Abstract
Several pathogens negatively affect the health of livestock, pets, poultry, and other animals of economic interest. In addition, some of these pathogens cause zoonotic diseases and thus become an interest in human health care. Vaccination is the most attractive alternative to prevent these infectious diseases but its cost is a critical aspect to address proper coverage. Algae species have entered in the race of developing attractive veterinary vaccines, offering the possibility of low cost production vaccines since they are produced in inexpensive media and many species are edible; allowing for the design of oral vaccines not requiring purification or specialized personnel and sterile devices for administration. Algae-based vaccines against the following pathogens have been evaluated in pilot studies: White spot syndrome virus, Avian influenza virus, Foot and mouth disease virus, Taenia solium, Porcine circovirus, and Classical swine fever virus. The algae species used as biofactories include Chlamydomonas reinhardtii, Schizochytrium sp., and Dunaliella salina. In general, these algae species have shown a proper biosynthetic capacity to produce functional antigenic proteins. Although the number of the targeted pathogens and the degree of vaccine characterization is still narrow, a perspective for this field is presented in this chapter. Interestingly some companies have adopted this technology, which will with no doubt accelerate the goals of defining and addressing a regulatory framework to achieve approval of algae-made vaccines making them a reality.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Arzt J, Baxt B, Grubman MJ, Jackson T, Juleff N, Rhyan J, Rieder E, Waters R, Rodriguez LL (2011) The pathogenesis of foot-and-mouth disease II: viral pathways in swine, small ruminants, and wildlife; myotropism, chronic syndromes, and molecular virus-host interactions. Transbound Emerg Dis 58:305–326
Avila-Calderón ED, Lopez-Merino A, Sriranganathan N, Boyle SM, Contreras-Rodríguez A (2013) A history of the development of Brucella vaccines. Biomed Res Int 2013:743509
Betancourt MA, de Aluja AS, Sciutto E, Hernández M, Bobes RJ, Rosas G, Hernández B, Fragoso G, Hallal-Calleros C, Aguilar L, Flores-Peréz I (2012) Effective protection induced by three different versions of the porcine S3Pvac anticysticercosis vaccine against rabbit experimental Taenia pisiformis cysticercosis. Vaccine 30:2760–2767
Cai K, Tu W, Liu Y, Li T, Wang H (2015) Novel fusion antigen displayed-bacterial ghosts vaccine candidate against infection of Escherichia coli O157:H7. Sci Rep 5:17479
Chae C (2005) A review of porcine circovirus 2-associated syndromes and diseases. Vet J 169:326–336
Cheng YS, Zheng Y, Labavitch JM, VanderGheynst JS (2013) Virus infection of Chlorella variabilis and enzymatic saccharification of algal biomass for bioethanol production. Bioresour Technol 137:326–331
Daszak P, Zambrana-Torrelio C, Bogich TL, Fernandez M, Epstein JH, Murray KA, Hamilton H (2013) Interdisciplinary approaches to understanding disease emergence: the past, present, and future drivers of Nipah virus emergence. Proc Natl Acad Sci U S A 110:3681–3688
Dórea FC, Elbers AR, Hendrikx P, Enoe C, Kirkeby C, Hoinville L, Lindberg A (2016) Vector-borne disease surveillance in livestock populations: a critical review of literature recommendations and implemented surveillance (BTV-8) in five European countries. Prev Vet Med 125:1–9, pii: S0167-5877(16)30002-2
Feng S, Feng W, Zhao L, Gu H, Li Q, Shi K, Guo S, Zhang N (2014) Preparation of transgenic Dunaliella salina for immunization against white spot syndrome virus in crayfish. Arch Virol 159:519–525
Ganter M (2015) Zoonotic risks from small ruminants. Vet Microbiol 181(1-2):53–65
Grubman MJ, Baxt B (2004) Foot-and-mouth disease. Clin Microbiol Rev 17:465–493
Guo X, Feilmeier B, Troupe KM, Bublot M, Cox K (2011) Foot and mouth disease virus recombinant vaccines and uses thereof. US patent application WO 2011112945 A2
