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Molecular cloning and expression profile of putative antilipopolysaccharide factor in Chinese shrimp (Fenneropenaeus chinensis)
Liu, F.; Liu, Y.; Li, F.; Dong, B.; Xiang, J. (2005). Molecular cloning and expression profile of putative antilipopolysaccharide factor in Chinese shrimp (Fenneropenaeus chinensis). Mar. Biotechnol. 7(6): 600-608. http://dx.doi.org/10.1007/s10126-005-5006-4
In: Marine Biotechnology. Springer-Verlag: New York. ISSN 1436-2228; e-ISSN 1436-2236, more
Peer reviewed article  

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Keywords
    Carbohydrates > Polysaccharides > Lipids > Antigens > Lipopolysaccharides
    Cloning
    Fenneropenaeus chinensis (Osbeck, 1765) [WoRMS]
    Marine/Coastal
Author keywords
    Fenneropenaeus chinensis; anti-lipopolysaccharide factor; antimicrobialpeptide; lipopolysaccharide cloning; expression

Authors  Top 
  • Liu, F.
  • Liu, Y.
  • Li, F.
  • Dong, B.
  • Xiang, J.

Abstract
    A new antimicrobial protein gene of the anti-lipopolysaccharide factor family (tentatively named as ALFFc) has been cloned from hemocytes of the Chinese shrimp Fenneropenaeus chinensis by rapid amplification of 3′ and 5′ complementary DNA ends with polymerase chain reaction. The full-length complementary DNA of ALFFc consists of 600 bp with a 369-bp open reading frame, encoding 123 amino acids. The deduced peptide contains a putative signal peptide of 25 amino acids and mature peptide of 98 amino acids. The molecular mass of the deduced mature peptide is 13799.16 Da. It is highly cationic, with a theoretical pI of 10.3. The deduced amino acid sequence of ALFFc showed 56% homology with sequences of Tachypleus tridentatus and L. polyhemus. The tissue expression profile of this gene was studied by Northern blot, and ALFFc transcripts were mainly detected in hemocytes, gill, and intestine. RNA in situ hybridization showed that ALFFc was constitutively expressed in hemocytes. Capillary electrophoresis reverse transcriptase PCR was used to quantify the variation of messenger RNA transcription level during the artificial infection process with Vibrio anguillarum. Significant enhancement of ALFFc transcription appeared during the first 24 hours in response to Vibrio infection. These results provide useful information for understanding the function of ALFFc in shrimp.

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