检验医学与临床
檢驗醫學與臨床
검험의학여림상
JOURNAL OF LABORATORY MEDICINE AND CLINICAL SCIENCES
2014年
18期
2505-2507
,共3页
缪敏慧%孟红委%倪红元%戴如顺%王敏%杜鸿
繆敏慧%孟紅委%倪紅元%戴如順%王敏%杜鴻
무민혜%맹홍위%예홍원%대여순%왕민%두홍
伤寒沙门菌%t4606基因%生长曲线%靶基因
傷寒沙門菌%t4606基因%生長麯線%靶基因
상한사문균%t4606기인%생장곡선%파기인
Salmonella typhi%t4606 gene%grow th curve%target gene
目的:研究 t4606基因在伤寒沙门菌适应高渗应激环境时的生物学作用,为临床治疗和预防伤寒沙门菌感染提供可能的靶向基因。方法采用原核生物基因同源重组技术制备伤寒沙门菌 t4606基因缺陷株及t4606基因缺陷回补株;以生长时间为横坐标,培养液600 nm处得吸光度值为纵坐标,绘制生长曲线,比较 t4606基因缺陷株、回补株及野生株在高渗应激(300 mmol/L NaCl)环境下的生长能力;统计学分析不同菌株间的吸光度值差异。结果成功制备伤寒沙门菌 t4606基因缺陷株和相应的回补株;生长曲线分析显示在高渗应激环境下, t4606基因缺陷株的生存能力明显弱于野生株。结论 t4606基因在伤寒沙门菌适应高渗应激环境方面发挥着重要的作用,t4606基因有可能作为临床治疗和预防伤寒沙门菌感染的靶向基因。
目的:研究 t4606基因在傷寒沙門菌適應高滲應激環境時的生物學作用,為臨床治療和預防傷寒沙門菌感染提供可能的靶嚮基因。方法採用原覈生物基因同源重組技術製備傷寒沙門菌 t4606基因缺陷株及t4606基因缺陷迴補株;以生長時間為橫坐標,培養液600 nm處得吸光度值為縱坐標,繪製生長麯線,比較 t4606基因缺陷株、迴補株及野生株在高滲應激(300 mmol/L NaCl)環境下的生長能力;統計學分析不同菌株間的吸光度值差異。結果成功製備傷寒沙門菌 t4606基因缺陷株和相應的迴補株;生長麯線分析顯示在高滲應激環境下, t4606基因缺陷株的生存能力明顯弱于野生株。結論 t4606基因在傷寒沙門菌適應高滲應激環境方麵髮揮著重要的作用,t4606基因有可能作為臨床治療和預防傷寒沙門菌感染的靶嚮基因。
목적:연구 t4606기인재상한사문균괄응고삼응격배경시적생물학작용,위림상치료화예방상한사문균감염제공가능적파향기인。방법채용원핵생물기인동원중조기술제비상한사문균 t4606기인결함주급t4606기인결함회보주;이생장시간위횡좌표,배양액600 nm처득흡광도치위종좌표,회제생장곡선,비교 t4606기인결함주、회보주급야생주재고삼응격(300 mmol/L NaCl)배경하적생장능력;통계학분석불동균주간적흡광도치차이。결과성공제비상한사문균 t4606기인결함주화상응적회보주;생장곡선분석현시재고삼응격배경하, t4606기인결함주적생존능력명현약우야생주。결론 t4606기인재상한사문균괄응고삼응격배경방면발휘착중요적작용,t4606기인유가능작위림상치료화예방상한사문균감염적파향기인。
Objective To investigate the biological effect of t4606 gene in Salmonella typhi (S .typhi) under hyperosmotic stress and provide target genes for therapy and prevention of infection disease caused by S .typhi . Methods t4606 deleted strains (Δt4606 strains) of S .typhi was prepared by homologious recombination .Supplemen-tal strains Δt4606 (pBADt4606) was also prepared with recombinant plasmid pBAD t4606 in the Δt4606 strains . Growth curves ware drawn as the X-axis with time and the Y-axis with the absorbance value at 600 nm .The survival ability of Δt4606 strains ,Δt4606 (pBADt4606) strains and wild-type strains under high osmolarity stress (300 mmol/L NaCl) were compared .The differences were statistically analyzed .Results The Δt4606 strains and Δt4606 (pBAD t4606) strains were successfully generated .Compared with wild-type strains ,the survival ability of Δt4606 strains was significantly compromised under high osmolarity stress .Conclusion It could be confirmed that t4606 gene might be important for S .typhi to overcome the high osmolarity ,which indicate that t4606 gene could be a target gene for therapy and prevention of infection diseases caused by S .typhi .