Andrews, J. M. (2007). BSAC standardized disc susceptibility testing method (version 6). J Antimicrob Chemother, 60, 20-41.

Blanco, M., Gutiérrez-Martin, C. B., Rodriguez-Ferri, E. F., Roberts, M. C. & Navas, J. (2006). Distribution of tetracycline resistance genes in Actinobacillus pleuropneumoniae isolates from Spain. Antimicrob Agents Chemother, 50, 702-708. Clark, N. C., Olsvik, 0., Swenson, J. M., Spiegel, C. A. & Tenover, F. C. (1999) Detection of a streptomycin/spectinomycin adenylyltransferase gene (aadA) in Enterococcus faecalis. Antimicrob Agents Chemother, 43, 157-160 Dabboussi, F., Hamze, M., Elomari, M., Verhille, S., Baida, N., Izard, D. & Leclerc, H. (1999) Pseudomonas libanensis sp. nov., a new species isolated from Lebanese spring waters. Int JSyst Bacteriol, 49, 1091-1101. Datta, N. & Hedges, R. W. (1972) Trimethoprim resistance conferred by W plasmid in

Enterobacteriaceae. J Gen Microbiol, 72, 349-355. Davies, J. (1994) Inactivation of antibiotics and the dissemination of resistance genes. Science, 264, 375-382.

D'Costa, V. M., McGrann, K. M., Hughes, D. W. & Wright, G. D. (2006) Sampling the antibiotic resistome. Science, 311 (5759), 374-377. Esiobu, N., Armenta, L. & Ike, J. (2002) Antibiotic resistance in soil and water environments.

Int J Environ Health Res, 12, 133-144. Fluit, A. C., Schmitz, F. J. & Verhoef, J. (2001). Multi-resistance to antimicrobial agents for the ten most frequently isolated bacterial pathogens. Int J Antimicrob Agents, 18, 147160.

Gilichinsky, D. A., Wilson, G. S., Friedmann, E. I., McKay, C. P., Sletten, R. S., Rivkina, E. M., Vishnivetskaya, T. A., Erokhina, L. G., Ivanushkina, N. E., Kochkina, G. A., Shcherbakova, V.A., Soina, V. S., Spirina, E. V., Vorobyova, E. A., Fyodorov-Davydov, D. G., Hallet, B., Ozerskaya, S. M., Sorokovikov, V. A., Laurinavichyus, K. S., Shatilovich, A. V., Chanton, J. P., Ostroumov, V. E. & Tiedje, J. M. (2007). Microbial populations in Antarctic permafrost: biodiversity, state, age, and implication for astrobiology. Astrobiology, 7, 275-311. Gomez, M. J. & Neyfakh, A. A. (2006) Genes involved in intrinsic antibiotic resistance of

Acinetobacter baylyi. Antimicrob Agents Chemother, 50, 3562-3567. Gould, V. C. & Avison, M. B. (2000) SmeDEF-mediated antimicrobial drug resistance in Stenotrophomonas maltophilia clinical isolates having defined phylogenetic relationships. J Antimicrob Chemother, 57, 1070-1076. Hall, R. M. & Collis, C. M. (1998) Antibiotic resistance in gram-negative bacteria: the role of gene cassettes and integrons. Drug Resist Updates, 1, 109-119. Hirai, K., Aoyama, H., Suzue, S., Irikura, T., Iyobe, S. & Mitsuhashi, S. (1986). Isolation and characterization of norfloxacin-resistant mutants of Escherichia coli K-12. Antimicrob Agents Chemother, 30, 248-253. Hughes, V. M. & Datta, N. (1983). Conjugative plasmids in bacteria of the 'preantibiotic era'. Nature, 302, 725-726.

Jacob, A. E., & Grinter, N. J. (1975). Plasmid RP4 as a vector replicon in genetic engineering.

Nature, 255, 504-506.

Juni, E. (1972). Interspecies transformation of Acinetobacter: genetic evidence for a ubiquitous genus. J Bacteriol, 112, 917-931. Kehrenberg, C., Salmon, S. A., Watts, J, L. & Schwarz, S. (2001). Tetracycline resistance genes in isolates of Pasteurella multocida, Mannheimia haemolytica, Mannheimia glucosida and Mannheimia varigena from bovine and swine respiratory disease: intergeneric spread of the tet(H) plasmid pMHT1. JAntimicrob Chemother, 48, 631-640.

Kholodii, G., Mindlin, S., Petrova, M. & Minakhina, S. (2003) Tn5060 from the Siberian permafrost is most closely related to the ancestor of Tn21 prior to integron acquisition. FEMSMicrobiol Lett, 226, 251-255.

Kontomichalou, P., Papachristou, E. & Angelatou, F. (1976) Multiresistant plasmids from Pseudomonas aeruginosa highly resistant to either or both gentamicin and carbenicillin. Antimicrob Agents Chemother. 9, 866-873.]

Magnet, S., Courvalin, P.,& Lambert, T. (2001). Resistance-nodulation-cell division-type efflux pump involved in aminoglycoside resistance in Acinetobacter baumannii strain BM4454. Antimicrob Agents Chemother, 45, 3375-3380.

Mindlin, S., Minakhin, L., Petrova, M., Kholodii, G., Minakhina, S., Gorlenko, Zh. & Nikiforov, V. (2005) Present-day mercury resistance transposons are common in bacteria preserved in permafrost grounds since the Upper Pleistocene. Res Microbiol, 156, 9941004.

