FN Archimer Export Format
PT J
TI Arbitrarily primed PCR to type Vibrio spp. Pathogenic for shrimp
BT 
AF GOARANT, Cyrille
   MERIEN, F
   BERTHE, Franck
   MERMOUD, I
   PEROLAT, P
AS 1:1;2:2;3:3;4:4;5:2;
FF 1:PDG-DOP-DCOP-AQNC;2:;3:PDG-DOP-DCN-AGSAE-LGP;4:;5:;
C1 Inst Pasteur, Lab Leptospires, Noumea 98845, New Caledonia.
   IFREMER, Lab Rech Aquacole, Noumea 98846, New Caledonia.
   CIRAD, EMVT, Programme Elevage, Noumea 98845, New Caledonia.
   IFREMER, Lab Biol & Ecol Invertebres Marins, F-17390 La Tremblade, France.
C2 INST PASTEUR, FRANCE
   IFREMER, FRANCE
   CIRAD, FRANCE
   IFREMER, FRANCE
SI NOUMEA
   LA TREMBLADE
SE PDG-DOP-DCOP-AQNC
   PDG-DOP-DCN-AGSAE-LGP
IF 3.389
TC 50
UR https://archimer.ifremer.fr/doc/1999/publication-2734.pdf
LA English
DT Article
AB A molecular typing study on Vibrio strains implicated in shrimp disease outbreaks in New Caledonia and Japan was conducted by using AP-PCR (arbitrarily primed PCR). It allowed rapid identification of isolates at the genospecies level and studies of infraspecific population structures of epidemiological interest. Clusters identified within the species Vibrio penaeicida were related to their area of origin, allowing discrimination between Japanese and New Caledonian isolates, as well as between those from two different bays in New Caledonia separated by only 50 km. Other subclusters of New Caledonian V. penaeicida isolates could be identified, but it was not possible to link those differences to accurate epidemiological features. This contribution of AP-PCR to the study of vibriosis in penaeid shrimps demonstrates its high discriminating power and the relevance of the epidemiological information provided. This approach would contribute to better knowledge of the ecology of Vibrio spp. and their implication in shrimp disease in aquaculture.
PY 1999
PD MAR
SO Applied And Environmental Microbiology
SN 0099-2240
PU Amer Soc Microbiology
VL 65
IS 3
UT 000078882000040
BP 1145
EP 1151
ID 2734
ER

EF