1. A phylogenetic analysis of the genus Leuconostoc based on reverse transcriptase sequencing of 16S rRNA. Martínez-Murcia, A.J . and Collins, M.D. 1990. FEMS Microbiol. Lett., 70: 73-84.
  2. 16S ribosomal ribonucleic acid sequence determination of members of the genus Carnobacterium and related lactic acid bacteria. Description of Vagococcus salmoninarum sp. nov. Wallbanks, S., Martínez-Murcia, A.J.,Fryer, J.L., Phillips, B.A. and Collins M.D. 1990. Int. J. System. Bacteriol., 40: 224-230.
  3. Phylogenetic analysis of the genus Lactobacillus and related lactic acid bacteria as determined by reverse transcriptase of 16S rRNA. Collins, M.D., Rodrigues, U., Ash, C., Aguirre, M., Farrow, J.A.E., Martínez-Murcia, A.J.,Phillips, B.A., Williams, A.M. and Wallbanks, S. 1990. FEMS Microbiol. Lett., 77: 5-12.
  4. Nucleotide sequence of 16S rRNA from Lactobacillus kandleri and Lactobacillus minor.Martínez-Murcia, A.J.and Collins, M.D. 1990. Nuc. Acids Res., 18: 3401.
  5. Nucleotide sequence of 16S rRNA from Lactobacillus confusus and Lactobacillus viridescens.Martínez-Murcia, A.J.and Collins, M.D. 1990. Nuc. Acids Res., 18: 3402.
  6. Enterococcus sulfureus, a new yellow-pigmented enterococci species.Martínez-Murcia, A.J.and Collins, M.D. 1991. FEMS Microbiol. Lett., 80: 69-73.
  7. A phylogenetic analysis of an atypical leuconostoc: description of Leuconostoc fallax sp. nov.Martínez-Murcia, A.J.and Collins, M.D. 1991. FEMS Microbiol. Lett., 82: 55-60.
  8.  An automated RNA extraction procedure and application for 16S rRNA sequencing of Leuconostoc amelobiosum.Martínez-Murcia, A.J. Microbiología SEM, 7: 106-112.
  9. Phylogenetic interrelationships of members of the genera Aeromonas and Plesiomonas as determined by 16S rDNA sequencing: lack of congruence with results of DNA-DNA hybridizations.Martínez-Murcia, A.J.,Benlloch, S. and Collins, M.D. 1992. Int. J. Sys. Bacteriol., 42 : 412-421.
  10. Aeromonas allosaccharophila sp. nov., a new mesophilic member of the genus Aeromonas.Martínez-Murcia, A.J.,Esteve, C., Garay, E. and Collins, M.D. 1992. FEMS Microbiol. Lett., 91, 199-206.
  11.  Phylogenetic analysis of some leuconostocs and related organisms as determined from large-subunit rRNA gene sequences: assessment of congruence of small- and large-subunit rRNA derived trees. Martinez-Murcia, A.J.,Harland, N.M. and Collins, M.D. 1993. J. Appl. Bacteriol., 74, 532-541.
  12. Identification of Aeromonas schubertii and Aeromonas jandaei by using a polymerase chain reaction-probe test. Martinez-Murcia, A.J.and Collins, M.D. 1993. FEMS Microbiol. Lett., 108, 151-156.
  13. Molecular identification of Aeromonas sobria by polymerase chain reaction. Ash, C., Martínez-Murcia, A.J.and Collins, M.D. 1993. Med. Microbiol. Lett., 2, 80-86.
  14. Aeromonas enteropelogenes and Aeromonas ichthiosmia are identical to Aeromonas trota and Aeromonas veronii, respectively, as revealed by small-subunit rRNA sequence analysis. Collins, M.D., Martínez-Murcia, A.J.and Cai, J. 1993. Int. J. Sys. Bacteriol., 43, 855-866.
  15. Random amplified polymorphic DNA of a group of halophilic archaeal isolates. Martínez-Murcia, A.J.and Rodríguez-Valera, F. 1994. System. Appl. Microbiol., 17, 395-401.

