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Frontiers of Environmental Science & Engineering

ISSN 2095-2201

ISSN 2095-221X(Online)

CN 10-1013/X

Postal Subscription Code 80-973

2018 Impact Factor: 3.883

Front. Environ. Sci. Eng.    2019, Vol. 13 Issue (3) : 44    https://doi.org/10.1007/s11783-019-1128-1
RESEARCH ARTICLE
Detection of presumed genes encoding beta-lactamases by sequence based screening of metagenomes derived from Antarctic microbial mats
Gastón Azziz1,2(), Matías Giménez1, Héctor Romero3, Patricia M. Valdespino-Castillo4, Luisa I. Falcón5,6, Lucas A. M. Ruberto7,8, Walter P. Mac Cormack7,8, Silvia Batista1
1. 1Molecular Microbiology Unit, Clemente Estable Biological Research Insitute, UdelaR, Montevideo 11600, Uruguay
2. Microbiology Laboratory, Faculty of Agronomy, UdelaR, Montevideo 12900, Uruguay
3. Genome Organization and Evolution Laboratory, Ecology and Evolution Department, Faculty of Sciences, UdelaR, Montevideo 11400, Uruguay
4. Molecular Biophysics and Integrated Bioimaging, BSISB Imaging Program, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA
5. Bacteial Ecology Laboratory, Ecology Institute, National Autonomous University of Mexico, CDMX 04510, Mexico
6. UNAM, Yucatan Technology and Science Park, Merida 97302, Mexico
7. Argentine Antarctic Institute, Buenos Aires 1650, Argentina
8. Biotechnology Unit, Faculty of Pharmacy and Biochemistry, Nanobiotec Institute UBA-CONICET, Buenos Aires 1113, Argentina
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Abstract

• Beta-lactamase genes were found in all samples from distant places in Antarctica.

• Class C beta-lactamase coding genes were the most frequently found.

• Diversity of sequences exceeds that of the beta-lactamases from clinical environment.

Analysis of environmental samples for bacterial antibiotic resistance genes may have different objectives and analysis strategies. In some cases, the purpose was to study diversity and evolution of genes that could be grouped within a mechanism of antibiotic resistance. Different protocols have been designed for detection and confirmation that a functional gene was found. In this study, we present a sequence-based screening of candidate genes encoding beta-lactamases in 14 metagenomes of Antarctic microbial mats. The samples were obtained from different sites, representing diverse biogeographic regions of maritime and continental Antarctica. A protocol was designed based on generation of Hidden Markov Models from the four beta-lactamase classes by Ambler classification, using sequences from the Comprehensive Antibiotic Resistance Database (CARD). The models were used as queries for metagenome analysis and recovered contigs were subsequently annotated using RAST. According to our analysis, 14 metagenomes analyzed contain A, B and C beta-lactamase genes. Class D genes, however, were identified in 11 metagenomes. The most abundant was class C (46.8%), followed by classes B (35.5%), A (14.2%) and D (3.5%). A considerable number of sequences formed clusters which included, in some cases, contigs from different metagenomes. These assemblies are clearly separated from reference clusters, previously identified using CARD beta-lactamase sequences. While bacterial antibiotic resistance is a major challenge of public health worldwide, our results suggest that environmental diversity of beta-lactamase genes is higher than that currently reported, although this should be complemented with gene function analysis.

