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Bacteriophages in the control of pathogenic vibrios

https://doi.org/10.1016/j.ejbt.2017.10.012

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Bacteriophage in the Treatment and Prevention of Cholera.

inferredcites →https://doi.org/10.1002/9781118806913.ch15openalex-snapshot

Vaccination against Vibriosis

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Novel Biopolymer Matrices for Microencapsulation of Phages: Enhanced Protection Against Acidity and Protease Activity

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Phage therapy treatment of the coral pathogen V ibrio coralliilyticus

inferredcites →https://doi.org/10.1007/bf01567009openalex-snapshot

Vibrio ordalii sp. nov.: A causative agent of vibriosis in fish

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Call for a Dedicated European Legal Framework for Bacteriophage Therapy

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An incidence of large foodborne outbreak associated with Vibrio mimicus

inferredcites →https://doi.org/10.1007/s10499-015-9948-xopenalex-snapshot

Progress in research on acute hepatopancreatic necrosis disease (AHPND)

inferredcites →https://doi.org/10.1007/s11356-016-8231-7openalex-snapshot

Environmental investigation for the presence of Vibrio species following a case of severe gastroenteritis in a touristic island

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Experimental infection of rainbow trout, Salmo gairdneri R., by dipping in suspensions of Vibrio anguillarum: ways of bacterial penetration; influence of temperature and salinity

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Mass mortality of Penaeus monodon larvae due to antibiotic-resistant Vibrio harveyi infection

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Phage Therapy Pharmacology

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Isolation of Vibrio harveyi bacteriophage with a potential for biocontrol of luminous vibriosis in hatchery environments

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Biocontrol of pathogens in shrimp hatcheries using bacteriophages

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Recently discovered Vibrio anguillarum phages can protect against experimentally induced vibriosis in Atlantic salmon, Salmo salar

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Outbreaks of vibriosis associated with Vibrio mimicus in freshwater catfish in China

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Diversity of Vibrio parahaemolyticus associated with disease outbreak among cultured Litopenaeus vannamei (Pacific white shrimp) in India

inferredcites →https://doi.org/10.1016/j.aquaculture.2015.09.024openalex-snapshot

Efficiency of a bacteriophage in controlling vibrio infection in the juvenile sea cucumber Apostichopus japonicus

inferredcites →https://doi.org/10.1016/j.aquaculture.2017.01.003openalex-snapshot

Bacteriophage therapy for the control of Vibrio harveyi in greenlip abalone (Haliotis laevigata)

inferredcites →https://doi.org/10.1016/j.biocel.2007.07.005openalex-snapshot

Vibrio cholerae: Cholera toxin

inferredcites →https://doi.org/10.1016/j.ejbt.2014.06.001openalex-snapshot

A note on stability in food matrices of Salmonella enterica serovar Enteritidis-controlling bacteriophages

inferredcites →https://doi.org/10.1016/j.ejbt.2015.09.007openalex-snapshot

Amplification of tlh gene in other Vibrionaceae specie by specie-specific multiplex PCR of Vibrio parahaemolyticus

inferredcites →https://doi.org/10.1016/j.fm.2016.02.008openalex-snapshot

Antibiotic resistance of Vibrio parahaemolyticus and Vibrio vulnificus in various countries: A review

inferredcites →https://doi.org/10.1016/j.foodhyd.2010.11.017openalex-snapshot

Enhanced alginate microspheres as means of oral delivery of bacteriophage for reducing Staphylococcus aureus intestinal carriage

inferredcites →https://doi.org/10.1016/j.foodres.2010.04.001openalex-snapshot

Climate anomalies and the increasing risk of Vibrio parahaemolyticus and Vibrio vulnificus illnesses

inferredcites →https://doi.org/10.1016/j.fsi.2015.11.008openalex-snapshot

Pathogenesis of acute hepatopancreatic necrosis disease (AHPND) in shrimp

inferredcites →https://doi.org/10.1016/j.fsi.2016.04.026openalex-snapshot

Use of phages to control Vibrio splendidus infection in the juvenile sea cucumber Apostichopus japonicus

inferredcites →https://doi.org/10.1016/j.ijantimicag.2008.10.034openalex-snapshot

Pathogenic potential of vibriophages against an experimental infection with Vibrio cholerae O1 in the RITARD model

inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2014.07.007openalex-snapshot