16. The use of arbitrarily primed PCR (AP-PCR) to develop taxa specific DNA probes of known sequence. Martínez-Murcia, A.J. and Rodríguez-Valera, F. 1994. FEMS Microbiol. Lett., 124, 265-270.

  1. Evaluation of the authenticity of haloarchaeal strains by Random-amplified polymorphic DNA. Martínez-Murcia, A.J.,Boan, I.J. and Rodríguez-Valera, F. 1995.  Appl. Microbiol., 21, 106-108.
  2. Sequencing of Bacterial and Archaeal 16S rRNA genes directly amplified from a hypersalineenvironment. Benlloch, S., Martínez-Murcia, A.J.and Rodríguez-Valera,F. 1995.  Appl. Microbiol., 18, 574-581.
  3. Evaluation of prokaryotic diversity by restrictase digestion of 16S rDNA directly amplified from hypersaline environments. Martínez-Murcia A.J.,Acinas, S.G. and Rodríguez-Valera, F. 1995. FEMS Microbiol. Ecol., 17, 247-256.
  4. Bacterial diversity in two coastal lagoons deduced from 16S rDNA PCR amplification and partial sequencing. Benlloch, S., Rodríguez-Valera,F and Martínez-Murcia, A.J.FEMS Microbiol. Ecol., 18, 267-280
  5. Molecular evidence supporting the existence of two major groups in uropathogenic Escherichia coli. García-Martínez, J., Martínez-Murcia, A.J.,Rodríguez-Valera, F. and Zorraquino, A. 1996. FEMS Immunol. Med. Microbiol., 14, 231-244.

22. 16S-23S rDNA intergenic sequences indicate that Leuconostoc oenos is phylogenetically homogeneous. Zavaleta, A., Martínez-Murcia, A.J. and Rodríguez-Valera,F. 1996. Microbiology-UK, 142, 2105-2114.

  1. Genetic diversity in uropathogenic Escherichia coli as shown by RAPD (Random Amplified Polymorphic DNA), 16S-23S rDNA spacers and adhesin gene restriction patterns. In Book: “Ecology of pathogenic bacteria: molecular and evolutionary aspects”. BAM van der Zeijst, WPM Hoekstra, JDA van Embden and AJW Alphen Editors. Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands. Rodríguez-Valera, F., García-Martínez, J., Zorraquino, A. and Martínez-Murcia, A.J.
  2. Intraspecific diversity in/strongspan bacteria. The case of Escherichia coli . Rodríguez-Valera, F. García-Martínez and Martínez-Murcia, A.J.Microbiología SEM, 11, 379-382.
  3. Heterotrophic bacteria activity and bacterial diversity in two coastal lagoons as detected by culture and 16S rDNA PCR amplification and partial sequencing. Benlloch, S., Rodríguez-Valera,F., Acinas, S.G. and Martínez-Murcia, A.J.Hydrobiology 329, 3-17.

26. Description of prokaryotic biodiversity along the salinity gradient of a multipond solar saltern by direct PCR amplification of 16S rDNA. Benlloch, S., Acinas, S.G., Martínez-Murcia, A.J. and Rodríguez-Valera,F. 1996. Hydrobiology 329, 19-31.

  1. Intraspecific Genetic Diversity of Oenococcus oeni as Derived from DNA Fingerprinting and Sequence Analyses. Zavaleta, A., Martínez-Murcia, A.J.and Rodríguez-Valera, F. 1997. Appl. Environ. Microbiol. 63, 1261-1267
  2. Heterotrophic bacteria activity and bacterial diversity in two coastal lagoons as detected by culture and 16S rDNA PCR amplification and partial sequencing. Benlloch, S., Rodríguez-Valera,F., Acinas, S.G. and Martínez-Murcia, A.J. 1996. Developments in Hydrobiology. “Coastal Lagoon Eutrophication and ANaerobic Processes (C.L.E.A.N.)”. Pierre Caumette, Jacques Castel and Rodney Herbert, Editors. Kluwer Academic Publishers, Dordrecht, The Netherlands.
