Please wait a minute...
Soil Ecology Letters

ISSN 2662-2289

ISSN 2662-2297(Online)

Soil Ecology Letters  2024, Vol. 6 Issue (3): 230222   https://doi.org/10.1007/s42832-023-0222-2
  本期目录
Prevention and control strategies for antibiotic resistance: from species to community level
Yan-Zi Wang1,2, Hu Li1,2(), Qing-Lin Chen1,2, Ting Pan1,2, Yong-Guan Zhu1,2,3, Dirk Springael4, Jian-Qiang Su1,2
1. Key Laboratory of Urban Environment and Health, Ningbo Observation and Research Station, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021, China
2. University of Chinese Academy of Sciences, Beijing 100049, China
3. State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China
4. Division of Soil and Water Management, KU Leuven, Kasteelpark Arenberg 20 Box 2459, 3001 Heverlee, Belgium
 全文: PDF(8303 KB)   HTML
Abstract

● ARGs and ARB in typical environments which exposed to antibiotics are prevalent.

● Nanoparticle- and photosensitizer-related technology can clear specific ARGs or ARB.

● CRISPR-Cas- and phage-related technology can eliminate particular ARGs or ARB.

● Antibiotic combination can be used to eliminate microbial resistance.

● Microbiome-specific technology can eradicate most types of ARGs or ARB in one shot.

Antibiotic resistance genes (ARGs) and antibiotic resistant bacteria (ARB) in the environment pose serious threats to environmental security and public health. There is an urgent need for methods to specifically and effectively control environmental pollution or pathogen infection associated with ARGs and ARB. This review aims to provide an overview of methods abating the prevalence and spread of ARGs and ARB from species to community level. At the species level, species-specific technologies, such as nanoparticle-, photosensitizer-, CRISPR-Cas-, and phage-related technology can be utilized to clear a particular class of ARGs or ARB, and in combination with low-dose antibiotics, a higher removal efficiency can be achieved. Moreover, the combination of antibiotics can be used to reverse microbial resistance and treat recurrent antibiotic resistant pathogen infections. At the community level, community-specific strategies, such as biochar, hyperthermophilic compost, and fecal microbiota transplantation can eradicate most types of ARGs or ARB in one shot, reducing the probability of resistance development. Though some progress has been made to eliminate ARGs and ARB in disease treatment or decontamination scenarios, further research is still needed to elucidate their mechanisms of action and scopes of application, and efforts should be made to explore novel strategies to counter the prevalence of antibiotic resistance.

Key wordsantibiotic resistance genes    antibiotic resistant bacteria    treatment strategy    disinfection
收稿日期: 2023-09-12      出版日期: 2024-01-26
Corresponding Author(s): Hu Li   
 引用本文:   
. [J]. Soil Ecology Letters, 2024, 6(3): 230222.
Yan-Zi Wang, Hu Li, Qing-Lin Chen, Ting Pan, Yong-Guan Zhu, Dirk Springael, Jian-Qiang Su. Prevention and control strategies for antibiotic resistance: from species to community level. Soil Ecology Letters, 2024, 6(3): 230222.
 链接本文:  
https://academic.hep.com.cn/sel/CN/10.1007/s42832-023-0222-2
https://academic.hep.com.cn/sel/CN/Y2024/V6/I3/230222
Category Technology Advantages Disadvantages
Species-specific Nanoparticle Control and modify molecular structures at the nanoscale to achieve intelligent, targeted, and controlled delivery. Neurotoxicity, genotoxicity, and cytotoxicity of nanomaterials are still unresolved.
Photosensitizer Cause both plasma membrane and DNA damage of specific bacteria. The specific wavelengths of light to excite many types of photosensitizers are needed.
CRISPR-Cas Selectively remove AMR-encoding plasmids or ARGs. Some microbes have evolved anti-CRISPR systems, which may aid HGT; side effects (e.g., target missing and gene toxicity) may occur.
Phage Specifically lyse the host bacteria and does not affect non-host bacteria. Co-evolution of bacteria and phages may happen; ARGs or toxin genes may be carried by phages; endotoxin exit.
Antibiotic combination Reverse the selective advantage of ARB in competing with sensitive bacteria and may reduce the antibiotic resistance evolution rate. The superposition between drugs is complex; the absorption and osmotic efficiency of different drugs in the body are not consistent.
Fecal microbiota transplantation Modify community structure at ecological niches, without antibiotic usage. The donor’s sample should be carefully examined, or superinfection may arise.
Community-specific Biochar Remove most ARGs by the sorption and electrostatic repulsion of some biochar. Different kinds of biochar have different effects; some kinds may result in an undesired outcome; certain types of biochar are less efficient.
Hyperthermophilic composting Remove ARGs effectively and cut down their half-lives as well. The mineralization and humification mechanisms of organic matter, and the migration and transformation mechanisms of pollutants during the process of hyperthermophilic composting remain unclear.
Tab.1  
Fig.1  
Fig.2  
Fig.3  
Fig.4  
1 M.S.E., Abigail Freedman, M.D., Stephen Eppes, 2014. 1805. Use of stool transplant to clear fecal colonization with carbapenem-resistant Enterobacteraciae (CRE): proof of concept. Open Forum Infectious Diseases1, S65.
2 T.J.B.S.P.G., Agrawal, 2013. Fecal microbiota transplantation: indications, methods, evidence, and future directions. Current Gastroenterology Reports15, 337.
https://doi.org/10.1007/s11894-013-0337-1
3 R., Al-Mutairi, A., Tovmasyan, I., Batinic-Haberle, L., Benov, 2018. Sublethal photodynamic treatment does not lead to development of resistance. Frontiers in Microbiology9, 1699.
https://doi.org/10.3389/fmicb.2018.01699
4 A., Anas, J., Sobhanan, K.M., Sulfiya, C., Jasmin, P.K., Sreelakshmi, V., Biju, 2021. Advances in photodynamic antimicrobial chemotherapy. Journal of Photochemistry and Photobiology C, Photochemistry Reviews49, 100452.
https://doi.org/10.1016/j.jphotochemrev.2021.100452
5 N.M.O., Andoy, K., Jeon, C.T., Kreis, R.M.A., Sullan, 2020. Multifunctional and stimuli-responsive polydopamine nanoparticle-based platform for targeted antimicrobial applications. Advanced Functional Materials30, 2004503.
https://doi.org/10.1002/adfm.202004503
6 P., Angsantikul, S., Thamphiwatana, Q., Zhang, K., Spiekermann, J., Zhuang, R.H., Fang, W., Gao, M., Obonyo, L., Zhang, 2018. Coating nanoparticles with gastric epithelial cell membrane for targeted antibiotic delivery against Helicobacter pylori infection. Advanced Therapeutics1, 1800016.
