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利用响应面法优化感染葡萄球菌噬菌体 vB_SauM-phiIPLA-RODI 在木糖葡萄球菌上的繁殖。

Optimizing Propagation of Staphylococcus aureus Infecting Bacteriophage vB_SauM-phiIPLA-RODI on Staphylococcus xylosus Using Response Surface Methodology.

机构信息

Instituto de Productos Lácteos de Asturias (IPLA-CSIC), Paseo Río Linares s/n, 33300 Villaviciosa, Spain.

Departamento de Biotecnología de Alimentos, Instituto de la Grasa (IG-CSIC), Campus Universitario Pablo de Olavide, Edificio 46. Ctra, Sevilla-Utrera, 1 km, 41013 Sevilla, Spain.

出版信息

Viruses. 2018 Mar 27;10(4):153. doi: 10.3390/v10040153.

DOI:10.3390/v10040153
PMID:29584701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5923447/
Abstract

The use of bacteriophages for killing pathogenic bacteria is a feasible alternative to antibiotics and disinfectants. To obtain the large quantities of phages required for this application, large-scale production of bacteriophages must be optimized. This study aims to define conditions that maximize the phage yield of the virulent and polyvalent staphylococcal bacteriophage vB_SauM-phiIPLA-RODI in broth culture, using the food-grade species Staphylococcus xylosus as the host strain to reduce the risk of growing massive quantities of pathogenic bacteria and therefore, to ensure the safety of the final phage stock. The effect of four variables, namely initial bacterial concentration (5.66-8.40 log colony-forming unit (CFU)/mL), initial phage concentration (5-8 log plaque-forming unit (PFU)/mL), temperature (21-40 °C) and agitation (20-250 rpm), on phage yield (response) was studied by using response surface methodology (RSM). Successive experimental designs showed that agitation did not significantly impact phage yield, while temperature did have a significant effect, with 38 °C being the optimum for phage propagation. The results allowed the design of a model to describe phage yield as a function of the initial bacterial and phage concentrations at fixed agitation (135 rpm), and optimum temperature (38 °C). The maximum experimental phage yield obtained was 9.3 log PFU/mL, while that predicted by the model under the optimized conditions (7.07 log CFU/mL initial bacterial population and 6.00 log PFU/mL initial phage titer) was 9.25 ± 0.30 log PFU/mL, with the desirability of 0.96. This yield is comparable to that obtained when the phage was propagated on the original host, Staphylococcus aureus. Bacteriophage phiIPLA-RODI showed the same host range and very similar biofilm removal ability regardless of the staphylococcal species used for its propagation. The results presented in this study show the suitability of using a food-grade strain of S. xylosus for the propagation of S. aureus infecting phages and the application of RSM to define the optimal propagation conditions.

摘要

噬菌体用于杀死致病菌是抗生素和消毒剂的可行替代品。为了获得这种应用所需的大量噬菌体,必须优化噬菌体的大规模生产。本研究旨在确定在肉汤培养中最大限度地提高毒性和多价葡萄球菌噬菌体 vB_SauM-phiIPLA-RODI 噬菌体产量的条件,使用食品级物种木糖葡萄球菌作为宿主菌株,以降低大量生长致病菌的风险,从而确保最终噬菌体库存的安全性。使用响应面法(RSM)研究了四个变量(初始细菌浓度(5.66-8.40 log 集落形成单位(CFU)/mL)、初始噬菌体浓度(5-8 log 噬菌斑形成单位(PFU)/mL)、温度(21-40°C)和搅拌(20-250 rpm))对噬菌体产量(响应)的影响。连续实验设计表明,搅拌对噬菌体产量没有显著影响,而温度有显著影响,噬菌体繁殖的最佳温度为 38°C。结果允许设计一个模型,将噬菌体产量描述为在固定搅拌(135 rpm)下初始细菌和噬菌体浓度的函数,并优化温度(38°C)。获得的最大实验噬菌体产量为 9.3 log PFU/mL,而在优化条件下(7.07 log CFU/mL 初始细菌种群和 6.00 log PFU/mL 初始噬菌体滴度)模型预测的最大产量为 9.25±0.30 log PFU/mL,可取性为 0.96。该产量与在原始宿主金黄色葡萄球菌上繁殖噬菌体时获得的产量相当。噬菌体 phiIPLA-RODI 显示出相同的宿主范围,并且无论用于其繁殖的葡萄球菌物种如何,都具有非常相似的生物膜去除能力。本研究中提出的结果表明,使用食品级木糖葡萄球菌菌株繁殖感染金黄色葡萄球菌的噬菌体是合适的,并且 RSM 可用于定义最佳繁殖条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/b4ee215c961b/viruses-10-00153-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/dfb622d4baaa/viruses-10-00153-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/c6ce6cbfad03/viruses-10-00153-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/7ee52ff4f411/viruses-10-00153-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/fb88aff850d6/viruses-10-00153-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/b4ee215c961b/viruses-10-00153-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/dfb622d4baaa/viruses-10-00153-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/c6ce6cbfad03/viruses-10-00153-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/7ee52ff4f411/viruses-10-00153-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/fb88aff850d6/viruses-10-00153-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d2/5923447/b4ee215c961b/viruses-10-00153-g005.jpg

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