1887

Abstract

1,4, [5],12:i:- strains with different antimicrobial resistance profiles have been associated with foodborne disease outbreaks in several countries. In Brazil, . 1,4, [5],12:i:- was identified as one of the most prevalent serovars in São Paulo State during 2004–2020.

However, few studies have characterized this serovar in Brazil.

This study aimed to determine the antimicrobial resistance profiles of . 1,4, [5],12:i:- strains isolated from different sources in Southeast Brazil and compare their genetic diversity.

We analysed 113 . 1,4, [5],12:i:- strains isolated from humans (=99), animals (=7), food (=5) and the environment (=2) between 1983 and 2020. Susceptibility testing against 13 antimicrobials was performed using the disc diffusion method for all the strains. Plasmid resistance genes and mutations in the quinolone resistance-determining regions were identified in phenotypically fluoroquinolone-resistant strains. Molecular typing was performed using enterobacterial repetitive intergenic consensus PCR (ERIC-PCR) for all strains and multilocus sequence typing (MLST) for 40 selected strains.

Of the 113 strains, 54.87 % were resistant to at least one antimicrobial. The highest resistance rates were observed against ampicillin (51.33 %), nalidixic acid (39.82 %) and tetracycline (38.05 %). Additionally, 39 (34.51 %) strains were classified as multidrug-resistant (MDR). Nine fluoroquinolone-resistant strains exhibited the mutation (Ser96→Tyr96) and contained the gene. The 113 strains were grouped into two clusters using ERIC-PCR, and most of strains were present in one cluster, with a genetic similarity of ≥80 %. Finally, 40 strains were typed as ST19 using MLST.

The prevalence of MDR strains is alarming because antimicrobial treatment against these strains may lead to therapeutic failure. Furthermore, the ERIC-PCR and MLST results suggested that most strains belonged to one main cluster. Thus, a prevalent subtype of 1,4, [5],12:i:- strains has probably been circulating among different sources in São Paulo, Brazil, over decades.

Funding
This study was supported by the:
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (Award 304803/2021-9)
    • Principle Award Recipient: JulianaPfrimer Falcao
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (Award Proc.304399/2018-3)
    • Principle Award Recipient: JulianaPfrimer Falcao
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Award 88887.523672/2020-00)
    • Principle Award Recipient: Giovanado Nascimento Pereira
  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Award 001)
    • Principle Award Recipient: JulianaPfrimer Falcao
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (Award 2022/07013-0)
    • Principle Award Recipient: JulianaPfrimer Falcao
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (Award 2019/19338-8)
    • Principle Award Recipient: JulianaPfrimer Falcao
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2024-02-20
2024-04-28
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References

  1. Troeger C, Blacker BF, Khalil IA, Rao PC, Cao S et al. Estimates of the global, regional, and national morbidity, mortality, and aetiologies of diarrhoea in 195 countries: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Infect Dis 2018; 18:1211–1228 [View Article]
    [Google Scholar]
  2. Qin X, Yang M, Cai H, Liu Y, Gorris L et al. Antibiotic resistance of Salmonella Typhimurium monophasic variant 1,4,[5],12:i:-in China: a systematic review and meta-analysis. Antibiotics 2022; 11:532 [View Article] [PubMed]
    [Google Scholar]