https://doi.org/10.1002/adtp.201800016
7 C., Antimicrobial Resistance, 2022. Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Lancet399, 629–655.
https://doi.org/10.1016/S0140-6736(21)02724-0
8 A.V., Anzalone, L.W., Koblan, D.R., Liu, 2020. Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors. Nature Biotechnology38, 824–844.
https://doi.org/10.1038/s41587-020-0561-9
9 M.S., Baptista, J., Cadet, A., Greer, A.H., Thomas, 2021. Photosensitization reactions of biomolecules: definition, targets and mechanisms. Photochemistry and Photobiology97, 1456–1483.
https://doi.org/10.1111/php.13470
10 F., Baquero, B.R., Levin, 2021. Proximate and ultimate causes of the bactericidal action of antibiotics. Nature Reviews Microbiology19, 123–132.
https://doi.org/10.1038/s41579-020-00443-1
11 F., Barancheshme, M., Munir, 2017. Strategies to combat antibiotic resistance in the wastewater treatment plants. Frontiers in Microbiology8, 2603.
https://doi.org/10.3389/fmicb.2017.02603
12 R., Barrangou, J.A., Doudna, 2016. Applications of CRISPR technologies in research and beyond. Nature Biotechnology34, 933–941.
https://doi.org/10.1038/nbt.3659
13 R., Barrangou, C., Fremaux, H., Deveau, M., Richards, P., Boyaval, S., Moineau, D.A., Romero, P., Horvath, 2007. CRISPR provides acquired resistance against viruses in prokaryotes. Science315, 1709–1712.
https://doi.org/10.1126/science.1138140
14 M., Baym, L.K., Stone, R., Kishony, 2016. Multidrug evolutionary strategies to reverse antibiotic resistance. Science351, aad3292.
https://doi.org/10.1126/science.aad3292
15 N., Benech, H., Sokol, 2020. Fecal microbiota transplantation in gastrointestinal disorders: time for precision medicine. Genome Medicine12, 58.
https://doi.org/10.1186/s13073-020-00757-y
16 G., Bertoloni, F.M., Lauro, G., Cortella, M., Merchat, 2000. Photosensitizing activity of hematoporphyrin on Staphylococcus aureus cells. Biochimica et Biophysica Acta. G, General Subjects1475, 169–174.
https://doi.org/10.1016/S0304-4165(00)00071-4
17 D., Bikard, C.W., Euler, W., Jiang, P.M., Nussenzweig, G.W., Goldberg, X., Duportet, V.A., Fischetti, L.A., Marraffini, 2014. Exploiting CRISPR-Cas nucleases to produce sequence-specific antimicrobials. Nature Biotechnology32, 1146–1150.
https://doi.org/10.1038/nbt.3043
18 J.M.A., Blair, M.A., Webber, A.J., Baylay, D.O., Ogbolu, L.J.V., Piddock, 2015. Molecular mechanisms of antibiotic resistance. Nature Reviews Microbiology13, 42–51.
https://doi.org/10.1038/nrmicro3380
19 L.J., Brandt, O.C., Aroniadis, M., Mellow, A., Kanatzar, C., Kelly, T., Park, N., Stollman, F., Rohlke, C., Surawicz, 2012. Long-term follow-up of colonoscopic fecal microbiota transplant for recurrent Clostridium difficile infection. American Journal of Gastroenterology107, 1079–1087.
https://doi.org/10.1038/ajg.2012.60
20 M.M.C., Buckner, M.L., Ciusa, L.J.V., Piddock, 2018. Strategies to combat antimicrobial resistance: anti-plasmid and plasmid curing. FEMS Microbiology Reviews42, 781–804.
https://doi.org/10.1093/femsre/fuy031
21 J.D., Buynak, 2013. Beta-lactamase inhibitors: a review of the patent literature (2010–2013). Expert Opinion on Therapeutic Patents23, 1469–1481.
https://doi.org/10.1517/13543776.2013.831071
22 S.J., Cameron, J., Sheng, F., Hosseinian, W.G., Willmore, 2022. Nanoparticle effects on stress response pathways and nanoparticle-protein interactions. International Journal of Molecular Sciences23, 7962.
https://doi.org/10.3390/ijms23147962
23 M., Camilleri, S. Dilmaghani, 2022. Treatment of irritable bowel syndrome using fecal microbiota transplantation: a step forward?. Gastroenterology163, 815–817.
https://doi.org/10.1053/j.gastro.2022.06.087
24 J., Carter, C., Hoffman, B., Wiedenheft, 2017. The interfaces of genetic conflict are hot spots for innovation. Cell168, 9–11.
https://doi.org/10.1016/j.cell.2016.12.007
25 A.P., Castano, P., Mroz, M.R., Hamblin, 2006. Photodynamic therapy and anti-tumour immunity. Nature Reviews Cancer6, 535–545.
https://doi.org/10.1038/nrc1894
26 S.R., Chatterjee, T.S., Srivastava, J.P., Kamat, T.P.A., Devasagayam, 1998. Photocleavage of plasmid pBR322 DNA by some anionic porphyrins. Journal of Porphyrins and Phthalocyanines2, 337–343.
https://doi.org/10.1002/(SICI)1099-1409(199807/10)2:4/5<337::AID-JPP80>3.0.CO;2-L
27 Q.L., Chen, H.L., Cui, J.Q., Su, J., Penuelas, Y.G., Zhu, 2019. Antibiotic resistomes in plant microbiomes. Trends in Plant Science24, 530–541.
https://doi.org/10.1016/j.tplants.2019.02.010
28 Q.L., Chen, X.T., Fan, D., Zhu, X.L., An, J.Q., Su, L., Cui, 2018. Effect of biochar amendment on the alleviation of antibiotic resistance in soil and phyllosphere of Brassica chinensis L. Soil Biology & Biochemistry119, 74–82.
https://doi.org/10.1016/j.soilbio.2018.01.015
29 A., Chevallereau, B.J., Pons, S., van Houte, E.R., Westra, 2021. Interactions between bacterial and phage communities in natural environments. Nature Reviews Microbiology20, 49–62.
https://doi.org/10.1038/s41579-021-00602-y
30 G., Cho, D., Lee, S.M., Kim, T.J., Jeon, 2022. Elucidation of the interactions of reactive oxygen species and antioxidants in model membranes mimicking cancer cells and normal cells. Membranes (Basel)12, 286.
https://doi.org/10.3390/membranes12030286
31 N.D., Chu, J.W., Crothers, L.T.T., Nguyen, S.M., Kearney, M.B., Smith, Z., Kassam, C., Collins, R., Xavier, P.L., Moses, E.J., Alm, 2021. Dynamic colonization of microbes and their functions after fecal microbiota transplantation for inflammatory bowel disease. mBio12, e00975–21.