  3. Description of prokaryotic biodiversity along the salinity gradient of a multipond solar saltern by direct PCR amplification of 16S rDNA. Benlloch, S., Acinas, S.G., Martínez-Murcia, A.J. and Rodríguez-Valera,F. 1996. Developments in Hydrobiology. “Coastal Lagoon Eutrophication and ANaerobic Processes (C.L.E.A.N.)”. Pierre Caumette, Jacques Castel and Rodney Herbert, Editors. Kluwer Academic Publishers, Dordrecht, The Netherlands.
  4. Patterns and sequencing analyses of DNA-fragments randomly amplified from Leuconostoc oenos. Zavaleta, A., Martínez-Murcia, A.J.and Rodríguez-Valera, F. 1997 Appl. Microbiol. 63, 1261-1267
  5. Comparison of the small 16S to 23S intergenic spacer region (ISR) of the rRNA operons of some Escherichia coli of the ECOR collection and E. coli K12. García-Martínez, J., Martínez-Murcia, A.J.,Anton, A.I., and Rodríguez-Valera,F. 1996.  of Bacteriol. 178, 6374-6377.
  6. Identification of Aeromonas clinical isolates by PCR-amplified 16S rDNA-restriction fragment length polymorphism. Borrell, N., Acinas, S.G., Figueras, M.J. and Martínez-Murcia, A.J.J. Clin. Microbiol. 35, 1671-1674.
  7. Patterns of sequence variation in two regions of the 16S rRNA multigene family of Escherichia coli.. Martinez-Murcia, A.J.,Anton, A.I. and Rodríguez-Valera, F. 1999. J. Sys. Bacteriol.49, 601-610.
  8. Sequence diversity in the 16S-23S Intergenic Spacer Region (ISR) of the rRNA operons in representatives of the Escherichiacoli ECOR collection. Antón, A.I., Martinez-Murcia,A.J. and Rodríguez-Valera, F. 1998. J. Mol. Evol. 47, 62-72.
  9. Intergenic spacer region (ISR) of the rRNA operons in representatives of the Escherichia coli ECOR collection. Antón, A.I., Martinez-Murcia,A.J.and Rodríguez-Valera, F. 1998.  Mol. Evol. 47, 62-72.
  10. Intraspecific diversity of the 23S rRNA gene and the spacer region downstream in Escherichia coli. Antón, A.I., Martinez-Murcia,A.J.and Rodríguez-Valera, F. 1999 J. Bacteriol. 181, 2703-2709.
  11. Phylogenetic positions of Aeromonas encheleia, Aeromonas popoffii, Aeromonas DNA Hybridization Group 11 and Aeromonas Group 501. Martinez-Murcia,A.J.Int. J. Syst. Bacteriol. 49, 1403-1408.
  12. Typing of clinical and environmental Aeromonas veronii strains based on the 16S-23S rDNA spacers. Martinez-Murcia,A.J.,Borrell, N. and Figueras, M.-J. 2000. FEMS Inmunol. Med. Microbiol. Lett. 28, 225-232.
  13. Extended method for discrimination of Aeromonas spp. By 16S rDNA RFLP analysis. Figueras, M.J., Soler, L., Chacón, M., Guarro, J. and Martínez-Murcia, A.J.2000 Int. J. Sys. Microbiol. 50, 2069-2073.
  14. Clynically relevant Aeromonas spp. Figueras, M.J., Guarro, J. and Martínez-Murcia, A.J.2000 Clin. Infect. Dis. 30, 988-989
  15. Restriction fragment length polymorphism of the PCR-amplified 16S rRNA gene for the identification of Aeromonas spp. Figueras, M.J., Guarro, J. and Martínez-Murcia, A.J.2000 J. Clin. 38, 2023-2025.
