Hf. Gomez et al., Antigenic cross-reactivity of venoms from medically important North American Loxosceles spider species, TOXICON, 39(6), 2001, pp. 817-824
We characterized the antigenic cross-reactivity of two medically important
North American Loxoxceles species: L. reclusa (native to southeastern US) a
nd L. deserta (native to southwestern US). Dermonecrosis resulting from bit
es from these two North American spider species are indistinguishable clini
cally. Polyclonal IgG antivenins directed against L. reclusa and L. deserta
were raised in rabbits and used to develop specific enzyme immunoassays (E
IAs). Antigenic differences in the two venoms were evaluated as follows: (I
) Comparison of the sensitivities and correlation coefficient (R-2) of anti
-L. reclusa (alpha LoxR) and anti-L. deserta antibodies (alpha LoxD) in the
detection of varying concentrations of the two venoms; (2) separation and
western blot comparison of venom components; (3) protein sequence analysis
of L. desertavenom and comparison to the L. reclusa protein sequence analys
is present in a US national database: and (4) in vivo evaluation of alpha L
oxR and alpha LoxD antivenins in attenuating dermal lesions (rabbit model).
Correlation coefficients for alpha LoxR (R-2 = 0.99) and alpha LoxD(R-2 =
0.99) polyclonal antibodies in the measurements of standard concentrations
of venoms were virtually identical. Western blot analysis revealed multiple
common bands between the two venoms. Amino acid data (amino acids 1-35, N-
terminal) of the active venom components of the two venoms revealed only th
ree non-identical amino acids. alpha LoxR and alpha LoxD antivenins were si
milarly effective in blocking the development of rabbit skin lesions (ANOVA
p < 0.05). In summary, L. reclusa and L deserta spider venoms possess seve
ral common protein bands as identified by western blot, greater than 90% am
ino acid sequence identity, and marked antigenic cross-reactivity. (C) 2001
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