https://doi.org/10.1128/mBio.00975-21
32 A.L., Clarke, S., De Soir, J.D., Jones, 2020. The safety and efficacy of phage therapy for bone and joint infections: a systematic review. Antibiotics (Basel, Switzerland)9, 795.
https://doi.org/10.3390/antibiotics9110795
33 A., Colavecchio, B., Cadieux, A., Lo, L.D., Goodridge, 2017. Bacteriophages contribute to the spread of antibiotic resistance genes among foodborne pathogens of the Enterobacteriaceae family−a review. Frontiers in Microbiology8, 1108.
https://doi.org/10.3389/fmicb.2017.01108
34 E., Cui, Y., Wu, Y., Zuo, H., Chen, 2016. Effect of different biochars on antibiotic resistance genes and bacterial community during chicken manure composting. Bioresource Technology203, 11–17.
https://doi.org/10.1016/j.biortech.2015.12.030
35 P., Cui, H., Liao, Y., Bai, X., Li, Q., Zhao, Z., Chen, Z., Yu, Z., Yi, S., Zhou, 2019. Hyperthermophilic composting reduces nitrogen loss via inhibiting ammonifiers and enhancing nitrogenous humic substance formation. Science of the Total Environment692, 98–106.
https://doi.org/10.1016/j.scitotenv.2019.07.239
36 M., Dai, Y.F., Liu, W., Chen, H., Buch, Y., Shan, L.H., Chang, Y., Bai, C., Shen, X., Zhang, Y., Huo, D., Huang, Z., Yang, Z., Hu, X., He, J., Pan, L., Hu, X., Pan, X., Wu, B., Deng, Z., Li, B., Cui, F., Zhang, 2019. Rescue fecal microbiota transplantation for antibiotic-associated diarrhea in critically ill patients. Critical Care (London, England)23, 324.
https://doi.org/10.1186/s13054-019-2604-5
37 Z.M., Dai, X.Q., Xiong, H., Zhu, H.J., Xu, P., Leng, J.H., Li, C., Tang, J., Xu, 2021. Association of biochar properties with changes in soil bacterial, fungal and fauna communities and nutrient cycling processes. Biochar3, 239–254.
https://doi.org/10.1007/s42773-021-00099-x
38 R.M., Dedrick, B.E., Smith, M., Cristinziano, K.G., Freeman, D., Jacobs-Sera, Y., Belessis, A., Whitney Brown, K.A., Cohen, R.M., Davidson, D., van Duin, A., Gainey, C.B., Garcia, C.R., Robert George, G., Haidar, W., Ip, J., Iredell, A., Khatami, J.S., Little, K., Malmivaara, B.J., McMullan, D.E., Michalik, A., Moscatelli, J.A., Nick, M.G., Tupayachi Ortiz, H.M., Polenakovik, P.D., Robinson, M., Skurnik, D.A., Solomon, J., Soothill, H., Spencer, P., Wark, A., Worth, R.T., Schooley, C.A., Benson, G.F., Hatfull, 2023. Phage therapy of Mycobacterium infections: compassionate use of phages in 20 patients with drug-resistant mycobacterial disease. Clinical Infectious Diseases76, 103–112.
https://doi.org/10.1093/cid/ciac453
39 E., Diaz, I., Martin-Loeches, J., Valles, 2013. Nosocomial pneumonia. Enfermedades Infecciosas y Microbiologia Clinica31, 692–698.
https://doi.org/10.1016/j.eimc.2013.04.014
40 J., Ding, Y., Yin, A.Q., Sun, S.B., Lassen, G., Li, D., Zhu, X., Ke, 2019. Effects of biochar amendments on antibiotic resistome of the soil and collembolan gut. Journal of Hazardous Materials377, 186–194.
https://doi.org/10.1016/j.jhazmat.2019.05.089
41 L., Du, S., Ahmad, L., Liu, L., Wang, J., Tang, 2023. A review of antibiotics and antibiotic resistance genes (ARGs) adsorption by biochar and modified biochar in water. Science of the Total Environment858, 159815.
https://doi.org/10.1016/j.scitotenv.2022.159815
42 M.L., Duan, H.C., Li, J., Gu, X.X., Tuo, W., Sun, X., Qian, X., Wang, 2017. Effects of biochar on reducing the abundance of oxytetracycline, antibiotic resistance genes, and human pathogenic bacteria in soil and lettuce. Environmental Pollution224, 787–795.
https://doi.org/10.1016/j.envpol.2017.01.021
43 M., El-Salhy, T., Hausken, J.G., Hatlebakk, 2021. Current status of fecal microbiota transplantation for irritable bowel syndrome. Neurogastroenterology and Motility33, e14157.
https://doi.org/10.1111/nmo.14157
44 F., Enault, A., Briet, L., Bouteille, S., Roux, M.B., Sullivan, M.A., Petit, 2017. Phages rarely encode antibiotic resistance genes: a cautionary tale for virome analyses. ISME Journal11, 237–247.
https://doi.org/10.1038/ismej.2016.90
45 X.T., Fan, H., Li, Q.L., Chen, Y.S., Zhang, J., Ye, Y.G., Zhu, J.Q., Su, 2019. Fate of antibiotic resistant Pseudomonas putida and broad host range plasmid in natural soil microcosms. Frontiers in Microbiology10, 194.
https://doi.org/10.3389/fmicb.2019.00194
46 F., Fatima, S., Siddiqui, W.A., Khan, 2020. Nanoparticles as novel emerging therapeutic antibacterial agents in the antibiotics resistant era. Biological Trace Element Research199, 2552–2564.
https://doi.org/10.1007/s12011-020-02394-3
47 R., Fekrazad, A, Kalhori, K.A.M., Nejat, 2017. Antimicrobial Photodynamic Therapy with Nanoparticles versus Conventional Photosensitizer in Oral Diseases. In: Ficai, A., Grumezescu, A.M., eds. Nanostructures for Antimicrobial Therapy. Elsevier
48 A., Fillol-Salom, A., Alsaadi, J.A.M., Sousa, L., Zhong, K.R., Foster, E.P.C., Rocha, J.R., Penadés, H., Ingmer, J., Haaber, 2019. Bacteriophages benefit from generalized transduction. PLoS Pathogens15, e1007888.
https://doi.org/10.1371/journal.ppat.1007888
49 M.A., Fischbach, 2011. Combination therapies for combating antimicrobial resistance. Current Opinion in Microbiology14, 519–523.
https://doi.org/10.1016/j.mib.2011.08.003
50 Y., Fu, M., Jia, F., Wang, Z., Wang, Z., Mei, Y., Bian, X., Jiang, M., Virta, J.M., Tiedje, 2021a. Strategy for mitigating antibiotic resistance by biochar and hyperaccumulators in cadmium and oxytetracycline co-contaminated soil. Environmental Science & Technology55, 16369–16378.
