21 research outputs found
CONSUMER PERCEPTION ON ALTERNATIVE POULTRY
Food Consumption/Nutrition/Food Safety, Livestock Production/Industries,
Human herpesvirus infections of the central nervous system: laboratory diagnosis based on Dna detection by nested Pcr in plasma and cerebrospinal fluid samples
Infections of the central nervous systems (CNS) present a diagnostic problem for which an accurate laboratory diagnosis is essential. Invasive practices, such as cerebral biopsy, have been replaced by obtaining a polymerase chain reaction (PCR) diagnosis using cerebral spinal fluid (CSF) as a reference method. Tests on DNA extracted from plasma are noninvasive, thus avoiding all of the collateral effects and patient risks associated with CSF collection. This study aimed to determine whether plasma can replace CSF in nested PCR analysis for the detection of CNS human herpesvirus (HHV) diseases by analysing the proportion of patients whose CSF nested PCR results were positive for CNS HHV who also had the same organism identified by plasma nested PCR. In this study, CSF DNA was used as the "gold standard," and nested PCR was performed on both types of samples. Fifty-two patients with symptoms of nervous system infection were submitted to CSF and blood collection. For the eight HHV, one positive DNA result-in plasma and/or CSF nested PCR-was considered an active HHV infection, whereas the occurrence of two or more HHVs in the same sample was considered a coinfection. HHV infections were positively detected in 27/52 (51.9%) of the CSF and in 32/52 (61.5%) of the plasma, difference not significant, thus nested PCR can be performed on plasma instead of CSF. In conclusion, this findings suggest that plasma as a useful material for the diagnosis of cases where there is any difficulty to perform a CSF puncture.Infections of the central nervous systems (CNS) present a diagnostic problem for which an accurate laboratory diagnosis is essential. Invasive practices, such as cerebral biopsy, have been replaced by obtaining a polymerase chain reaction (PCR) diagnosis874648655sem informaçãosem informaçãoAbele, S.W., Puchhammer-Stöckl, E., Diagnosis of herpesvirus infections of the central nervous system (2002) J Clin Virol, 25, pp. S79-S85Altman, D.G., (1991) Practical statistics for medical research, pp. 410-411. , London: Chapman and hallBig, C., Reineck, L.A., Aronoff, D.M., Viral infections of the central nervous system: A case-based review (2009) J Clin Med Res, 7, pp. 142-146Boivin, G., Diagnosis of herpesvirus infections of the central nervous system (2004) Herpes, 11, pp. 48-56Calvario, A., Bozzi, A., Scarasciulli, M., Ventola, C., Stomati, D., Brancasi, B., Herpes consensus PCR test: A useful diagnostic approach to the screening of viral diseases of the central nervous system (2002) J Clin Virol, 25, pp. S71-S78Cassinotti, P., Siegl, G., A Nested-PCR assay for the simultaneous amplification of HSV-1, HSV-2, and HCMV genomes in patients with presumed herpetic CNS infections (1998) J Virol Methods, 71, pp. 105-114Chan, P.K., Ho-Keung, N.G., Cheung, J.L.K., Cheng, A.F., Survey for presence and distribuition of human herpesvirus 8 in healthy brain (2000) J Clin Microbiol, 38, pp. 2772-2773Cinque, P., Brytting, M., Vago, L., Castagna, A., Parravicini, C., Zanchetta, N., D'Arminio, M., Linde, A., Epstein-Barr virus DNA in cerebrospinal fluid from patients with Aids related primary lymphoma of the central nervous system (1993) Lancet, 342, pp. 398-401Danise, A., Cinque, P., Vergani, S., Candino, M., Racca, S., De Bona, A., Novati, R., Lazzarin, A., Use of polymerase chain reaction assays of aqueous humor in the differential diagnosis of retinitis in patients infected with human immunodeficiency virus (1997) Clin Infect Dis, 24, pp. 1100-1106Davies, N.W.S., Brown, L.J., Gonde, J., Irish, D., Robinson, R.O., Swan, A.V., Banatvala, J., Muir, P., Factors influencing PCR detection of viruses in cerebrospinal fluid of patients with suspected CNS infections (2005) J Neurol Neurosurg Psychiatry, 76, pp. 82-87DeBiasi, R., Kleinschmidt-Demasters, B., Weinberg, A., Tyler, K., Use of PCR for the diagnosis of herpesvirus infections of the central nervous system (2002) J Clin Virol, 25, pp. S5-S11Ehrnst, A., Barkholt, L., Lewensohhn-Fuchs, I., Ljungman, P., Teodosiu, O., Staland, A., Ringdén, O., Johansson, B., HCMV PCR monitoring in leukocytes of transplant patients (1995) Clin Diagn Virol, 3, pp. 139-153Fujimoto, H., Asaoka, K., Imaizumi, T., Ayabe, M., Shoji, H., Kaji, M., Epstein-Barr