Eating oysters without risk of vibriosis: Application of a bacteriophage against Vibrio parahaemolyticus in oysters

inferredcites →https://doi.org/10.1016/j.ijid.2014.03.594openalex-snapshot

Antibiotic resistant patterns amongst clinical Vibrio cholerae O1 isolates from the Greater Accra Region, Ghana-2013

inferredcites →https://doi.org/10.1016/j.ijmm.2014.02.007openalex-snapshot

Comparative analysis of different oral approaches to treat Vibrio cholerae infection in adult mice

inferredcites →https://doi.org/10.1016/j.medmal.2008.06.023openalex-snapshot

Phage therapy experience at the Eliava Institute

inferredcites →https://doi.org/10.1016/j.micinf.2012.11.002openalex-snapshot

Efficacy of cocktail phage therapy in treating Vibrio cholerae infection in rabbit model

inferredcites →https://doi.org/10.1017/s0950268804002705openalex-snapshot

Genetic diversity and antibiotic resistance of clinical and environmental Vibrio cholerae suggests that many serogroups are reservoirs of resistance

inferredcites →https://doi.org/10.1038/21119openalex-snapshot

Marine viruses and their biogeochemical and ecological effects

inferredcites →https://doi.org/10.1038/nature11723openalex-snapshot

Bacteriophage genes that inactivate the CRISPR/Cas bacterial immune system

inferredcites →https://doi.org/10.1038/nature15254openalex-snapshot

Multiple mechanisms for CRISPR–Cas inhibition by anti-CRISPR proteins

inferredcites →https://doi.org/10.1038/nature15386openalex-snapshot

CRISPR-Cas immunity in prokaryotes

inferredcites →https://doi.org/10.1038/ncomms14187openalex-snapshot

A cocktail of three virulent bacteriophages prevents Vibrio cholerae infection in animal models

inferredcites →https://doi.org/10.1038/nmicrobiol.2017.92openalex-snapshot

A decade of discovery: CRISPR functions and applications

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Marine viruses — major players in the global ecosystem

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Bacteriophage resistance mechanisms

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A century of the phage: past, present and future

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A new bacteriophage, VHML, isolated from a toxin-producing strain of Vibrio harveyi in tropical Australia

inferredcites →https://doi.org/10.1046/j.1365-2761.2003.00413.xopenalex-snapshot

Association of a bacteriophage with virulence in Vibrio harveyi

inferredcites →https://doi.org/10.1056/nejmoa1012928openalex-snapshot

The Origin of the Haitian Cholera Outbreak Strain

inferredcites →https://doi.org/10.1080/08905430500524275openalex-snapshot

Vibrio parahaemolyticus, a Notably Lethal Human Pathogen Derived From Seafood: A Review of its Pathogenicity, Characteristics, Subspecies Characterization, and Molecular Methods of Detection

inferredcites →https://doi.org/10.1089/153531404323143594openalex-snapshot

Epidemiology, Pathogenesis, and Prevention of Foodborne Vibrio parahaemolyticus Infections

inferredcites →https://doi.org/10.1089/fpd.2014.1792openalex-snapshot

Association of CRISPR/Cas Evolution with Vibrio parahaemolyticus Virulence Factors and Genotypes

inferredcites →https://doi.org/10.1093/femsle/fnv222openalex-snapshot

Genetic diversity ofVibrio parahaemolyticusstrains isolated from farmed Pacific white shrimp and ambient pond water affected by acute hepatopancreatic necrosis disease outbreak in Thailand

inferredcites →https://doi.org/10.1093/infdis/jiu059openalex-snapshot

Bacteriophage Therapy of a Vibrio parahaemolyticus Infection Caused by a Multiple-Antibiotic–Resistant O3:K6 Pandemic Clinical Strain

inferredcites →https://doi.org/10.1093/jhmas/48.3.275openalex-snapshot

Cholera and Plague in India: The Bacteriophage Inquiry of 1927–1936

inferredcites →https://doi.org/10.1097/qco.0b013e32834a88afopenalex-snapshot

Cholera in the 21st century

inferredcites →https://doi.org/10.1099/ijs.0.02402-0openalex-snapshot

Vibrio coralliilyticus sp. nov., a temperature-dependent pathogen of the coral Pocillopora damicornis