Keywords Beta-lactamases      Antibiotic resistance coding genes      Metagenomes      Antarctic microbial mats     
Corresponding Author(s): Gastón Azziz   
Issue Date: 26 June 2019
 Cite this article:   
Gastón Azziz,Matías Giménez,Héctor Romero, et al. Detection of presumed genes encoding beta-lactamases by sequence based screening of metagenomes derived from Antarctic microbial mats[J]. Front. Environ. Sci. Eng., 2019, 13(3): 44.
 URL:  
https://academic.hep.com.cn/fese/EN/10.1007/s11783-019-1128-1
https://academic.hep.com.cn/fese/EN/Y2019/V13/I3/44
Sample Geographic reference Latitude Longitude
Sample 1 King George Island (Fildes Peninsula) 62°09′31” S 58°56′31’ W
Sample 2 King George Island (Fildes Peninsula) 62°09′59” S 58°58′33” W
Sample 3 King George Island (Fildes Peninsula) 62°12′14” S 58°57′16” W
Sample 4 King George Island (Fildes Peninsula) 62°10′0” S 58°58′34” W
Sample 5 King George Island (Potter Peninsula) 62°14′35” S 58°40′39” W
Sample 6 King George Island (Potter Peninsula) 62°14′34” S 58°40′26” W
Sample 7 Antarctic Peninsula (Trinity Peninsula) 63°28′13” S 57°12′3” W
Sample 8 Antarctic Peninsula (Danco Coast) 64°09′22” S 60°57′30” W
Sample 9 Antarctic Peninsula (Fallieres Coast) 68°07′45” S 67°06′2” W
Sample 10 McMurdo Dry Valleys 78°01′24” S 163°55′03” E
Sample 11 McMurdo Dry Valleys 78°01′23” S 163°54′56” E
Sample 12 McMurdo Dry Valleys 78°01′23” S 163°54′07” E
Sample 13 McMurdo Dry Valleys 78°01′30” S 164°06′02” E
Sample 14 McMurdo Dry Valleys 77°39′40” S 163°05′31” E
Tab.1  Geographic location of sampling sites
Class A Class B
Samplea) Primary Hits (n) Confirmed Hits (n) Confirmed
Hits (‰)
Primary Hits (n) Confirmed Hits (n) Confirmed
Hits (‰)
Metagenome 1 (14344) 4 2 0.139 17 6 0.418
Metagenome 2 (3760) 10 3 0.798 33 5 1.330
Metagenome 3 (3724) 8 1 0.269 14 6 1.611
Metagenome 4 (4706) 7 4 0.850 28 8 1.700
Metagenome 5 (15035) 42 13 0.865 78 21 1.397
Metagenome 6 (11962) 32 8 0.669 66 15 1.254
Metagenome 7 (9291) 21 8 0.861 67 16 1.722
Metagenome 8 (10127) 39 12 1.185 72 19 1.876
Metagenome 9 (7315) 14 5 0.684 64 34 4.648
Metagenome 10 (6973) 20 7 1.004 53 15 2.151
Metagenome 11 (9269) 22 13 1.403 68 24 2.589
Metagenome 12 (8972) 7 2 0.223 76 15 1.672
Metagenome 13 (7187) 13 5 0.696 58 16 2.226
Metagenome 14 (11580) 21 10 0.864 71 32 2.763
Tab.2  Number and per mille of beta-lactamase hits found for classes A and B in each metagenome
Class C Class D
Samplea) Primary Hits (n) Confirmed Hits (n) Confirmed
Hits (‰)
Primary Hits (n) Confirmed Hits (n) Confirmed
Hits (‰)
Metagenome 1 (14344) 19 12 0.837 0 0 0
Metagenome 2 (3760) 27 10 2.660 9 2 0.532
Metagenome 3 (3724) 17 7 1.880 4 1 0.269
Metagenome 4 (4706) 21 10 2.125 8 0 0
Metagenome 5 (15035) 58 19 1.264 22 1 0.067
Metagenome 6 (11962) 75 26 2.174 28 1 0.084
Metagenome 7 (9291) 36 14 1.507 21 2 0.215
Metagenome 8 (10127) 70 26 2.567 26 5 0.494
Metagenome 9 (7315) 86 44 6.015 10 3 0.410
Metagenome 10 (6973) 51 23 3.298 14 2 0.287
Metagenome 11 (9269) 64 32 3.452 14 3 0.324
Metagenome 12 (8972) 62 19 2.118 9 2 0.223
Metagenome 13 (7187) 43 25 3.479 8 1 0.139
Metagenome 14 (11580) 79 39 3.368 15 0 0
Tab.3  Number and per mille of beta-lactamase hits found for classes C and D in each metagenome
Fig.1  Phylogenetic tree constructed with deduced amino acid sequences of class A beta-lactamases identified in Antarctic microbial mat metagenomes. Representative reference sequences were also included in the tree. The tree was constructed using Neighbor Joining algorithm.
Fig.2  Phylogenetic tree constructed with deduced amino acid sequences of class B beta-lactamases identified in Antarctic microbial mat metagenomes. Representative reference sequences were also included in the tree. The tree was constructed using Neighbor Joining algorithm.