  16. Sequence microdiversity at the ribosomal RNA operons of Escherichia coli pyelonephritogenic strains. Antón, A.I., Martinez-Murcia,A.J., Dalet, F. and Rodríguez-Valera, F. 2001. Clinical Microbiology and Infection 7, 345-351
  17. 16S ribosomal DNA and 16S-23S spacer diversity of Escherichia coli isolates causing human acute pyelonephritis. Antón, A.I., Martinez-Murcia,A.J.,Dalet, F. and Rodríguez-Valera, F. 2001. Clinical Microbiology and Infection 7, 1-7
  18. Potential virulence and antimicrobial susceptibility of Aeromonas popofii, recovered from freshwater and seawater. Soler, L., Figueras, M.J., Chacón, M., Vila, J., Marco, F., Martínez-Murcia, A.J.and Guarro, J.2002 FEMS Immunol. Microbiol. Letts. 32, 243-247
  19. Comparison of three molecular methods for typing Aeromonas popoffii isolates. Soler L., Figueras M.J., Chacón M.R., Guarro J. & Martinez-Murcia A.J.(2003). Antonie van Leeuwenhoek. 83, 341-349
  20. Phylogenetic analysis of the genus Aeromonas based on gyrB gene sequences. Yánez, M.A., Catalán, V., Apráiz, D., Figueras, M.J. and Martínez-Murcia A.J.2003 Int. J. System. Microbiol. 53, 875-883.
  21. Phylogenetic analysis of the genus Aeromonas based on two housekeeping genes.  Soler3, M.A. Yáñez2,4, M.R. Chacon3, M.G. Aguilera-Arreola3,5, V. Catalan4, M.J. Figueras3, and A. J.Martinez-Murcia1,2. 2004. Int. J. System. Evol. Microbiol. 54, 1511-1519
  22. Resistance to &-lactam antibiotics in Aeromonas hydrophila isolated from rainbow trout (Oncorhynchus mykiss). Saavedra , Guedes-Novais, Alves, Rema, Tacão, Correia, and Martínez-Murcia. International Microbiology 7, 207-211.
  23. First record of the rare species Aeromonas culicicola from a drinking water supply. Figueras, M.J., Suarez-Franquet, A., Chacón, M.R., Soler, L., Navarro, M., Alejandre, C., Grasa, B., Martínez-Murcia, A.J., and Guarro, J. 2005 Appl. Microbiol. 71, 538-541.
  24. Phenotypifont-size: genotypic and phylogenetic discrepancies to differentiate Aeromonas salmonicida and Aeromonas bestiarum from each other. J. Martínez-Murcia* 1, L. Soler2, M.J. Saavedra1,3, M.R. Chacón, J. Guarro2, E. Stackebrandt4, and M.J. Figueras2. 2005 International Microbiology 8, 259-270
  25. Microbiota associated to Posidonia oceanica in Western Mediterranean sea. Ester Marco-Noales*,1, Mónica Ordax1, Armando Delgado1, María Milagros López1, María José Saavedra2, Antonio Martínez-Murcia2,Neus Garcias3, Núria Marbà3, Carlos M. Duarte3 2006. Modern Multidisciplinary Applied Microbiology. Exploiting Microbes and Their Interactions. Mendez-Vilas, Antonio (ed.) 1ª Edition , páginas 114-119. ©2006 Wiley-VCH Verlag GmbH & Co. KGaA
  26. Genotyping of isolates included in the description of a novel species should be mandatory. Figueras, M. J., Alperi, A., Guarro J. & Martinez-Murcia A. J.(2006). International Journal of Systematic and Evolutionary Microbiology, 56, 1183-1184
  27. Updated phylogeny of the genus Aeromonas M.J. Saavedra1, 2, M.J. Figueras3, and J. Martínez-Murcia1*(2006) International Journal of Systematic and Evolutionary Microbiology, 56, 2481-2487.
  28. Phylogenetic identification of new Aeromonas allosaccharophila strains isolated from pigs, a species not detected since first description. Saavedra, M. J., Perea, V., Fontes, M. C., Martins, C. & Martínez-Murcia, A. J. (2007). Antonie van Leeuwenhoek, 91, 159-167.