https://doi.org/10.1021/acs.est.1c03434
51 Y.H., Fu, F., Wang, H.J., Sheng, F., Hu, Z.Q., Wang, M., Xu, Y., Bian, X., Jiang, J.M., Tiedje, 2021b. Removal of extracellular antibiotic resistance genes using magnetic biochar/quaternary phosphonium salt in aquatic environments: a mechanistic study. Journal of Hazardous Materials411, 125048.
https://doi.org/10.1016/j.jhazmat.2021.125048
52 A.M., Ginsberg, M., Spigelman, 2007. Challenges in tuberculosis drug research and development. Nature Medicine13, 290–294.
https://doi.org/10.1038/nm0307-290
53 A.A., Gomaa, H.E., Klumpe, M.L., Luo, K., Selle, R., Barrangou, C.L., Beisel, 2014. Programmable removal of bacterial strains by use of genome-targeting CRISPR-Cas systems. mBio5, e00928–13.
https://doi.org/10.1128/mBio.00928-13
54 C., Gomez-Gomez, P., Blanco-Picazo, M., Brown-Jaque, P., Quiros, L., Rodriguez-Rubio, M., Cerda-Cuellar, M., Muniesa, 2019. Infectious phage particles packaging antibiotic resistance genes found in meat products and chicken feces. Scientific Reports9, 11.
https://doi.org/10.1038/s41598-019-49898-0
55 C., Gonzalez-Bello, D., Rodriguez, M., Pernas, A., Rodriguez, E., Colchon, 2020. Beta-lactamase inhibitors to restore the efficacy of antibiotics against superbugs. Journal of Medicinal Chemistry63, 1859–1881.
https://doi.org/10.1021/acs.jmedchem.9b01279
56 M.T., Guo, Y., Gao, Y.B., Xue, Y.P., Liu, X.Y., Zeng, Y.Q., Cheng, J., Ma, H., Wang, J., Sun, Z., Wang, Y., Yan, 2021. Bacteriophage cocktails protect dairy cows against mastitis caused by drug resistant Escherichia coli infection. Frontiers in Cellular and Infection Microbiology11, 690377.
https://doi.org/10.3389/fcimb.2021.690377
57 M.T., Guo, Q.B., Yuan, J., Yang, 2015. Distinguishing effects of ultraviolet exposure and chlorination on the horizontal transfer of antibiotic resistance genes in municipal wastewater. Environmental Science & Technology49, 5771–5778.
https://doi.org/10.1021/acs.est.5b00644
58 J., Hrenovic, T., Ivankovic, D., Ivekovic, S., Repec, D., Stipanicev, M., Ganjto, 2017. The fate of carbapenem-resistant bacteria in a wastewater treatment plant. Water Research126, 232–239.
https://doi.org/10.1016/j.watres.2017.09.007
59 Y., Hu, T., Zhang, L., Jiang, Y., Luo, S., Yao, D., Zhang, K., Lin, C., Cui, 2019. Occurrence and reduction of antibiotic resistance genes in conventional and advanced drinking water treatment processes. Science of the Total Environment669, 777–784.
https://doi.org/10.1016/j.scitotenv.2019.03.143
60 Y., Hua, T., Luo, Y., Yang, D., Dong, R., Wang, Y., Wang, M., Xu, X., Guo, F., Hu, P., He, 2017. Phage therapy as a promising new treatment for lung infection caused by carbapenem-resistant Acinetobacter baumannii in mice. Frontiers in Microbiology8, 2659.
https://doi.org/10.3389/fmicb.2017.02659
61 C., Huang, Z., Tang, B., Xi, W., Tan, W., Guo, W., Wu, C., Ma, 2021. Environmental effects and risk control of antibiotic resistance genes in the organic solid waste aerobic composting system: a review. Frontiers of Environmental Science & Engineering15, 127.
https://doi.org/10.1007/s11783-021-1415-5
62 F.Y., Huang, Q.L., Chen, X., Zhang, R., Neilson, J.Q., Su, S.Y.D., Zhou, 2021. Dynamics of antibiotic resistance and its association with bacterial community in a drinking water treatment plant and the residential area. Environmental Science and Pollution Research International28, 55690–55699.
https://doi.org/10.1007/s11356-021-14896-1
63 I.C., Iakovides, I., Michael-Kordatou, N.F.F., Moreira, A.R., Ribeiro, T., Fernandes, M.F.R., Pereira, O.C., Nunes, C.M., Manaia, A.M.T., Silva, D., Fatta-Kassinos, 2019. Continuous ozonation of urban wastewater: removal of antibiotics, antibiotic-resistant Escherichia coli and antibiotic resistance genes and phytotoxicity. Water Research159, 333–347.
https://doi.org/10.1016/j.watres.2019.05.025
64 C., Jacobs, J.M., Frere, S., Normark, 1997. Cytosolic intermediates for cell wall biosynthesis and degradation control inducible beta-lactam resistance in gram-negative bacteria. Cell88, 823–832.
https://doi.org/10.1016/S0092-8674(00)81928-5
65 Q., Jiang, H., Yin, G., Li, H., Liu, T., An, P.K., Wong, H., Zhao, 2017. Elimination of antibiotic-resistance bacterium and its associated/dissociative blaTEM-1 and aac(3)-II antibiotic-resistance genes in aqueous system via photoelectrocatalytic process. Water Research125, 219–226.
https://doi.org/10.1016/j.watres.2017.08.050
66 W., Jiao, R., Du, M., Ye, M., Sun, Y., Feng, J., Wan, Y., Zhao, Z., Zhang, D., Huang, D., Du, X., Jiang, 2018. ‘Agricultural Waste to Treasure’−Biochar and eggshell to impede soil antibiotics/antibiotic resistant bacteria (genes) from accumulating in Solanum tuberosum L. Environmental Pollution242, 2088–2095.
https://doi.org/10.1016/j.envpol.2018.06.059
67 E.W., Jones, J.M., Carlson, 2018. In silico analysis of antibiotic-induced Clostridium difficile infection: remediation techniques and biological adaptations. PLoS Computational Biology14, e1006001.
https://doi.org/10.1371/journal.pcbi.1006001
68 G., Jori, C., Fabris, M., Soncin, S., Ferro, O., Coppellotti, D., Dei, L., Fantetti, G., Chiti, G., Roncucci, 2006. Photodynamic therapy in the treatment of microbial infections: basic principles and perspective applications. Lasers in Surgery and Medicine38, 468–481.
https://doi.org/10.1002/lsm.20361
69 Z., Kassam, C.H., Lee, Y.H., Yuan, R.H., Hunt, 2013. Fecal microbiota transplantation for Clostridium difficile infection: systematic review and meta-analysis. American Journal of Gastroenterology108, 500–508.