inferredcites →https://doi.org/10.1099/jmm.0.023051-0openalex-snapshot

Antibiotic resistance mechanisms of Vibrio cholerae

inferredcites →https://doi.org/10.1099/mic.0.26797-0openalex-snapshot

Molecular identification of Vibrio harveyi-related isolates associated with diseased aquatic organisms

inferredcites →https://doi.org/10.1111/1462-2920.12420openalex-snapshot

Quorum sensing positively regulates flagellar motility in pathogenic V ibrio harveyi

inferredcites →https://doi.org/10.1111/1462-2920.12484openalex-snapshot

Aquatic ecology of the oyster pathogens V ibrio splendidus and V ibrio aestuarianus

inferredcites →https://doi.org/10.1111/1574-6976.12072openalex-snapshot

Bacteria–phage coevolution as a driver of ecological and evolutionary processes in microbial communities

inferredcites →https://doi.org/10.1111/are.12846openalex-snapshot

Characterization of two bacteriophages for specific treatment of biofilm formed by aVibriosp. isolated from an abalone farm

inferredcites →https://doi.org/10.1111/are.12923openalex-snapshot

The first record of acute hepatopancreatic necrosis disease in the Philippines

inferredcites →https://doi.org/10.1111/j.1365-2672.2004.02362.xopenalex-snapshot

The ability of two different Vibrio spp. bacteriophages to infect Vibrio harveyi, Vibrio cholerae and Vibrio mimicus

inferredcites →https://doi.org/10.1111/j.1365-2672.2006.03250.xopenalex-snapshot

Cloning and expression of gene encoding the thermostable direct hemolysin from Vibrio alginolyticus strain HY9901, the causative agent of vibriosis of crimson snapper (Lutjanus erythopterus)

inferredcites →https://doi.org/10.1111/j.1365-2672.2009.04578.xopenalex-snapshot

Isolation of lytic bacteriophage againstVibrio harveyi

inferredcites →https://doi.org/10.1111/j.1365-2672.2010.04743.xopenalex-snapshot

An in vitro and in vivo assessment of the potential of Vibrio spp. as probiotics for the Pacific White shrimp, Litopenaeus vannamei

inferredcites →https://doi.org/10.1111/j.1365-2761.1994.tb00221.xopenalex-snapshot

Vibrio anguillarum serovars associated with vibriosis in fish

inferredcites →https://doi.org/10.1111/j.1365-2761.2007.00878.xopenalex-snapshot

First description of serotype O3 in Vibrio anguillarum strains isolated from salmonids in Chile

inferredcites →https://doi.org/10.1111/j.1365-2761.2011.01279.xopenalex-snapshot

Vibrio anguillarum as a fish pathogen: virulence factors, diagnosis and prevention

inferredcites →https://doi.org/10.1111/j.1365-2761.2011.01336.xopenalex-snapshot

Diversity of Flavobacterium psychrophilum and the potential use of its phages for protection against bacterial cold water disease in salmonids

inferredcites →https://doi.org/10.1111/j.1462-2920.2005.00847.xopenalex-snapshot

Pathogenicity of vibrios to rainbow trout ( Oncorhynchus mykiss , Walbaum) and Artemia nauplii

inferredcites →https://doi.org/10.1111/j.1462-2920.2006.01006.xopenalex-snapshot

Genetic richness of vibriophages isolated in a coastal environment

inferredcites →https://doi.org/10.1111/j.1462-2920.2006.01054.xopenalex-snapshot

Heavy use of prophylactic antibiotics in aquaculture: a growing problem for human and animal health and for the environment

inferredcites →https://doi.org/10.1111/j.1462-2920.2006.01140.xopenalex-snapshot

Molecular characterization of Vibrio harveyi bacteriophages isolated from aquaculture environments along the coast of India

inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02143.xopenalex-snapshot

A new group of cosmopolitan bacteriophages induce a carrier state in the pandemic strain of Vibrio parahaemolyticus

inferredcites →https://doi.org/10.1111/j.1462-2920.2012.02883.xopenalex-snapshot

Rise and fall of pandemic V ibrio parahaemolyticus serotype O3 : K6 in southern C hile

