Cloning, expression and sequence diversity of iss gene from avian pathogenic Escherichia coli (APEC) isolated in Brazil

被引:0
作者
Sampaio Baptista, Ana Angelita [4 ]
Takayama Kobayashi, Renata Katsuko [3 ]
Venancio, Emerson Jose [2 ]
Vidotto, Marilda Carlos [1 ]
机构
[1] Univ Estadual Londrina, Ctr Ciencias Agr, Depto Med Vet Prevent, BR-86055900 Londrina, PR, Brazil
[2] Univ Estadual Londrina, Ctr Ciencias Biol, Depto Ciencias Patol, BR-86055900 Londrina, PR, Brazil
[3] Univ Estadual Londrina, Ctr Ciencias Biol, Depto Microbiol, BR-86055900 Londrina, PR, Brazil
[4] Univ Estadual Londrina, Ctr Ciencias Agr, Programa Posgrad Ciencia Anim, BR-86055900 Londrina, PR, Brazil
来源
SEMINA-CIENCIAS AGRARIAS | 2010年 / 31卷 / 03期
关键词
Avian pathogenic E. coli (APEC); gene iss; cloning; RIss; serum resistance; SERUM RESISTANCE; VIRULENCE FACTORS; PLASMID; COLIBACILLOSIS; PROTEIN; POULTRY; TRAITS; STRAIN; HENS; TRAT;
D O I
10.5433/1679-0359.2010v31n3p723
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The Iss (Increased serum survival) protein is an important characteristic of resistance to complement system of avian pathogenic Escherichia coli (APEC). The objectives of this work were to cloning and verify the sequence diversity of iss gene from APEC and characterize the recombinant Iss protein. The iss gene of 309 bp was amplified by PCR, cloned and expressed in E. coli BL21 (DE3) using the pET SUMO vector. The iss gene from APEC9 strain was classified as iss type 1 by differentiation of the three iss gene allele types. The protein was expressed by induction of IPTG and purified in resin charged with the nickel ion. Antibodies IgY anti rIss reacted with rIss showing a molecular mass of 22 kDa, corresponding 11KDa of Iss protein and 11 KDa SUMO protein.
引用
收藏
页码:723 / 731
页数:9
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