Andréia Henzel
Universidade Feevale
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Featured researches published by Andréia Henzel.
Ciencia Rural | 2005
Andrea Pinto Loguercio; Alice Battistin; Agueda Castagna de Vargas; Andréia Henzel; Niura Mazzini Witt
The antimicrobial activity of medicinal plants has been searched in diverse species, as much in Brazil as in other countries. The aim of this study was to evaluate the existence of hydro-alcoholic extract jambolan leaves 10% (w/v) antibacterial effect. Seventeen Gram positive and Gram negative isolated bacterial were used. The antibacterial action was evaluated through the inoculation of Mueller Hinton agar plates, with a bacterial inoculate of 3x10 8 cell/ mL, with four paper discs, being the first of commercial antimicrobial and the others embedded with 25µL of the extract, saline or ethanol. The plates were incubated at 37°C for 24 hours, and their reading of inhibition hales diameter was done. The extract inhibited the growth of 100% of the tested bacteria; the Gram positive isolates had presented an average hale of 19.5mm, while of the Gram negative was of 18.8mm. There was not significant inhibition of growth in treatments with saline and ethanol. As verified in this study, the tested extract presents antibacterial activity against all the isolates, without sensitivity difference among Gram positive and Gram negative microorganisms.
Brazilian Journal of Microbiology | 2012
Andréia Henzel; Mário Celso Sperotto Brum; Claudia Lautert; Mathias Martins; Luciane Teresinha Lovato; Rudi Weiblen
Feline calicivirus (FCV) and feline herpesvirus type 1 (FHV-1) are the two primary causes of upper respiratory tract disease in cats. The aim of this study was to demonstrate the distribution of FCV and FHV-1 among the feline population of several counties in Rio Grande do Sul State, Brazil. To this end, conjunctival and nasal swabs were collected from 302 cats from different locations, including households, breeding catteries, veterinary clinics, animal hospitals and experimental research facilities. The samples were collected between July 2006 to June 2009. The virus isolation was performed in CRFK cells and, subsequently, the identification was confirmed by PCR. FCV, FHV-1, or both were isolated from 55 cats from 28 different locations. FCV alone was isolated from 52.7% (29/55) of the animals that tested positively, FHV-1 alone was isolated from 38.2% (21/55) of the animals that tested positively, and co-infection were detected in 9.1% (5/55) of the animals that tested positively. Virus detection was more prevalent in cats that were less than 1 year old, among animals that shared a living space with other cats, and females. FCV and FHV-1 were isolated from vaccinated cats. In addition, both viruses were isolated from cats that showed no signs of disease. The results suggest that a carrier state is common for both viruses in the evaluated population. A search for other causes of respiratory disease in that population is necessary; and further studies relating to the molecular characterization of viruses and vaccine efficacy are also necessary.
Pesquisa Veterinaria Brasileira | 2008
Sandra Arenhart; Letícia Frizzo da Silva; Andréia Henzel; Rogério Ferreira; Rudi Weiblen; Eduardo Furtado Flores
This paper reports the antibody response and fetal protection in pregnant cows conferred by an experimental vaccine containing two attenuated strains of bovine viral diarrhea virus (BVDV-1 and BVDV-2). Cows (n=19) were vaccinated twice, with a 34 days-interval, with the experimental vaccine and together with non-vaccinated controls (n=18), were mated and challenged between days 60 and 90 of gestation by intranasal inoculation of four heterologous BVDV-1 and BVDV-2 isolates. The antibody response was evaluated by serum-neutralization tests performed at different intervals after vaccination (days 34, 78 and 138 post-vaccination [pv]). Fetal protection was monitored by ultrassonographic and clinical examination of the dams and fetuses during the rest of gestation; and through virological and serological examination of pre-colostral blood obtained from aborted and/or recently born fetuses/calves. At the day of challenge (day 138 pv), all vaccinated cows had neutralizing antibodies in high titers against BVDV-1 (1,280->10,240), and with one exception (titer 20), presented moderate to high titers to BVDV-2 (80-1,280). At the end of the monitoring, only three out of 18 control cows (16.6%) delivered healthy, virus-free calves. Fifteen non-vaccinated cows (83.3%) presented signs of fetal infection and/or had reproductive losses. Seven of these cows (38.8%) delivered virus-positive calves; five were healthy and survived (27.7%); two were premature or weak and lasted three and 15 days, respectively. The other eight cows (44.4%) aborted between day 30 post-challenge and the parturition; or delivered premature or stillbirth calves. In contrast, 17 out of 19 (89.4%) vaccinated cows delivery virus-free, healthy calves. One vaccinated cow aborted around day 130 post-challenge, yet this fetus could not be examined for the presence of virus. Another cow delivered a virus-positive calf (5.2%). In summary, the experimental vaccine induced adequate antibody titers in most animals and the immunological response induced by vaccination was able to prevent fetal infection and reproductive losses upon challenge with a pool of heterologous BVDV isolates. Hence, this experimental vaccine may be an attractive alternative for the prevention of reproductive losses associated with BVDV infection.
