Ses. Because our antibodies recognize an epitope that are distinct from other flu subtypes, they could be combined with these novel detection technologies to 86168-78-7 chemical information develop rapid, specific and sensitive diagnostic methods for HPAI H5N1. All HPAI H5N1 viruses 22948146 in the A/goose/Guangdong/1/96 (H5N1) lineage have multiple basic residues at the HA CS [27], and almost all HPAI H5N1 viruses are characterized by the CS structure. Thus, diagnosis via the CS provides important information about viral pathogenicity. Although CS-specific detection of H5N1 virus by PCR-based method has been reported [28] and sequence analysis of the CS with reverse transcriptionPCR is MedChemExpress SR-3029 essential for the molecular pathotyping of H5 get CAL-120 subtype viruses [29], this is the first immunological CS detection that is potentially applicable to many popular antibody-based diagnostic platforms. Namely, these Fab fragments can be applied to rapid pathotyping assays such as ELISA and immunochromatography. Although almost all the H5 subtype viruses containing a multibasic sequence are highly pathogenic, there are a few exceptions [30]. For example, the A/goose/Guangdong/2/96 strain was coisolated with A/goose/Guangdong/1/96 from geese in 1996. While both strains have multibasic sequences, A/goose/Guangdong/2/96 cannot replicate in chickens [31]. Nevertheless, the recombinant Fab fragments we report will be useful novel reagents for the rapid and specific detection of emerging highly pathogenic viruses.Materials and Methods MaterialsThe E. coli XL10-Gold strain for phagemid cloning and amplification was obtained from Agilent (La Jolla, CA, USA). TG-1 and HB2151 bacteria were obtained from GE purchase AZ-876 Healthcare (Tokyo, Japan) and used for phage production and Fab expression, respectively. Recombinant HA proteins derived from influenza A virus H1N1 (A/California/04/09), H5N1 (A/Vietnam/1194/04, A/Anhui/1/05, and A/Turkey/1/05) and H7N7 (A/Netherlands/219/03), and HA-Fc fusion protein (A/Vietnam/1194/ 2004(H5N1), in which the cleavage site RERRRKKR was mutated to TETR) were purchased from Sino Biological Inc.Antibodies for HPAI H5N1 Viruses(Beijing, China), as well as a mouse monoclonal 
antibody against H5N1. Synthetic 7-mer peptides used for epitope scanning were from Peptide 2.0 Inc. (Chantilly, VA). Restriction and modification enzymes were obtained from Takara-Bio (Shiga, Japan), Toyobo 1662274 (Osaka, Japan), Roche Diagnostics (Tokyo, Japan), or New England Biolabs (Ipswich, MA). Oligonucleotides were synthesized by Fasmac Co. (Kanagawa, Japan) or Invitrogen (Tokyo, Japan). Other chemicals, reagents and antibodies, unless otherwise indicated, were obtained from Sigma (St. Louis, MO) or Wako Pure Chemicals (Osaka, Japan).Fab antibody phage displayE. coli TG-1 cells transformed with the phagemid were cultivated in 4 ml of 2YTAG overnight at 37uC. Ten milliliters of 2YTAG was inoculated with 100 ml of the overnight culture and incubated at 37uC with shaking at 200 rpm until the OD600 reached ,0.5, when the helper phage KM13 [32] was added with a multiplicity of infection (MOI) of 20. After incubation at 37uC for 30 min without shaking, the culture was centrifuged at 3,7006 g for 15 min. The E. coli pellet was resuspended in 50 ml of 2YTAK (2YT medium containing 100 mg/ml ampicillin and 50 mg/ml kanamycin) and incubated overnight with shaking at 30uC. The overnight culture was centrifuged at 10,8006 g for 30 min. Ten milliliters of PEG/NaCl (20 polyethylene glycol 6000, 2.5 M NaCl) was added to 40 ml of supernat.Ses. Because our antibodies recognize an epitope that are distinct from other flu subtypes, they could be combined with these novel detection technologies to develop rapid, specific and sensitive diagnostic methods for HPAI H5N1. All HPAI H5N1 viruses 22948146 in the A/goose/Guangdong/1/96 (H5N1) lineage have multiple basic residues at the HA CS [27], and almost all HPAI H5N1 viruses are characterized by the CS structure. Thus, diagnosis via the CS provides important information about viral pathogenicity. Although CS-specific detection of H5N1 virus by PCR-based method has been reported [28] and sequence analysis of the CS with reverse transcriptionPCR is essential for the molecular pathotyping of H5 subtype viruses [29], this is the first immunological CS detection that is potentially applicable to many popular antibody-based diagnostic platforms. Namely, these Fab fragments can be applied to rapid pathotyping assays such 
