福建水产
福建水產
복건수산
JOURNAL OF FUJIAN FISHERIES
2014年
2期
87-95
,共9页
郭睿%刘年锋%江小斌%张善霹%王伟%郑晨晖%杨小强
郭睿%劉年鋒%江小斌%張善霹%王偉%鄭晨暉%楊小彊
곽예%류년봉%강소빈%장선벽%왕위%정신휘%양소강
嗜水气单胞菌%分子鉴定%gyrB%毒力基因%序列分析
嗜水氣單胞菌%分子鑒定%gyrB%毒力基因%序列分析
기수기단포균%분자감정%gyrB%독력기인%서렬분석
Aeromonas hydrophila%molecular characterization%gyrB%virulence gene%sequence analysis
为了分子鉴定6株鱼源嗜水气单胞菌,并从分子层面验证通过检测毒力基因以推测嗜水气单胞菌潜在致病性的可行性。实验采用PCR扩增16 S rDNA和gyrB基因并结合系统发育树的构建和分析进行菌种的分子鉴定,检测气溶素( aerolysin, aer)、溶血素( haemoly-sin, hly)、丝氨酸蛋白酶( serine protease, ahp)、热稳定细胞肠毒素( heat-stable cytotonic enterotoxin, ast)和热敏感细胞肠毒素( heat-labile cytotonic enterotoxin, alt)5种毒力基因,且使用Mega 5.2对核苷酸和氨基酸序列进行分析。结果显示6株菌均为嗜水气单胞菌Aero-monas hydrophila,检测出5种毒力基因中的至少4种,其中均检测出溶血素和2种肠毒素,序列分析表明气溶素、溶血素和丝氨酸蛋白酶的氨基酸序列高度保守。本研究基于16 S rD-NA和gyrB基因可以准确地对嗜水气单胞菌进行分子鉴定,6株菌的毒力基因丰富预示着一定的致病性, aer、 hly和ahp基因相对保守,编码的毒力因子高度同源,在临床分子诊断中建议使用aer、 ahp和hly基因对嗜水气单胞菌的潜在致病性进行检测。
為瞭分子鑒定6株魚源嗜水氣單胞菌,併從分子層麵驗證通過檢測毒力基因以推測嗜水氣單胞菌潛在緻病性的可行性。實驗採用PCR擴增16 S rDNA和gyrB基因併結閤繫統髮育樹的構建和分析進行菌種的分子鑒定,檢測氣溶素( aerolysin, aer)、溶血素( haemoly-sin, hly)、絲氨痠蛋白酶( serine protease, ahp)、熱穩定細胞腸毒素( heat-stable cytotonic enterotoxin, ast)和熱敏感細胞腸毒素( heat-labile cytotonic enterotoxin, alt)5種毒力基因,且使用Mega 5.2對覈苷痠和氨基痠序列進行分析。結果顯示6株菌均為嗜水氣單胞菌Aero-monas hydrophila,檢測齣5種毒力基因中的至少4種,其中均檢測齣溶血素和2種腸毒素,序列分析錶明氣溶素、溶血素和絲氨痠蛋白酶的氨基痠序列高度保守。本研究基于16 S rD-NA和gyrB基因可以準確地對嗜水氣單胞菌進行分子鑒定,6株菌的毒力基因豐富預示著一定的緻病性, aer、 hly和ahp基因相對保守,編碼的毒力因子高度同源,在臨床分子診斷中建議使用aer、 ahp和hly基因對嗜水氣單胞菌的潛在緻病性進行檢測。
위료분자감정6주어원기수기단포균,병종분자층면험증통과검측독력기인이추측기수기단포균잠재치병성적가행성。실험채용PCR확증16 S rDNA화gyrB기인병결합계통발육수적구건화분석진행균충적분자감정,검측기용소( aerolysin, aer)、용혈소( haemoly-sin, hly)、사안산단백매( serine protease, ahp)、열은정세포장독소( heat-stable cytotonic enterotoxin, ast)화열민감세포장독소( heat-labile cytotonic enterotoxin, alt)5충독력기인,차사용Mega 5.2대핵감산화안기산서렬진행분석。결과현시6주균균위기수기단포균Aero-monas hydrophila,검측출5충독력기인중적지소4충,기중균검측출용혈소화2충장독소,서렬분석표명기용소、용혈소화사안산단백매적안기산서렬고도보수。본연구기우16 S rD-NA화gyrB기인가이준학지대기수기단포균진행분자감정,6주균적독력기인봉부예시착일정적치병성, aer、 hly화ahp기인상대보수,편마적독력인자고도동원,재림상분자진단중건의사용aer、 ahp화hly기인대기수기단포균적잠재치병성진행검측。
Six strains of Aeromonas hydrophila isolated from dying fish were molecularly characterized as well as five virulence genes were detected and analyzed in order to evaluate the feasibility of detecting the virulence genes to infer the potential pathogenicity of A. hydrophila at the molecular lever. 16S rDNA and gyrB gene were used to characterize A. hydrophila,five virulence genes including aerolysin( aer) ,haemolysin( hly) ,serine protease(ahp),heat-stable cytotonic enterotoxin(ast) and heat-labile cytotonic enterotoxin(alt) were de-tected by PCR,and the sequences of gene and virulence were analyzed using Mega 5. 2. All of the strains were characterized as A. hydrophila,and four of five virulence genes at least were detected as positive,including the genes of haemolysin and two kinds of cytotonic enterotoxin. By the sequences analysis, we found the amino acid sequences of high similarity among aerolysin,haemolysin and serine protease. A. hydrophila could be well characterized using 16S rDNA and gyrB gene sequences,and the varied virulence genes indicated the potential pathogenicity. Through the sequences analysis,the genes of aer,hly and ahp were relatively conservative,and the encoding virulences were highly conserved. Detecting the virulence genes of aer,hly and ahp could infer the potential pathogenicity of A. hydrophila in the clinical molecular diagnosis.