Pesquisa Veterinaria Brasileira | 2008
Andréia Henzel; Diego Gustavo Diel; Sandra Arenhart; Fernanda Silveira Flores Vogel; Rudi Weiblen; Eduardo Furtado Flores
ABSTRACT.- Henzel A., Diel D.G., Arenhart S., Vogel F.S.F., Weiblen R. & Flores E.F.2008. [ Virological and clinico-pathological features of acute vulvovaginitis and latentinfection by bovine herpesvirus 1.2 in heifers experimentally infected .] Aspectosvirologicos e clinico-patologicos da infeccao genital aguda e latente pelo herpesvirusbovino tipo 1.2 em bezerras experimentalmente infectadas. Pesquisa Veterinaria Brasileira28(3):140-148. Departamento de Medicina Veterinaria Preventiva, Universidade Federalde Santa Maria, 97105-900 Santa Maria, RS, Brazil. E-mail: [email protected] infection of heifers and cows with bovine herpesvirus type 1.2 (BoHV-1.2)may result in vulvovaginitis and transient infertility. The acute infection is followed bythe establishment of latent infection which can be periodically reactivated. We hereindescribe the virology and clinico-pathological aspects of acute and recrudescentvulvovaginitis in heifers inoculated with a Brazilian BoHV-1.2 isolate recovered froman outbreak of balanoposthitis. Genital inoculation of isolate SV-56/90 (10
Brazilian Journal of Microbiology | 2015
Michele Regina Vetter; Rodrigo Staggemeier; Andréia Dalla Vecchia; Andréia Henzel; Caroline Rigotto; Fernando Rosado Spilki
Human adenoviruses (HAdV), members of the Adenoviridae family, are excreted through the fecal route and may be present in the feces of humans consuming contaminated food or water. The presence of HAdV from different serotypes in the feces of healthy individuals was already reported using conventional polymerase chain reaction; however, real-time PCR (qPCR) may reveal not only the rates of detection as well as demonstrate the viral loads excreted by healthy persons. Aiming to identify and characterize the presence of adenoviruses in stool samples, 147 fecal samples from patients with no records of diarrhea were analyzed (74 from winter season and 73 from summer) by Real-Time PCR (qPCR) assay and conventional PCR. HAdV genome was present in 43.8% (32/73) of stools samples collected during summer season and 21.6% (16/74) during winter. The rate of detection of genomic copies (gc) ranged from 4.04×102 to 6.72×105gc/g of feces among the 147 samples analyzed, of which the ranged of genomic copies of DNA HAdV was major in summer. All samples were negative when tested for rotaviruses (RV) and noroviruses (NoV) by PCR conventional and qPCR respectively. HAdV is excreted constantly by infected individuals in the absence of clinical signs and the occurrence may vary seasonally.
Journal of Water and Health | 2014
Mariana Kluge; Juliane Deise Fleck; Mayra Cristina Soliman; Roger Bordin da Luz; Rafael Bandeira Fabres; Juliana Comerlato; Joseane Vanessa dos Santos da Silva; Rodrigo Staggemeier; Andréia Dalla Vecchia; Roberta Capalonga; Ana Beatriz Almeida de Oliveira; Andréia Henzel; Caroline Rigotto; Fernando Rosado Spilki
The effects of viral gastroenteritis are more devastating in children than in any other age category. Thus, children exposed to the consumption of low quality water are at an increased risk of infection, especially in regions where sanitation is inadequate. The present study aimed to provide a survey of the occurrence of representative enteric viruses: human adenovirus (HAdV), human enteroviruses (hEV), and genogroup A rotavirus (GARV) in tap water samples collected in public schools located at six municipalities of Rio Grande do Sul, southern Brazil. Seventy-three schools were included in the study and tap water samples were analyzed by conventional PCR for the presence of HAdV, hEV, and GARV genomes. hEV showed the highest detection rate (27.4%), followed by HAdV (23.3%), and GARV (16.4%). New approaches to water monitoring should be considered to promote a better water quality and reduce the risk of waterborne diseases, especially considering drinking water to be served to vulnerable individuals.
Brazilian Journal of Microbiology | 2015
Roger Bordin da Luz; Rodrigo Staggemeier; Rafael Bandeira Fabres; Mayra Cristina Soliman; Fernanda Gil de Souza; Raoni da Silva Gonçalves; Ivone Veiga Fausto; Caroline Rigotto; Ls Heinzelmann; Andréia Henzel; Juliane Deise Fleck; Fernando Rosado Spilki
Adenoviruses are among the most promising viral markers of fecal contamination. They are frequently found in the water, sediment and soil of regions impacted by human activity. Studies of the bioaccumulation of enteric viruses in shrimp are scarce. The cities located in the northern coast of the lake systems in Southern Brazil have high urbanization and intensive farming rates, and poor sewage collection and treatment. One hundred (n = 100) Farfantepenaeus paulensis pink-shrimp specimens and 48 water samples were collected from coastal lagoons between June 2012 and May 2013. Water samples were concentrated and the shrimp, mashed. After DNA extraction, samples were analyzed by real time polymerase chain reaction (qPCR) in order to detect and quantify viral genomes. Thirty-five percent of shrimp samples were positive for contamination, predominantly by avian adenoviruses. A total of 91.7% of water samples contained adenoviruses DNA, with the human form being the most frequent. Our results provided evidence of significant bioaccumulation of adenoviruses in shrimp, showing the extent of the impact of fecal pollution on aquatic ecosystems.