  29. The recently proposed species Aeromonas sharmana sp. nov., isolate GPTSA-6, is not a member of the genus Aeromonas. J. Martínez-Murcia1*,M.J. Figueras3, M.J. Saavedra1, 2 and E. Stackebrandt (2007) International Microbiology, 10, 61-64.
  30. Controversial data on the association of Aeromonas with diarrhoea in a recent Hong Kong study. M. J. Figueras, A. J. Horneman, J. Martinez-Murciaand A.J. Guarro (2007) Journal of Medical Microbiology, 56, 996-998.
  31. Aeromonas tecta sp. nov., isolated from clinical and environmental sources. Antonella Demarta,1 Mara Küpfer,1 Philippe Riegel2, Colette Harf-Monteil,2 Mauro Tonolla1, Raffaele Peduzzi1, M.J. Saavedra3, J. Martínez-Murcia(2008) Syst. Appl. Microbiol. 31, 278–286
  32. Aeromonas aquariorum species nova, isolated from aquaria of ornamental fish.  J. Martınez-Murcia,M. J. Saavedra, V. R. Mota, T. Maier, E. Stackebrandt and S. Cousin (2008) International Journal of Systematic and Evolutionary Microbiology, 58, 1169–1175
  33. Analysis of 16S rRNA gene mutations in a subset of Aeromonas strains and their impact in species delineation (2008) Anabel Alperi, Maria J. Figueras, Isabel Inza, Antonio J. Martínez-Murcia International Microbiology, 11:185-194
  34. Phylogenetic evidence indicated that Aeromonas hydrophila subsp. dhakensis Huys et al. 2002 is a synonym of Aeromonas aquariorum sp. nov. Martínez-Murcia et al. 2008. Antonio Martínez-Murcia, Arturo Monera, Anabel Alperi, Maria-Jose Figueras, Maria-Jose Saavedra (2009) Current Microbiology 58: 76-80.
  35. Cultivar identification using 18S–28S rDNA intergenic spacer-RFLP in pomegranate (Punica granatum L.) P. Melgarejo J.J. Martínez, Fca. Hernández a, R. Martínez,*, P. Legua, R. Oncina, J. Martínez-Murcia(2009) Scientia Horticulturae 120: 500–503
  36. Clinical Relevance of the Recently Described Species Aeromonas aquariorum_ M. Jose Figueras,* Anabel Alperi, M. Jose Saavedra, Wen-Chien Ko, Nieves Gonzalo, Maria Navarro, and Antonio J. Martínez-Murcia(2009) Journal of Clinical Microbiology 47: 3742-3746
  37. Phylogenetic identification of Aeromonas simiae from a pig, first isolate since species description Maria Conceicao Fontes, Maria Jose Saavedra, Arturo Monera, Conceicao Martins, Antonio Martınez-Murcia(2010)Veterinary Microbiology 142: 313-316.
  38. Aeromonas fluvialis sp. nov., isolated from a Spanish river. Anabel Alperi, Antonio J. Martínez-Murcia, Arturo Monera, Maria J. Saavedra and Maria J. Figueras Int J Syst Evol Microbiol (2010); 60, 72–77
  39. Aeromonas taiwanensis sp. nov. and Aeromonas sanarellii sp. nov., two new clinical species from Taiwan Anabel Alperi, Antonio J. Martínez-Murcia, Wen-Chien Ko, Arturo Monera, Maria J. Saavedra and Maria J. Figueras Int J Syst Evol Microbiol (2010) 60, 2048 – 2055.
  40. Aeromonas rivuli sp. nov., isolated from the upstream region of a karst water rivulet in Germany . Maria J. Figueras Anabel Alperi, Roxana Beaz-Hidalgo, Erko Stackebrandt, E. Brambilla, Arturo Monera, and Antonio J. Martínez-Murcia Int J Syst Evol Microbiol (2011) 61, 242-248.