inferredcites →https://doi.org/10.1111/j.1472-765x.2006.01989.xopenalex-snapshot

Vibrio harveyi: a significant pathogen of marine vertebrates and invertebrates

inferredcites →https://doi.org/10.1111/j.1574-6968.2009.01755.xopenalex-snapshot

Analysis of 16S–23S rRNA gene internal transcribed spacer ofVibrio anguillarumandVibrio ordaliistrains isolated from fish

inferredcites →https://doi.org/10.1111/j.1574-6968.2009.01850.xopenalex-snapshot

Vibrio owensii sp. nov., isolated from cultured crustaceans in Australia

inferredcites →https://doi.org/10.1111/j.1753-5131.2012.01061.xopenalex-snapshot

Pathogenesis, virulence factors and virulence regulation of vibrios belonging to the Harveyi clade

inferredcites →https://doi.org/10.1111/jfd.12659openalex-snapshot

Virulence‐associated factors in Vibrio cholerae non‐O1/non‐O139 and V. mimicus strains isolated in ornamental fish species

inferredcites →https://doi.org/10.1111/jwas.12177openalex-snapshot

Effect of Bacteriophages on Vibrio alginolyticus Infection in the Sea Cucumber, Apostichopus japonicus (Selenka)

inferredcites →https://doi.org/10.1111/lam.12175openalex-snapshot

Isolation and characterization of broad spectrum bacteriophages lytic to Vibrio harveyi from shrimp farms of Kerala, India

inferredcites →https://doi.org/10.1111/raq.12188openalex-snapshot

A comprehensive review of Vibrio ( Listonella ) anguillarum : ecology, pathology and prevention

inferredcites →https://doi.org/10.1126/science.272.5270.1910openalex-snapshot

Lysogenic Conversion by a Filamentous Phage Encoding Cholera Toxin

inferredcites →https://doi.org/10.1128/aac.30.4.622openalex-snapshot

Antibiotic resistance patterns of Vibrio mimicus isolated from human and environmental sources in Bangladesh

inferredcites →https://doi.org/10.1128/aac.49.7.2874-2878.2005openalex-snapshot

Human Volunteers Receiving Escherichia coli Phage T4 Orally: a Safety Test of Phage Therapy

inferredcites →https://doi.org/10.1128/aem.00509-13openalex-snapshot

Dispersal and Survival of Flavobacterium psychrophilum PhagesIn Vivoin Rainbow Trout andIn Vitrounder Laboratory Conditions: Implications for Their Use in Phage Therapy

inferredcites →https://doi.org/10.1128/aem.00620-16openalex-snapshot

Multilocus Sequence Analysis of Close Relatives Vibrio anguillarum and Vibrio ordalii

inferredcites →https://doi.org/10.1128/aem.01421-13openalex-snapshot

Evolution of Pseudomonas aeruginosa Virulence as a Result of Phage Predation

inferredcites →https://doi.org/10.1128/aem.01995-08openalex-snapshot

Enhancement of UV Light Sensitivity of a Vibrio parahaemolyticus O3:K6 Pandemic Strain Due to Natural Lysogenization by a Telomeric Phage

inferredcites →https://doi.org/10.1128/aem.02386-14openalex-snapshot

Detection and Quantification of Flavobacterium psychrophilum-Specific Bacteriophages In Vivo in Rainbow Trout upon Oral Administration: Implications for Disease Control in Aquaculture

inferredcites →https://doi.org/10.1128/aem.02930-14openalex-snapshot

Mortalities of Eastern and Pacific Oyster Larvae Caused by the Pathogens Vibrio coralliilyticus and Vibrio tubiashii

inferredcites →https://doi.org/10.1128/aem.62.4.1141-1144.1996openalex-snapshot

Vibrio mimicus diarrhea following ingestion of raw turtle eggs

inferredcites →https://doi.org/10.1128/aem.63.2.408-413.1997openalex-snapshot

Chitin Degradation Proteins Produced by the Marine Bacterium Vibrio harveyi Growing on Different Forms of Chitin

inferredcites →https://doi.org/10.1128/aem.64.11.4269-4275.1998openalex-snapshot

Pathogenicity of Vibrio alginolyticus for Cultured Gilt-Head Sea Bream ( Sparus aurata L.)

