Classification of circulating hemocytes from the red swamp crayfish Procambarus clarkii and their susceptibility to the novel pathogen Spiroplasma eriocheiris in vitro

Aquaculture

Volumn 356-357, Issue , 2012, Pages 371-380

  Ding, Zhengfeng ^a,b   Du, Jie ^a   Ou, Jiangtao ^a   Li, Wenjie ^a   Wu, Ting ^a   Xiu, Yunji ^a   Meng, Qingguo ^a   Ren, Qian ^a   Gu, Wei ^a   Xue, Hui ^b   Tang, Jianqing ^b   Wang, Wen ^a  

^a NANJING NORMAL UNIVERSITY   (China)

^b FRESHWATER FISHERIES RESEARCH INSTITUTE OF JIANGSU PROVINCE   (China)

Author keywords

Cell culture; Hemocyte; Immune related gene; Procambarus clarkii; Real time PCR; Spiroplasma eriocheiris

Indexed keywords

CELL ORGANELLE; CRAB; CRAYFISH; FLOW CYTOMETRY; GENE EXPRESSION; HOST-PATHOGEN INTERACTION; IMMUNE SYSTEM; INOCULATION; MORPHOLOGY; POLYMERASE CHAIN REACTION; QUANTITATIVE ANALYSIS; SERUM;

ASTACOIDEA; BOVINAE; CRUSTACEA; HEXAPODA; PROCAMBARUS CLARKII; SPIROPLASMA;

EID: 84863332086     PISSN: 00448486     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.aquaculture.2012.04.042     Document Type: Article

References (60)