  3. Xie X, Wang Z, Zhang K, Li Y, Hu Y et al. Pig as a reservoir of CRISPR type TST4 Salmonella enterica serovar Typhimurium monophasic variant during 2009-2017 in China. Emerg Microbes Infect 2020; 9:1–4 [View Article] [PubMed]
    [Google Scholar]
  4. Sun H, Wan Y, Du P, Bai L. The epidemiology of monophasic Salmonella Typhimurium. Foodborne Pathog Dis 2020; 17:87–97 [View Article]
    [Google Scholar]
  5. Hauser E, Tietze E, Helmuth R, Junker E, Blank K et al. Pork contaminated with Salmonella enterica serovar 4,[5],12:i:-, an emerging health risk for humans. Appl Environ Microbiol 2010; 76:4601–4610 [View Article] [PubMed]
    [Google Scholar]
  6. Clemente L, Manageiro V, Ferreira E, Jones-Dias D, Correia I et al. Occurrence of extended-spectrum β-lactamases among isolates of Salmonella enterica subsp. enterica from food-producing animals and food products, in Portugal. Int J Food Microbiol 2013; 167:221–228 [View Article] [PubMed]
    [Google Scholar]
  7. Fois F, Piras F, Torpdahl M, Mazza R, Consolati SG et al. Occurrence, characterization, and antimicrobial susceptibility of Salmonella enterica in slaughtered pigs in Sardinia. J Food Sci 2017; 82:969–976 [View Article] [PubMed]
    [Google Scholar]
  8. Lund S, Tahir M, Vohra LI, Hamdana AH, Ahmad S. Outbreak of monophasic Salmonella Typhimurium sequence type 34 linked to chocolate products. Ann Med Surg 2022; 82:104597 [View Article] [PubMed]
    [Google Scholar]
  9. Larkin L, Pardos de la Gandara M, Hoban A, Pulford C, Jourdan-Da Silva N et al. Investigation of an international outbreak of multidrug-resistant monophasic Salmonella Typhimurium associated with chocolate products, EU/EEA and United Kingdom, February to April 2022. Euro Surveill 2022; 27:15 [View Article] [PubMed]
    [Google Scholar]
  10. Fernandes SA, Tavechio AT, Ghilardi ÂCR, Almeida EA de, Silva JML da et al. Salmonella enterica serotypes from human and nonhuman sources in Sao Paulo State, Brazil, 2004-2020. Rev Inst Med trop S Paulo 2004; 64: [View Article]
    [Google Scholar]
  11. Gut AM, Vasiljevic T, Yeager T, Donkor ON. Salmonella infection – prevention and treatment by antibiotics and probiotic yeasts: a review. Microbiology 2018; 164:1327–1344 [View Article]
    [Google Scholar]
  12. McDermott PF, Zhao S, Tate H. Antimicrobial resistance in nontyphoidal Salmonella. Microbiol Spectr 2018; 6: [View Article] [PubMed]
    [Google Scholar]
  13. Medalla F, Gu W, Mahon BE, Judd M, Folster J et al. Estimated incidence of antimicrobial drug-resistant nontyphoidal Salmonella infections, United States, 2004-2012. Emerg Infect Dis 2016; 23:29–37 [View Article] [PubMed]
    [Google Scholar]
  14. Wen SCH, Best E, Nourse C. Non‐typhoidal Salmonella infections in children: review of literature and recommendations for management. J Paediatrics Child Health 2017; 53:936–941 [View Article]
    [Google Scholar]
  15. Proroga YTR, Mancusi A, Peruzy MF, Carullo MR, Montone AMI et al. Characterization of Salmonella Typhimurium and its monophasic variant 1,4, [5],12:i:- isolated from different sources. Folia Microbiol 2019; 64:711–718 [View Article] [PubMed]
    [Google Scholar]
  16. Kongsoi S, Chumsing S, Satorn D, Noourai P. Serotypes and antimicrobial resistance profiles of Salmonella enterica recovered from clinical swine samples. Vet World 2020; 13:2312–2318 [View Article] [PubMed]
    [Google Scholar]
  17. Chaudhari R, Singh K, Kodgire P. Biochemical and molecular mechanisms of antibiotic resistance in Salmonella spp. Res Microbiol 2023; 174:103985 [View Article] [PubMed]
    [Google Scholar]
  18. Urban-Chmiel R, Marek A, Stępień-Pyśniak D, Wieczorek K, Dec M et al. Antibiotic resistance in bacteria-a review. Antibiotics 2022; 11:1079 [View Article] [PubMed]