https://doi.org/10.1038/ajg.2013.59
70 C.R., Kelly, S., Kahn, P., Kashyap, L., Laine, D., Rubin, A., Atreja, T., Moore, G., Wu, 2015. Update on fecal microbiota transplantation 2015: indications, methodologies, mechanisms, and outlook. Gastroenterology149, 223–237.
https://doi.org/10.1053/j.gastro.2015.05.008
71 G.B., Kharkwal, S.K., Sharma, Y.Y., Huang, T., Dai, M.R., Hamblin, 2011. Photodynamic therapy for infections: clinical applications. Lasers in Surgery and Medicine43, 755–767.
https://doi.org/10.1002/lsm.21080
72 H.J., Kim, J.W., Jun, S.S., Giri, S.G., Kim, S.W., Kim, J., Kwon, S.B., Lee, C., Chi, S.C., Park, 2020. Bacteriophage cocktail for the prevention of multiple-antibiotic-resistant and mono-phage-resistant Vibrio coralliilyticus infection in pacific oyster (Crassostrea gigas) larvae. Pathogens (Basel, Switzerland)9, 831.
https://doi.org/10.3390/pathogens9100831
73 K.E., Kollef, G.E., Schramm, A.R., Wills, R.M., Reichley, S.T., Micek, M.H., Kollef, 2008. Predictors of 30-day mortality and hospital costs in patients with ventilator-associated pneumonia attributed to potentially antibiotic-resistant Gram-negative bacteria. Chest134, 281–287.
https://doi.org/10.1378/chest.08-1116
74 S.J., Labrie, J.E., Samson, S., Moineau, 2010. Bacteriophage resistance mechanisms. Nature Reviews Microbiology8, 317–327.
https://doi.org/10.1038/nrmicro2315
75 M., Laffin, B., Millan, K.L., Madsen, 2017. Fecal microbial transplantation as a therapeutic option in patients colonized with antibiotic resistant organisms. Gut Microbes8, 221–224.
https://doi.org/10.1080/19490976.2016.1278105
76 D.G.J., Larsson, C.F., Flach, 2022. Antibiotic resistance in the environment. Nature Reviews Microbiology20, 257–269.
https://doi.org/10.1038/s41579-021-00649-x
77 J.D., Laskin, 1994. Cellular and molecular mechanisms in photochemical sensitization−studies on the mechanism of action of psoralens. Food and Chemical Toxicology32, 119–127.
https://doi.org/10.1016/0278-6915(94)90172-4
78 A., Lewies, J.F., Wentzel, A., Jordaan, C., Bezuidenhout, L.H., Du Plessis, 2017. Interactions of the antimicrobial peptide nisin Z with conventional antibiotics and the use of nanostructured lipid carriers to enhance antimicrobial activity. International Journal of Pharmaceutics526, 244–253.
https://doi.org/10.1016/j.ijpharm.2017.04.071
79 H., Liao, X., Lu, C., Rensing, V.P., Friman, S., Geisen, Z., Chen, Z., Yu, Z., Wei, S., Zhou, Y., Zhu, 2018. Hyperthermophilic composting accelerates the removal of antibiotic resistance genes and mobile genetic elements in sewage sludge. Environmental Science & Technology52, 266–276.
https://doi.org/10.1021/acs.est.7b04483
80 H.P., Liao, Q., Zhao, P., Cui, Z., Chen, Z., Yu, S., Geisen, V.P., Friman, S., Zhou, 2019. Efficient reduction of antibiotic residues and associated resistance genes in tylosin antibiotic fermentation waste using hyperthermophilic composting. Environment International133, 105203.
https://doi.org/10.1016/j.envint.2019.105203
81 B.N., Limketkai, S., Hendler, P., Ting, A.M., Parian, 2019. Fecal microbiota transplantation for the critically ill patient. Nutrition in Clinical Practice34, 73–79.
https://doi.org/10.1002/ncp.10228
82 G.W., Liu, Q.P., Lin, S., Jin, C.X., Gao, 2022. The CRISPR-Cas toolbox and gene editing technologies. Molecular Cell82, 333–347.
https://doi.org/10.1016/j.molcel.2021.12.002
83 X.H., Liu, S.Y., Lu, W., Guo, B.D., Xi, W.L., Wang, 2018. Antibiotics in the aquatic environments: a review of lakes, China. Science of the Total Environment627, 1195–1208.
https://doi.org/10.1016/j.scitotenv.2018.01.271
84 Y., Liu, H.J., Busscher, B.R., Zhao, Y.F., Li, Z.K., Zhang, H.C., van der Mei, Y., Ren, L., Shi, 2016a. Surface-adaptive, antimicrobially loaded, micellar nanocarriers with enhanced penetration and killing efficiency in staphylococcal biofilms. ACS Nano10, 4779–4789.
https://doi.org/10.1021/acsnano.6b01370
85 Y.Y., Liu, Y., Wang, T.R., Walsh, L.X., Yi, R., Zhang, J., Spencer, Y., Doi, G., Tian, B., Dong, X., Huang, L.F., Yu, D., Gu, H., Ren, X., Chen, L., Lv, D., He, H., Zhou, Z., Liang, J.H., Liu, J. Shen, , 2016b. Emergence of plasmid-mediated colistin resistance mechanism MCR-1 in animals and human beings in China: a microbiological and molecular biological study. Lancet Infectious Diseases 16, 161–168
86 Z., Liu, H., Dong, Y., Cui, L., Cong, D., Zhang, 2020. Application of different types of CRISPR/Cas-based systems in bacteria. Microbial Cell Factories19, 172.
https://doi.org/10.1186/s12934-020-01431-z
87 C., Lu, J., Gu, X., Wang, J., Liu, K., Zhang, X., Zhang, R., Zhang, 2018. Effects of coal gasification slag on antibiotic resistance genes and the bacterial community during swine manure composting. Bioresource Technology268, 20–27.
https://doi.org/10.1016/j.biortech.2018.07.086
88 T., Luong, A.C., Salabarria, R.A., Edwards, D.R., Roach, 2020. Standardized bacteriophage purification for personalized phage therapy. Nature Protocols15, 2867–2890.
https://doi.org/10.1038/s41596-020-0346-0
89 M., Mahler, A.R., Costa, S.P.B., van Beljouw, P.C., Fineran, S.J.J., Brouns, 2023. Approaches for bacteriophage genome engineering. Trends in Biotechnology41, 669–685.
https://doi.org/10.1016/j.tibtech.2022.08.008
90 K.S., Makarova, Y.I., Wolf, O.S., Alkhnbashi, F., Costa, S.A., Shah, S.J., Saunders, R., Barrangou, S.J.J., Brouns, E., Charpentier, D.H., Haft, P., Horvath, S., Moineau, F.J.M., Mojica, R.M., Terns, M.P., Terns, M.F., White, A.F., Yakunin, R.A., Garrett, J., van der Oost, R., Backofen, E.V., Koonin, 2015. An updated evolutionary classification of CRISPR-Cas systems. Nature Reviews Microbiology13, 722–736.