Fig.3  Phylogenetic tree constructed with deduced amino acid sequences of class C beta-lactamases identified in Antarctic microbial mat metagenomes. Representative reference sequences were also included in the tree. The tree was constructed using Neighbor Joining algorithm.
Fig.4  Phylogenetic tree constructed with deduced amino acid sequences of class D beta-lactamases identified in Antarctic microbial mat metagenomes. Representative reference sequences were also included in the tree. The tree was constructed using Neighbor Joining algorithm.
Class Shannon index of metagenome sequences Shannon index of database sequences
Class Aa) 2.94 (n = 93) 1.35 (n = 660)
Class Ba) 3.32 (n = 232) 2.30 (n = 163)
Class Ca) 4.85 (n = 306) 0.72 (n = 226)
Class Da) 1.54 (n = 23) 1.66 (n = 292)
Tab.4  Shannon diversity indexes for each class of beta-lactamases for sequences retrieved from the Antarctic metagenomes and from CARD database
1 C Al Bayssari, A O Olaitan, F Dabboussi, M Hamze, J M Rolain (2015). Emergence of OXA-48-producing Escherichia coli clone ST38 in fowl. Antimicrobial Agents and Chemotherapy, 59(1): 745–746
https://doi.org/10.1128/AAC.03552-14 pmid: 25348536
2 H K Allen, J Donato, H H Wang, K A Cloud-Hansen, J Davies, J Handelsman (2010). Call of the wild: Antibiotic resistance genes in natural environments. Nature Reviews. Microbiology, 8(4): 251–259
https://doi.org/10.1038/nrmicro2312 pmid: 20190823
3 H K Allen, L A Moe, J Rodbumrer, A Gaarder, J Handelsman (2009). Functional metagenomics reveals diverse b-lactamases in a remote Alaskan soil. The ISME Journal, 3(2): 243–251
https://doi.org/10.1038/ismej.2008.86 pmid: 18843302
4 R K Aziz, D Bartels, A A Best, M DeJongh, T Disz, R A Edwards, K Formsma, S Gerdes, E M Glass, M Kubal, F Meyer, G J Olsen, R Olson, A L Osterman, R A Overbeek, L K McNeil, D Paarmann, T Paczian, B Parrello, G D Pusch, C Reich, R Stevens, O Vassieva, V Vonstein, A Wilke, O Zagnitko (2008). The RAST Server: rapid annotations using subsystems technology. BMC Genomics, 9(1): 75–90
https://doi.org/10.1186/1471-2164-9-75 pmid: 18261238
5 M Babic, A M Hujer, R A Bonomo (2006). What’s new in antibiotic resistance? Focus on beta-lactamases. Drug Resistance Updates: Reviews and Commentaries in Antimicrobial and Anticancer Chemotherapy, 9(3): 142–156
https://doi.org/10.1016/j.drup.2006.05.005 pmid: 16899402
6 J W Bennett, K T Chung (2001). Alexander Fleming and the discovery of penicillin. Advances in Applied Microbiology, 49: 163–184
https://doi.org/10.1016/S0065-2164(01)49013-7 pmid: 11757350
7 F Berglund, T Österlund, F Boulund, N P Marathe, D G J Larsson, E Kristiansson (2019). Identification and reconstruction of novel antibiotic resistance genes from metagenomes. Microbiome, 7(1): 52–66
https://doi.org/10.1186/s40168-019-0670-1 pmid: 30935407
8 R Bonnet (2004). Growing group of extended-spectrum b-lactamases: The CTX-M enzymes. Antimicrobial Agents and Chemotherapy, 48(1): 1–14
https://doi.org/10.1128/AAC.48.1.1-14.2004 pmid: 14693512
9 M Boolchandani, A W D’Souza, G Dantas (2019). Sequencing-based methods and resources to study antimicrobial resistance. Nature Reviews. Genetics,
https://doi.org/10.1038/s41576-019-0108-4 pmid: 30886350
10 K Bush, P Courvalin, G Dantas, J Davies, B Eisenstein, P Huovinen, G A Jacoby, R Kishony, B N Kreiswirth, E Kutter, S A Lerner, S Levy, K Lewis, O Lomovskaya, J H Miller, S Mobashery, L J Piddock, S Projan, C M Thomas, A Tomasz, P M Tulkens, T R Walsh, J D Watson, J Witkowski, W Witte, G Wright, P Yeh, H I Zgurskaya (2011). Tackling antibiotic resistance. Nature Reviews. Microbiology, 9(12): 894–896