inferredcites →https://doi.org/10.1128/cmr.00025-06openalex-snapshot

Global Dissemination of Vibrio parahaemolyticus Serotype O3:K6 and Its Serovariants

inferredcites →https://doi.org/10.1128/iai.01046-08openalex-snapshot

Vibrio vulnificus: Disease and Pathogenesis

inferredcites →https://doi.org/10.1128/iai.70.11.6251-6262.2002openalex-snapshot

Phage Therapy of Local and Systemic Disease Caused by Vibrio vulnificus in Iron-Dextran-Treated Mice

inferredcites →https://doi.org/10.1128/jb.00378-11openalex-snapshot

Protection and Attachment of Vibrio cholerae Mediated by the Toxin-Coregulated Pilus in the Infant Mouse Model

inferredcites →https://doi.org/10.1128/jb.00747-15openalex-snapshot

Functional Analysis of Bacteriophage Immunity through a Type I-E CRISPR-Cas System in Vibrio cholerae and Its Application in Bacteriophage Genome Engineering

inferredcites →https://doi.org/10.1128/jcm.00092-11openalex-snapshot

Vibrio furnissii: an Unusual Cause of Bacteremia and Skin Lesions after Ingestion of Seafood

inferredcites →https://doi.org/10.1128/jcm.10.5.666-668.1979openalex-snapshot

Vibrio alginolyticus infections in humans

inferredcites →https://doi.org/10.1128/jcm.25.11.2200-2203.1987openalex-snapshot

Toxin production by Vibrio mimicus strains isolated from human and environmental sources in Bangladesh

inferredcites →https://doi.org/10.1128/jvi.00672-09openalex-snapshot

The Linear Plasmid Prophage Vp58.5 of Vibrio parahaemolyticus Is Closely Related to the Integrating Phage VHML and Constitutes a New Incompatibility Group of Telomere Phages

inferredcites →https://doi.org/10.1128/microbiolspec.ve-0001-2014openalex-snapshot

The Biology of Vibrio vulnificus

inferredcites →https://doi.org/10.1128/mmbr.62.4.1301-1314.1998openalex-snapshot

Epidemiology, Genetics, and Ecology of Toxigenic Vibrio cholerae

inferredcites →https://doi.org/10.1128/mmbr.68.3.403-431.2004openalex-snapshot

Biodiversity of Vibrios

inferredcites →https://doi.org/10.1136/vr.162.3.94openalex-snapshot

Clinical vibriosis in farmed Atlantic cod ( Gadus morhua ) in Ireland

inferredcites →https://doi.org/10.1186/gb-2007-8-4-r61openalex-snapshot

Evolutionary conservation of sequence and secondary structures in CRISPR repeats

inferredcites →https://doi.org/10.1300/j109v08n01_06openalex-snapshot

European Patent Office

inferredcites →https://doi.org/10.1371/journal.pone.0031698openalex-snapshot

A Method for Generation Phage Cocktail with Great Therapeutic Potential

inferredcites →https://doi.org/10.1371/journal.pone.0053157openalex-snapshot

Phage-Driven Loss of Virulence in a Fish Pathogenic Bacterium

inferredcites →https://doi.org/10.1371/journal.pone.0081800openalex-snapshot

An Improved Detection and Quantification Method for the Coral Pathogen Vibrio coralliilyticus

inferredcites →https://doi.org/10.1371/journal.pone.0114197openalex-snapshot

Phage Therapy as an Approach to Prevent Vibrio anguillarum Infections in Fish Larvae Production

inferredcites →https://doi.org/10.1371/journal.pone.0144885openalex-snapshot

Molecular and Genomic Characterization of Vibrio mimicus Isolated from a Frozen Shrimp Processing Facility in Mexico

inferredcites →https://doi.org/10.1371/journal.pone.0151101openalex-snapshot

Isolation and Characterization of Two Lytic Bacteriophages, φSt2 and φGrn1; Phage Therapy Application for Biological Control of Vibrio alginolyticus in Aquaculture Live Feeds

inferredcites →https://doi.org/10.2174/138920110790725401openalex-snapshot

Phage Therapy in Clinical Practice: Treatment of Human Infections

inferredcites →https://doi.org/10.2217/17460913.2.3.335openalex-snapshot

Regulation of Virulence in Vibrio Cholerae : The Toxr Regulon

inferredcites →https://doi.org/10.2217/fvl.15.3openalex-snapshot

Bacteriophage Therapy: History and Future Prospects

inferredcites →https://doi.org/10.2225/vol10-issue4-fulltext-14openalex-snapshot

Phage-resistance of Salmonella enterica serovar Enteritidis and pathogenesis in Caenorhabditis elegans is mediated by the lipopolysaccharide

