TY - JOUR
T1 - Proteomic profiling of integral membrane proteins associated to pathogenicity in Vibrio parahaemolyticus strains
AU - Pérez-Acosta, Jesús A.
AU - Martínez-Porchas, Marcel
AU - Elizalde-Contreras, José M.
AU - Leyva, Juan Manuel
AU - Ruiz-May, Eliel
AU - Gollas-Galván, Teresa
AU - Martínez-Córdova, Luis R.
AU - Huerta-Ocampo, José Ángel
N1 - Publisher Copyright:
© 2017 The Societies and John Wiley & Sons Australia, Ltd
PY - 2018/1
Y1 - 2018/1
N2 - Vibrio parahaemolyticus has been recognized as the causal agent of early mortality syndrome and is currently considered an emerging shrimp disease causing losses of millions in the aquaculture industry. Integral membrane proteins are widely recognized as pathogenicity factors involved in essential mechanisms for V. parahaemolyticus infection, which makes them attractive as therapeutic targets. However, their physico-chemical properties and weak expression has resulted in under-representation of these proteins in conventional bottom-up proteomics, making integral membrane proteomics a challenging task. Integral membrane proteins from a bacterial strain isolated from the hepatopancreases of white shrimp with early mortality syndrome and identified by 16S rRNA sequencing as V. parahaemolyticus and an ATCC strain that is pathogenic for humans were obtained by a sequential extraction method and subjected to relative quantification and identification by isobaric Tags for Relative and Absolute Quantitation. A homology database search resulted in identification of more than two hundred proteins, 35 of which are recognized as pathogenic factors showed statistically significant differential accumulation between the strains. These proteins are mainly associated with adherence, secretion systems, cell division, transport, lysogenization, movement and virulence. Identification of pathogenicity-related proteins in V. parahaemolyticus provides valuable information for developing strategies based on molecular mechanisms that inhibit these proteins, which may be useful therapeutic targets for assisting the shrimp and aquaculture industry.
AB - Vibrio parahaemolyticus has been recognized as the causal agent of early mortality syndrome and is currently considered an emerging shrimp disease causing losses of millions in the aquaculture industry. Integral membrane proteins are widely recognized as pathogenicity factors involved in essential mechanisms for V. parahaemolyticus infection, which makes them attractive as therapeutic targets. However, their physico-chemical properties and weak expression has resulted in under-representation of these proteins in conventional bottom-up proteomics, making integral membrane proteomics a challenging task. Integral membrane proteins from a bacterial strain isolated from the hepatopancreases of white shrimp with early mortality syndrome and identified by 16S rRNA sequencing as V. parahaemolyticus and an ATCC strain that is pathogenic for humans were obtained by a sequential extraction method and subjected to relative quantification and identification by isobaric Tags for Relative and Absolute Quantitation. A homology database search resulted in identification of more than two hundred proteins, 35 of which are recognized as pathogenic factors showed statistically significant differential accumulation between the strains. These proteins are mainly associated with adherence, secretion systems, cell division, transport, lysogenization, movement and virulence. Identification of pathogenicity-related proteins in V. parahaemolyticus provides valuable information for developing strategies based on molecular mechanisms that inhibit these proteins, which may be useful therapeutic targets for assisting the shrimp and aquaculture industry.
KW - epizootic disease
KW - mass spectrometry
KW - shrimp pathogen
KW - virulence factor
UR - http://www.scopus.com/inward/record.url?scp=85039703973&partnerID=8YFLogxK
U2 - 10.1111/1348-0421.12556
DO - 10.1111/1348-0421.12556
M3 - Artículo
C2 - 29171072
SN - 0385-5600
VL - 62
SP - 14
EP - 23
JO - Microbiology and Immunology
JF - Microbiology and Immunology
IS - 1
ER -