He DM, Qian KX, Shen GF, Zhang ZF, Li YN, Su ZL, Shao HB (2007) Recombination and expression of classical swine fever virus (CSFV) structural protein E2 gene in Chlamydomonas reinhardtii chroloplasts. Colloids Surf B Biointerfaces 55:26–30
Hotez PJ, Ferris MT (2006) The antipoverty vaccines. Vaccine 24(31-32):5787–5799
Ito A, Yanagida T, Nakao M (2015) Recent advances and perspectives in molecular epidemiology of Taenia solium cysticercosis. Infect Genet Evol. 40:357–367 doi:10.1016/j.meegid.2015.06.022
Kahn LH (2011) The need for one health degree programs. Infect Ecol Epidemiol 1:7919
Karesh WB, Dobson A, Lloyd-Smith JO, Lubroth J, Dixon MA, Bennett M, Aldrich S, Harrington T, Formenty P, Loh EH, Machalaba CC, Thomas MJ, Heymann DL (2012) Ecology of zoonoses: natural and unnatural histories. Lancet 380:1936–1945
Kolotilin I, Topp E, Cox E, Devriendt B, Conrad U, Joensuu J, Stöger E, Warzecha H, McAllister T, Potter A, McLean MD, Hall JC, Menassa R (2014) Plant-based solutions for veterinary immunotherapeutics and prophylactics. Vet Res 45:117
Langridge W, Dénes B, Fodor I (2010) Cholera toxin B subunit modulation of mucosal vaccines for infectious and autoimmune diseases. Curr Opin Investig Drugs 11:919–928
Laughlin RC, Drake KL, Morrill JC, Adams LG (2016) Correlative Gene Expression to Protective Seroconversion in Rift Valley Fever Vaccinates. PLoS One 11(1):e0147027
Lightner DV, Redman RM (1998) Shrimp diseases and current diagnostic methods. Aquaculture 164:201–220
Mabbott NA (2015) Prospects for safe and effective vaccines against prion diseases. Expert Rev Vaccines 14(1):1–4
MacDonald J, Doshi K, Dussault M, Hall JC, Holbrook L, Jones G, Kaldis A, Klima CL, Macdonald P, McAllister T, McLean MD, Potter A, Richman A, Shearer H, Yarosh O, Yoo HS, Topp E, Menassa R (2015) Bringing plant-based veterinary vaccines to market: managing regulatory and commercial hurdles. Biotechnol Adv 33(8):1572–1581
Mackey TK, Liang BA, Cuomo R, Hafen R, Brouwer KC, Lee DE (2014) Emerging and reemerging neglected tropical diseases: a review of key characteristics, risk factors, and the policy and innovation environment. Clin Microbiol Rev 27(4):949–979
Manam S, Chaganty BK, Evani SJ, Zafiratos MT, Ramasubramanian AK, Arulanandam BP, Murthy AK (2013) Intranasal vaccination with Chlamydia pneumoniae induces cross-species immunity against genital Chlamydia muridarum challenge in mice. PLoS One 8(5):e64917
Manuell AL, Beligni MV, Elder JH, Siefker DT, Tran M, Weber A, McDonald TL, Mayfield SP (2007) Robust expression of a bioactive mammalian protein in Chlamydomonas chloroplast. Plant Biotechnol J 5:402–412
Mihaliak CA, Webb S, Miller T et al (2005) Development of plant cell produced vaccines for animal health applications. Proceedings of the 108th Annual Meeting of the United States Animal Health Association. Greensboro NC 158–163
Muñoz-González S, Perez-Simó M, Muñoz M, Bohorquez JA, Rosell R, Summerfield A, Domingo M, Ruggli N, Ganges L (2015) Efficacy of a live attenuated vaccine in classical swine fever virus postnatally persistently infected pigs. Vet Res 46:78
O’Keefe KA, Eberhard ML, Shafir SC, Wilkins P, Ash LR, Sorvillo FJ (2015) Cysticercosis-related hospitalizations in the United States, 1998-2011. Am J Trop Med Hyg 92:354–359
Onyango J, Mata F, McCormick W, Chapman S (2014) Prevalence, risk factors and vaccination efficacy of contagious ovine ecthyma (orf) in England. Vet Rec 175(13):326
Phan HT, Floss DM, Conrad U (2013) Veterinary vaccines from transgenic plants: highlights of two decades of research and a promising example. Curr Pharm Des 19:5601–5611
Potter A, Gerdts V, Litte-van den Hurk S (2008) Veterinary vaccines: alternatives to antibiotics? Anim Health Res Rev 9:187–199
Rabinowitz PM, Kock R, Kachani M, Kunkel R, Thomas J, Gilbert J, Wallace R, Blackmore C, Wong D, Karesh W, Natterson B, Dugas R, Rubin C, Stone Mountain One Health Proof of Concept Working Group (2013) Toward proof of concept of a one health approach to disease prediction and control. Emerg Infect Dis 19(12):10–3201