as ELISA and immunochromatography. Although almost all the H5 subtype viruses containing a multibasic sequence are highly pathogenic, there are a few exceptions [30]. For example, the A/goose/Guangdong/2/96 strain was coisolated with A/goose/Guangdong/1/96 from geese in 1996. While both strains have multibasic sequences, A/goose/Guangdong/2/96 cannot replicate in chickens [31]. Nevertheless, the recombinant Fab fragments we report will be useful novel reagents for the rapid and specific detection of emerging highly pathogenic viruses.Materials and Methods MaterialsThe E. coli XL10-Gold strain for phagemid cloning and amplification was obtained from Agilent (La Jolla, CA, USA). TG-1 and HB2151 bacteria were obtained from GE Healthcare (Tokyo, Japan) and used for phage production and Fab expression, respectively. Recombinant HA proteins derived from influenza A virus H1N1 (A/California/04/09), H5N1 (A/Vietnam/1194/04, A/Anhui/1/05, and A/Turkey/1/05) and H7N7 (A/Netherlands/219/03), and HA-Fc fusion protein (A/Vietnam/1194/ 2004(H5N1), in which the cleavage site RERRRKKR was mutated to TETR) were purchased from Sino Biological Inc.Antibodies for HPAI H5N1 Viruses(Beijing, China), as well as a mouse monoclonal antibody against H5N1. Synthetic 7-mer peptides used for epitope scanning were from Peptide 2.0 Inc. (Chantilly, VA). Restriction and modification enzymes were obtained from Takara-Bio (Shiga, Japan), Toyobo 1662274 (Osaka, Japan), Roche Diagnostics (Tokyo, Japan), or New England Biolabs (Ipswich, MA). Oligonucleotides were synthesized by Fasmac Co. (Kanagawa, Japan) or Invitrogen (Tokyo, Japan). Other chemicals, reagents and antibodies, unless otherwise indicated, were obtained from Sigma (St. Louis, MO) or Wako Pure Chemicals (Osaka, Japan).Fab antibody phage displayE. coli TG-1 cells transformed with the phagemid were cultivated in 4 ml of 2YTAG overnight at 37uC. Ten milliliters of 2YTAG was inoculated with 100 ml of the overnight culture and incubated at 37uC with shaking at 200 rpm until the OD600 reached ,0.5, when the helper phage KM13 [32] was added with a multiplicity of infection (MOI) of 20. After incubation at 37uC for 30 min without shaking, the culture was centrifuged at 3,7006 g for 15 min. The E. coli pellet was resuspended in 50 ml of 2YTAK (2YT medium containing 100 mg/ml ampicillin and 50 mg/ml kanamycin) and incubated overnight with shaking at 30uC. The overnight culture was 
centrifuged at 10,8006 g for 30 min. Ten milliliters of PEG/NaCl (20 polyethylene glycol 6000, 2.5 M NaCl) was added to 40 ml of supernat.Ses. Because our antibodies recognize an epitope that are distinct from other flu subtypes, they could be combined with these novel detection technologies to develop rapid, specific and sensitive diagnostic methods for HPAI H5N1. All HPAI H5N1 viruses 22948146 in the A/goose/Guangdong/1/96 (H5N1) lineage have multiple basic residues at the HA CS [27], and almost all HPAI H5N1 viruses are characterized by the CS structure. Thus, diagnosis via the CS provides important information about viral pathogenicity. Although CS-specific detection of H5N1 virus by PCR-based method has been reported [28] and sequence analysis of the CS with reverse transcriptionPCR is essential for the molecular pathotyping of H5 subtype viruses [29], this is the first immunological CS detection that is potentially applicable to many popular antibody-based diagnostic platforms. Namely, these Fab fragments can be applied to rapid pathotyping assays such as ELISA and immunochromatography. Although almost all the H5 subtype viruses containing a multibasic sequence are highly pathogenic, there are a few exceptions [30]. For example, the A/goose/Guangdong/2/96 strain was coisolated with A/goose/Guangdong/1/96 from geese in 1996. While both strains have multibasic sequences, A/goose/Guangdong/2/96 cannot replicate in chickens [31]. Nevertheless, the recombinant Fab fragments we report will be useful novel reagents for the rapid and specific detection of emerging highly pathogenic viruses.Materials and Methods MaterialsThe E. coli XL10-Gold strain for phagemid cloning and amplification was obtained from Agilent (La Jolla, CA, USA). TG-1 and HB2151 bacteria were obtained from GE Healthcare (Tokyo, Japan) and used for phage production and Fab expression, respectively. Recombinant HA proteins derived from influenza A virus H1N1 (A/California/04/09), H5N1 (A/Vietnam/1194/04, A/Anhui/1/05, and A/Turkey/1/05) and H7N7 (A/Netherlands/219/03), and HA-Fc fusion protein (A/Vietnam/1194/ 2004(H5N1), in which the cleavage site RERRRKKR was mutated to TETR) were purchased from Sino Biological Inc.Antibodies for HPAI H5N1 Viruses(Beijing, China), as well as a mouse monoclonal antibody against H5N1. Synthetic 7-mer peptides used for epitope scanning were from Peptide 2.0 Inc. (Chantilly, VA). Restriction and modification enzymes