رسالة جامعية

Proteomic analysis reveals stress-responsive proteins of Photobacterium damselae under different salt concentrations and during invasion of fish kidney cells

التفاصيل البيبلوغرافية
العنوان: Proteomic analysis reveals stress-responsive proteins of Photobacterium damselae under different salt concentrations and during invasion of fish kidney cells
العنوان البديل: 以蛋白質體學方法分析雀鯛發光桿菌在鹽濃度改變與入侵魚類腎細胞過程中產生之壓力調節蛋白質
المؤلفون: Min-Yuan Chuang, 莊閔元
مرشدي الرسالة: Wei-Jung Chen, 陳威戎
سنة النشر: 2009
المجموعة: National Digital Library of Theses and Dissertations in Taiwan
الوصف: 97
Being an island surrounded by sea, Taiwan’s fisheries are well developed and net-cage fish farming becomes a promising economic sector. However, an outbreak of fish photobacteriosis is recognized as one of the most threatening bacterial diseases in aquaculture worldwide due to its wide host range and massive mortality. Photobacterium damselae subsp. piscicida is the causative agent of this serious fish disease. The astonishing flexibility and adaptability of the bacterial cell has enabled many marine pathogenic species to freely transition between dramatically different environmental conditions, especially osmotic pressure. In the current study, 0.85% and 3.5% NaCl concentrations were used to mimic the osmotic conditions in host and marine water bodies, respectively. Proteomic approaches were applied to investigate the expression pattern of the sub-proteomes of P. damselae subsp. piscicida in different salinities. Proteins significantly altered were analyzed by 2-DE and LC-ESI-Q-TOF MS/MS, thus resulted in 16 outer membrane proteins (OMPs), 12 inner membrane proteins (IMPs), and 20 cytoplasmic proteins (CPs), respectively. COG analysis revealed that when shifting from 3.5% to 0.85% salinity, the majority of the up-regulated proteins were involved in posttranslational modification, protein turnover, and chaperones, while the down-regulated proteins were related to energy production and conversion. Quantitative real-time PCR was performed to confirm the proteomic results. Furthermore, The protein profile changes that underlie this ability can determine the success of the pathogen in the host. An investigation of the differential protein expression of this pathogen during invasion was undertaken utilizing fish kidney cell line. However, it is apparent that 39 identified proteins are not directly involved in damaging or injuring host cells. Rather, these proteins seem to be primarily involved in the metabolism and utilization of nutrients in the host environments. These results will be helpful for expanding our knowledge on the mechanism of survival between a host and seawater for P. damselae subsp. piscicida and open very promising prospects towards the development of an effective anti-photobacteriosis vaccine.
Original Identifier: 097NIU07108012
نوع الوثيقة: 學位論文 ; thesis
وصف الملف: 112
الإتاحة: http://ndltd.ncl.edu.tw/handle/60106678775713123468Test
رقم الانضمام: edsndl.TW.097NIU07108012
قاعدة البيانات: Networked Digital Library of Theses & Dissertations