Literature DB >> 11137541

Antigenic cross-reactivity of venoms from medically important North American Loxosceles spider species.

H F Gomez1, M J Miller, M W Waggener, H A Lankford, J S Warren.   

Abstract

We characterized the antigenic cross-reactivity of two medically important North American Loxoxceles species: L. reclusa (native to southeastern US) and L. deserta (native to southwestern US). Dermonecrosis resulting from bites from these two North American spider species are indistinguishable clinically. Polyclonal IgG antivenins directed against L. reclusa and L. deserta were raised in rabbits and used to develop specific enzyme immunoassays (EIAs). Antigenic differences in the two venoms were evaluated as follows: (1) 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 analysis present in a US national database; and (4) in vivo evaluation of alpha LoxR 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 three non-identical amino acids. alpha LoxR and alpha LoxD antivenins were similarly effective in blocking the development of rabbit skin lesions (ANOVA p<0.05). In summary, L. reclusa and L deserta spider venoms possess several common protein bands as identified by western blot, greater than 90% amino acid sequence identity, and marked antigenic cross-reactivity.

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Year:  2001        PMID: 11137541     DOI: 10.1016/s0041-0101(00)00212-9

Source DB:  PubMed          Journal:  Toxicon        ISSN: 0041-0101            Impact factor:   3.033


  5 in total

1.  Diagnosis of loxoscelism in a child confirmed with an enzyme-linked immunosorbent assay and noninvasive tissue sampling.

Authors:  William V Stoecker; Jonathan A Green; Hernan F Gomez
Journal:  J Am Acad Dermatol       Date:  2006-09-01       Impact factor: 11.527

2.  A new assay for the detection of Loxosceles species (brown recluse) spider venom.

Authors:  Hernan F Gomez; Diann M Krywko; William V Stoecker
Journal:  Ann Emerg Med       Date:  2002-05       Impact factor: 5.721

3.  Duration of Loxosceles reclusa venom detection by ELISA from swabs.

Authors:  David L McGlasson; Jonathon A Green; William V Stoecker; James L Babcock; David A Calcara
Journal:  Clin Lab Sci       Date:  2009

4.  Molecular evolution, functional variation, and proposed nomenclature of the gene family that includes sphingomyelinase D in sicariid spider venoms.

Authors:  Greta J Binford; Melissa R Bodner; Matthew H J Cordes; Katherine L Baldwin; Melody R Rynerson; Scott N Burns; Pamela A Zobel-Thropp
Journal:  Mol Biol Evol       Date:  2008-11-28       Impact factor: 16.240

5.  First report of in vitro selection of RNA aptamers targeted to recombinant Loxosceles laeta spider toxins.

Authors:  Amalia Sapag; Catalina Salinas-Luypaert; Carlos Constenla-Muñoz
Journal:  Biol Res       Date:  2014-03-26       Impact factor: 5.612

  5 in total

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