  41. Multilocus phylogenetic analysis of the genus Aeromonas. Martinez-Murcia, A. J.,Monera, A., Saavedra, M. J., Oncina, R., Lopez-Alvarez, M., Lara, E. and Figueras M. J. (2011) Syst Appl Microbiol 34; 189–199
  42. Phylogenetic identification of Aeromonas from pigs slaughtered for consumption in slaughterhouses at the North of Portugal M.C. Fontes, M.J. Saavedra, C. Martins and J. Martínez-Murcia.(2011) International Journal of Food Microbiology 146: 118–122
  43. Recommendations for a new bacterial species description based on analyses of the unrelated genera Aeromonas and Arcobacter. María José Figueras, Roxana Beaz-Hidalgo, Luis Collado andAntonio Martínez-Murcia.The Bulletin of BISMiS (2011), Volume 2, part 1, pp. 1–16. (Published by Bergey’s International Society for Microbial Systematics)
  44. Antibacterial effects of glucosinolate derived hydrolysis products against enterobacteria and enterococci isolated from pig ileum segments. Saavedra, MJ., Dias, C., Martinez-Murcia, A., Bennett, R., Aires, A., Rosa, E.(2012). Foodborne Pathogens and Disease. April 2012, Vol. 9, No. 4: 338-345.
  45. Phylogenetic diversity, antibiotic resistance and virulence traits of Aeromonas spp. from untreated waters for human consumption. Maria João Carvalho, Antonio Martínez-Murcia, Ana Cristina Esteves, António Correia, Maria José Saavedra. International Journal of Food Microbiology 159 (2012) 230–239

72. Aeromonas australiensis  sp. nov., isolated from irrigation water in Western Australia. Max Aravena-Román, Roxana Beaz-Hidalgo, Timothy J.J. Inglis,  T. V. Riley, A. J. Martínez-Murcia, Barbara J. Chang,  and Maria Jose Figueras. Int J Syst Evol Microbiol 2013 Jun;63 (Pt 6):2270-6

  1. Aeromonas cavernicola sp. nov., isolated from fresh water of a brook in a cavern.  J. Martínez-Murcia, R. Beaz-Hidalgo, Pavel Svec, M. Jose Saavedra, M. J. Figueras, and Ivo SedlacekCurr Microbiol 2013 Feb;66(2):197-204
  2. Reclassification of Aeromonas hydrophila subsp. dhakensis Huys et al. 2002 and Aeromonas aquariorum Martínez-Murcia et al. 2008 as Aeromonas dhakensis sp. nov. comb nov. and emendation of the species Aeromonas hydrophila. Roxana Beaz-Hidalgo, Antonio Martínez-Murcia& Maria José Figueras Syst Appl Microbiol  2013 May;36(3):171-6.

75. Detection of Legionella spp. in Natural and Man-made Water Systems Using Standard Guidelines Borges A., Simões M., Martínez-Murcia A., Saavedra M. J. Journal of Microbiology Research 2012, 2(4): 95-102

  1. Corrigendum to “Reclassification of Aeromonas hydrophila subsp. dhakensis Huys et al. 2002 and Aeromonas aquariorum Martínez-Murcia et al. 2008 as Aeromonas dhakensis sp. nov. comb nov. and emendation of the species Aeromonas hydrophila” [Syst. Appl. Microbiol. 36 (2013) 171–176] Roxana Beaz-Hidalgo, Antonio Martínez-Murcia, María José Figueras Systematic and Applied Microbiology, Volume 37, Issue 7, October 2014, Page 543
  2. Aeromonas lusitana sp. nov., isolated from untreated water and vegetables A. J. Martínez-Murcia, A. Navarro, R. Beaz-Hidalgo, Maria João Carvalho, Max Aravena-Román,  Antonio Correia, M. J. Figueras, and M. Jose Saavedra Current  Microbiol (2016) 72:795–803
  3. Arcobacter ebronensis sp. nov. and Arcobacter aquimarinus sp. nov., two new species isolated from marine environment Arturo Levican; Sara Rubio-Arcos; Antonio Martinez-Murcia; Luis Collado; Maria Jose Figueras Systematic and Applied Microbiology – 2015, 38 (1) Pages 30–35
  4. Molecular Diagnostics by Genetic Methods. Martínez-Murcia, A.J.and Lamy, B. (2015). BOOK:  Aeromonas. Graf, J. (Ed.) pp. 155-200. Caister Academic Press. Norfolk, UK.
