Jm. Janda et al., BIOCHEMICAL INVESTIGATIONS OF BIOGROUPS AND SUBSPECIES OF MORGANELLA-MORGANII, Journal of clinical microbiology, 34(1), 1996, pp. 108-113
We determined the subspecies and biogroup designations for 73 strains
of Morganella morganii principally recovered from routine clinical spe
cimens. On the basis of trehalose fermentation, 90% of all strains wer
e identified as M. morganii subsp, morganii (trehalose negative), whit
e the remaining 10% were designated M. morganii subsp, sibonii (trehal
ose positive). Using three tests (ornithine decarboxylase [ODC] and ly
sine decarboxylase [LDC] activities and susceptibility to tetracycline
), we determined the biogroup designations for these 73 strains, Four
of the seven recognized biogroups within the genus Morganella were fou
nd in the study, with biogroup A (ODC positive [ODC+], LDC negative [L
DC(-)]) predominating (78%); all M. morganii subsp. sibonii strains we
re found to belong to biogroup G (ODC+, LDC(-)). Rapid glycerol fermen
tation (24 h) was linked to nonmotility and biogroup B strains (ODC+,
LDC(+)), LDC activity but not tetracycline resistance appeared to be a
ssociated with the possession of a 40- to 45-MDa plasmid, The use of t
hree commercial systems (API ZYM, API 50 CH, and Biolog GN) failed to
detect any new biochemical tests useful for subspecies identification,
with the possible exception of L-phenylalanine utilization as a sole
carbon source in the Biolog GN system, No Morganella strain was found
to invade either HEp-2 or Vero cell lines, but four of seven M. morgan
ii subsp, morganii strains were cytotoxic on sheets of both cells. Thi
s cytotoxic activity appeared to correlate with the rapid expression o
f beta-hemolytic activity.