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Appl. Environ. Microbiol., 04 1995, 1431-1437, Vol 61, No. 4
NM Balayeva, ME Eremeeva, H Tissot-Dupont, IA Zakharov and D Raoult
The male-killing ladybird beetle (LB) bacterium (AB bacterium) was analyzed
with specific rickettsial molecular biology tools in the LB Adalia
bipunctata strains. Eight phenotype-positive LB strains showing mortality
of male embryos were amplified with rickettsial genus- specific primers
from the gene for citrate synthase (CS) and the gene for a 17-kDa protein
and spotted fever group-specific primers from the gene for the 120-kDa
outer membrane protein (ompB). The specificity of amplification was
confirmed by Southern hybridization and the absence of the above-listed
gene products in three phenotype-negative LB strains. Restriction
polymorphism patterns of three examined amplicons from the CS gene,
17-kDa-protein gene, and ompB gene were identical among the eight
phenotype-positive LB strains and were unique among all known rickettsiae
of the spotted fever and typhus groups. Amplified fragments of the CS genes
of the AB bacterium, Rickettsia prowazekii Breinl, Rickettsia typhi
Wilmington, Rickettsia canada 2678, and Rickettsia conorii 7 (Malish) were
sequenced. The greatest differences among the above-listed rickettsial and
AB bacterium CS gene sequences were between bp 1078 and 1110. Numerical
analysis based on CS gene fragment sequences shows the close relationships
of the AB bacterium to the genus Rickettsia. Expanding of knowledge about
rickettsial arthropod vectors and participation of rickettsiae in the
cytoplasmic maternal inheritance of arthropods is discussed.
Copyright © 1995, American Society for Microbiology
Genotype characterization of the bacterium expressing the male-killing trait in the ladybird beetle Adalia bipunctata with specific rickettsial molecular tools [published erratum appears in Appl Environ Microbiol 1996 Oct;62(10):3914]
Unite des Rickettsies, Centre National de la Recherche Scientifique EP J0054, Faculte de Medecine, Marseille, France.
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