1. Bachere E., Gueguen Y., Gonzalez M., De Lorgeril J., Garnier J., Romestand B. Insights into the anti-microbial defense of marine invertebrates: the penaeid shrimps and the oyster Crassostrea gigas. Immunological Reviews 2004, 198:149-168.
2. Battison A., Cawthorn R., Horney B. Classification of Homarus americanus hemocytes and the use of differential hemocyte counts in lobsters infected with Aerococcus viridans var. homari (Gaffkemia). Journal of Invertebrate Pathology 2003, 84:177-197.
3. Beetz S., Brinkmann M., Trenczek T. Differences between larval and pupal hemocytes of the tobacco hornworm, Manduca sexta, determined by monoclonal antibodies and density centrifugation. Journal of Insect Physiology 2004, 50:805-819.
4. Cárdenas W., Dankert J.R., Jenkins J.A. Flow cytometric analysis of crayfish haemocytes activated by lipopolysaccharides. Fish & Shellfish Immunology 2004, 17:223-233.
5. Chen S., Wang C. Establishment of cell culture systems from penaeid shrimp and their susceptibility to white spot disease and yellow head viruses. Methods in Cell Science 1999, 21:199-206.
6. Cheng W., Chen J.C. Effects of intrinsic and extrinsic factors on the haemocyte profile of the prawn, Macrobrachium rosenbergii. Fish & Shellfish Immunology 2001, 11:53-63.
7. Ding Z., Bi K., Wu T., Gu W., Wang W., Chen J. A simple PCR method for the detection of pathogenic spiroplasmas in crustaceans and environmental samples. Aquaculture 2007, 265:49-54.
8. Du J., Ou J., Li W., Ding Z., Wu T., Meng Q., Gu W., Wang W. Primary hemocyte culture of the freshwater prawn Macrobrachium rosenbergii and its susceptibility to the novel pathogen spiroplasma strain MR-1008. Aquaculture 2012, 330-333:21-28.
9. Ellender R., Najafabadi A., Middlebrooks B. Observations on the primary culture of hemocytes of Penaeus. Journal of Crustacean Biology 1992, 178-185.
10. Fan T.J., Wang X.F. In vitro culture of embryonic cells from the shrimp, Penaeus chinensis. Journal of Experimental Marine Biology and Ecology 2002, 267:175-184.
11. Frerichs G. In vitro culture of embryonic cells from the freshwater prawn Macrobrachium rosenbergii. Aquaculture 1996, 143:227-232.
12. Gargioni R., Barracco M.A. Hemocytes of the palaemonids Macrobrachium rosenbergii and M. acanthurus, and of the penaeid Penaeus paulensis. Journal of Morphology 1998, 236:209-221.
13. Georgopoulos C., Welch W. Role of the major heat shock proteins as molecular chaperones. Annual Review of Cell Biology 1993, 9:601-634.
14. Ghosh D., Dasmahapatra A.K., Ray A.K. Primary culture of prawn hepatocytes in serum free media. In Vitro Cellular & Developmental Biology. Animal 1995, 31:811-813.
15. Giulianini P.G., Bertolo F., Battistella S., Amirante G. Ultrastructure of the hemocytes of Cetonischema aeruginosa larvae (Coleoptera, Scarabaeidae): involvement of both granulocytes and oenocytoids in in vivo phagocytosis. Tissue & Cell 2003, 35:243-251.
16. Giulianini P.G., Bierti M., Lorenzon S., Battistella S., Ferrero E.A. Ultrastructural and functional characterization of circulating hemocytes from the freshwater crayfish Astacus leptodactylus: cell types and their role after in vivo artificial non-self challenge. Micron 2007, 38:49-57.
17. Holmblad T., Söderhäll K. Cell adhesion molecules and antioxidative enzymes in a crustacean, possible role in immunity. Aquaculture 1999, 172:111-123.
18. Hsu P.I., Liu C.H., Tseng D.Y., Lee P.P., Cheng W. Molecular cloning and characterisation of peroxinectin, a cell adhesion molecule, from the giant freshwater prawn Macrobrachium rosenbergii. Fish & Shellfish Immunology 2006, 21:1-10.
19. Itami T., Maeda M., Kondo M., Takahashi Y. Primary culture of lymphoid organ cells and haemocytes of kuruma shrimp, Penaeus japonicus. Methods in Cell Science 1999, 21:237-244.
20. Jiang Y.S., Zhan W.B., Wang S.B., Xing J. Development of primary shrimp hemocyte cultures of Penaeus chinensis to study white spot syndrome virus (WSSV) infection. Aquaculture 2006, 253:114-119.