virus infections of the central nervous system (2003) Intern Med, 42, pp. 33-40Gilden, D., Mahalingam, R., Cohrs, R., Tyler, K., Herpesvirus infection of the nervous system (2007) Nat Clin Pract Neuro, 3, pp. 82-94Gregoire, S.M., Van Pesch, V., Goffete, S., Peeters, A., Sindic, C.J., Polymerase chain reaction analysis and oligoclonal antibody in the cerebrospinal fluid from 34 patients with Varicella-Zoster virus infection of the nervous system (2006) J Neurol Neurosurg Psychiatry, 77, pp. 938-942Imai, S., Usui, N., Sugiura, M., Osato, T., Sato, T., Tsutsumi, H., Tachi, N., Chiba, S., Epstein-Barr virus genomic sequences and specific antibodies in cerebrospinal fluid in children with neurologic complications of acute and reactivated EBV infections (1993) J Med Virol, 40, pp. 278-284Jeffery, K.J.M., Read, S.J., Peto, T.E.A., Mayon-White, R.T., Bangham, C.R.M., Diagnosis of viral infections of central nervous system: Clinical interpretation of PCR results (1997) Lancet, 249, pp. 313-317Juhl, D., Mosel, C., Nawroth, F., Funke, A.M., Dadgar, S.M., Hagenstrom, H., Kirchner, H., Hennig, H., Detection of herpes simplex virus DNA in plasma of patients with primary but not with recurrent infection: Implications for transfusion medicine (2010) Transfusion Med, 20, pp. 38-47Kaji, M., Shoji, H., Detection of Epstein-Barr virus genome in peripheral leucocytes and CSF by the polymerase chain reaction in two patients with Epstein-Barr virus related to aseptic meningitis (1995) J Neurol Neurosurg Psychiatry, 59, p. 99Kleinschmidt-DeMasters, B.K., De Biasi, R.L., Tyler, K.L., Polymerase chain reaction as a diagnostic adjunct in herpesvirus infections of the nervous system (2001) Brain Pathol, 11. , 452-446Landgren, M., Kyllerman, M., Bergstrom, T., Dotevall, L., Ljungstrom, L., Ricksten, A., Diagnosis of Epstein-Barr virus-induced central nervous system infections by DNA amplification from cerebrospinal fluid (1994) Ann Neurol, 35, pp. 631-635Leong, H.N., Tuke, P.W., Tedder, R.S., Khanom, A.B., Eglin, R.P., Atkinson, C.E., The prevalence of chromosomally integrated human herpesvirus 6 genomes in the blood of UK blood donors (2007) J Med Virol, 79, pp. 45-51Martelius, T., Lappalainen, M., Palomäki, M., Anttila, V.J., Clinical characteristics of patients with Epstein Barr virus in cerebrospinal fluid (2011) BMC Infect Dis, 11, pp. 281-287Meyding-Lamadè, U., Strank, C., Herpesvirus infections of the central nervous system in immunocompromised patients (2012) Ther Adv Neurol Disord, 5, pp. 279-296Mitchell, P.S., Espy, M.J., Smith, T.F., Persing, D.H., Molecular diagnosis of herpes simplex virus infections in the central nervous system (1999) J Clin Microbiol, 37, pp. 2127-2136Portolani, M., Pietrosemoli, P., Meacci, M., Sabbatini, A.M., Pecorari, M., Mantovani, G., Cermelli, C., Detection of Epstein-Barr virus DNA in cerebrospinal fluid from immunocompetent individuals with brain disorders (1998) New Microbiol, 21, pp. 77-79Prösch, S., Schielke, E., Reip, A., Meisel, H., Volk, H.D., Einhäupl, K.M., Krüger, D.H., Human cytomegalovirus (HCMV) encephalitis in an immunocompetent young person and diagnostic reliability of HCMV DNA PCR using cerebrospinal fluid of nonimmunosuppressed patients (1998) J Clin Microbiol, 36, pp. 3636-3640Sauerbrei, A., Wutzler, P., Laboratory diagnosis of central nervous system infections caused by herpesviruses (2002) J Clin Virol, 25, pp. S45-S51Schäfer, P., Tenschert, W., Schröter, M., Gutensohn, K., Laufs, R., False-positive results of plasma PCR for cytomegalovirus DNA due to delayed sample preparation (2000) J Clin Microbiol, 9, pp. 3249-3253Schmutzhard, E., Viral infections of the CNS with special emphasis on herpes simplex infections (2001) J Neurol, 248, pp. 469-477Schovoerer, E., Frechin, V., Fritsch, S., Freitag, R., Fuchs, A., Gutt, J.P., Stoll-Keller, F., Atypical symptoms in patients with herpesvirus DNA detected by PCR in cerebrospinal fluid (2006) J Clin Virol, 35, pp. 458-462Sghaier, W., Bahri, O., Kedous, E., Fazaa, O., Rezig, D., Touzi, H., Ben, Y., Triki, H., Retrospective study of viral causes of central nervous system infections in Tunisia (2003-2009) (2012) Med Sante Trop, 2, pp. 373-378Shoji, H., Wakasugi, K., Miura, Y., Imaizumi, T., Kazuyama, Y., Herpesvirus infections of the central nervous system (2002) Jpn J Infect Dis, 55, pp. 6-13Stahl, H.D., Hubner, B., Seid, B., Liebert, U., van der Heijden, I.M., Wilbrink, B., Kraan, M.C., Tak, P.P., Detection of multiple viral DNA species in synovial tissue and fluid of patients with early