designed by using the insertion of new gene sequences into these thymine genes, causing a strict thyminedependent growth. 2 This concept is used for the first time in the present study to introduce an antigen or virulence factor from the human pathogenic bacterium Helicobacter pylori, a major risk factor for stomach cancer, 6 on the surface of B. subtilis spores.This may lead to the creation and advancement of recombinant vaccines against this pathogen that are environmentally sound, ultimately enhancing both human and environmental health.

Bacterial strains and medium
B. subtilis strain PY79 is a prototrophic laboratory strain derived from the type strain 168. 7The two-step transformation approach and other standard methods for working with B. subtilis were carried out as previously mentioned. 8SM is the recommended medium for the growth and sporulation of B. subtilis, 9 supplemented with thymine (50 μg/ml) and trimethoprim (3 μg/ml).Escherichia coli DH5α (Invitrogen) was cultured in Luria-Bertani (LB).Competent cells of E. coli DH5α were prepared as described by Sambrook and Russell 10 and those of B. subtilis PY79 were performed according to Zhang et al. 11 H. pylori strains (HP24, HP28, HP30, HP34, and HP37) isolated from patients with chronic gastritis in 2020 and provided by the Hospital of University of Medicine and Pharmacy, Hue University, Vietnam, were used for the amplification of gene sequence encoding for urease A antigen.H. pylori strains were cultured using either selective Horse Blood Agar (HBA) or Brain Heart Infusion (BHI) medium (Oxoid) containing 5% (v/v) fetal bovine serum (FBS, Thermofisher Scientific).Incubation was made in a microaerophilic chamber using an Oxoid CampyGen 2.5 L Sachet (5-7% O2, 5-10% CO2, and 85% N2) at 37°C, with passaging every 48 h.The strains were preserved in BHI supplemented with 15% (v/v) glycerol at -80°C.

Oligonucleotides, plasmids, and enzymes
Table provides a list of the DNA primers used for PCR amplification.Plasmid pThyA (4,274 bp) (Life Technologies) composes of the thyA gene that is located around a multiple cloning site (MCS).Enzymes such as Vent DNA polymerase (New England Biolabs, USA), My Taq DNA polymerase (Bioline, UK), T4 DNA ligase (New England Biolabs, USA) and restriction enzymes BamHI, NdeI, ScaI and EcoRI (New England Biolabs, USA) were used.

Construction of cotB-ureA gene fusion in B. subtilis
The cotB gene was amplified by PCR from B. subtilis PY79.The cotB gene was then cloned into plasmid pThyA in E. coli DH5α and confirmed by colony PCR and digestion of restriction enzymes.For cloning in pThyA-cotB, the ureA gene was isolated from clinical H. pylori strains by PCR.Two steps made up the cloning process.E. coli DH5 cells were employed in the first stage for heat shock transformation at 42°C.After being linearized using ScaI digestion and electroporation into B. subtilis PY79, recombinant pThyA plasmids containing the cotB-ureA fused gene were used.Cells were then plated on Supplemented Minimal Medium agar (SMM) added with thymine (50 µg/ ml) and trimethoprim (3 µg/ml).Single colonies were purified after 48 hours of culture and tested for growth on SMM added with trimethoprim (3 µg/ml) and with or without thymine (50 µg/ ml) at 37°C and 46°C.A cotB-ureA chimeric gene at the thyA locus allowed cells to grow at 37°C with or without thymine but not at 46°C without additional thymine.The resulting thyA:: insertion strain is a trimethoprim-resistant transformant that is thymine-dependent.To confirm the existence of the chimeric gene from transformants, the insert DNA fragment was amplified using colony PCR and then sequenced.Fused cotB-ureA strains were also confirmed by spore preparation, spore coat protein extraction, sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and dot blot analysis.

Spore preparation
The exhaustion method was used to cause sporulation as described previously in B. subtilis strains. 9After being incubated at 37°C for 48 hours, spores were harvested, thoroughly washed, and purified using lysozyme to break down any remaining sporangial cells. 9To guarantee that there were no viable vegetative cells, each batch of spores was heated at 65°C for one hour.They were then floated in cool, sterile water and kept in aliquots (1×10 10 spores/mL) at -20°C until they were needed.Serial dilution and plate counting were used to calculate spore counts.