Rosales-Mendoza S, Govea-Alonso DO, Monreal-Escalante E, Fragoso G, Sciutto E (2012) Developing plant-based vaccines against neglected tropical diseases: where are we? Vaccine 31:40–48
Rosales-Mendoza S, Angulo C, Meza B (2015) Food-Grade Organisms as Vaccine Biofactories and Oral Delivery Vehicles. Trends Biotechnol 34:124–136
Salazar-González JA, Bañuelos-Hernández B, Rosales-Mendoza S (2015) Current status of viral expression systems in plants and perspectives for oral vaccines development. Plant Mol Biol 87(3):203–217
Scallan E, Hoekstra RM, Angulo FJ, Tauxe RV, Widdowson MA, Roy SL, Jones JL, Griffin PM (2011) Foodborne illness acquired in the United States—major pathogens. Emerg Infect Dis 17(1):7–15
Schulze LS, Borchardt S, Ouellet V, Heuwieser W (2016) Effect of a phase I Coxiella burnetii inactivated vaccine on body temperature and milk yield in dairy cows. J Dairy Sci 99(1):541–550
Sciutto E, Morales J, Martinez JJ, Toledo A, Villalobos MN, Cruz-Revilla C, Meneses G, Hernández M, Díaz A, Rodarte LF, Acero G, Gevorkian G, Manoutcharian K, Paniagua J, Fragoso G, Fleury A, Larralde R, De Aluja AS, Larralde C (2007) Further evaluation of the synthetic peptide vaccine S3Pvac against Taenia solium cysticercosis in pigs in an endemic town of Mexico. Parasitology 134:129–133
Segura-Velázquez R, Pérez-Torres A, Rosas G, Toledo A, Restelli M, Acosta E, Corral R, Rosetti F, Fragoso G, Grinstein S, Sciutto E (2006) A novel synthetic adjuvant effectively enhances the immunogenicity of the influenza vaccine. Vaccine 24:1073–1080
Statistics Canada (2006) Canada’s beef industry and BSE [Internet] [updated 2006 Jun 28; cited 2014 Jan 31]. Retrieved from: http://www41.statcan.gc.ca/2006/0920/ceb0920_001-eng.htm
Sun M, Qian K, Su N, Chang H, Liu J, Shen G (2003) Foot-and-mouth disease virus VP1 protein fused with cholera toxin B subunit expressed in Chlamydomonas reinhardtii chloroplast. Biotechnol Lett 25:1087–1092
Surzycki R, Greenham K, Kitayama K, Dibal F, Wagner R, Rochaix JD, Ajam T, Surzycki S (2009) Factors effecting expression of vaccines in microalgae. Biologicals 37:133–138
Taylor LH, Latham SM, Woolhouse ME (2001) Risk factors for human disease emergence. Philos Trans R Soc Lond B Biol Sci 356:983–989
Toledo A, Larralde C, Fragoso G, Gevorkian G, Manoutcharian K, Hernández M, Acero G, Rosas G, López-Casillas F, Garfias CK, Vázquez R, Terrazas I, Sciutto E (1999) Towards a Taenia solium cysticercosis vaccine: an epitope shared by Taenia crassiceps and Taenia solium protects mice against experimental cysticercosis. Infect Immun 67:2522–2530
Toledo A, Fragoso G, Rosas G, Hernandez M, Gevorkian G, López-Casillas F, Hernández B, Acero G, Huerta M, Larralde C, Sciutto E (2001) Two epitopes shared by Taenia crassiceps and Taenia solium confer protection against murine T. crassiceps cysticercosis along with a prominent T1 response. Infect Immun 69(3):1766–1773
Van Etten JL, Dunigan DD (2012) Chloroviruses: not your everyday plant virus. Trends Plant Sci 17:1–8
Van Etten JL, Lane LC, Meints RH (1991) Viruses and virus like particles of eukaryotic algae. Microbiol Rev 55:586–620
Woolhouse ME, Gowtage-Sequeria S (2005) Host range and emerging and reemerging pathogens. Emerg Infect Dis 11:1842–1847
Yang Z, Wang J, Cheng X, Jiang Y, Liang Z (2013) Making porcine circovirus vaccine to prevent/treat porcine circovirus infection involves coding porcine circovirus type 2 antigen gene in Chlamydomonas chloroplasts, constructing chloroplasts in expression box; selecting antigen; screening. Patent CN103007269-A
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2016 Springer International Publishing Switzerland
About this chapter
Cite this chapter
Rosales-Mendoza, S. (2016). Algae-Made Vaccines Targeting Animal Pathogens. In: Algae-Based Biopharmaceuticals. Springer, Cham. https://doi.org/10.1007/978-3-319-32232-2_4
Download citation
DOI: https://doi.org/10.1007/978-3-319-32232-2_4
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-32230-8
Online ISBN: 978-3-319-32232-2
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)