inferredcites →https://doi.org/10.3147/jsfp.46.1openalex-snapshot

Genetic Determinants of Virulence in the Marine Fish Pathogen Vibrio anguillarum

inferredcites →https://doi.org/10.3201/eid1502.071269openalex-snapshot

Epidemiology ofVibrio parahaemolyticusOutbreaks, Southern Chile

inferredcites →https://doi.org/10.3201/eid1701.p11101openalex-snapshot

Foodborne Illness Acquired in the United States—Major Pathogens

inferredcites →https://doi.org/10.3201/eid2207.151896openalex-snapshot

Outbreak ofVibrio parahaemolyticusSequence Type 120, Peru, 2009

inferredcites →https://doi.org/10.3354/dao01982openalex-snapshot

Re-emergence of Vibrio tubiashii in bivalve shellfish aquaculture: severity, environmental drivers, geographic extent and management

inferredcites →https://doi.org/10.3354/dao027157openalex-snapshot

Effect of strain origin on siderophore production in Vibrio harveyi isolates

inferredcites →https://doi.org/10.3354/dao02806openalex-snapshot

Simulated hatchery system to assess bacteriophage efficacy against Vibrio harveyi

inferredcites →https://doi.org/10.3354/dao03005openalex-snapshot

Survival behaviour and virulence of the fish pathogen Vibrio ordalii in seawater microcosms

inferredcites →https://doi.org/10.3354/dao053033openalex-snapshot

Bacteriophage control of Pseudomonas plecoglossicida infection in ayu, Plectoglossis altivelis

inferredcites →https://doi.org/10.3354/dao054187openalex-snapshot

Experimental bacteriophage-mediated virulence in strains of Vibrio harveyi

inferredcites →https://doi.org/10.3354/dao057147openalex-snapshot

Vibrio alginolyticus associated with white spot disease of Penaeus monodon

inferredcites →https://doi.org/10.3354/meps120089openalex-snapshot

Genetic diversity of related vibriophages isolated from marine environments around Florida and Hawaii, USA

inferredcites →https://doi.org/10.3389/fmicb.2014.00091openalex-snapshot

Vibrio fluvialis: an emerging human pathogen

inferredcites →https://doi.org/10.3389/fmicb.2015.00144openalex-snapshot

The pathogenesis, detection, and prevention of Vibrio parahaemolyticus

inferredcites →https://doi.org/10.3389/fmicb.2015.00343openalex-snapshot

Virulence reduction in bacteriophage resistant bacteria

inferredcites →https://doi.org/10.3389/fmicb.2016.00567openalex-snapshot

Sero-Prevalence and Genetic Diversity of Pandemic V. parahaemolyticus Strains Occurring at a Global Scale

inferredcites →https://doi.org/10.3389/fmicb.2016.01209openalex-snapshot

Adapting Drug Approval Pathways for Bacteriophage-Based Therapeutics

inferredcites →https://doi.org/10.3389/fmicb.2016.01473openalex-snapshot

RETRACTED: First Report of Vibrio tubiashii Associated with a Massive Larval Mortality Event in a Commercial Hatchery of Scallop Argopecten purpuratus in Chile

inferredcites →https://doi.org/10.3389/fmicb.2017.00528openalex-snapshot

Functional Characterization and Conditional Regulation of the Type VI Secretion System in Vibrio fluvialis

inferredcites →https://doi.org/10.3389/fmicb.2017.00762openalex-snapshot

New Insights into Pathogenic Vibrios Affecting Bivalves in Hatcheries: Present and Future Prospects

inferredcites →https://doi.org/10.4067/s0717-34582007000400015openalex-snapshot

Phage-resistance of Salmonella enterica serovar Enteritidis and pathogenesis in Caenorhabditis elegans is mediated by the lipopolysaccharide

inferredcites →https://doi.org/10.4161/bact.1.2.14590openalex-snapshot

Pros and cons of phage therapy

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Synergy as a rationale for phage therapy using phage cocktails

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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