Spore coat protein extraction and SDS-PAGE analysis
Aliquots of 1×10 10 spores suspended in distilled water were used to extract spore coat proteins in B. subtilis by addition of 100 µl extraction buffer (0.05 M Tris-HCl pH 6.8, 1% SDS (sodium dodecyl sulphate), 0.05 M DTT (dithiothreitol)) to spore pellet and then incubation at 68°C for 1 h, as previously reported.9These supernatant protein samples were mixed 1:1 (v/v) with the 2X treatment sample buffer (1% DTT used instead of 2-ME) for SDS-PAGE and then heated for 15 min at 98°C.Using a Mini Protein II device (Bio-Rad Laboratories, Inc., Richmond, CA, USA), protein samples are loaded onto polyacrylamide gels with a 12% running gel and a 4% stacking gel before being electrophoresed at 15 mA/gel of steady-state current.The gels were stained with 0.05% Coomassie Blue in a solution of 25% v/v ethanol and 10% v/v acetic acid for 4 hours after electrophoresis.The gels were finally destained with destaining solution (25% (v/v) methanol and 10% (v/v) acetic acid).

Dot blotting assay
Spore coat protein extracts were 2-fold serially diluted with phosphate-buffered saline (PBS) and blotted onto nitrocellulose membrane.The experiments were replicated three times.For negative controls, either PBS or supernatant of PY79 cells was used.For positive controls, either UreA protein or supernatant of H. pylori HP37 cells was used.The membrane was blocked overnight at 4°C by immersion in 5% Skim milk and PBST (PBS with 0.05% Tween-20), and then three PBST washes on the membrane were performed.The membrane was probed with rabbit anti-UreA primary antibody (PA14347A0Rb, Cusabio, USA) at 1:4000 ratio for 1 h at room temperature, and then three washed with PBST.Goat anti-rabbit IgG-HRP (Sigma-Aldrich, Germany) at 1:40,000 ratio was used as the secondary antibody, and the membrane was incubated for 1 hour at room temperature with this antibody in PBST containing

The stability of spore surface expression
The stability of spore surface expression of UreA on A1.13 by using dot blots were tested at different preservation/delivery temperatures (-20°C, 4°C, 25°C and 37°C) for 28 days, as well as in the conditions treated with simulated gastric fluids (SGF) (Merck, Germany) or simulated intestinal fluids (SIF) (Merck, Germany) at 1:1 (v/v) ratio for 1 h and then stored at 4°C for the same days.