arthritis (2000) Ann Rheum Dis, 59, pp. 342-346Studahl, M., Bergstrom, T., Hagberg, L., Acute viral encephalitis in adults - A prospective study (1998) Scand J Infect Dis, 30, pp. 215-220Studahl, M., Hagberg, L., Rekabdar, E., Bergström, T., Herepesvirus DNA detection in cerebral spinal fluid: Differences in clinical presentation between Alpha-, Beta- and Gamma-herpesviruses (2000) Scand J Infect Dis, 32, pp. 237-238Studahl, M., Richsten, A., Sandberg, T., Elowson, S., Herner, S., Sall, C., Bergstrom, T., Cytomegalovirus infection of the CNS in non-compromised patients (1994) Acta Neurol Scand, 89, pp. 451-457Thorén, A., Widell, A., PCR for the diagnosis of enteroviral meningitis (1994) Scand J Infect Dis, 26, pp. 249-254Vrioni, G., Kalogeropoulos, C., Gartzonika, C., Priavali, E., Levidiotou, S., Usefulness of Herpes Consensus PCR methodology to routine diagnostic testing for herpesviruses infections in clinical specimens (2007) Virol J, 4, pp. 59-62Wada, K., Kubota, N., Ito, Y., Yagasaki, H., Kato, K., Yoshikawa, T., Yasuyuki, O., Hiroshi, K., Simultaneous quantification of Epstein-Barr virus, Cytomegalovirus, and Human Herpesvirus 6 DNA in samples from transplant recipients by multiplex real-time PCR Assay (2007) J Clin Microbiol, 45, pp. 1426-1432Ward, K.N., Leong, H.N., Thiruchelvam, A.D., Atkinson, C.E., Clark, D.A., Human herpesvirus 6 DNA levels in cerebrospinal fluid due to primary infection differ from those due to chromosomal viral integration and have implications for diagnosis of encephalitis (2007) J Clin Microbiol, 45, pp. 1298-1304Wang, F.Z., Dahl, H., Linde, A., Brytting, M., Ehrnst, A., Ljungman, P., Lymphotropic herpesviruses in allogeneic bone marrow transplantation (1996) Blood, 88, pp. 3615-3620Whitley, R.J., Gnann, J., Viral encephalitis: Familiar infections and emerging pathogens (2002) Lancet, 359, pp. 507-513Yalcin, S., Karpuzoglu, T., Suleymanlar, G., Mutlu, G., Mukai, T., Yamamoto, T., Isegawa, Y., Yamanishi, K., Human herpesvirus 6 and human herpesvirus 7 infections in renal transplant recipients and healthy adults in Turkey (1994) Arch Virol, 136, pp. 183-19
Silicato de potasio como elicitor de resistencia en las características de rendimiento de maíz dulce bajo estrés hídrico
Plant water stress is a major problem in the Cerrado biome of Brazil. Dry periods and random climatic events cause quality and yield losses in sweet corn plants. Compounds, such as silicon (Si), are being studied to reduce the negative impacts of water stress on agricultural crops. Further tests may allow farmers to increase the use of silicon-based compounds. The objective of this study was to evaluate the production parameters of the sweet corn (Zea mays var. saccharata) (Poaceae) Tropical Plus® hybrid with water stress and potassium silicate doses applied with foliar spraying. A randomized block design with four soil water tensions (15, 30, 45 and 60 kPa) and four potassium silicate doses (0, 6, 12 and 24 L ha-1) was used in a greenhouse. The studied factors, alone or in interaction with each other, did not affect most of the sweet corn yield parameters. The hypothesis that these results may have been partially affected by the presence of silicon are discussed. The sweet corn plant yield was affected mainly by the soil water tension of 60 kPa.El estrés hídrico en la planta es un problema importante en el bioma Cerrado de Brasil. Los períodos secos y los eventos climáticos aleatorios causan pérdidas de calidad y productividad en las plantas de maíz dulce. Compuestos como el silicio (Si), pueden ser estudiados para reducir los impactos negativos del estrés hídrico en los cultivos agrícolas. Pruebas adicionales pueden permitir a los agricultores aumentar el uso de compuestos a base de silicio. El objetivo de este trabajo fue evaluar los parámetros de producción de maíz dulce (Zea mays var. Saccharata, híbrido Tropical Plus®) con niveles de estrés hídrico y dosis de silicato de potasio aplicadas por pulverización foliar. El diseño experimental fue un diseño de bloques al azar con cuatro tensiones hídricas en el suelo (15, 30, 45 y 60 kPa) y cuatro dosis de silicato de potasio (0, 6, 12 y 24 L ha-1) en invernadero. Los factores estudiados solos o en interacción no afectaron la mayoría de los parámetros de producción de maíz dulce. Se discute la hipótesis de que estos resultados pueden haber sido parcialmente afectados por la presencia de silicio. El rendimiento de la planta de maíz dulce se vio afectado principalmente por el estrés hídrico del suelo a 60 kPa