  5. Purification and quantification of circulating cell-free DNA from body fluids with DANAGENE Circulating System applied to Liquid Biopsy David Navarro, A. Navarro, A. Martinez-Murcia, and Adriana Lasa BioTechniques, Vol. 60, No. 4, April 2016, p. 212
  6. Phylogenetic analyses of the genus Aeromonasbased on housekeeping gene sequencing and its influence on systematics. Aaron Navarro,  Antonio Martínez-Murcia (2018). Journal of Applied Microbiology 125, 622-631 
  7. Draft Genome Sequence of Aeromonas lusitana sp. nov. Strain DSM 24905T, Isolated from a Hot Spring in Vila-Real, Portugal. S. M. Colston,A. Navarro, A. J. Martinez-Murcia, J. Graf (2018). Genome Announc. 6: e00226-18.
  8. Draft Genome Sequence of Aeromonas cavernicola sp. nov. DSM 24474T, Isolated from a Cavern Brook in the Moravia Region of the Czech Republic. S. M. Colston, A. Navarro, A. J. Martinez-Murcia, J. Graf (2018). Genome Announc. 6: e00227-18.
  9. Biofilms and antibiotic susceptibility of multidrug-resistant bacteria from wild animals. Carla Dias1,2,3, Anabela Borges1,3,4, Diana Oliveira1Antonio Martinez-Murcia5, Maria José Saavedra2,3and Manuel Simões (2018). PeerJ 6:e4974;DOI10.7717/peerj. 4974
  10. 85. Detección discriminativa de Mycoplasma gallisepticum y la cepa vacunal 6/85 mediante qPCR. Antonio Martínez-Murcia1,2, Aarón Navarro2, Gema Bru2, Rosa Amejiras3– 1Universidad Miguel Hernández. 2genetic PCR solutions™ 03206 Elche, Alicante. 3Trow Nutrition (Nutreco) 28760 Tres Cantos, Madrid.
  11. Certifcation by Genova University of GPS™ qPCR Kits.
  12. Carbon footprint evaluation of GPS™qPCR  kits by the frame of – the AQUAVALENS project.Presented in Society of Environmental Toxicology and Chemistry (SETAC) Europe 26th Annual Meeting, Nantes, France, 2016.Presented in LCM2017: Liife Cycle Management Conference, 3rd-6th September. Luxemburg, Luxemburg 2017. Torres C.M.1, Castells F.a, MaríaJ. Figueras2    1Departament d’Enginyeria Química,Universitat Rovira i Virgili Av. PaïssosCatalans 26, Tarragona 43007 Phone: (+34) 977558553 2Departament de Ciències Médiques Bàsiques, Universitat Rovira i Virgili, C/Sant Llorenç 21, 43021, Reus, Spain
  13. Validation of Commercial PCR Kits for the Detection of Bacteria and Viruses. C. Stange1, V. Simon1, F. Loisy-Hamon2A. Martínez-Murcia3, A. Tiehm11DVGW-Technologiezentrum Wasser (TZW), Karlsruhe, Germany. 2Ceeram S.A.S, 1 La Chapelle sur Erdre Cédex, France. 3Genetic PCR Solutions™ and Universidad Miguel Hernández, Elche (Alicante), Spain.
