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Registro Completo |
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Biblioteca(s): |
Embrapa Caprinos e Ovinos. |
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Data corrente: |
09/12/2021 |
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Data da última atualização: |
10/12/2021 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
PEIXOTO, R. M.; SOUSA, A. L. M. de; ARAÚJO, J. F.; PINHEIRO, R. R. |
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Afiliação: |
RENATO MESQUITA PEIXOTO; ANA LÍDIA MADEIRA DE SOUSA; JUSCILÂNIA FURTADO ARAÚJO; RAYMUNDO RIZALDO PINHEIRO, CNPC. |
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Título: |
Western Blot no imunodiagnóstico de lentivírus de pequenos ruminantes. |
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Ano de publicação: |
2021 |
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Fonte/Imprenta: |
Acta Scientiae Veterinariae, v. 49, pub. 1781, p. 1-11, 2021. |
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Idioma: |
Português |
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Conteúdo: |
Background: Small ruminant lentivirus (SRLV) belong to genus Lentivirus, family Retroviridae. These viruses cause caprine arthritis encephalitis (CAE) and maedi visna (MV), infectious diseases that cause economic, production, and reproductive losses. There are no effective treatments or vaccines for these diseases. Thus, early detection via serology has great importance for control of SRLV. Therefore, the objective of this review is to demonstrate the potential of the western blot (WB) test as an immunodiagnostic test for SRLV. Review: In general, immunodiagnosis of SRLV is performed via agar gel immunodiffusion (AGID) and indirect enzyme linked immunosorbent assay (ELISA), which can detect antibodies in several different biological samples but is used pref- erably with serum and blood plasma. However, WB has demonstrated efficacy in the early diagnosis of immunoglobulins against SRLV, presenting higher sensitivity and specificity than the serological tests usually used, because this technique can detect antibodies at a dilution as much as 256 times greater than that of AGID and 32 times greater than that of ELISA. SRLV infection and consequent immunological activation result in the induction of cellular and humoral responses. Ad-ditionally, around the third week, production of antibodies directed mainly toward viral capsid proteins (p25 and p28) occurs. After the fifth week, production of immunoglobulins directed toward other viral proteins occurs. Because of the persistence of SRLV infection, serology is considered to be the most practical means to diagnosis. Each serological test has a percentage specificity and distinct sensitivity, as well as advantages and disadvantages in its applicability. It should be noted that there is no gold standard test for diagnosis of SRLV infection. Moreover, SRLV are characterized by escape mechanisms such as genetic diversity, mutagenic potential, viral intermittence, and the process of compartmentalization, which make immunodiagnosis more difficult. In addition, positive animals tend to present unstable levels of antibodies over weeks, months, and even years. In this context, WB, with early antibody detection, has been proven to be a refined and more accurate technique than other immunodiagnostic tests for SRLV. WB allows the simultaneous resolution of several immunogenic antigens present in a sample, and this feature provides it with greater reliability, differentiates it from other immunological methods, and accredits it as a test of wide applicability. Epidemiological and immunological dynamics studies often use WB in the immunodynamic diagnosis of SRLV. Serum, blood plasma, and seminal plasma are typical biological materials used in the serological diagnosis of SRLV with WB, expanding its potential as an immunodiagnosis method. Conclusion: WB is the most accurate serological technique for SRLV. It is more capable of accurate diagnosis because the genetic diversity that characterizes such lentiviruses and their various immune system escape mechanisms routinely hinder traditional diagnosis. Additionally, this test has been used widely in studies of SRLV for various purposes, but mainly in studies of epidemiological and immunological dynamics, using serum, blood plasma, or seminal plasma. However, independently of the biological sample tested, WB maintains high sensitivity and precision in immunodiagnosis, making it a refined and valid technique for SRLV control programs. MenosBackground: Small ruminant lentivirus (SRLV) belong to genus Lentivirus, family Retroviridae. These viruses cause caprine arthritis encephalitis (CAE) and maedi visna (MV), infectious diseases that cause economic, production, and reproductive losses. There are no effective treatments or vaccines for these diseases. Thus, early detection via serology has great importance for control of SRLV. Therefore, the objective of this review is to demonstrate the potential of the western blot (WB) test as an immunodiagnostic test for SRLV. Review: In general, immunodiagnosis of SRLV is performed via agar gel immunodiffusion (AGID) and indirect enzyme linked immunosorbent