Evaluation of Sulfadiazine Degradation in Three Newly Isolated Pure Bacterial Cultures

PLoS One. 2016 Oct 18;11(10):e0165013. doi: 10.1371/journal.pone.0165013. eCollection 2016.

Abstract

This study is aimed to assess the biodegradation of sulfadiazine (SDZ) and characterization of heavy metal resistance in three pure bacterial cultures and also their chemotactic response towards 2-aminopyrimidine. The bacterial cultures were isolated from pig manure, activated sludge and sediment samples, by enrichment technique on SDZ (6 mg L-1). Based on the 16S rRNA gene sequence analysis, the microorganisms were identified within the genera of Paracoccus, Methylobacterium and Kribbella, which were further designated as SDZ-PM2-BSH30, SDZ-W2-SJ40 and SDZ-3S-SCL47. The three identified pure bacterial strains degraded up to 50.0, 55.2 and 60.0% of SDZ (5 mg L-1), respectively within 290 h. On the basis of quadrupole time-of-flight mass spectrometry and high performance liquid chromatography, 2-aminopyrimidine and 4-hydroxy-2-aminopyrimidine were identified as the main intermediates of SDZ biodegradation. These bacteria were also able to degrade the metabolite, 2-aminopyrimidine, of the SDZ. Furthermore, SDZ-PM2-BSH30, SDZ-W2-SJ40 and SDZ-3S-SCL47 also showed resistance to various heavy metals like copper, cadmium, chromium, cobalt, lead, nickel and zinc. Additionally, all three bacteria exhibited positive chemotaxis towards 2-aminopyrimidine based on the drop plate method and capillary assay. The results of this study advanced our understanding about the microbial degradation of SDZ, which would be useful towards the future SDZ removal in the environment.

MeSH terms

  • Actinobacteria / classification
  • Actinobacteria / drug effects
  • Actinobacteria / genetics
  • Actinobacteria / isolation & purification
  • Animals
  • Anti-Infective Agents / analysis
  • Anti-Infective Agents / metabolism*
  • Anti-Infective Agents / pharmacology
  • Bacteria / drug effects
  • Bacteria / genetics
  • Bacteria / isolation & purification
  • Bacteria / metabolism*
  • Chemotaxis
  • Chromatography, High Pressure Liquid
  • Drug Resistance, Bacterial
  • Geologic Sediments / microbiology
  • Manure / microbiology
  • Mass Spectrometry
  • Metals, Heavy / toxicity
  • Methylobacterium / classification
  • Methylobacterium / drug effects
  • Methylobacterium / genetics
  • Methylobacterium / isolation & purification
  • Microbial Sensitivity Tests
  • Paracoccus / classification
  • Paracoccus / drug effects
  • Paracoccus / genetics
  • Paracoccus / isolation & purification
  • Phylogeny
  • Pyrimidines / analysis
  • Pyrimidines / isolation & purification
  • RNA, Ribosomal, 16S / chemistry
  • RNA, Ribosomal, 16S / metabolism
  • Sequence Analysis, DNA
  • Sewage / microbiology
  • Sulfadiazine / analysis
  • Sulfadiazine / metabolism*
  • Sulfadiazine / pharmacology
  • Swine

Substances

  • Anti-Infective Agents
  • Manure
  • Metals, Heavy
  • Pyrimidines
  • RNA, Ribosomal, 16S
  • Sewage
  • Sulfadiazine
  • 2-aminopyrimidine

Grants and funding

This research was supported by the Hundred Talents Program of Fujian Province, China, National Natural Science Foundation of China (31370503, 31470539), International Young Scientists by National Natural Science Foundation of China (31450110426), Youth Innovation Promotion Association CAS and the financial assistance from The World Academy of Sciences-Chinese Academy of Sciences (TWAS-CAS) under its Post-Doctoral fellowships for Young International Scientists (2013FFZB0003). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.