inPhocus: “Virus Amigos?” The Journey of the Development of Phage-Based Biocontrol in the Latin American Poultry and Aquaculture Industries

European Centre for Disease Prevention and Control. Antibiotic resistance—an increasing threat to human health. European Antibiotic Awareness Day. 2018. Available at https://antibiotic.ecdc.europa.eu/en/publications-data/antibiotic-resistance-increasing-threat-human-health (last accessed February 2, 2021).

O'Neill J . Review on Antimicrobial Resistance . Antimicrobial Resistance: Tackling a crisis for the health and wealth of nations. 2014. Available at http://www.jpiamr.eu/wp-content/uploads/2014/12/AMR-Review-Paper-Tackling-a-crisis-for-the-health-and-wealth-of-nations_1–2.pdf (last accessed September 30, 2019).

Jonas OB , Irwin A , Berthe FCJ , et al. Drug-resistant infections: A threat to our economic future (Vol. 2): Final report. 2017. Available at https://documents.worldbank.org/en/publication/documents-reports/documentdetail/323311493396993758/final-report (last accessed February 2, 2021).

Rossi F , Baquero F , Hsueh P-R , et al. In vitro susceptibilities of aerobic and facultatively anaerobic Gram-negative bacilli isolated from patients with intra-abdominal infections worldwide: 2004 results from SMART (Study for Monitoring Antimicrobial Resistance Trends). J Antimicrob Chemother. 2006; 58(1):205–210.

Organizacion Panamericana de la Salud . Magnitude and trends of antimicrobial resistance in Latin America [in Spanish]. RELAVRA 2014, 2015, 2016. 2020. Available at https://www.paho.org/es/documentos/magnitud-tendencias-resistencia-antimicrobianos-latinoamerica-relavra-2014-2015-2016 (last accessed February 5, 2021).

Donado-Godoy P , Byrne BA , León M , et al. Prevalence, resistance patterns, and risk factors for antimicrobial resistance in bacteria from retail chicken meat in Colombia. J Food Prot. 2015; 78:751–759.

Vinueza-Burgos C , Wautier M , Martiny D , et al. Prevalence, antimicrobial resistance and genetic diversity of Campylobacter coli and Campylobacter jejuni in Ecuadorian broilers at slaughter age. Poult Sci. 2017; 96(7):2366–2374.

Ferro ID , Benetti TM , Oliveira TCRM , et al. Evaluation of antimicrobial resistance of Campylobacter spp. isolated from broiler carcasses. Br Poult Sci. 2015; 56(1):66–71.

Boeckel TPV , Glennon EE , Chen D , et al. Reducing antimicrobial use in food animals. Science. 2017; 357(6358):1350–1352.

World Health Organization. Global action plan on antimicrobial resistance. Available at https://www.who.int/publications-detail-redirect/global-action-plan-on-antimicrobial-resistance (last accessed February 9, 2021).

Pan American Health Organization. CD54/12 Plan of action on antimicrobial resistance; 2015—PAHO/WHO | Pan American Health Organization. Available at https://www.paho.org/en/documents/cd5412-plan-action-antimicrobial-resistance-2015 (last accessed February 9, 2021).

Da Silva Jr JB , Espinal M , Ramon-Pardo P . Antimicrobial resistance: Time for action [in Spanish]. Rev Panam Salud Publica. 2020.

Ventura da Silva M. Poultry and poultry products—Risks for human health. In: Poultry Development Review. Food and Agriculture Organization of the United Nations; 2013: 15.

Farell D . The role of poultry in human nutrition. In: Poultry Development Review. Rome, Italy: Food and Agriculture Organization of the United Nations; 2013:. 2.

Bryan FL , Doyle MP . Health risks and consequences of Salmonella and Campylobacter jejuni in raw poultry. J Food Prot. 1995; 58(3):326–344.