    [Google Scholar]
  19. Hussain HI, Aqib AI, Seleem MN, Shabbir MA, Hao H et al. Genetic basis of molecular mechanisms in β-lactam resistant gram-negative bacteria. Microb Pathog 2021; 158:105040 [View Article] [PubMed]
    [Google Scholar]
  20. Marin C, Chinillac MC, Cerdà-Cuéllar M, Montoro-Dasi L, Sevilla-Navarro S et al. Contamination of pig carcass with Salmonella enterica serovar Typhimurium monophasic variant 1,4[5],12:i:- originates mainly in live animals. Sci Total Environ 2020; 703:134609 [View Article] [PubMed]
    [Google Scholar]
  21. Murase T, Ozaki H, Phuektes P, Angkititrakul S. Genotypic and phenotypic characterization of Salmonella enterica subsp. enterica serovar Typhimurium monophasic variants isolated in Thailand and Japan. J Vet Med Sci 2018; 80:1839–1846 [View Article] [PubMed]
    [Google Scholar]
  22. Kaczorek-Łukowska E, Sowińska P, Franaszek A, Dziewulska D, Małaczewska J et al. Can domestic pigeon be a potential carrier of zoonotic Salmonella?. Transbound Emerg Dis 2021; 68:2321–2333 [View Article] [PubMed]
    [Google Scholar]
  23. Olive DM, Bean P. Principles and applications of methods for DNA-based typing of microbial organisms. J Clin Microbiol 1999; 37:1661–1669 [View Article] [PubMed]
    [Google Scholar]
  24. Casas MRT, Camargo CH, Soares FB, da Silveira WD, Fernandes SA. Presence of plasmid-mediated quinolone resistance determinants and mutations in gyrase and topoisomerase in Salmonella enterica isolates with resistance and reduced susceptibility to ciprofloxacin. Diagn Microbiol Infect Dis 2016; 85:85–89 [View Article] [PubMed]
    [Google Scholar]
  25. de Quadros CL, Manto L, Mistura E, Webber B, Ritterbusch GA et al. Antimicrobial and disinfectant susceptibility of Salmonella serotypes isolated from swine slaughterhouses. Curr Microbiol 2020; 77:1035–1042 [View Article] [PubMed]
    [Google Scholar]
  26. Meneguzzi M, Pissetti C, Rebelatto R, Trachsel J, Kuchiishi SS et al. Re-emergence of salmonellosis in hog farms: outbreak and bacteriological characterization. Microorganisms 2021; 9:947 [View Article] [PubMed]
    [Google Scholar]
  27. Possebon FS, Tiba Casas MR, Nero LA, Yamatogi RS, Araújo JP Jr et al. Prevalence, antibiotic resistance, PFGE and MLST characterization of Salmonella in swine mesenteric lymph nodes. Prev Vet Med 2020; 179:105024 [View Article] [PubMed]
    [Google Scholar]
  28. Tavechio AT, Ghilardi ACR, Fernandes SA. Multiplex PCR” identification of the atypical and monophasic Salmonella enterica subsp. enterica serotype 1,4,[5],12:i:- in São Paulo State, Brazil: frequency and antibiotic resistance patterns. Rev Inst Med Trop Sao Paulo 2004; 46:115–117 [View Article] [PubMed]
    [Google Scholar]
  29. Tavechio AT, Fernandes SA, Ghilardi ÂC, Soule G, Ahmed R et al. Tracing lineage by phenotypic and genotypic markers in Salmonella enterica subsp. enterica serovar 1,4,[5],12:i:- and Salmonella Typhimurium isolated in state of São Paulo, Brazil. Mem Inst Oswaldo Cruz 2009; 104:1042–1046 [View Article]
    [Google Scholar]
  30. Clinical and Laboratory Standards Institute (CLSI) Performance Standards for Antimicrobial Susceptibility Testing, 30rd. edn Wayne: CLSI supplement M100; 2020
    [Google Scholar]
  31. Campioni F, Falcão JP. Genotypic diversity and virulence markers of Yersinia enterocolitica biotype 1A strains isolated from clinical and non-clinical origins. APMIS 2014; 122:215–222 [View Article] [PubMed]
    [Google Scholar]
  32. Sambrook J, Russell D. Molecular Cloning: A Laboratory Manual, 3rd edition. New York: Cold Spring Harbor Laboratory Press; 2001
    [Google Scholar]