assay (ELISA), which can detect antibodies in several different biological samples but is used pref- erably with serum and blood plasma. However, WB has demonstrated efficacy in the early diagnosis of immunoglobulins against SRLV, presenting higher sensitivity and specificity than the serological tests usually used, because this technique can detect antibodies at a dilution as much as 256 times greater than that of AGID and 32 times greater than that of ELISA. SRLV infection and consequent immunological activation result in the induction of cellular and humoral responses. Ad-ditionally, around the third week, production of antibodies directed mainly toward viral capsid proteins (p25 and p28) occurs. After the fifth week, production of immunoglobulins directed toward other viral proteins occurs. Because of the persistenc... Mostrar Tudo |
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Palavras-Chave: |
Diagnóstico sorológico; Lentivirose; Lentiviruses; LVPR; Serological diagnosis; SRLV. |
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Thesagro: |
Caprino; Doença Animal; Imunoglobulina; Ovino. |
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Thesaurus Nal: |
Caprine arthritis-encephalitis; Disease diagnosis; Goat diseases; Goats; Immunoglobulins; Serodiagnosis; Sheep diseases; Visna maedi virus; Western blotting. |
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Categoria do assunto: |
H Saúde e Patologia |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/228882/1/cnpc-2021-Art-91.pdf
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Marc: |
LEADER 04531naa a2200385 a 4500
001 2137467
005 2021-12-10
008 2021 bl uuuu u00u1 u #d
100 1 $aPEIXOTO, R. M.
245 $aWestern Blot no imunodiagnóstico de lentivírus de pequenos ruminantes.$h[electronic resource]
260 $c2021
520 $aBackground: Small ruminant lentivirus (SRLV) belong to genus Lentivirus, family Retroviridae. These viruses cause caprine arthritis encephalitis (CAE) and maedi visna (MV), infectious diseases that cause economic, production, and reproductive losses. There are no effective treatments or vaccines for these diseases. Thus, early detection via serology has great importance for control of SRLV. Therefore, the objective of this review is to demonstrate the potential of the western blot (WB) test as an immunodiagnostic test for SRLV. Review: In general, immunodiagnosis of SRLV is performed via agar gel immunodiffusion (AGID) and indirect enzyme linked immunosorbent assay (ELISA), which can detect antibodies in several different biological samples but is used pref- erably with serum and blood plasma. However, WB has demonstrated efficacy in the early diagnosis of immunoglobulins against SRLV, presenting higher sensitivity and specificity than the serological tests usually used, because this technique can detect antibodies at a dilution as much as 256 times greater than that of AGID and 32 times greater than that of ELISA. SRLV infection and consequent immunological activation result in the induction of cellular and humoral responses. Ad-ditionally, around the third week, production of antibodies directed mainly toward viral capsid proteins (p25 and p28) occurs. After the fifth week, production of immunoglobulins directed toward other viral proteins occurs. Because of the persistence of SRLV infection, serology is considered to be the most practical means to diagnosis. Each serological test has a percentage specificity and distinct sensitivity, as well as advantages and disadvantages in its applicability. It should be noted that there is no gold standard test for diagnosis of SRLV infection. Moreover, SRLV are characterized by escape mechanisms such as genetic diversity, mutagenic potential, viral intermittence, and the process of compartmentalization, which make immunodiagnosis more difficult. In addition, positive animals tend to present unstable levels of antibodies over weeks, months, and even years. In this context, WB, with early antibody detection, has been proven to be a refined and more accurate technique than other immunodiagnostic tests for SRLV. WB allows the simultaneous resolution of several immunogenic antigens present in a sample, and this feature provides it with greater reliability, differentiates it from other immunological methods, and accredits it as a test of wide applicability. Epidemiological and immunological dynamics studies often use WB in the immunodynamic diagnosis of SRLV. Serum, blood plasma, and seminal plasma are typical biological materials used in the serological diagnosis of SRLV with WB, expanding its potential as an immunodiagnosis method. Conclusion: WB is the most accurate serological technique for SRLV. It is more capable of accurate diagnosis because the genetic diversity that characterizes such lentiviruses and their various immune system escape mechanisms routinely hinder traditional diagnosis. Additionally, this test has been used widely in studies of SRLV for various purposes, but mainly in studies of epidemiological and immunological dynamics, using serum, blood plasma, or seminal plasma. However, independently of the biological sample tested, WB maintains high sensitivity and precision in immunodiagnosis, making it a refined and valid technique for SRLV control programs.