https://doi.org/10.1038/nrmicro2693 pmid: 22048738
11 Y P Chen, S H Lee, C H Chou, H J Tsai (2012). Detection of florfenicol resistance genes in Riemerella anatipestifer isolated from ducks and geese. Veterinary Microbiology, 154(3–4): 325–331
https://doi.org/10.1016/j.vetmic.2011.07.012 pmid: 21820820
12 P E Coudron, E S Moland, K S Thomson (2000). Occurrence and detection of AmpC beta-lactamases among Escherichia coli, Klebsiella pneumoniae, and Proteus mirabilis isolates at a veterans medical center. Journal of Clinical Microbiology, 38(5): 1791–1796
pmid: 10790101
13 J Davies, D Davies (2010). Origins and evolution of antibiotic resistance. Microbiology and Molecular Biology Reviews : MMBR, 74(3): 417–433
https://doi.org/10.1128/MMBR.00016-10 pmid: 20805405
14 M de Been, V F Lanza, M de Toro, J Scharringa, W Dohmen, Y Du, J Hu, Y Lei, N Li, A Tooming-Klunderud, D J Heederik, A C Fluit, M J Bonten, R J Willems, F de la Cruz, W van Schaik (2014). Dissemination of cephalosporin resistance genes between Escherichia coli strains from farm animals and humans by specific plasmid lineages. PLOS Genetics, 10(12): e1004776–e1004793
https://doi.org/10.1371/journal.pgen.1004776 pmid: 25522320
15 B A Evans, S G Amyes (2014). OXA b-lactamases. Clinical Microbiology Reviews, 27(2): 241–263 PMID:24696435
https://doi.org/10.1128/CMR.00117-13
16 L Fu, B Niu, Z Zhu, S Wu, W Li (2012). CD-HIT: accelerated for clustering the next-generation sequencing data. Bioinformatics (Oxford, England), 28(23): 3150–3152
https://doi.org/10.1093/bioinformatics/bts565 pmid: 23060610
17 G Garau, I García-Sáez, C Bebrone, C Anne, P Mercuri, M Galleni, J M Frère, O Dideberg (2004). Update of the standard numbering scheme for class B b-lactamases. Antimicrobial Agents and Chemotherapy, 48(7): 2347–2349
https://doi.org/10.1128/AAC.48.7.2347-2349.2004 pmid: 15215079
18 M K Gibson, K J Forsberg, G Dantas (2015). Improved annotation of antibiotic resistance determinants reveals microbial resistomes cluster by ecology. The ISME Journal, 9(1): 207–216
https://doi.org/10.1038/ismej.2014.106 pmid: 25003965
19 B G Hall, M Barlow (2004). Evolution of the serine b-lactamases: Past, present and future. Drug Resistance Updates: Reviews and Commentaries in Antimicrobial and Anticancer Chemotherapy, 7(2): 111–123 doi:10.1016/j.drup.2004.02.003
pmid: 15158767
20 B G Hall, M Barlow (2005). Revised Ambler classification of b-lactamases. The Journal of Antimicrobial Chemotherapy, 55(6): 1050–1051
https://doi.org/10.1093/jac/dki130 pmid: 15872044
21 L D Högberg, A Heddini, O Cars (2010). The global need for effective antibiotics: Challenges and recent advances. Trends in Pharmacological Sciences, 31(11): 509–515
https://doi.org/10.1016/j.tips.2010.08.002 pmid: 20843562
22 K A Hughes, A Thompson (2004). Distribution of sewage pollution around a maritime Antarctic research station indicated by faecal coliforms, Clostridium perfringens and faecal sterol markers. Environmental Pollution (Barking, Essex: 1987), 127(3): 315–321
https://doi.org/10.1016/j.envpol.2003.09.004 pmid: 14638291
23 G A Jacoby (2009). AmpC b-lactamases. Clinical Microbiology Reviews, 22(1): 161–182
https://doi.org/10.1128/CMR.00036-08 pmid: 19136439
24 S H Jeong, I K Bae, J H Lee, S G Sohn, G H Kang, G J Jeon, Y H Kim, B C Jeong, S H Lee (2004). Molecular characterization of extended-spectrum beta-lactamases produced by clinical isolates of Klebsiella pneumoniae and Escherichia coli from a Korean nationwide survey. Journal of Clinical Microbiology, 42(7): 2902–2906
https://doi.org/10.1128/JCM.42.7.2902-2906.2004 pmid: 15243036
25 C M June, B C Vallier, R A Bonomo, D A Leonard, R A Powers (2014). Structural origins of oxacillinase specificity in class D b-lactamases. Antimicrobial Agents and Chemotherapy, 58(1): 333–341
