2012
DOI: 10.1177/1040638711434322
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Differential reactivity of serum immunoglobulins from Brazilian wild mammals to staphylococcal A and streptococcal G proteins

Abstract: Abstract. Human pathogens have evolved to infect vertebrate hosts other than human beings without causing symptoms of the disease, thus permitting them to complete their life cycle and to develop into infectious forms. The identification and management of infected animals are alternatives to control dissemination of the disease and to prevent human illness. In the current study, the potential use of staphylococcal A or streptococcal G proteins was evaluated with enzyme-linked immunosorbent assays (ELISAs) for … Show more

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Cited by 6 publications
(2 citation statements)
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References 12 publications
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“…Evolutionary distance is likely to play a significant role for inter-species variation in binding patterns with protein A/G in marsupials due to variation of protein A/G binding domains present in immunoglobulins [ 31 , 39 ]. Similar differences along taxonomic lines are observed between eutherian mammal species [ 31 , 40 ]. However, the results presented here show that taxonomic distance is not always a reliable predictor of immunoglobulin-binding affinity.…”
Section: Discussionsupporting
confidence: 72%
See 1 more Smart Citation
“…Evolutionary distance is likely to play a significant role for inter-species variation in binding patterns with protein A/G in marsupials due to variation of protein A/G binding domains present in immunoglobulins [ 31 , 39 ]. Similar differences along taxonomic lines are observed between eutherian mammal species [ 31 , 40 ]. However, the results presented here show that taxonomic distance is not always a reliable predictor of immunoglobulin-binding affinity.…”
Section: Discussionsupporting
confidence: 72%
“…However, the results presented here show that taxonomic distance is not always a reliable predictor of immunoglobulin-binding affinity. Therefore, it is important to assess the species-specific binding capability of protein A/G before developing serological assays [ 40 ] or use any commercially available kits using protein A/G as a conjugate, particularly with wildlife species where limited affinity data is available.…”
Section: Discussionmentioning
confidence: 99%