21. Jiravanichpaisal P., Sricharoen S., Söderhäll I., Söderhäll K. White spot syndrome virus (WSSV) interaction with crayfish haemocytes. Fish & Shellfish Immunology 2006, 20:718-727.
22. Johansson M.W. Cell adhesion molecules in invertebrate immunity. Developmental and Comparative Immunology 1999, 23:303-315.
23. Johansson M.W., Söderhäll K. A cell adhesion factor from crayfish haemocytes has degranulating activity towards crayfish granular cells. Insect Biochemistry 1989, 19:183-190.
24. Johansson M.W., Lind M.I., Holmblad T., Thornqvist P.O., Soderhall K. Peroxinectin, a novel cell adhesion protein from crayfish blood. Biochemical and Biophysical Research Communications 1995, 216:1079-1087.
25. Jose S., Mohandas A., Philip R., Bright Singh I. Primary hemocyte culture of Penaeus monodon as an in vitro model for white spot syndrome virus titration, viral and immune related gene expression and cytotoxicity assays. Journal of Invertebrate Pathology 2010, 105:312-321.
26. Kobayashi M., Johansson M.W., Söderhäll K. The 76kD cell-adhesion factor from crayfish haemocytes promotes encapsulation in vitro. Cell and Tissue Research 1990, 260:13-18.
27. Laake J.H., Haug F.-M., Wieloch T., Ottersen O.P. A simple in vitro model of ischemia based on hippocampal slice cultures and propidium iodide fluorescence. Brain Research Protocols 1999, 4:173-184.
28. Lang G.H., Nomura N., Wang B.Z., Matsumura M. Penaeid (Penaeus japonicus) lymphoid cells replicate by cell division in vitro. In Vitro Cellular & Developmental Biology. Animal 2002, 38:142-145.
29. Le Moullac G., Le Groumellec M., Ansquer D., Froissard S., Levy P. Haematological and phenoloxidase activity changes in the shrimp Penaeus stylirostrisin relation with the moult cycle: protection against vibriosis. Fish & Shellfish Immunology 1997, 7:227-234.
30. Leignel V., Cibois M., Moreau B., Chénais B. Identification of new subgroup of HSP70 in Bythograeidae (hydrothermal crabs) and Xanthidae. Gene 2007, 396:84-92.
31. Li C., Shields J.D. Primary culture of hemocytes from the Caribbean spiny lobster, Panulirus argus, and their susceptibility to Panulirus argus Virus 1 (PaV1). Journal of Invertebrate Pathology 2007, 94:48-55.
32. Liang T., Li X., Du J., Yao W., Sun G., Dong X., Liu Z., Ou J., Meng Q., Gu W., Wang W. Identification and isolation of a spiroplasma pathogen from diseased freshwater prawns, Macrobrachium rosenbergii, in China: a new freshwater crustacean host. Aquaculture 2011, 318:1-6.
33. Lin X., Söderhäll I. Crustacean hematopoiesis and the astakine cytokines. Blood 2011, 117:6417.
34. Liu C.H., Cheng W., Chen J.C. The peroxinectin of white shrimp Litopenaeus vannamei is synthesised in the semi-granular and granular cells, and its transcription is up-regulated with Vibrio alginolyticus infection. Fish & Shellfish Immunology 2005, 18:431-444.
35. Livak K.J., Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2-[Delta][Delta] CT method. Methods 2001, 25:402-408.
36. Maeda M., Mizuki E., Itami T., Ohba M. Ovarian primary tissue culture of the kuruma shrimp Marsupenaeus japonicus. In Vitro Cellular & Developmental Biology. Animal 2003, 39:208-212.
37. Matozzo V., Marin M.G. The role of haemocytes from the crab Carcinus aestuarii (Crustacea, Decapoda) in immune responses: a first survey. Fish & Shellfish Immunology 2010, 28:534-541.
38. Moseley P.L. Heat shock proteins and heat adaptation of the whole organism. Journal of Applied Physiology 1997, 83:1413-1417.
39. Nunan L.M., Lightner D.V., Oduori M.A., Gasparich G.E. Spiroplasma penaei sp. nov., associated with mortalities in Penaeus vannamei, Pacific white shrimp. International Journal of Systematic and Evolutionary Microbiology 2005, 55:2317-2322.
40. Persson M., Vey A., Söderhäll K. Encapsulation of foreign particles in vitro by separated blood cells from crayfish, Astacus leptodactylus. Cell and Tissue Research 1987, 247:409-415.
41. Ranford J., Henderson B. Chaperonins in disease: mechanisms, models, and treatments. Molecular Pathology 2002, 55:209-213.