Mindlin, S., Soina, V., Petrova, M. & Gorlenko, Z. (2008). Isolation of antibiotic resistance bacterial strains from East Siberia permafrost sediments. Russian J Genetics, 44, 27-34.

Ochi, K. (1995). Comparative ribosomal protein sequence analyses of a phylogenetically defined genus, Pseudomonas, and its relatives. Int J Syst Bacteriol, 45, 268-273.

Petrova, M. A., Mindlin,S. Z., Gorlenko, Zh. M., Kalyaeva, E. S., Soina, V. S.& Bogdanova, E. S. (2002) Mercury-resistant bacteria from permafrost sediments and prospects for their use in comparative studies of mercury resistance determinants. Russian J Genetics, 38, 1569-1574.

Petrova, M. A., Gorlenko, Zh. M., Soina, V. S, Mindlin,S. Z. (2008) Association of the strA-strB genes with plasmids and transposons in the present-day bacteria and in bacterial strains from permafrost. Russian J Genetics, 44, 1281-1286.

Piddock, L. J. (2006) Clinically relevant chromosomally encoded multidrug resistance efflux pumps in bacteria. Clin Microbiol Rev, 19, 382-402.

Poole, K. (1994) Bacterial multidrug resistance - emphasis on efflux mechanisms and Pseudomonas aeruginosa. . J Antimicrob Chemother,34, 453-456.

Poole, K. (2005) Efflux-mediated antimicrobial resistance. J Antimicrob Chemother, 56, 2051.

Riesenfeld, S. C., Goodman, R. M. & Handelsman, J. (2004). Uncultural soil bacteria are a reservoir of new antibiotic resistance genes. Environ Microbiol, 6, 981-989.

Sambrook J., Fritsch, E.F. & Maniatis T. (1989) Molecular cloning: a laboratory manual. Cold Spring Harbor, NY. Cold Spring Harbor Laboratory Press.

Soina, V. S. & Vorobyova, E. A. (2004). Adaptation of bacteria to the terrestrial permafrost environment: a biomodel for Astrobiology. In J. Seckbach (Ed), Origins:genesis, evolution and biodiversity of life (pp. 427-444). Netherlands, Kluver Academic publishers.

Sunde, M. & Norstrom, M. (2005). The genetic background for streptomycin resistance in Escherichia coli influences the distribution of MICs. J Antimicrob Chemother, 56, 87-90.

Sundin, G. W. (2002). Distinct recent lineage of the strA-strB streptomycin-resistance genes in clinical and environmental bacteria. Curr. Microbiol, 45, 63-69.

Tenover, F.C. (2006). Mechanisms of antimicrobial resistance in bacteria. Am J Med, 119, Suppl. 1, S3-10.

Tiedje, J., Smith, G. B., Simkins, S., Holben, W. E., Finney, C. & Gilichinsky, D. A. (1994). Recovery of DNA, denitrifiers and patterns of antibiotic sensitivity in microorganisms from ancient permafrost soils of Eastern Siberia. In D. A. Gilichinsky (Ed.), Viable microorganisms from permafrost. ( pp. 83-98). Puschino. (in Russian).

Vishnivetskaya, T., Kathariou S., McGrath J., Gilichinsky, D. & Tiedje, J. M. (2000) Low-temperature recovery strategies for the isolation of bacteria from ancient permafrost sediments. Extremophiles, 4, 165-173.

Vishnivetskaya, T. A., Petrova, M. A., Urbance, J., Ponder, M., Moyer, C. L., Gilichinsky, D. A. & Tiedje, J. M. (2006). Bacterial community in ancient siberian permafrost as characterized by culture and culture-independent methods. Astrobiology, 6, 400-414.

Vorobyova, E., Soina, V., Gorlenko, M., Minkovskaya, N., Zalinova, N., Mamukelashvili, A., Gilichinsky, D., Rivkina, E. & Vishnivetskaya, T. (1997). The deep cold biosphere: facts and hypothesis. FEMSMicrobiol Rev, 20, 277-290.

Vorobyova, E. A., Soina, V. S., Mamukelashvili, A. G., Bolshakova A., Yaminsky I. V.& Mulyukin A. L. (2005). Living Cells in Permafrost as Models for Astrobiology Research. (Chapter 19). In J.D Castello and S.O. Rogers (Eds.), Life in Ancient Ice. pp. 277-288, Princeton University Press.

Yabuuchi, E., Yano, I., Oyaizu, H., Hashimoto, Y., Ezaki, T. & Yamamoto, H. (1990). Proposals of Sphingomonas paucimobilis gen. nov. and comb. nov., Sphingomonas parapaucimobilis sp. nov., Sphingomonas yanoikuyae sp. nov., Sphingomonas adhaesiva sp. nov., Sphingomonas capsulata comb. nov., and two genospecies of the genus Sphingomonas. Microbiol Immunol, 34, 99-119.

Reviewed by Mulyukin (Muliukin) A. L. Institute of Microbiology, Russian Academy of Sciences, Moscow, Russia.

In: New Permafrost and Glacier Research Editors: Max I. Krugger and Harry P. Stern

ISBN: 978-1-60692-616-1 ©2009 Nova Science Publishers, Inc.

Chapter 4

Similarities Between the Recent Permafrost in North-Western Canada and the Pleistocene Relict Cryogenic Forms in Central Europe (Hungary)

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