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Applied and Environmental Microbiology, September 1998, p. 3214-3219, Vol. 64, No. 9
Department of Biological Sciences, Simon
Fraser University, Burnaby, Vancouver, British Columbia, Canada V5A
1S6
Received 6 April 1998/Accepted 6 June 1998
A small-colony variant (Vsm) of the primary form (Vp) of
Photorhabdus luminescens MD from in vitro and in vivo
cultures is described. Unlike the primary form, Vp, the Vsm variant is
not the preferred diet of its nematode symbiont, a
Heterorhabditis sp., does not support development and
reproduction of the nematode, and is less pathogenic than Vp to
Galleria mellonella larvae. Vsm cells were carried by 25%
of infective juveniles, but they comprised a very low percentage
(~0.4%) of the total cells carried by the juvenile. In vitro
subculture and in vivo injection into the larvae with either Vp or Vsm
always produced a mixture of both Vp and Vsm. In
nematode-bacterium-infected G. mellonella larvae, the Vp
population in the hemocoel was high (4 × 109 to
5 × 109 CFU/g of wet insect tissue) at 24 h
after infection, decreased about 10-fold by 48 h, and then
regained a high level at day 5 before decreasing at day 7 and then
remaining relatively constant through day 15 postinfection. The Vsm
population, under the same conditions as those of Vp, increased
gradually to a high level (9 × 108 CFU/g of wet
insect tissue) at day 5 postinfection and then declined gradually
through day 15.
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
In Vitro and In Vivo Characterization of a Small-Colony
Variant of the Primary Form of Photorhabdus luminescens
MD (Enterobacteriaceae)
*
Corresponding author. Mailing address: Department of
Biological Sciences, Simon Fraser University, Burnaby, Vancouver, BC V5A 1S6, Canada. Phone: (604) 291-4105. Fax: (604) 291-3496. E-mail: Kaiji{at}sfu.ca.
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