  33. Falcão JP, Falcão DP, Pitondo-Silva A, Malaspina AC, Brocchi M. Molecular typing and virulence markers of Yersinia enterocolitica strains from human, animal and food origins isolated between 1968 and 2000 in Brazil. J Med Microbiol 2006; 55:1539–1548 [View Article] [PubMed]
    [Google Scholar]
  34. Jacoby GA, Gacharna N, Black TA, Miller GH, Hooper DC. Temporal appearance of plasmid-mediated quinolone resistance genes. Antimicrob Agents Chemother 2009; 53:1665–1666 [View Article]
    [Google Scholar]
  35. Kim HB, Park CH, Kim CJ, Kim E-C, Jacoby GA et al. Prevalence of plasmid-mediated quinolone resistance determinants over a 9-year period. Antimicrob Agents Chemother 2009; 53:639–645 [View Article]
    [Google Scholar]
  36. Tamang MD, Nam H-M, Kim A, Lee H-S, Kim T-S et al. Prevalence and mechanisms of quinolone resistance among selected nontyphoid Salmonella isolated from food animals and humans in Korea. Foodborne Pathog Dis 2011; 8:1199–1206 [View Article] [PubMed]
    [Google Scholar]
  37. Chen X, Zhang W, Pan W, Yin J, Pan Z et al. Prevalence of qnr, aac(6’)-Ib-cr, qepA, and oqxAB in Escherichia coli isolates from humans, animals, and the environment. Antimicrob Agents Chemother 2012; 56:3423–3427 [View Article] [PubMed]
    [Google Scholar]
  38. Park CH, Robicsek A, Jacoby GA, Sahm D, Hooper DC. Prevalence in the United States of aac(6’)-Ib-cr encoding a ciprofloxacin-modifying enzyme. Antimicrob Agents Chemother 2006; 50:3953–3955 [View Article] [PubMed]
    [Google Scholar]
  39. Pitout JDD, Hossain A, Hanson ND. Phenotypic and molecular detection of CTX-M-beta-lactamases produced by Escherichia coli and Klebsiella spp. J Clin Microbiol 2004; 42:5715–5721 [View Article] [PubMed]
    [Google Scholar]
  40. Saladin M, Cao VTB, Lambert T, Donay J-L, Herrmann J-L et al. Diversity of CTX-M beta-lactamases and their promoter regions from Enterobacteriaceae isolated in three Parisian hospitals. FEMS Microbiol Lett 2002; 209:161–168 [View Article] [PubMed]
    [Google Scholar]
  41. Rasheed JK, Jay C, Metchock B, Berkowitz F, Weigel L et al. Evolution of extended-spectrum beta-lactam resistance (SHV-8) in a strain of Escherichia coli during multiple episodes of bacteremia. Antimicrob Agents Chemother 1997; 41:647–653 [View Article] [PubMed]
    [Google Scholar]
  42. Clímaco EC, Oliveira ML de, Pitondo-Silva A, Oliveira MG, Medeiros M et al. Clonal complexes 104, 109 and 113 playing a major role in the dissemination of OXA-carbapenemase-producing Acinetobacter baumannii in Southeast Brazil. Infect Genet Evol 2013; 19:127–133 [View Article] [PubMed]
    [Google Scholar]
  43. Souza RA, Pitondo-Silva A, Falcão DP, Falcão JP. Evaluation of four molecular typing methodologies as tools for determining taxonomy relations and for identifying species among Yersinia isolates. J Microbiol Methods 2010; 82:141–150 [View Article] [PubMed]
    [Google Scholar]
  44. Jeong HS, Kim JA, Shin JH, Chang CL, Jeong J et al. Prevalence of plasmid-mediated quinolone resistance and mutations in the gyrase and topoisomerase IV genes in Salmonella isolated from 12 tertiary-care hospitals in Korea. Microb Drug Resist 2011; 17:551–557 [View Article] [PubMed]
    [Google Scholar]
  45. O’Regan E, Quinn T, Pagès J-M, McCusker M, Piddock L et al. Multiple regulatory pathways associated with high-level ciprofloxacin and multidrug resistance in Salmonella enterica serovar enteritidis: involvement of RamA and other global regulators. Antimicrob Agents Chemother 2009; 53:1080–1087 [View Article] [PubMed]
    [Google Scholar]
  46. Fàbrega A, Vila J. Salmonella enterica serovar Typhimurium skills to succeed in the host: virulence and regulation. Clin Microbiol Rev 2013; 26:308–341 [View Article] [PubMed]