Fernandez J , Fica A , Ebensperger G , et al. Analysis of molecular epidemiology of Chilean Salmonella enterica serotype Enteritidis isolates by pulsed-field gel electrophoresis and bacteriophage typing. J Clin Microbiol. 2003; 41(4):1617–1622.

dos Santos LR , do Nascimento VP , de Oliveira SD , et al. Phage types of Salmonella Enteritidis isolated from clinical and food samples, and from broiler carcasses in Southern Brazil. Rev Inst Med Trop São Paulo. 2003; 45(1):1–4.

Anderson ES , Williams REO . Bacteriophage typing of enteric pathogens and Staphylococci and its use in epidemiology: A review. J Clin Pathol. 1956; 9(2):94–127.

Andreatti Filho RL , Higgins JP , Higgins SE , et al. Ability of Bacteriophages isolated from different sources to reduce Salmonella enterica Serovar Enteritidis in vitro and in vivo. Poult Sci. 2007; 86(9):1904–1909.

Borie C , Albala I , Sánchez P , et al. Bacteriophage treatment reduces Salmonella colonization of infected chickens. Avian Dis. 2008; 52(1):64–67.

Borie C , Sánchez ML , Navarro C , et al. Aerosol spray treatment with bacteriophages and competitive exclusion reduces Salmonella enteritidis infection in chickens. Avian Dis. 2009; 53(2):250–254.

Holguin-Moreno AV , Vives-Flores MJ , Jimenez-Sanchez AP . Composition comprising bacteriophages for reducing, eliminating and/or preventing Salmonella Enteritidis, Salmonella Typhimurium and Salmonella Paratyphi b [in Spanish]. Universidad de los Andes, assignee. Colombian Pat. No.. 15281747.

Clavijo V , Baquero D , Hernandez S , et al. Phage cocktail SalmoFREE^® reduces Salmonella on a commercial broiler farm. Poult Sci. 2019; 98(10):5054–5063.

Torres-Acosta MA , Clavijo V , Vaglio C , et al. Economic evaluation of the development of a phage therapy product for the control of Salmonella in poultry. Biotechnol Prog. 2019; 35(5):e2852.

Wurmann CG . Regional review on status and trends in aquaculture development in latin america and the caribbean—2015. FAO Fish Aquac Circ. 2017;(C1135/3):III,IV,V,1–36.

Lafferty KD , Harvell CD , Conrad JM , et al. Infectious diseases affect marine fisheries and aquaculture economics. Annu Rev Mar Sci. 2015; 7(1):471–496.

Nematollahi A , Decostere A , Pasmans F , et al. Flavobacterium psychrophilum infections in salmonid fish. J Fish Dis. 2003; 26(10):563–574.

Castillo D , Higuera G , Villa M , et al. Diversity of Flavobacterium psychrophilum and the potential use of its phages for protection against bacterial cold water disease in salmonids. J Fish Dis. 2012; 35(3):193–201.

Toranzo AE , Magariños B , Romalde JL . A review of the main bacterial fish diseases in mariculture systems. Aquaculture. 2005; 246(1):37–61.

Higuera G , Bastías R , Tsertsvadze G , et al. Recently discovered Vibrio anguillarum phages can protect against experimentally induced vibriosis in Atlantic salmon, Salmo salar. Aquaculture. 2013; 392–395:128–133.

Mikkelsen H , Lund V , Martinsen L-C , et al. Variability among Vibrio anguillarum O2 isolates from Atlantic cod (Gadus morhua L.): Characterisation and vaccination studies. Aquaculture. 2007; 266(1):16–25.

Rivas AJ , Lemos ML , Osorio CR . Photobacterium damselae subsp. damselae, a bacterium pathogenic for marine animals and humans. Front Microbiol. 2013; 4. Available at https://www.frontiersin.org/articles/10.3389/fmicb.2013.00283/full (last accessed February 14, 2021).

Veyrand-Quirós B , Gómez-Gil B , Lomeli-Ortega CO , et al. Use of bacteriophage vB_Pd_PDCC-1 as biological control agent of Photobacterium damselae subsp. damselae during hatching of longfin yellowtail (Seriola rivoliana) eggs. J Appl Microbiol. 2020; 129(6):1497–1510.