https://doi.org/10.1128/AAC.01483-13 pmid: 24165180
26 M N Lisa, A R Palacios, M Aitha, M M González, D M Moreno, M W Crowder, R A Bonomo, J Spencer, D L Tierney, L I Llarrull, A J Vila (2017). A general reaction mechanism for carbapenem hydrolysis by mononuclear and binuclear metallo-b-lactamases. Nature Communications, 8(1): 538–549
https://doi.org/10.1038/s41467-017-00601-9 pmid: 28912448
27 J L Martínez (2008). Antibiotics and antibiotic resistance genes in natural environments. Science, 321(5887): 365–367
https://doi.org/10.1126/science.1159483 pmid: 18635792
28 T Naas, L Poirel, P Nordmann (2008). Minor extended-spectrum b-lactamases. Clinical Microbiology and Infection, 14(Suppl 1): 42–52
https://doi.org/10.1111/j.1469-0691.2007.01861.x pmid: 18154527
29 J Nesme, S Cécillon, T O Delmont, J M Monier, T M Vogel, P Simonet (2014). Large-scale metagenomic-based study of antibiotic resistance in the environment. Current Biology: CB, 24(10): 1096–1100
https://doi.org/10.1016/j.cub.2014.03.036 pmid: 24814145
30 Y Peng, H C Leung, S M Yiu, F Y Chin (2012). IDBA-UD: a de novo assembler for single-cell and metagenomic sequencing data with highly uneven depth. Bioinformatics (Oxford, England), 28(11): 1420–1428
https://doi.org/10.1093/bioinformatics/bts174 pmid: 22495754
31 F J Pérez-Pérez, N D Hanson (2002). Detection of plasmid-mediated AmpC b-lactamase genes in clinical isolates by using multiplex PCR. Journal of Clinical Microbiology, 40(6): 2153–2162
https://doi.org/10.1128/JCM.40.6.2153-2162.2002 pmid: 12037080
32 C Quince, A W Walker, J T Simpson, N J Loman, N Segata (2017). Shotgun metagenomics, from sampling to analysis. Nature Biotechnology, 35(9): 833–844
https://doi.org/10.1038/nbt.3935 pmid: 28898207
33 E Ruppé, A Ghozlane, J Tap, N Pons, A S Alvarez, N Maziers, T Cuesta, S Hernando-Amado, I Clares, J L Martínez, T M Coque, F Baquero, V F Lanza, L Máiz, T Goulenok, V de Lastours, N Amor, B Fantin, I Wieder, A Andremont, W van Schaik, M Rogers, X Zhang, R J L Willems, A G de Brevern, J M Batto, H M Blottière, P Léonard, V Léjard, A Letur, F Levenez, K Weiszer, F Haimet, J Doré, S P Kennedy, S D Ehrlich (2019). Prediction of the intestinal resistome by a three-dimensional structure-based method. Nature Microbiology, 4(1): 112–123
https://doi.org/10.1038/s41564-018-0292-6 pmid: 30478291
34 T Segawa, N Takeuchi, A Rivera, A Yamada, Y Yoshimura, G Barcaza, K Shinbori, H Motoyama, S Kohshima, K Ushida (2013). Distribution of antibiotic resistance genes in glacier environments. Environmental Microbiology Reports, 5(1): 127–134
https://doi.org/10.1111/1758-2229.12011 pmid: 23757141
35 S Shaikh, J Fatima, S Shakil, S M D Rizvi, M A Kamal (2015). Antibiotic resistance and extended spectrum beta-lactamases: Types, epidemiology and treatment. Saudi Journal of Biological Sciences, 22(1): 90–101
https://doi.org/10.1016/j.sjbs.2014.08.002 pmid: 25561890
36 M W Van Goethem, R Pierneef, O K I Bezuidt, Y Van De Peer, D A Cowan, T P Makhalanyane (2018). A reservoir of ‘historical’ antibiotic resistance genes in remote pristine Antarctic soils. Microbiome, 6(1): 40–52
https://doi.org/10.1186/s40168-018-0424-5 pmid: 29471872
37 J C Wallace, J A Port, M N Smith, E M Faustman (2017). FARME DB: A functional antibiotic resistance element database. Database (Oxford), 2017: baw165–7
https://doi.org/10.1093/database/baw165 pmid: 28077567
38 G D Wright (2010). Antibiotic resistance in the environment: A link to the clinic? Current Opinion in Microbiology, 13(5): 589–594
https://doi.org/10.1016/j.mib.2010.08.005 pmid: 20850375
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