    [Google Scholar]
  47. Carrique-Mas JJ, Papadopoulou C, Evans SJ, Wales A, Teale CJ et al. Trends in phage types and antimicrobial resistance of Salmonella enterica serovar Enteritidis isolated from animals in Great Britain from 1990 to 2005. Vet Rec 2008; 162:541–546 [View Article] [PubMed]
    [Google Scholar]
  48. Almeida F, Medeiros MIC, Rodrigues DDP, Falcão JP. Genotypic diversity, pathogenic potential and the resistance profile of Salmonella Typhimurium strains isolated from humans and food from 1983 to 2013 in Brazil. J Med Microbiol 2015; 64:1395–1407 [View Article] [PubMed]
    [Google Scholar]
  49. Versalovic J, Koeuth T, Lupski JR. Distribution of repetitive DNA sequences in eubacteria and application to fingerprinting of bacterial genomes. Nucleic Acids Res 1991; 19:6823–6831 [View Article] [PubMed]
    [Google Scholar]
  50. Pereira G do N, Seribelli AA, Gomes CN, Vilela FP, Tonani L et al. Virulence potential of Salmonella 1,4, [5],12:i:- strains isolated during decades from different sources in the Southeast region of Brazil. Braz J Microbiol 2023; 54:2827–2843 [View Article]
    [Google Scholar]
  51. Zhou Z, Alikhan N-F, Sergeant MJ, Luhmann N, Vaz C et al. GrapeTree: visualization of core genomic relationships among 100,000 bacterial pathogens. Genome Res 2018; 28:1395–1404 [View Article]
    [Google Scholar]
  52. Hunter PR, Gaston MA. Numerical index of the discriminatory ability of typing systems: an application of Simpson’s index of diversity. J Clin Microbiol 1988; 26:2465–2466 [View Article] [PubMed]
    [Google Scholar]
  53. Elnekave E, Hong S, Mather AE, Boxrud D, Taylor AJ et al. Salmonella enterica serotype 4,[5],12:i:- in swine in the United States Midwest: an emerging multidrug-resistant clade. Clin Infect Dis 2018; 66:877–885 [View Article] [PubMed]
    [Google Scholar]
  54. García P, Malorny B, Rodicio MR, Stephan R, Hächler H et al. Horizontal acquisition of a multidrug-resistance module (R-type ASSuT) is responsible for the monophasic phenotype in a widespread clone of Salmonella Serovar 4,[5],12:i:-. Front Microbiol 2016; 7:680 [View Article]
    [Google Scholar]
  55. Nadimpalli M, Fabre L, Yith V, Sem N, Gouali M et al. CTX-M-55-type ESBL-producing Salmonella enterica are emerging among retail meats in Phnom Penh, Cambodia. J Antimicrob Chemother 2019; 74:342–348 [View Article] [PubMed]
    [Google Scholar]
  56. Sun R-Y, Ke B-X, Fang L-X, Guo W-Y, Li X-P et al. Global clonal spread of mcr-3-carrying MDR ST34 Salmonella enterica serotype Typhimurium and monophasic 1,4,[5],12:i:- variants from clinical isolates. J Antimicrob Chemother 2020; 75:1756–1765 [View Article] [PubMed]
    [Google Scholar]
  57. Listorti V, Garcia-Vozmediano A, Pitti M, Maurella C, Adriano D et al. Antimicrobial resistance of Salmonella strains isolated from human, Wild boar, and environmental samples in 2018–2020 in the Northwest of Italy. Pathogens 2022; 11:1446 [View Article]
    [Google Scholar]
  58. Abgottspon H, Zurfluh K, Nüesch-Inderbinen M, Hächler H, Stephan R. Quinolone resistance mechanisms in Salmonella enterica serovars Hadar, Kentucky, Virchow, Schwarzengrund, and 4,5,12:i:-, isolated from humans in Switzerland, and identification of a novel qnrD variant, qnrD2, in S. Hadar. Antimicrob Agents Chemother 2014; 58:3560–3563 [View Article] [PubMed]
    [Google Scholar]
  59. Sriyapai T, Pulsrikarn C, Chansiri K, Sriyapai P. Molecular characterization of extended-spectrum cephalosporin and fluoroquinolone resistance genes in Salmonella and Shigella isolated from clinical specimens in Thailand. Heliyon 2022; 8:e12383 [View Article] [PubMed]
    [Google Scholar]