American Journal of Infection Control | 2014
Joseane Vanessa dos Santos da Silva; Mateus Henrique de Mello; Rodrigo Staggemeier; Andréia Henzel; Caroline Rigotto; Fernando Rosado Spilki
Internship units Pediatric section Computer desk Positive Light switch Positive Front desk Positive Table for preparation of drugs products Positive Medical clinic A Front desks* Both negative Light switch Positive Table for preparation of drugs products Positive Sink (handwashing) Positive Medical clinic B Sinks (handwashing)* Both positive Front desk Negative Light switches Negative Mouse Negative Medical clinic C Sink (handwashing) Positive Front desk Positive Table for preparation of medications Positive Mouse Negative Emergency room Tables for preparation of medications* Both positive Mouse Positive Sinks (handwashing)y One positive Light switches* One positive Door handle Negative Computer table Positive Operating room Light switches Negative Computer table Positive Anesthesia cart Positive Support table Negative Total 32 20
Environmental Monitoring and Assessment | 2017
J. S. Gularte; Rodrigo Staggemeier; Meriane Demoliner; Tatiana Moraes da Silva Heck; F. H. Heldt; Rute Gabriele Fischoeder Ritzel; Caroline Rigotto; Andréia Henzel; Fernando Rosado Spilki
Human adenovirus (HAdV) is resistant to environment and can be used as a marker to detect fecal contamination. Considering the importance of freshwater snails in the aquatic environment, their use as concentrators for HAdV is a complementary tool for viral analysis of water. The goal of the study was to detect HAdV in snails and surface water collected from wetlands of the Sinos River (Rio Grande do Sul, Brazil) basin and to compare rates and viral loads found in both samples. HAdV was detected through real-time PCR. Total and fecal coliforms were detected by Colilert® kit, and viral infectivity of positive samples of the DNA genome was performed in A549 human cell line. All wetlands presented bacterial and viral contamination, but no viral particle was considered viable. The wetland that showed lower fecal coliform mean was Campo Bom, and São Leopoldo (both cities in Rio Grande do Sul) was representative of the highest mean. HAdV was detected in water samples (53%), gastropods’ hemolymph (31%) and tissues (16%). Wetlands proved to be environments already altered by human action. Water samples exhibited a higher frequency of HAdV detection; however, in some instances, the target viral genomes were only found in gastropod biological samples. This was a pioneer study in the use of freshwater snails for human enteric viral assessment thus demonstrating that the human organism can retain fecal contamination, complementing and assisting in microbiological water analyzes.
Revista Da Sociedade Brasileira De Medicina Tropical | 2015
Deise Nascimento de Freitas; Henrique Ataíde Isaía; Andréia Henzel; Éder Maiquel Simão; Rodrigo Benedetti Gassen; Luiz Carlos Rodrigues Junior
INTRODUCTION While no single factor is sufficient to guarantee the success of influenza vaccine programs, knowledge of the levels of immunity in local populations is critical. Here, we analyzed influenza immunity in a population from Southern Brazil, a region with weather conditions that are distinct from those in the rest of country, where influenza infections are endemic, and where greater than 50% of the population is vaccinated annually. METHODS Peripheral blood mononuclear cells were isolated from 40 individuals. Of these, 20 had received the H1N1 vaccine, while the remaining 20 were unvaccinated against the disease. Cells were stimulated in vitro with the trivalent post-pandemic influenza vaccine or with conserved major histocompatibility complex I (MHC I) peptides derived from hemagglutinin and neuraminidase. Cell viability was then analyzed by [3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide)]-based colorimetric assay (MTT), and culture supernatants were assayed for helper T type 1 (Th1) and Th2-specific cytokine levels. RESULTS Peripheral blood lymphocytes from vaccinated, but not unvaccinated, individuals exhibited significant proliferation in vitro in the presence of a cognate influenza antigen. After culturing with vaccine antigens, cells from vaccinated individuals produced similar levels of interleukin (IL)-10 and interferon (IFN)-γ, while those from unvaccinated individuals produced higher levels of IFN-γ than of IL-10. CONCLUSIONS Our data indicate that peripheral blood lymphocytes from vaccinated individuals are stimulated upon encountering a cognate antigen, but did not support the hypothesis that cross-reactive responses related to previous infections can ameliorate the immune response. Moreover, monitoring IL-10 production in vaccinated individuals could comprise a valuable tool for predicting disease evolution.