650 $aCaprine arthritis-encephalitis
650 $aDisease diagnosis
650 $aGoat diseases
650 $aGoats
650 $aImmunoglobulins
650 $aSerodiagnosis
650 $aSheep diseases
650 $aVisna maedi virus
650 $aWestern blotting
650 $aCaprino
650 $aDoença Animal
650 $aImunoglobulina
650 $aOvino
653 $aDiagnóstico sorológico
653 $aLentivirose
653 $aLentiviruses
653 $aLVPR
653 $aSerological diagnosis
653 $aSRLV
700 1 $aSOUSA, A. L. M. de
700 1 $aARAÚJO, J. F.
700 1 $aPINHEIRO, R. R.
773 $tActa Scientiae Veterinariae$gv. 49, pub. 1781, p. 1-11, 2021.
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Registro original: |
Embrapa Caprinos e Ovinos (CNPC) |
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Registro Completo
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Biblioteca(s): |
Embrapa Meio Ambiente. |
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Data corrente: |
19/03/1994 |
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Data da última atualização: |
15/02/2017 |
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Autoria: |
MEDUGNO, C. C.; CAPALBO, D. M. F.; ONAGA, H.; GONZALES, G. M. |
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Afiliação: |
CLAUDIA CONTI MEDUGNO, CNPMA; DEISE MARIA FONTANA CAPALBO, CNPMA; H. ONAGA; G. M. ONAGA, CENPES/PETROBRÁS. |
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Título: |
Bacillus thuringiensis israelensis para o controle de vetores: preparação de unidades flutuantes. |
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Ano de publicação: |
1993 |
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Fonte/Imprenta: |
In: CONGRESSO BRASILEIRO DE MICROBIOLOGIA, 17., 1993, Santos. Resumos. [S.l.: s.n.], 1993. |
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Páginas: |
p.41 |
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Idioma: |
Português |
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Palavras-Chave: |
Bacillus thuringiensis israelensis; Hidrofobicidade; Inseto vetor. |
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Thesagro: |
Controle Biológico; Doença; Toxina. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/155711/1/1993PL006-Capalbo-Bacillus-1970.PDF
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Marc: |
LEADER 00728naa a2200229 a 4500
001 1011337
005 2017-02-15
008 1993 bl uuuu u00u1 u #d
100 1 $aMEDUGNO, C. C.
245 $aBacillus thuringiensis israelensis para o controle de vetores$bpreparação de unidades flutuantes.$h[electronic resource]
260 $c1993
300 $ap.41
650 $aControle Biológico
650 $aDoença
650 $aToxina
653 $aBacillus thuringiensis israelensis
653 $aHidrofobicidade
653 $aInseto vetor
700 1 $aCAPALBO, D. M. F.
700 1 $aONAGA, H.
700 1 $aGONZALES, G. M.
773 $tIn: CONGRESSO BRASILEIRO DE MICROBIOLOGIA, 17., 1993, Santos. Resumos. [S.l.: s.n.], 1993.
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Embrapa Meio Ambiente (CNPMA) |
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