  60. Cao C, Zhao W, Z, Mo Y, Hu W et al. Microbiological analysis and characterization of Salmonella and ciprofloxacin-resistant Escherichia coli isolates recovered from retail fresh vegetables in Shaanxi Province, China. Int J Food Microbiol 2023; 387:110053 [View Article] [PubMed]
    [Google Scholar]
  61. Rau RB, de Lima-Morales D, Wink PL, Ribeiro AR, Barth AL. Salmonella enterica mcr-1 positive from food in Brazil: detection and characterization. Foodborne Pathog Dis 2020; 17:202–208 [View Article] [PubMed]
    [Google Scholar]
  62. Lee S, Park N, Yun S, Hur E, Song J et al. Presence of plasmid-mediated quinolone resistance (PMQR) genes in non-typhoidal Salmonella strains with reduced susceptibility to fluoroquinolones isolated from human salmonellosis in Gyeonggi-do, South Korea from 2016 to 2019. Gut Pathog 2021; 13:35 [View Article] [PubMed]
    [Google Scholar]
  63. He J, Sun F, Sun D, Wang Z, Jin S et al. Multidrug resistance and prevalence of quinolone resistance genes of Salmonella enterica serotypes 4,[5],12:i:- in China. Int J Food Microbiol 2020; 330:108692 [View Article] [PubMed]
    [Google Scholar]
  64. Long L, You L, Wang D, Wang M, Wang J et al. Highly prevalent MDR, frequently carrying virulence genes and antimicrobial resistance genes in Salmonella enterica serovar 4,[5],12:i:- isolates from Guizhou Province, China. PLoS One 2022; 17:e0266443 [View Article] [PubMed]
    [Google Scholar]
  65. Tzouvelekis LS, Lukova V, Tassios PT, Fluit AC, Jones RN et al. Resistance to beta-lactams among blood isolates of Salmonella spp. in European hospitals: results from the SENTRY antimicrobial Surveillance Program 1997-98. Clin Microbiol Infect 2003; 9:149–152 [View Article] [PubMed]
    [Google Scholar]
  66. Win AT, Supa-Amornkul S, Orsi RH, Carey JH, Wolfgang WJ et al. Sequence analyses and phenotypic characterization revealed multidrug resistant gene insertions in the genomic region encompassing phase 2 flagellin encoding fljAB genes in monophasic variant Salmonella enterica serovar 4,5,12:i:- isolates from various sources in Thailand. Front Microbiol 2021; 12:720604 [View Article] [PubMed]
    [Google Scholar]
  67. Diaconu EL, Alba P, Feltrin F, Di Matteo P, Iurescia M et al. Emergence of IncHI2 plasmids with mobilized colistin resistance (mcr)-9 gene in ESBL-producing, multidrug-resistant Salmonella Typhimurium and its monophasic variant ST34 from food-producing animals in Italy. Front Microbiol 2021; 12:705230 [View Article]
    [Google Scholar]
  68. Marin C, Torres C, Marco-Jiménez F, Cerdà-Cuéllar M, Sevilla S et al. Supplementary feeding stations for conservation of vultures could be an important source of monophasic Salmonella Typhimurium 1,4,[5],12:i. Sci Total Environ 2018; 636:449–455 [View Article] [PubMed]
    [Google Scholar]
  69. Calarga AP, Gontijo MTP, de Almeida LGP, de Vasconcelos ATR, Nascimento LC et al. Antimicrobial resistance and genetic background of non-typhoidal Salmonella enterica strains isolated from human infections in São Paulo, Brazil (2000–2019). Braz J Microbiol 2022; 53:1249–1262 [View Article]
    [Google Scholar]
  70. Moura Q, Fernandes MR, Silva KC, Monte DF, Esposito F et al. Virulent nontyphoidal Salmonella producing CTX-M and CMY-2 β-lactamases from livestock, food and human infection, Brazil. Virulence 2018; 9:281–286 [View Article] [PubMed]
    [Google Scholar]
  71. Yang X, Wu Q, Zhang J, Huang J, Guo W et al. Prevalence and characterization of monophasic Salmonella serovar 1,4,[5],12:i:- of food origin in China. PLoS One 2015; 10:e0137967 [View Article] [PubMed]
    [Google Scholar]
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