High rates of CTX-M-15-producing Escherichia coli and Klebsiella pneumoniae in wild boars and Barbary macaques in Algeria

Journal of Global Antimicrobial Resistance

Volumn 8, Issue , 2017, Pages 35-40

  Bachiri, Taous ^a,b   Bakour, Sofiane ^b   Ladjouzi, Rabia ^a   Thongpan, Leangapichart ^b   Rolain, Jean Marc ^b   Touati, Abdelaziz ^a  

^a UNIVERSITY OF BEJAIA   (Algeria)

^b AIX MARSEILLE UNIVERSITY   (France)

Author keywords

Algeria; Barbary macaques; Enterobacteriaceae; ESBL; MLST; Wild boars

Indexed keywords

AMIKACIN; AMOXICILLIN; AMOXICILLIN PLUS CLAVULANIC ACID; AZTREONAM; CEFEPIME; CEFOTAXIME; CEFOXITIN; CEFTAZIDIME; CEFTRIAXONE; CIPROFLOXACIN; COLISTIN; COTRIMOXAZOLE; ERTAPENEM; FOSFOMYCIN; GENTAMICIN; IMIPENEM; TETRACYCLINE; TIMENTIN; ANTIINFECTIVE AGENT; BACTERIAL DNA; BACTERIAL PROTEIN; BETA LACTAMASE; BETA-LACTAMASE CTX-M-15; BETA-LACTAMASE TEM-1;

ALGERIA; ANTIBIOTIC RESISTANCE; ANTIBIOTIC SENSITIVITY; ARTICLE; DISK DIFFUSION; DNA SEQUENCE; ESCHERICHIA COLI; EUROPEAN WILD BOAR; FECES; KLEBSIELLA PNEUMONIAE; MACACA; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; MULTILOCUS SEQUENCE TYPING; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; ANIMAL; DRUG EFFECT; ENTEROBACTERIACEAE; ENTEROBACTERIACEAE INFECTION; GENETICS; GEOGRAPHIC MAPPING; ISOLATION AND PURIFICATION; METABOLISM; MICROBIOLOGY; MOLECULAR EPIDEMIOLOGY; PIG; SEQUENCE ANALYSIS; VETERINARY MEDICINE; WILD ANIMAL;

ALGERIA; ANIMALS; ANIMALS, WILD; ANTI-BACTERIAL AGENTS; BACTERIAL PROTEINS; BETA-LACTAMASES; DNA, BACTERIAL; ENTEROBACTERIACEAE; ENTEROBACTERIACEAE INFECTIONS; ESCHERICHIA COLI; FECES; GEOGRAPHIC MAPPING; KLEBSIELLA PNEUMONIAE; MACACA; MOLECULAR EPIDEMIOLOGY; MULTILOCUS SEQUENCE TYPING; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; SEQUENCE ANALYSIS, DNA; SUS SCROFA;

EID: 85003945943     PISSN: 22137165     EISSN: 22137173     Source Type: Journal    
DOI: 10.1016/j.jgar.2016.10.005     Document Type: Article

References (39)