https://doi.org/10.1038/nrmicro3569
91 S.L., Manoto, D.O., Oluwole, R., Malabi, C., Maphanga, S., Ombinda-Lemboumba, T., Nyokong, P., Mthunzi-Kufa, 2017. Phototodynamic activity of zinc monocarboxyphenoxy phthalocyane (ZnMCPPc) conjugated to gold silver (AuAg) nanoparticles in melanoma cancer cells. Conference on Optical Methods for Tumor Treatment and Detection - Mechanisms and Techniques in Photodynamic Therapy XXVI. 10047, San Francisco, CA,
92 L.A., Marraffini, 2013. CRISPR-Cas immunity against phages: its effects on the evolution and survival of bacterial pathogens. PLoS Pathogens9, e1003765.
https://doi.org/10.1371/journal.ppat.1003765
93 J.L., Martinez, F., Baquero, 2000. Mutation frequencies and antibiotic resistance. Antimicrobial Agents and Chemotherapy44, 1771–1777.
https://doi.org/10.1128/AAC.44.7.1771-1777.2000
94 J.L., Martínez, T.M., Coque, F., Baquero, 2014. What is a resistance gene? Ranking risk in resistomes. Nature Reviews Microbiology13, 116–123.
https://doi.org/10.1038/nrmicro3399
95 L.M., McMurry, M., Oethinger, S.B., Levy, 1998. Triclosan targets lipid synthesis. Nature394, 531–532.
https://doi.org/10.1038/28970
96 S., Mousa, M., Magdy, D.Y., Xiong, R., Nyaruabaa, S.M., Rizk, J.P., Yu, H., Wei, 2022. Microbial profiling of potato-associated rhizosphere bacteria under bacteriophage therapy. Antibiotics (Basel, Switzerland)11, 1117.
https://doi.org/10.3390/antibiotics11081117
97 Y., Nitzan, M., Salmon-Divon, E., Shporen, Z., Malik, 2004. ALA induced photodynamic effects on Gram positive and negative bacteria. Photochemical & Photobiological Sciences3, 430–435.
https://doi.org/10.1039/b315633h
98 J., Oh, D.E., Salcedo, C.A., Medriano, S., Kim, 2014. Comparison of different disinfection processes in the effective removal of antibiotic-resistant bacteria and genes. Journal of Environmental Sciences (China)26, 1238–1242.
https://doi.org/10.1016/S1001-0742(13)60594-X
99 M.O., Ojemaye, M.A., Adefisoye, A.I., Okoh, 2020. Nanotechnology as a viable alternative for the removal of antimicrobial resistance determinants from discharged municipal effluents and associated watersheds: a review. Journal of Environmental Management275, 111234.
https://doi.org/10.1016/j.jenvman.2020.111234
100 T., Oshima, T., Moriya, 2008. A Preliminary Analysis of Microbial and Biochemical Properties of High-Temperature Compost. In: Wiegel, J., Maier, R.J., Adams, M.W.W., eds. Incredible Anaerobes: From Physiology to Genomics to Fuels. 1125. Blackwell Publishing, Oxford, pp. 338–344
101 W.Y., Ouyang, F.Y., Huang, Y., Zhao, H., Li, J.Q., Su, 2015. Increased levels of antibiotic resistance in urban stream of Jiulongjiang River, China. Applied Microbiology and Biotechnology99, 5697–5707.
https://doi.org/10.1007/s00253-015-6416-5
102 A.C., Palmer, R., Kishony, 2013. Understanding, predicting and manipulating the genotypic evolution of antibiotic resistance. Nature Reviews Genetics14, 243–248.
https://doi.org/10.1038/nrg3351
103 S.V., Patwardhan, F.S., Emami, R.J., Berry, S.E., Jones, R.R., Naik, O., Deschaume, H., Heinz, C.C., Perry, 2012. Chemistry of aqueous silica nanoparticle surfaces and the mechanism of selective peptide adsorption. Journal of the American Chemical Society134, 6244–6256.
https://doi.org/10.1021/ja211307u
104 D.P., Pires, S., Cleto, S., Sillankorva, J., Azeredo, T.K., Lu, 2016. Genetically engineered phages: a review of advances over the last decade. Microbiology and Molecular Biology Reviews80, 523–543.
https://doi.org/10.1128/MMBR.00069-15
105 I.M., Proenca, W.M., Bernardo, A.M., da Ponte, C.O., Matsubayashi, A.P.S., Kotinda, M.M., Flor, D.T., de Moura, E.G., de Moura, 2020. Fecal microbiota transplantation for metabolic syndrome and obesity: a systematic review and meta-analysis based on randomized clinical trials. Gastroenterology158, S480–S481.
https://doi.org/10.1016/S0016-5085(20)31880-1
106 A., Pruden, D.G., Larsson, A., Amezquita, P., Collignon, K.K., Brandt, D.W., Graham, J.M., Lazorchak, S., Suzuki, P., Silley, J.R., Snape, E., Topp, T., Zhang, Y.G., Zhu, 2013. Management options for reducing the release of antibiotics and antibiotic resistance genes to the environment. Environmental Health Perspectives121, 878–885.
https://doi.org/10.1289/ehp.1206446
107 Q., Pu, L.X., Zhao, Y.T., Li, J.Q., Su, 2020. Manure fertilization increase antibiotic resistance in soils from typical greenhouse vegetable production bases, China. Journal of Hazardous Materials391, 122267.
https://doi.org/10.1016/j.jhazmat.2020.122267
108 E., Pursey, D., Sunderhauf, W.H., Gaze, E.R., Westra, S., van Houte, 2018. CRISPR-Cas antimicrobials: challenges and future prospects. PLoS Pathogens14, e1006990.
https://doi.org/10.1371/journal.ppat.1006990
109 G., Qing, X., Zhao, N., Gong, J., Chen, X., Li, Y., Gan, Y., Wang, Z., Zhang, Y., Zhang, W., Guo, Y., Luo, X.J., Liang, 2019. Thermo-responsive triple-function nanotransporter for efficient chemo-photothermal therapy of multidrug-resistant bacterial infection. Nature Communications10, 4336.
https://doi.org/10.1038/s41467-019-12313-3
110 M., Raffi, S., Mehrwan, T.M., Bhatti, J.I., Akhter, A., Hameed, W., Yawar, M.M., ul Hasan, 2010. Investigations into the antibacterial behavior of copper nanoparticles against Escherichia coli. Annals of Microbiology60, 75–80.
https://doi.org/10.1007/s13213-010-0015-6
111 S., Ranghar, P., Sirohi, P., Verma, V., Agarwal, 2014. Nanoparticle-based drug delivery systems: promising approaches against infections. Brazilian Archives of Biology and Technology57, 209–222.