42. Ravaux J., Toullec J.-Y., Léger N., Lopez P., Gaill F., Shillito B. First hsp70 from two hydrothermal vent shrimps, Mirocaris fortunata and Rimicaris exoculata: characterization and sequence analysis. Gene 2007, 386:162-172.
43. Roulston C., Smith V.J. Isolation and in vitro characterisation of prohaemocytes from the spider crab; Hyas araneus (L.). Developmental and Comparative Immunology 2010, 35:537-544.
44. Shimizu C., Shike H., Klimpel K.R., Burns J.C. Hemolymph analysis and evaluation of newly formulated media for culture of shrimp cells (Penaeus stylirostris). In Vitro Cellular & Developmental Biology. Animal 2001, 37:322-329.
45. Soderhall K., Smith V.J. Separation of the haemocyte populations of and other marine decapods, and prophenoloxidase distribution. Developmental and Comparative Immunology 1983, 7:229-239.
46. Söderhäll K., Smith V.J., Johansson M.W. Exocytosis and uptake of bacteria by isolated haemocyte populations of two crustaceans: evidence for cellular co-operation in the defence reactions of arthropods. Cell and Tissue Research 1986, 245:43-49.
47. Song L., Wu L., Ni D., Chang Y., Xu W., Xing K. The cDNA cloning and mRNA expression of heat shock protein 70 gene in the haemocytes of bay scallop (Argopecten irradians, Lamarck 1819) responding to bacteria challenge and naphthalin stress. Fish & Shellfish Immunology 2006, 21:335-345.
48. Sperstad S.V., Smith V.J., Stensvåg K. Expression of antimicrobial peptides from Hyas araneus haemocytes following bacterial challenge in vitro. Developmental and Comparative Immunology 2010, 34:618-624.
49. Sritunyalucksana K., Wongsuebsantati K., Johansson M., Söderhäll K. Peroxinectin, a cell adhesive protein associated with the proPO system from the black tiger shrimp, Penaeus monodon. Developmental and Comparative Immunology 2001, 25:353-363.
50. Thornqvist P.O., Johansson M.W., Soderhall K. Opsonic activity of cell adhesion proteins and [beta]-1,3-glucan binding proteins from two crustaceans. Developmental and Comparative Immunology 1994, 18:3-12.
51. Tsan M.F., Gao B. Heat shock protein and innate immunity. Cellular & Molecular Immunology 2004, 1:274-279.
52. Wang W., Gu W., Ding Z., Ren Y., Chen J., Hou Y. A novel Spiroplasma pathogen causing systemic infection in the crayfish Procambarus clarkii (Crustacea: Decapod), in China. FEMS Microbiology Letters 2005, 249:131-137.
53. Wang Z., Wu Z., Jian J., Lu Y. Cloning and expression of heat shock protein 70 gene in the haemocytes of pearl oyster (Pinctada fucata, Gould 1850) responding to bacterial challenge. Fish & Shellfish Immunology 2009, 26:639-645.
54. Wang W., Gu W., Gasparich G.E., Bi K., Ou J., Meng Q., Liang T., Feng Q., Zhang J., Zhang Y. Spiroplasma eriocheiris sp. nov., associated with mortality in the Chinese mitten crab, Eriocheir sinensis. International Journal of Systematic and Evolutionary Microbiology 2011, 61:703-708.
55. Watthanasurorot A., Jiravanichpaisal P., Soderhall I., Soderhall K. A gC1qR prevents white spot syndrome virus replication in the freshwater crayfish Pacifastacus leniusculus. Journal of Virology 2010, 84:10844-10851.
56. Xian J.A., Wang A.L., Tian J.X., Huang J.W., Ye C.X., Wang W.N., Sun R.Y. Morphologic, physiological and immunological changes of haemocytes from Litopenaeus vannamei treated by lipopolysaccharide. Aquaculture 2009, 298:139-145.
57. Xue Q., Renault T., Cochennec N., Gerard A. Separation of European flat oyster, Ostrea edulis, haemocytes by density gradient centrifugation and SDS-PAGE characterisation of separated haemocyte sub-populations. Fish & Shellfish Immunology 2000, 10:155-165.
58. Yip E.C.H., Wong J.T.Y. Fluorescence activated cell-sorting of haemocytes in penaeid prawns. Aquaculture 2002, 204:25-31.
59. Zhang Z.F., Shao M., Ho Kang K. Classification of haematopoietic cells and haemocytes in Chinese prawn Fenneropenaeus chinensis. Fish & Shellfish Immunology 2006, 21:159-169.
60. Zhou J., Wang W.N., He W.Y., Zheng Y., Wang L., Xin Y., Liu Y., Wang A.L. Expression of HSP60 and HSP70 in white shrimp, Litopenaeus vannamei in response to bacterial challenge. Journal of Invertebrate Pathology 2010, 103:170-178.