1. [1] Da Costa, P.M., Loureiro, L., Matos, A.J.F., Transfer of multidrug-resistant bacteria between intermingled ecological niches: the interface between humans, animals and the environment. Int J Environ Res Public Health 10 (2013), 278–294.
2. [2] Wellington, E.M., Boxall, A.B., Cross, P., Feil, E.J., Gaze, W.H., Hawkey, P.M., et al. The role of the natural environment in the emergence of antibiotic resistance in Gram-negative bacteria. Lancet Infect Dis 13 (2013), 155–165.
3. [3] Benavides, J.A., Godreuil, S., Bodenham, R., Ratiarison, S., Devos, C., Petretto, M., et al. No evidence for transmission of antibiotic-resistant Escherichia coli strains from humans to wild western lowland gorillas in Lopé National Park, Gabon. Appl Environ Microbiol 78 (2012), 4281–4287.
4. [4] Jamborova, I., Dolejska, M., Vojtech, J., Guenther, S., Uricariu, R., Drozdowska, J., et al. Plasmid-mediated resistance to cephalosporins and fluoroquinolones in various Escherichia coli sequence types isolated from rooks wintering in Europe. Appl Environ Microbiol 81 (2015), 648–657.
5. [5] Schaumburg, F., Mugisha, L., Peck, B., Becker, K., Gillespie, T.R., Peters, G., et al. Drug-resistant human Staphylococcus aureus in sanctuary apes pose a threat to endangered wild ape populations. Am J Primatol 74 (2012), 1071–1075.
6. [6] Dobiasova, H., Dolejska, M., Jamborova, I., Brhelova, E., Blazkova, L., Papousek, I., et al. Extended spectrum β-lactamase and fluoroquinolone resistance genes and plasmids among Escherichia coli isolates from zoo animals, Czech Republic. FEMS Microbiol Ecol 85 (2013), 604–611.
7. [7] Gao, L., Hu, J., Zhang, X., Wei, L., Li, S., Miao, Z., et al. Application of swine manure on agricultural fields contributes to extended-spectrum β-lactamase-producing Escherichia coli spread in Tai'an, China. Front Microbiol, 6, 2015, 313.
8. [8] Costa, D., Poeta, P., Saenz, Y., Vinue, L., Rojo-Bezares, B., Jouini, A., et al. Detection of Escherichia coli harbouring extended-spectrum β-lactamases of the CTX-M, TEM and SHV classes in faecal samples of wild animals in Portugal. J Antimicrob Chemother 58 (2006), 1311–1312.
9. [9] Brahmi, S., Dunyach-Rémy, C., Touati, A., Lavigne, J.P., CTX-M-15-producing Escherichia coli and the pandemic clone O25b-ST131 isolated from wild fish in Mediterranean Sea. Clin Microbiol Infect 21 (2014), 18–20.
10. [10] Literak, I., Dolejska, M., Radimersky, T., Klimes, J., Friedman, M., Aarestrup, F.M., et al. Antimicrobial-resistant faecal Escherichia coli in wild mammals in wild mammals in central Europe: multiresistant Escherichia coli producing extended-spectrum β-lactamases in wild boars. J Appl Microbiol 108 (2009), 1702–1711.
11. [11] Poeta, P., Radhouani, H., Pinto, L., Martinho, A., Rego, V., Rodrigues, R., et al. Wild boars as reservoirs of extended-spectrum β-lactamase (ESBL) producing Escherichia coli of different phylogenetic groups. J Basic Microbiol 49 (2009), 584–588.
12. [12] Ho, P.L., Lo, W.U., Lai, E.L., Law, P.Y., Leung, S.M., Wang, Y., et al. Clonal diversity of CTX-M-producing, multidrug-resistant Escherichia coli from rodents. J Med Microbiol 64 (2015), 185–190.
13. [13] Gonçalves, A., Igrejas, G., Radhouani, H., Estepa, V., Alcaide, E., Zorrilla, I., et al. Detection of extended-spectrum β-lactamase-producing Escherichia coli isolates in faecal samples of Iberian lynx. Lett Appl Microbiol 54 (2012), 73–77.
14. [14] Van Veen, S.Q., Claas, E.C., Kuijper, E.J., High-throughput identification of bacteria and yeast by matrix-assisted laser desorption ionization-time of flight mass spectrometry in conventional medical microbiology laboratories. J Clin Microbiol 48 (2010), 900–907.
15. [15] Jarlier, V., Nicolas, M.H., Fournier, G., Philippon, A., Extended broad-spectrum β-lactamases conferring transferable resistance to newer β-lactam agents in Enterobacteriaceae: hospital prevalence and susceptibility patterns. Rev Infect Dis 10 (1988), 867–878.
16. [16] European Committee on Antimicrobial Susceptibility Testing, Breakpoint tables for interpretation of MICs and zone diameters. Version 5.0, 2015. 2015, EUCAST, Basel, Switzerland http://www.eucast.org/ [Accessed 1 December 2016].
17. [17] Kermas, R., Touati, A., Brasme, L., Le Magrex-Debar, E., Mehrane, S., Weill, F.X., et al. Characterization of extended-spectrum β-lactamase-producing Salmonella enterica serotype Brunei and Heidelberg at the Hussein Dey Hospital in Algiers (Algeria). Foodborne Pathog Dis 9 (2012), 803–808.
18. [18] Santos, T., Silva, N., Igrejas, G., Rodrigues, P., Micael, J., Rodrigues, T., et al. Dissemination of antibiotic resistant Enterococcus spp. and Escherichia coli from wild birds of Azores Archipelago. Anaerobe 24 (2013), 25–31.
19. [19] Moreno, H., Bello, H., Guggiana, D., Dominguez, M., Gonzalez, G., Extended-spectrum β-lactamases belonging to CTX-M group produced by Escherichia coli strains isolated from companion animals treated with enrofloxacin. Vet Microbiol 129 (2008), 203–208.