  14. Implementation of newly developed pathogen detection methods in a large water system. S. Fernández1, R. Juárez1, C.Puigdomènech1, S.González1, G.Saucedo2,MJ. Arnedo2and B.Galofré2.1Cetaqua, Water Technology Center, Ctra d’Esplugues, 75, 08940-Cornellà de Llobregat, Barcelona. 2Aigües de Barcelona, Empresa Metropolitana de Gestió del Cicle Integral de l’Aigua, SA. Carrer General Batet 5-7, 08028-Barcelona. (Poster link)
  15. New concentration method for drinking water samples improving Legionella detection developed in Aquavalens project. 1Saucedo G, 2Puigdomènech C, 1Arnedo MJ, 2Juárez R, 1Galofré B,2González S. 1Aigües de Barcelona, Empresa Metropolitana de Gestió del Cicle Integral de l’Aigua, SA. Carrer General Batet 5-7, 08028 –BARCELONA, SPAIN. 2Cetaqua, Water Technology Center, Ctra. d’Esplugues, 75,08940 -Cornellà de Llobregat,BARCELONA, SPAIN
  16. Trans-European study on the implementation of novel water testing methodologies to assess the safety of irrigation water. CM Burgess1, B Machado-Moreira1,2, R O’Malley1, K Richards3, R Santos4, S Monteiro4, A Rajkovic5, N Smigic5, L Avery6, E Pagaling6, S Pedley7, A Lopez-Aviles7, M Byrne8and A Martinez-Murcia9.  (1) Teagasc Food Research Centre, Ashtown, Ireland, (2) National University of Ireland Galway, Ireland, (3) Teagasc Johnstown Castle, Ireland, (4) Instituto Superior Técnico, Lisbon, Portugal, (5) University of Belgrade, Serbia, (6) James Hutton Institute, Scotland, (7) University of Surrey, England, (8) City Analysts Limited, Ireland (9) Genetic PCR SolutionsTM and University Miguel Hernández, Alicante, Spain.
  17. Internal validation of GPS™ MONODOSE CanAur dtec-qPCR kit following the UNE/EN ISO/IEC 17025:2005 for detection of the emerging yeast Candida auris.Antonio Martínez-Murcia1,2 Aaron Navarro2 Gema Bru2 Anuradha Chowdhary3 Ferry Hagen4,5 Jacques F. Meis4,6 (1)Department of Microbiology, University Miguel Hernández, Orihuela, Alicante, Spain (2)Genetic PCR Solutions™, Elche, Alicante, Spain (3)Department of Medical Mycology, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, India (4)Department of Medical Microbiology and Infectious Diseases, ECMM Excellence Center, Canisius-Wilhelmina Hospital (CWZ), Nijmegen, The Netherlands (5)Department of Medical Mycology, Westerdijk Fungal Biodiversity Institute, Utrecht, The Netherlands (6)Centre of Expertise in Mycology Radboudumc/CWZ, Nijmegen, The Netherlands.
  18. Impact of beef extract used for sample concentration on the detection of Escherichia coli DNA in water samples via qPCR. Bernardino Machado-Moreira1,2, Silvia Monteiro3, Ricardo Santos3Antonio Martinez-Murcia4, Andreja Rajkovic5,6, Nada Smigic5, Karl G. Richards7, Florence Abram2, Catherine M. Burgess – 1 Teagasc Food Research Centre, Ashtown, Dublin, Ireland, 2 Functional Environmental Microbiology, National University of Ireland Galway, Galway, Ireland, 3 Laboratório de Análises, Instituto Superior Técnico, Universidade de Lisboa, Lisbon, Portugal, 4 University Miguel Hernandez and Genetic PCR SolutionsTM, Alicante, Spain, 5 Department of Food Safety and Food Quality Management, University of Belgrade-Faculty of Agriculture, Serbia, 6 Department of Food Technology, Safety and Health, Faculty of Bioscience Engineering, Ghent University; Belgium, 7 Teagasc Johnstown Castle Environmental Research Centre, Wexford, Ireland.
  19. Validación interna del panel GPS™ Mycoplasmas Contagious Agalactia dtec-qPCR siguiendo la norma UNE-EN ISO/IEC 17025:2005 para la detección en pequeños rumiantes. Gema Bru1, Aaron Navarro1y Antonio Martínez-Murcia1, 2 *  1 Genetic PCR Solutions™, 03206-Elche 2Universidad Miguel Hernández, 03300-Orihuela, Alicante, España.