were obtained from Takara-Bio (Shiga, Japan), Toyobo 1662274 (Osaka, Japan), Roche Diagnostics (Tokyo, Japan), or New England Biolabs (Ipswich, MA). Oligonucleotides were synthesized by Fasmac Co. (Kanagawa, Japan) or Invitrogen (Tokyo, Japan). Other chemicals, reagents and antibodies, unless otherwise indicated, were obtained from Sigma (St. Louis, MO) or Wako Pure Chemicals (Osaka, Japan).Fab antibody phage displayE. coli TG-1 cells transformed with the phagemid were cultivated in 4 ml of 2YTAG overnight at 37uC. Ten milliliters of 2YTAG was inoculated with 100 ml of the overnight culture and incubated at 37uC with shaking at 200 rpm until the OD600 reached ,0.5, when the helper phage KM13 [32] was added with a multiplicity of infection (MOI) of 20. After incubation at 37uC for 30 min without shaking, the culture was centrifuged at 3,7006 g for 15 min. The E. coli pellet was resuspended in 50 ml of 2YTAK (2YT medium containing 100 mg/ml ampicillin and 50 mg/ml kanamycin) and incubated overnight with shaking at 30uC. The overnight culture was centrifuged at 10,8006 g for 30 min. Ten milliliters of PEG/NaCl (20 polyethylene glycol 6000, 2.5 M NaCl) was added to 40 ml of supernat.Ses. Because our antibodies recognize an epitope that are distinct from other flu subtypes, they could be combined with these novel detection technologies to develop rapid, specific and sensitive diagnostic methods for HPAI H5N1. All HPAI H5N1 viruses 22948146 in the A/goose/Guangdong/1/96 (H5N1) lineage have multiple basic residues at the HA CS [27], and almost all HPAI H5N1 viruses are characterized by the CS structure. Thus, diagnosis via the CS provides important information about viral pathogenicity. Although CS-specific detection of H5N1 virus by PCR-based method has been reported [28] and sequence analysis of the CS with 
reverse transcriptionPCR is essential for the molecular pathotyping of H5 subtype viruses [29], this is the first immunological CS detection that is potentially applicable to many popular antibody-based diagnostic platforms. Namely, these Fab fragments can be applied to rapid pathotyping assays such as ELISA and immunochromatography. Although almost all the H5 subtype viruses containing a multibasic sequence are highly pathogenic, there are a few exceptions [30]. For example, the A/goose/Guangdong/2/96 strain was coisolated with A/goose/Guangdong/1/96 from geese in 1996. While both strains have multibasic sequences, A/goose/Guangdong/2/96 cannot replicate in chickens [31]. Nevertheless, the recombinant Fab fragments we report will be useful novel reagents for the rapid and specific detection of emerging highly pathogenic viruses.Materials and Methods MaterialsThe E. coli XL10-Gold strain for phagemid cloning and amplification was obtained from Agilent (La Jolla, CA, USA). TG-1 and HB2151 bacteria were obtained from GE Healthcare (Tokyo, Japan) and used for phage production and Fab expression, respectively. Recombinant HA proteins derived from influenza A virus H1N1 (A/California/04/09), H5N1 (A/Vietnam/1194/04, A/Anhui/1/05, and A/Turkey/1/05) and H7N7 (A/Netherlands/219/03), and HA-Fc fusion protein (A/Vietnam/1194/ 2004(H5N1), in which the cleavage site RERRRKKR was mutated to TETR) were purchased from Sino Biological Inc.Antibodies for HPAI H5N1 Viruses(Beijing, China), as well as a mouse monoclonal antibody against H5N1. Synthetic 7-mer peptides used for epitope scanning were from Peptide 2.0 Inc. (Chantilly, VA). Restriction and modification enzymes were obtained from Takara-Bio (Shiga, Japan), Toyobo 1662274 (Osaka, Japan), Roche Diagnostics (Tokyo, Japan), or New England Biolabs (Ipswich, MA). Oligonucleotides were synthesized by Fasmac Co. (Kanagawa, Japan) or Invitrogen (Tokyo, Japan). Other chemicals, reagents and antibodies, unless otherwise indicated, were obtained from Sigma (St. Louis, MO) or Wako Pure Chemicals (Osaka, Japan).Fab antibody phage displayE. coli TG-1 cells transformed with the phagemid were cultivated in 4 ml of 2YTAG overnight at 37uC. Ten milliliters of 2YTAG was inoculated with 100 ml of the overnight culture and incubated at 37uC with shaking at 200 rpm until the OD600 reached ,0.5, when the helper phage KM13 [32] was added with a multiplicity of infection (MOI) of 20. After incubation at 37uC for 30 min without shaking, the culture was centrifuged at 3,7006 g for 15 min. The E. coli pellet was resuspended in 50 ml of 2YTAK (2YT medium containing 100 mg/ml ampicillin and 50 mg/ml kanamycin) and incubated overnight with shaking at 30uC. The overnight culture was centrifuged at 10,8006 g for 30 min. Ten milliliters of PEG/NaCl (20 polyethylene glycol 6000, 2.5 M NaCl) was added to 40 ml of supernat.