20. [20] Amos, G.C., Hawkey, P.M., Gaze, W.H., Wellington, E.M., Waste water effluent contributes to the dissemination of CTX-M-15 in the natural environment. J Antimicrob Chemother 69 (2014), 1785–1791.
21. [21] Guenther, S., Ewers, C., Wieler, L.H., Extended-spectrum β-lactamases producing E. coli in wildlife, yet another form of environmental pollution?. Front Microbiol, 2, 2011, 246.
22. [22] Rossolini, G.M., D'Andrea, M.M., Mugnaioli, C., The spread of CTX-M-type extended-spectrum β-lactamases. Clin Microbiol Infect 1 (2008), 33–41.
23. [23] Lahlaoui, H., Ben Haj Khalifa, A., Ben Moussa, M., Epidemiology of Enterobacteriaceae producing CTX-M type extended spectrum β-lactamase (ESBL). Med Mal Infect 44 (2014), 400–404.
24. [24] Ewers, C., Bethe, A., Semmler, T., Guenther, S., Wieler, L.H., Extended-spectrum β-lactamase-producing and AmpC-producing Escherichia coli from livestock and companion animals, and their putative impact on public health: a global perspective. Clin Microbiol Infect 18 (2012), 646–655.
25. [25] Seiffert, S.N., Hilty, M., Perreten, V., Endimiani, A., Extended-spectrum cephalosporin-resistant Gram-negative organisms in livestock: an emerging problem for human health?. Drug Resist Updat 16 (2013), 22–45.
26. [26] Wang, Y., He, T., Han, J., Wang, J., Foley, S.L., Yang, G., et al. Prevalence of ESBLs and PMQR genes in fecal Escherichia coli isolated from the non-human primates in six zoos in China. Vet Microbiol 159 (2012), 53–59.
27. [27] Janatova, M., Albrechtova, K., Petrzelkova, K.J., Dolejska, M., Papousek, I., Masarikova, M., et al. Antimicrobial-resistant Enterobacteriaceae from humans and wildlife in Dzanga-Sangha Protected Area, Central African Republic. Vet Microbiol 171 (2014), 422–431.
28. [28] Johnson, J.R., Johnston, B., Clabots, C., Kuskowski, M.A., Castanheira, M., Escherichia coli sequence type ST131 as the major cause of serious multidrug resistant E. coli infections in the United States. Clin Infect Dis 51 (2010), 286–294.
29. [29] Abgottspon, H., Nüesch-Inderbinen, M.T., Zurfluh, K., Althaus, D., Hächler, H., Stephan, R., Enterobacteriaceae with extended-spectrum- and pAmpC-type β-lactamase-encoding genes isolated from fresh water fish from two lakes in Switzerland. Antimicrob Agents Chemother 58 (2014), 2482–2484.
30. [30] D'Andrea, M.M., Venturelli, C., Giani, T., Arena, F., Conte, V., Bresciani, P., et al. Persistent carriage and infection by multidrug-resistant Escherichia coli ST405 producing NDM-1 carbapenemase: report on the first Italian cases. J Clin Microbiol 49 (2011), 2755–2758.
31. [31] Colomer-Lluch, M., Mora, A., Lopez, C., Mamani, R., Dahbi, G., Marzoa, J., et al. Detection of quinolone-resistant Escherichia coli isolates belonging to clonal groups O25b:H4-B2-ST131 and O25b:H4-D-ST69 in raw sewage and river water in Barcelona, Spain. J Antimicrob Chemother 68 (2012), 758–765.
32. [32] Stolle, I., Prenger-Berninghoff, E., Stamm, I., Scheufen, S., Hassdenteufel, E., Guenther, S., et al. Emergence of OXA-48 carbapenemase-producing Escherichia coli and Klebsiella pneumoniae in dogs. J Antimicrob Chemother 68 (2013), 2802–2808.
33. [33] Chen, Y., Chen, X., Zheng, S., Yu, F., Kong, H., Yang, Q., et al. Serotypes, genotypes and antimicrobial resistance patterns of human diarrhoeagenic Escherichia coli isolates circulating in southeastern China. Clin Microbiol Infect 20 (2013), 52–58.
34. [34] Dolejska, M., Masarikova, M., Dobiasova, H., Jamborova, I., Karpiskova, R., Havlicek, M., et al. High prevalence of Salmonella and IMP-4-producing Enterobacteriaceae in the silver gull on Five Islands, Australia. J Antimicrob Chemother 71 (2015), 63–70.
35. [35] Radhouani, H., Silva, N., Poeta, P., Torres, C., Correia, S., Igrejas, G., Potential impact of antimicrobial resistance in wildlife, environment and human health. Front Microbiol, 5, 2014, 23.
36. [36] Rwego, I.B., Isabirye-Basuta, G., Gillespie, T.R., Goldberg, T.L., Gastrointestinal bacterial transmission among humans, mountain gorillas, and livestock in Bwindi Impenetrable National Park, Uganda. Conserv Biol 22 (2008), 1600–1607.
37. [37] Cristobal-Azkarate, J., Dunn, J.C., Day, J.M.W., Amabile-Cuevas, C.F., Resistance to antibiotics of clinical relevance of the fecal microbiota of Mexican wildlife. PLoS One, 9, 2014, e107719.
38. [38] Ho, P.L., Chow, K.H., Lai, E.L., Lo, W.U., Yeung, M.K., Chan, J., et al. Extensive dissemination of CTX-M-producing Escherichia coli with multidrug resistance to critically important antibiotics among food animals in Hong Kong, 2008–10. J Antimicrob Chemother 66 (2011), 765–768.
39. [39] Gazin, M., Paasch, F., Goossens, H., Malhotra-Kumar, S., MOSAR WP2 and SATURN WP1 Study Teams, Current trends in culture-based and molecular detection of extended-spectrum-β-lactamase-harboring and carbapenem-resistant Enterobacteriaceae. J Clin Microbiol 50 (2012), 1140–1146.