Synthesis and integration of the cotB-ureA gene fusion in the B. subtilis chromosome
3][14] In this study, CotB was designed as a carrier protein in order to create recombinant B. subtilis spores with UreA expressed on their surface.In order to do this, the coding portion of the cotB gene and the ureA gene of H. pylori were fused in frame.In particular, the cotB gene fragment (1130 bp) was cloned from B. subtilis PY79 with primer pair CotB-F and CotB-R (Figure 1A), in which three 27 amino acid repeats at the C-terminus were removed because these fragments cause genetic instability of CotB, 12 and an upstream sequence of the cotB gene and a restriction enzyme recognition sequence at the two ends were added.The ureA gene (732 bp), which consists of the entire nucleotide sequence coding for the urease A subunit and restriction enzyme recognition sequences added at both ends, was PCR amplified successfully from different clinical H. pylori strains by using primer pair UreAV-F1 and UreAV-R and the results of single PCR product band were shown (Figure 1B).The cotB gene was then purified from PCR, cleaved by NdeI and BamHI enzymes before incorporated into the pThyA vector.The ureA gene, after also being purified from PCR, was cut with BamHI and EcoRI enzymes before being inserted into the pThyA-cotB vector.
The pThyA vector and the cotB gene were joined with the T4 DNA ligase enzyme to generate the recombinant pThyA-cotB vector, which is followed by the transformation into competent cells E. coli DH5α cloned on LB agar including ampicillin (100 µg/ml) (Figure 1C,D).Colonies obtained after 24 h of culture at 37 °C were further screened by colony PCR with the same primer pair CotB-F and CotB-R to identify recombinant strains.
The ureA gene and the pThyA-cotB vector were linked by T4 DNA ligase to generate a plasmid called pThyA-cotB-ureA which is then also transformed into E. coli on ampicillinsupplemented LB agar (Figure 1C,E).The colonies obtained after 24 h of culture at 37°C were further screened by colony PCR method with the same primer pairs UreAV-F1 and UreAV-R to identify E. coli strains carrying the recombinant gene.
After transformation in B. subtilis, cells that successfully performed double-crossover of homologous segments of the thyA gene cannot survive in the medium without thymine because of the inactivation of the thyA gene. 2 Individual clones with the presence of ureA gene were detected by PCR (Figure 1F).Also, to verify the sequence of ureA gene, these clones were sequenced by using the same primers.The results indicated that a selected clone carrying the ureA gene from H. pylori strain HP37 shared 100% identity with that of H. pylori strain dRdM2addM2 (Genbank Accession No. CP026515) (not shown).This clone is named A1.13 and used for further analysis.
The isogenic parental strain PY79 and the ).The number of spores was 2×10 7 spores per sample recombinant strain A1.13 both displayed similar levels of sporulation, germination efficiency, and spore resistance to trimethoprim and heat (not shown), which is relevant to a previous study. 13uthors in that research developed a fusion of CotB with an N-terminal length of 275 amino acid residues (825 bp) and a shortened UreA sequence that lacked 49 amino acids at the N-terminal end, but failed to generate any fusion products of CotB with the entire protein UreA.Although still removed DNA region encoding the three repeats in the C terminus of CotB, this study used a longer fragment of cotB (1130 bp) with additional upstream sequences, thus likely contributing to improved genetic stability to successfully clone the entire protein UreA in B. subtilis.
In addition, compared to E. coli expression system, B. subtilis host is more relatively difficult in plasmid transformation and less stability of plasmids. 15In the present study, the plasmid pThyA-cotB which was firstly transformed in E. coli before fused with ureA and then transformed in B. subtilis, thus, possibly improved transformation efficiency in the latter host.
To verify that the gene fusion was surface expressed, spore coat protein extraction, SDS-PAGE and dot blot analysis were performed with the use of anti-UreA antibodies.An approximately 58.2-kDa band was found after SDS-PAGE examination of spore coat protein extracts from wild type and recombinant strains bearing the cotB-ureA fusion (Figure 2B), which is relevant to the gene structure designed and amino acid sequences deduced from DNA sequences (Figure 2A).Dot blot analysis showed the surface expression of UreA on spores A1.13 and its stability maintained in the different conditions of temperatures and simulated harsh environments of gastrointestinal (GI) tract for a minimum of 28 days (Figure 3).
In order to further test a robust immune response, an oral vaccine candidate must overcome preservation conditions (e.g.-20°C, 4°C) and multiple physicochemical and biological barriers in the GI tract such as the human body temperature at 37°C, a high acidity in the stomach, an alkaline pH in the intestine tract, and proteolytic enzymes available for the degradation of antigenic proteins or peptides. 16In this study, combined with genetic structure stability, the surface expression stability of the recombinant spores at different oral vaccine preservation and delivery conditions has proven spore as a cutting-edge and effective mucosal vaccination delivery method, 13,14 and suggested A1.13 as a spore vectored vaccine candidate against H. pylori.Findings from this study indicate that CotB is an appropriate carrier for displaying the full protein UreA on the surface of spores.However, further immunological experiments, preclinical and clinical trials will now be required to assess protective immune responses and its application potential.
Finally, following genetic manipulation, an environmentally sustainable and innovative gene-based solution for a critical problem of GEMs in the environment has been introduced here to be applied for the development of next-generation vaccines against H. pylori and other pathogens.If discharged, the recombinant spores A1.13 would spawn bacteria that could not survive in the environment habitats in the absence of thymine since they were made to be dependent on thymine, thus likely stopping potential risks and controversies surrounding the use of GEMs.However, it now still lacks evidence for a "permanent" thymine-less death of microbes in nature.

CONCLUSION
We used here the N-terminal fragment of spore coat protein CotB in B. subtilis and the entire antigen UreA in H. pylori as examples showing that chimeric proteins comprised of these two heterologous proteins/peptides can be displayed on the spore surface with high stability of genetic structure and expression.The ureA gene was inserted into the thyA gene in the wild type strain, thus the recombinant spores A1.13 grows dependently on thymine and become a promising spore vectored vaccine candidate for oral administration against H. pylori with higher safety when released in the environment.

Figure 2 .Figure 3 .
Figure 2. Gene structure and deduced amino acid sequences of the cotB-ureA fusion region (A) and SDS -PAGE (12% gel) of CotB-UreA (1-238) recombinant protein from spores B. subtilis A1.13 (B).Chimeric genes inserted at the B. subtilis thyA loci are shown.Urease A from H. pylori HP37 was fused in frame to the C-terminus of the spore coat protein CotB.The estimated MW of the chimera are shown.Lane 1: extracted protein of B. subtilis PY79 spores; lane 2: extracted protein of B. subtilis A1.13 spores; M: Protein marker

Table .
PCR primer list