https://doi.org/10.1590/S1516-89132013005000011
112 A., Rineh, M.J., Kelso, F., Vatansever, G.P., Tegos, M.R., Hamblin, 2014. Clostridium difficile infection: molecular pathogenesis and novel therapeutics. Expert Review of Anti-Infective Therapy12, 131–150.
https://doi.org/10.1586/14787210.2014.866515
113 A.L., Romo, R., Quiros, 2019. Appropriate use of antibiotics: an unmet need. Therapeutic Advances in Urology11, 9.
https://doi.org/10.1177/1756287219832174
114 L.K., Ruddaraju, S.V.N., Pammi, G.S., Guntuku, V.S., Padavala, V.R.M., Kolapalli, 2020. A review on anti-bacterials to combat resistance: from ancient era of plants and metals to present and future perspectives of green nano technological combinations. Asian J Pharm Sci15, 42–59.
https://doi.org/10.1016/j.ajps.2019.03.002
115 M., Salmon-Divon, Y., Nitzan, Z., Malik, 2004. Mechanistic aspects of Escherichia coli photodynamic inactivation by cationic tetra-meso (N-methylpyridyl)porphine. Photochemical & Photobiological Sciences3, 423–429.
https://doi.org/10.1039/b315627n
116 V.P., Sandanayaka, A.S., Prashad, 2002. Resistance to beta-lactam antibiotics: structure and mechanism based design of beta-lactamase inhibitors. Current Medicinal Chemistry9, 1145–1165.
https://doi.org/10.2174/0929867023370031
117 E., Sanganyado, W., Gwenzi, 2019. Antibiotic resistance in drinking water systems: occurrence, removal, and human health risks. Science of the Total Environment669, 785–797.
https://doi.org/10.1016/j.scitotenv.2019.03.162
118 V.K., Sharma, N., Johnson, L., Cizmas, T.J., McDonald, H., Kim, 2016. A review of the influence of treatment strategies on antibiotic resistant bacteria and antibiotic resistance genes. Chemosphere150, 702–714.
https://doi.org/10.1016/j.chemosphere.2015.12.084
119 S., Shehreen, T.y., Chyou, P.C., Fineran, C.M., Brown, 2019. Genome-wide correlation analysis suggests different roles of CRISPR-Cas systems in the acquisition of antibiotic resistance genes in diverse species. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences374, 20180384.
https://doi.org/10.1098/rstb.2018.0384
120 A.F., Shorr, M.D., Zilberberg, S.T., Micek, M.H., Kollef, 2008. Prediction of infection due to antibiotic-resistant bacteria by select risk factors for health care-associated pneumonia. Archives of Internal Medicine168, 2205–2210.
https://doi.org/10.1001/archinte.168.20.2205
121 M., Soncin, C., Fabris, A., Busetti, D., Dei, D., Nistri, G., Roncucci, G., Jori, 2002. Approaches to selectivity in the Zn(II)-phthalocyanine-photosensitized inactivation of wild-type and antibiotic-resistant Staphylococcus aureus. Photochemical & Photobiological Sciences1, 815–819.
https://doi.org/10.1039/b206554a
122 M., Sun, M., Ye, Z., Zhang, S., Zhang, Y., Zhao, S., Deng, L., Kong, R., Ying, B., Xia, W., Jiao, J., Cheng, Y., Feng, M., Liu, F., Hu, 2019. Biochar combined with polyvalent phage therapy to mitigate antibiotic resistance pathogenic bacteria vertical transfer risk in an undisturbed soil column system. Journal of Hazardous Materials365, 1–8.
https://doi.org/10.1016/j.jhazmat.2018.10.093
123 E., Tacconelli, 2006. New strategies to identify patients harbouring antibiotic-resistant bacteria at hospital admission. Clinical Microbiology and Infection12, 102–109.
https://doi.org/10.1111/j.1469-0691.2005.01326.x
124 T.L., Tagliaferri, N.R., Guimaraes, M.P.M., Pereira, L.F.F., Vilela, H.P., Horz, S.G., dos Santos, T.A.O., Mendes, 2020. Exploring the potential of CRISPR-Cas9 under challenging conditions: facing high-copy plasmids and counteracting beta-lactam resistance in clinical strains of Enterobacteriaceae. Frontiers in Microbiology11, 578.
https://doi.org/10.3389/fmicb.2020.00578
125 A.K., Thabit, J.L., Crandon, D.P., Nicolau, 2015. Antimicrobial resistance: impact on clinical and economic outcomes and the need for new antimicrobials. Expert Opinion on Pharmacotherapy16, 159–177.
https://doi.org/10.1517/14656566.2015.993381
126 C.M., Thomas, K.M., Nielsen, 2005. Mechanisms of, and barriers to, horizontal gene transfer between bacteria. Nature Reviews Microbiology3, 711–721.
https://doi.org/10.1038/nrmicro1234
127 J., Walter, M.X., Maldonado-Gomez, I., Martinez, 2018. To engraft or not to engraft: an ecological framework for gut microbiome modulation with live microbes. Current Opinion in Biotechnology49, 129–139.
https://doi.org/10.1016/j.copbio.2017.08.008
128 J.L., Wang, D.Q., Mao, Q.H., Mu, Y., Luo, 2015. Fate and proliferation of typical antibiotic resistance genes in five full-scale pharmaceutical wastewater treatment plants. Science of the Total Environment526, 366–373.
https://doi.org/10.1016/j.scitotenv.2015.05.046
129 L., Wang, C., Hu, L., Shao, 2017. The antimicrobial activity of nanoparticles: present situation and prospects for the future. International Journal of Nanomedicine12, 1227–1249.
https://doi.org/10.2147/IJN.S121956
130 X.F., Wang, Z., Wei, K.M., Yang, J.N., Wang, A., Jousset, Y.C., Xu, Q., Shen, V.-P., Friman, 2019. Phage combination therapies for bacterial wilt disease in tomato. Nature Biotechnology37, 1513–1520.
https://doi.org/10.1038/s41587-019-0328-3
131 Y.Z., Wang, X.L., An, X.T., Fan, Q., Pu, H., Li, W.Z., Liu, Z., Chen, J.Q., Su, 2024. Visible light-activated photosensitizer inhibits the plasmid-mediated horizontal gene transfer of antibiotic resistance genes. Journal of Hazardous Materials461, 132564.
https://doi.org/10.1016/j.jhazmat.2023.132564
132 Y.Z., Wang, S.Y.D., Zhou, X.Y., Zhou, X.L., An, J.Q., Su, 2022. Manure and biochar have limited effect on lettuce leaf endophyte resistome. Science of the Total Environment860, 160515–160515.
