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Table 2 Applications of bioengineering

From: Probiotic engineering: towards development of robust probiotic strains with enhanced functional properties and for targeted control of enteric pathogens

Applications

Probiotics

Genes/receptors expressed

Action

References

Improvement of stress tolerance

L. paracasei

Heat shock protein chaperones (GroES and GroEL)

Improved thermotolerance (heat tolerance) of probiotic; increased solvent resistance by the probiotic strain

[104]

L. salivarius

Listerial betaine uptake system (BetL)

Increase in the resistance of the probiotic to several stresses

[110]

L. lactis

Trehalose synthesis gene (ostAB)

Enhanced probiotic’s resistance to gastric acid protection of the probiotic against damage caused by acid, cold, or heat shock

[114, 115]

Production of antimicrobial peptides

L. lactis

A3APO and alyteserin

Successfully inhibited E. coli and Salmonella

[31]

Probiotic E. coli

Cell receptor (ganglioside) for cholera toxin or ETEC heat-labile toxin

Enterotoxins are sequestered by the probiotic E. coli thus protecting host against diarrheal infection

[12]

L. reuteri

Heat-stable (ST) and heat-labile (LT) enterotoxins

Successfully bound to the enterotoxins and prevented enterotoxicity in a mouse model

[12]

Enhancement of anti-inflammatory response

L. lactis

Elafin

Significant reduction in inflammation

[118]

L. lactis

TGF-β

Overall reduction of inflammation and colitis

[120]

L. lactis

IL-10

Successfully prevented colitis in murine models

[121]

L. lactis

Anti-TNF-α nanobodies

Reduced the colonic inflammation

[123]

L. lactis

Internalin A

Enhanced efficient internalization of L. lactis in the human intestinal cell line Caco-2

[124]

Enhancement of colonization exclusion

L. paracasei

Listeria adhesion protein (LAP)

Inhibited the adhesion of Listeria to host cells

[94]

L. lactis

Surface-associated flagellin

Inhibited the binding and adhesion of pathogenic E. coli and S. enterica

[126]

L. acidophilus

K99 fimbriae

Reduced the attachment of ETEC to porcine intestinal brush border

[129]

Receptor mimicry system and toxin neutralization

E. coli Nissle 1917; L. lactis

Galactosyl-transferase genes; Tetanus toxin fragment C (TTFC)

Recombinant bacteria neutralized shiga toxins, Stx1 or Stx2

[132]

Increased IgA levels led to protection of the host against the infections of the mucous membrane

[135, 136]

E. coli Nissle 1917

Receptor GM1

Protected infant mice from challenge with virulent V. cholerae

[139]

E. coli Nissle 1917; L. casei

AI-2 co-expressed CAI-1

80% reduction in Ctx binding to the intestines of mice which reduced numbers of V. cholerae in treated mouse intestines

[140]

Adhesins K99

Protected 80% of the vaccinated mice after challenge with a lethal dose of strains of ETEC K99 and K88

[142]

Vaccination

L. lactis

Virus spike protein VP8

Provided 100% protection against rotavirus infection

[145]