https://doi.org/10.1016/j.scitotenv.2022.160515
133 Z., Wang, D., Wu, Y., Lin, X., Wang, 2021. Role of temperature in sludge composting and hyperthermophilic systems: a review. BioEnergy Research15, 962–976.
https://doi.org/10.1007/s12155-021-10281-5
134 P.J., Weldrick, S., Iveson, M.J., Hardman, V.N., Paunov, 2019. Breathing new life into old antibiotics: overcoming antibacterial resistance by antibiotic-loaded nanogel carriers with cationic surface functionality. Nanoscale11, 10472–10485.
https://doi.org/10.1039/C8NR10022E
135 X., Wittebole, S., De Roock, S.M., Opal, 2014. A historical overview of bacteriophage therapy as an alternative to antibiotics for the treatment of bacterial pathogens. Virulence5, 226–235.
https://doi.org/10.4161/viru.25991
136 R.J., Worthington, C., Melander, 2013. Combination approaches to combat multidrug-resistant bacteria. Trends in Biotechnology31, 177–184.
https://doi.org/10.1016/j.tibtech.2012.12.006
137 G.D., Wright, 2016. Antibiotic adjuvants: rescuing antibiotics from resistance. Trends in Microbiology24, 862–871.
https://doi.org/10.1016/j.tim.2016.06.009
138 W., Yang, J., Shang, B., Li, M., Flury, 2020. Surface and colloid properties of biochar and implications for transport in porous media. Critical Reviews in Environmental Science and Technology50, 2484–2522.
https://doi.org/10.1080/10643389.2019.1699381
139 M., Ye, M., Sun, Y., Feng, J., Wan, S., Xie, D., Tian, Y., Zhao, J., Wu, F., Hu, H., Li, X., Jiang, 2016. Effect of biochar amendment on the control of soil sulfonamides, antibiotic-resistant bacteria, and gene enrichment in lettuce tissues. Journal of Hazardous Materials309, 219–227.
https://doi.org/10.1016/j.jhazmat.2015.10.074
140 M., Ye, M., Sun, D., Huang, Z., Zhang, H., Zhang, S., Zhang, F., Hu, X., Jiang, W., Jiao, 2019. A review of bacteriophage therapy for pathogenic bacteria inactivation in the soil environment. Environment International129, 488–496.
https://doi.org/10.1016/j.envint.2019.05.062
141 M., Ye, M., Sun, Y., Zhao, W., Jiao, B., Xia, M., Liu, Y., Feng, Z., Zhang, D., Huang, R., Huang, J., Wan, R., Du, X., Jiang, F., Hu, 2018. Targeted inactivation of antibiotic-resistant Escherichia coli and Pseudomonas aeruginosa in a soil-lettuce system by combined polyvalent bacteriophage and biochar treatment. Environmental Pollution241, 978–987.
https://doi.org/10.1016/j.envpol.2018.04.070
142 Y., Yoon, H.J., Chung, D.Y., Wen Di, M.C., Dodd, H.G., Hur, Y., Lee, 2017. Inactivation efficiency of plasmid-encoded antibiotic resistance genes during water treatment with chlorine, UV, and UV/H2O2. Water Research123, 783–793.
https://doi.org/10.1016/j.watres.2017.06.056
143 I., Yosef, M., Manor, R., Kiro, U., Qimron, 2015. Temperate and lytic bacteriophages programmed to sensitize and kill antibiotic-resistant bacteria. Proceedings of the National Academy of Sciences of the United States of America112, 7267–7272.
https://doi.org/10.1073/pnas.1500107112
144 B., Zeina, J., Greenman, D., Corry, W.M., Purcell, 2002. Cytotoxic effects of antimicrobial photodynamic therapy on keratinocytes in vitro. British Journal of Dermatology146, 568–573.
https://doi.org/10.1046/j.1365-2133.2002.04623.x
145 F., Zhang, T., Zhang, H., Zhu, T.J., Borody, 2019a. Evolution of fecal microbiota transplantation in methodology and ethical issues. Current Opinion in Pharmacology49, 11–16.
https://doi.org/10.1016/j.coph.2019.04.004
146 T.Y., Zhang, Y.R., Hu, L., Jiang, S.J., Yao, K.F., Lin, Y.B., Zhou, C., Cui, 2019b. Removal of antibiotic resistance genes and control of horizontal transfer risk by UV, chlorination and UV/chlorination treatments of drinking water. Chemical Engineering Journal358, 589–597.
https://doi.org/10.1016/j.cej.2018.09.218
147 Y., Zhang, P., Huang, D., Wang, J., Chen, W., Liu, P., Hu, M., Huang, X., Chen, Z., Chen, 2018. Near-infrared-triggered antibacterial and antifungal photodynamic therapy based on lanthanide-doped upconversion nanoparticles. Nanoscale10, 15485–15495.
https://doi.org/10.1039/C8NR01967C
148 Y., Zhao, Z.T., Lu, X.M., Dai, X.S., Wei, Y.J., Yu, X.L., Chen, X., Zhang, C., Li, 2018. Glycomimetic-conjugated photosensitizer for specific Pseudomonas aeruginosa recognition and targeted photodynamic therapy. Bioconjugate Chemistry29, 3222–3230.
https://doi.org/10.1021/acs.bioconjchem.8b00600
149 Y., Zhao, M., Ye, X., Zhang, M., Sun, Z., Zhang, H., Chao, D., Huang, J., Wan, S., Zhang, X., Jiang, D., Sun, Y., Yuan, F., Hu, 2019. Comparing polyvalent bacteriophage and bacteriophage cocktails for controlling antibiotic-resistant bacteria in soil-plant system. Science of the Total Environment657, 918–925.
https://doi.org/10.1016/j.scitotenv.2018.11.457
150 G., Zheng, Y., Lu, D., Wang, L., Zhou, 2019. Importance of sludge conditioning in attenuating antibiotic resistance: removal of antibiotic resistance genes by bioleaching and chemical conditioning with Fe[III]/CaO. Water Research152, 61–73.
https://doi.org/10.1016/j.watres.2018.12.053
151 J., Zheng, C., Su, J., Zhou, L., Xu, Y., Qian, H., Chen, 2017. Effects and mechanisms of ultraviolet, chlorination, and ozone disinfection on antibiotic resistance genes in secondary effluents of municipal wastewater treatment plants. Chemical Engineering Journal317, 309–316.
https://doi.org/10.1016/j.cej.2017.02.076
152 Y.G., Zhu, Y., Zhao, B., Li, C.L., Huang, S.Y., Zhang, S., Yu, Y.S., Chen, T., Zhang, M.R., Gillings, J.Q., Su, 2017. Continental-scale pollution of estuaries with antibiotic resistance genes. Nature Microbiology2, 16270.
https://doi.org/10.1038/nmicrobiol.2016.270
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed