Thesis (Ph. D.)--University of Missouri-Columbia, 1996. / Typescript. Vita. Includes bibliographical references (leaves 129-157). Also available on the Internet.

Thesis (Ph. D.)--University of Missouri-Columbia, 1996. / Typescript. Vita. Includes bibliographical references (leaves 129-157). Also available on the Internet.

Submitted by Ana Borges (ana.azevedo@udesc.br) on 2017-06-09T11:56:55Z No. of bitstreams: 1 Cristiane Mezaroba.pdf: 9118688 bytes, checksum: 7706a8529180fd844f20da89e3df3d57 (MD5) / Made available in DSpace on 2017-06-09T11:56:55Z (GMT). No. of bitstreams: 1 Cristiane Mezaroba.pdf: 9118688 bytes, checksum: 7706a8529180fd844f20da89e3df3d57 (MD5) Previous issue date: 2017-02-23 / CAPES / Plasma sterilization present effective and extensive microbial lethality, fast action, compatibility with various materials, high diffusion through porous substances and are non-polluting systems. The objective of this study was to evaluate if the inductive RF plasma and N2-O2 mixture is efficient for use in sterilization of polymer medical-hospital and dental materials, represented in this study by the polymer HDPE. It was also the objective of this study to evaluate the possible superficial modifications of HDPE after sterilization. HDPE films were used with spores of Geobacillus stearothermophilus, with ≅5,73x107 UFC/film. In the microbiological tests were used 20W and 40W power, 0.5 Torr pressure and exposure times of 2,5,10,15 and 20 minutes. Low temperature was maintained (T<40°C), and the results demonstrated sterilization efficiency. The samples were characterized by contact angle measurements, atomic force microscopy (AFM), scanning electron microscopy field emission (FEG-SEM) and Fourier transform infrared spectroscopy in the "Attenuated Total Reflectance" (FTIR-ATR) mode. The active species formed in plasma were identified by a system of optical emission spectroscopy (OES). / A esterilização por plasma têm oferecido vantagens em relação a outros métodos à baixa temperatura utilizados, a começar por alta eficácia e abrangente letalidade microbiana, ação rápida, compatibilidade com vários materiais, alta difusibilidade e é um sistema não poluente. O objetivo deste trabalho foi avaliar se o plasma RF indutivo (ICP) e mistura de N2-O2 é eficiente para uso em esterilização de materiais poliméricos médico-hospitalares e odontológicos, representado neste estudo pelo polímero PEAD. Também foi objetivo deste trabalho avaliar as possíveis modificações superficiais do PEAD após a esterilização. Foram utilizados filmes de PEAD com esporos de Geobacillus stearothermophilus, com ≅5,73x107 UFC/filme. Nos testes microbiológicos foram utilizadas potências de 20W e 40W, pressão de 0,5 Torr e tempos de exposição de 2,5,10,15 e 20 minutos. Foi mantida baixa temperatura (T<40°C), e os resultados demonstraram eficiência de esterilização. Os filmes de PEAD após esterilização foram caracterizados por medidas do ângulo de contato, microscopia de força atômica (AFM), microscopia eletrônica de varredura por emissão de campo (FEG-MEV) e espectroscopia no infravermelho por transformada de Fourier no modo “Refletância Total Atenuada” (FTIR-ATR). As espécies ativas formadas no plasma foram identificadas por um sistema de espectroscopia óptica de emissão (OES).

Esporos de Bacillus subtilis podem ser utilizados como veículos vacinais capazes de expressar ou adsorver proteínas heterólogas em sua superfície. Estudos recentes indicaram que esporos de B. subtilis também conferem um forte efeito adjuvante para vacinas baseadas em proteínas purificadas administradas por via parenteral. Nesse cenário, o objetivo do presente projeto foi avaliar o papel adjuvante dos esporos de B. subtilis e viabilizar sua utilização como carregadores de vacinas de DNA pelo método da biobalística (gene gun). Nesta metodologia, os esporos foram utilizados como substitutos das micropartículas de ouro usualmente empregadas, mantendo a capacidade de transfecção de células eucarióticas in vitro, e produção de anticorpos específicos em camundongos C57BL/6 imunizados com o plasmídeo vacinal pgDE7h (que codifica para uma forma atóxica da oncoproteína E7 do HPV-16). Além disso, esporos de B. subtilis foram capazes de ativar células dendríticas in vitro e, quando coadministrados a pgDE7h pela via intramuscular, conferiram um aumento de 50% na proteção anti-tumoral de animais previamente transplantados com a linhagem tumoral TC-1 (que expressa a proteína E7 do HPV-16), em uma relação dose-dependente. / Bacillus subtilis spores can be used as vaccine vehicles capable of to display or adsorb heterologous proteins in its surface. Recent studies have indicated that spores of B. subtilis confer a strong adjuvant effect for vaccines based on purified proteins administered by the parenteral route. In this scenario, the objective of this project is to evaluate the adjuvant role of B. subtilis spores e viabilize its use as DNA vaccine carriers of biolistic method (gene gun). In this methodology, the spores are used as gold microparticles substitutes usually employed, maintaining the ability to transfect eukaryotic cells in vitro and production of specific antibodies in C57BL / 6 mice immunized with the vaccine plasmid pgDE7h (encoding a non-toxic form of the E7oncoprotein of HPV-16). Additionally, spores of B. subtilis were able to activate dendritic cells in vitro when co-administered intramuscularly to pgDE7h, conferring an increase of 50% of anti-tumor protection in animals previously transplanted with the TC-1 tumor cell line (expressing the E7 protein of HPV-16) in a dose-dependent manner.

O S. mutans é o agente etiológico da cárie dental humana, uma doença com ampla distribuição mundial. A adesão à superfície dental depende da interação entre a proteína de superfície P1 e a aglutinina salivar (SAG) adsorvida ao dente. A região N-terminal da P1 é um alvo vacinal importante que está diretamente associada às funções de adesão e agregação. Este trabalho teve o objetivo de avaliar estratégias vacinais contra o S. mutans baseadas na proteína P1 usando linhagens recombinantes de B. subtilis. O B. subtilis é uma bactéria gram positiva, formadora de esporos, não patogênica, empregada como sistema de expressão de proteínas heterólogas e como veículo vacinal administrado por vias de mucosas. Empregamos o B. subtilis para expressar e purificar a proteína P139-512 derivada da proteína P1 de S. mutans UA159. O antígeno P139-512 apresentou epítopos lineares e conformacionais semelhantes aos presentes na proteína P1 nativa. O sítio de ligação à SAG está preservado nessa proteína assim como suas propriedades imunogênicas. A coadministração parenteral do antígeno com adjuvantes vacinais promoveu resposta sistêmica específica com anticorpos eficazes no bloqueio da adesão de S. mutans. Por fim, usamos esporos de B. subtilis como veículo de entrega de mucosa para o antígeno alvo de S. mutans. Esporos de B. subtilis foram modificados para expressar na superfície adesinas bacterianas (SlpA, InvA ou Inv600) com capacidade de ligação ao epitélio intestinal e, quando no estágio de célula vegetativa, expressar intracelularmente o antígeno P139-512. A imunização oral com os esporos adesivos induziu altas concentrações de anticorpos sistêmicos e de mucosa. A imunização nasal ou sublingual com os esporos recombinantes induziu níveis de anticorpos sistêmicos maiores do que aqueles obtidos após a imunização oral. Além disso, esses anticorpos foram mais eficientes em bloquear a adesão de S. mutans à SAG imobilizada, sem interferir com a agregação. Em conclusão, os resultados obtidos abrem perspectivas interessantes para o desenvolvimento de vacinas anti-cárie baseadas em linhagens de B. subtilis. / S. mutans is the major etiologic agent of human dental caries, a disease with worldwide distribution. The adhesion to the tooth surface is dependent on the interaction of the P1 surface protein and salivary agglutinin (SAG) adsorbed to the tooth. The N-terminal region of P1 is an important vaccine target that is directly associated with adhesion and aggregation functions. This study aimed to evaluate vaccination strategies against S. mutans based on the P1 protein using recombinant B. subtilis strains. B. subtilis is a gram positive, spore-forming, non-pathogenic bacterium used as expression system for heterologous proteins and as a vaccine vehicle administered by mucosal routes. Inicially, we employed a recombinant B. subtilis strain to express and purify the P139-512 protein derived from the S. mutans UA159 P1 protein. The P139-512 antigen showed important conformational and linear epitopes similar to those present in the native P1 protein. The SAG-binding site is preserved in P139-512 as well as immunological properties. The parenteral co-administration of antigen with vaccine adjuvants stimulated systemic antibodies effective in blocking adhesion of S. mutans to SAG. Lastly, we used B. subtilis spores as a mucosal delivery vehicle for antigen targeting. B. subtilis endospores were modified to display bacterial adhesins (SlpA, InvA or Inv600), capable to bind to the intestinal epithelium, on the spore surface and to express intracellularly the P139-512 antigen during the vegetative cell stage. Oral immunization with adhesives spores induced high systemic and mucosal specific antibodies levels. The nasal or sublingual immunization with B. subtilis recombinant spores induced higher amounts of systemic antibodies than the oral immunization. Furthermore, the specific antibodies were highly effective in blocking the adherence of S. mutans to immobilized SAG, without interfering with aggregation. In conclusion, the results open interesting perspectives for the development of anti-caries vaccines based on B. subtilis strains.

No description available.

A transmissão de parasitas da malária por mosquitos vetores é dependente do desenvolvimento bem sucedido das formas infectantes de Plasmodium sp., especialmente os esporozoítas, que são as formas que infectam o hospedeiro vertebrado. A manipulação genética de mosquitos vetores tem sido uma estratégia alternativa na tentativa de controle da malária. Um componente extremamente importante desta estratégia é a escolha de uma molécula efetora capaz de reduzir a transmissão do patógeno. Microplusina é um peptídeo antimicrobiano rico em cisteína, originalmente descrito como um componente antimicrobiano da hemolinfa e dos ovos de carrapato bovino Rhipicephalus (Boophilus) microplus. Testes anteriores utilizando o modelo experimental mosquito Aedes aegypti infectado por Plasmodium gallinaceum mostraram que a microplusina é altamente tóxico para esporozoítas de Plasmodium gallinaceum em concentração relativamente baixa, sem apresentar toxicidade aos mosquitos vetores Aedes aegypti. Nosso objetivo foi analisar a expressão da microplusina e seu efeito na infecção de P. gallinaceum em mosquitos transgênicos. Obtivemos quatro linhagens através da integração de um transgene contendo a região promotora do gene da vitelogenina de Ae. aegypti, peptídeo sinal maltase-like I de Ae. aegypti e a sequência codificadora da microplusina (PMOS [3xP3-EGFP-AeVg Micro]). A atividade anti esporozoítas da microplusina expressa pelos mosquitos transgênicos mostrou diferença significante as linhagens. O desenho de novas moléculas utilizando como molde moléculas efetoras existentes e testadas, possibilitará o aperfeiçoamento da expressão de genes exógenos em mosquitos transgênicos, tornando-os refratários ao parasita. / Transmission of malaria parasites by mosquito vectors is dependent on the successful development of Plasmodium sp. infective forms, particularly the sporozoites, which are the forms that enter the vertebrate host. The genetic manipulation of mosquito vectors has been a strategy for malaria control. An extremely important component of this strategy is the effector molecule of choice which reduces parasite transmission. Microplusin is a cysteine-rich antimicrobial peptide originally described as an hemolymph and eggs antimicrobial component of the cattle tick Boophilus microplus. Previous tests using the experimental model Plasmodium gallinaceum infected Aedes aegypti showed that microplusin is highly toxic to P. gallinaceum sporozoites in relatively low concentration, without showing toxicity to the mosquito vector A. aegypti. Our goal was to analyze transgenic mosquitoes expressing microplusin and its effect on infection of P. gallinaceum. We obtained four lines through the integration of transgene that containing the promoter region of the A. aegypti vitelogenin gene, the maltase-like I signal peptide of A. aegypti and microplusin coding sequence (pMos[3xP3-EGFPAeVg-Micro]). The activity anti sporozoites microplusin expressed by transgenic mosquitoes showed significant differences between strains. The design of effector molecules using information from existing and tested molecules as template will enable the improvement of the expression of foreign genes in transgenic mosquitoes, making them resistant to the parasite.

A transmissão de parasitas da malária por mosquitos vetores é dependente do desenvolvimento bem sucedido das formas infectantes de Plasmodium sp., especialmente os esporozoítas, que são as formas que infectam o hospedeiro vertebrado. A manipulação genética de mosquitos vetores tem sido uma estratégia alternativa na tentativa de controle da malária. Um componente extremamente importante desta estratégia é a escolha de uma molécula efetora capaz de reduzir a transmissão do patógeno. Microplusina é um peptídeo antimicrobiano rico em cisteína, originalmente descrito como um componente antimicrobiano da hemolinfa e dos ovos de carrapato bovino Rhipicephalus (Boophilus) microplus. Testes anteriores utilizando o modelo experimental mosquito Aedes aegypti infectado por Plasmodium gallinaceum mostraram que a microplusina é altamente tóxico para esporozoítas de Plasmodium gallinaceum em concentração relativamente baixa, sem apresentar toxicidade aos mosquitos vetores Aedes aegypti. Nosso objetivo foi analisar a expressão da microplusina e seu efeito na infecção de P. gallinaceum em mosquitos transgênicos. Obtivemos quatro linhagens através da integração de um transgene contendo a região promotora do gene da vitelogenina de Ae. aegypti, peptídeo sinal maltase-like I de Ae. aegypti e a sequência codificadora da microplusina (PMOS [3xP3-EGFP-AeVg Micro]). A atividade anti esporozoítas da microplusina expressa pelos mosquitos transgênicos mostrou diferença significante as linhagens. O desenho de novas moléculas utilizando como molde moléculas efetoras existentes e testadas, possibilitará o aperfeiçoamento da expressão de genes exógenos em mosquitos transgênicos, tornando-os refratários ao parasita. / Transmission of malaria parasites by mosquito vectors is dependent on the successful development of Plasmodium sp. infective forms, particularly the sporozoites, which are the forms that enter the vertebrate host. The genetic manipulation of mosquito vectors has been a strategy for malaria control. An extremely important component of this strategy is the effector molecule of choice which reduces parasite transmission. Microplusin is a cysteine-rich antimicrobial peptide originally described as an hemolymph and eggs antimicrobial component of the cattle tick Boophilus microplus. Previous tests using the experimental model Plasmodium gallinaceum infected Aedes aegypti showed that microplusin is highly toxic to P. gallinaceum sporozoites in relatively low concentration, without showing toxicity to the mosquito vector A. aegypti. Our goal was to analyze transgenic mosquitoes expressing microplusin and its effect on infection of P. gallinaceum. We obtained four lines through the integration of transgene that containing the promoter region of the A. aegypti vitelogenin gene, the maltase-like I signal peptide of A. aegypti and microplusin coding sequence (pMos[3xP3-EGFPAeVg-Micro]). The activity anti sporozoites microplusin expressed by transgenic mosquitoes showed significant differences between strains. The design of effector molecules using information from existing and tested molecules as template will enable the improvement of the expression of foreign genes in transgenic mosquitoes, making them resistant to the parasite.

The development of bio-resorbable implant materials is rapidly going on. Sterilization of those materials is inevitable to assure the hygienic requirements for critical medical devices according to the medical device directive (MDD, 93/42/EG). Biopolymer-containing biomaterials are often highly sensitive towards classical sterilization procedures like steam, ethylene oxide treatment or gamma irradiation. Supercritical CO2 (scCO2) treatment is a promising strategy for the terminal sterilization of sensitive biomaterials at low temperature. In combination with low amounts of additives scCO2 treatment effectively inactivates microorganisms including bacterial spores. We established a scCO2 sterilization procedure under addition of 0.25% water, 0.15% hydrogen peroxide and 0.5% acetic anhydride. The procedure was successfully tested for the inactivation of a wide panel of microorganisms including endospores of different bacterial species, vegetative cells of gram positive and negative bacteria including mycobacteria, fungi including yeast, and bacteriophages. For robust testing of the sterilization effect with regard to later application of implant materials sterilization all microorganisms were embedded in alginate/agarose cylinders that were used as Process Challenge Devices (PCD). These PCD served as surrogate models for bioresorbable 3D scaffolds. Furthermore, the impact of scCO2 sterilization on mechanical properties of polysaccharide-based hydrogels and collagen-based scaffolds was analyzed. The procedure was shown to be less compromising on mechanical and rheological properties compared to established low-temperature sterilization methods like gamma irradiation and ethylene oxide exposure as well as conventional steam sterilization. Cytocompatibility of alginate gels and scaffolds from mineralized collagen was compared after sterilization with ethylene oxide, gamma irradiation, steam sterilization and scCO2 treatment. Human mesenchymal stem cell viability and proliferation were not compromised by scCO2 treatment of these materials and scaffolds. We conclude that scCO2 sterilization under addition of water, hydrogen peroxide and acetic anhydride is a very effective, gentle, non-cytotoxic and thus a promising alternative sterilization method especially for biomaterials.

Thesis (PhD (Food Science))--University of Stellenbosch, 2009. / ENGLISH ABSTRACT: Species of Alicyclobacillus are acid-tolerant and heat-resistant bacteria that cause spoilage of heat-treated fruit juices stored at room temperature. During the past decade, Alicyclobacillus spp. have become a major cause of spoilage in pasteurised fruit juices leading to significant economic losses world-wide. Spoilage has been reported in apple, pear, orange, peach, mango and white grape juice, as well as in fruit juice blends, fruit juice containing drinks and tomato products, such as tomato juice and canned tomatoes. Spoilage is characterised by a medicinal smell and guaiacol production. These endospore-formers have been shown to survive pasteurisation conditions of 95 °C for 2 min, grow at temperatures between 25° and 60 °C and a pH range of 2.5 to 6.0. Knowledge of this organism is limited, both locally and internationally and the route of contamination to the final product is not well established. In this study the fruit concentrate processing environment was investigated as a potential source and route of contamination for the final product. Species of Alicyclobacillus were isolated from orchard soil, various stages during processing and from fruit juice and concentrates. The isolates were identified based on morpholological, biochemical and physiological properties. Identification to species level was done by 16S ribosomal RNA gene sequencing and strain differentiation by RAPD-PCR. Results indicate that species of A. acidoterrestris and Alicyclobacillus acidocaldarius were found in orchard soil and throughout the processing environment. This is the first report on the isolation of these species from orchard soil, vinegar flies and the fruit processing environment. The 16 isolates identified as A. acidoterrestris grouped into four clusters based on RAPD-PCR banding patterns, suggesting that they belong to at least four genotypic groups. Isolates from the fruit concentrate, wash water and soil located outside of the fruit processing plant grouped into one cluster. Concluded from these results, A. acidoterrestris found in the wash water and soil outside of the factory could act as a potential reservoir of organisms for the contamination of the final fruit concentrate. Thus good manufacturing practices play an essential role in controlling incidence of spoilage caused by these bacteria. Fruit juices can be treated using ultraviolet (UV-C) light with a wavelength of 254 nm, which has a germicidal effect against micro-organisms. Alicyclobacillus acidoterrestris spores were inoculated into tap water, used wash water from a fruit processing plant and grape juice concentrate. Ultraviolet dosage levels (J L−1) of 0, 61, 122, 183, 244, 305 and 367 were applied using a novel UV-C turbulent flow system. The UV treatment method was shown to reliably achieve in excess of a 4 log10 reduction (99.99%) per 0.5 kJ L-1 of UV-C dosage in all the liquids inoculated with A. acidoterrestris. The applied novel UV technology could serve as an alternative to thermal treatments of fruit juices for the inactivation of Alicyclobacillus spores or in the treatment of contaminated processing wash water. Finally, the thermal inactivation at 95 °C for two strains of A. acidoterrestris isolated from contaminated fruit juice concentrates were investigated in a 0.1% (m/v) peptone buffer solution (pH 7.04) and grape juice (pH 4.02, 15.5 °Brix). The thermal inactivation of A. acidoterrestris spores followed first-order kinetics, suggesting that as the microbial population is exposed to a specific high temperature, the spores inactivated at a constant rate. D-values determined in the buffer solution were calculated to be 1.92 min and 2.29 min, while in grape juice D-values were found to be 2.25 min and 2.58 min for the two strains tested. From this study it is clear that the D-value is dependant on the strain tested, but also on the soluble solids of the solution the cells are suspended in. The results indicated that the spores of A. acidoterrestris isolated from South African fruit juice concentrate may survive after the pasteurisation treatment commonly applied during manufacturing. / AFRIKAANSE OPSOMMING: Spesies van Alicyclobacillus is suur-tolerante en hittebestande bakterieë wat bederf veroorsaak in hitte-behandelde vrugtesappe wat teen kamertemperatuur gestoor word. Gedurende die afgelope dekade het Alicyclobacillus spp. ‘n belangrike oorsaak van bederf in gepasteuriseerde vrugtesappe geword en beduidende ekonomiese verliese wêreldwyd veroorsaak. Bederf is aangeteken in appel-, peer-, lemoen-, perske-, mango- en witdruiwesap, sowel as in vrugtesapversnitte, vrugtesapbevattende drankies en in tamatieprodukte soos tamatiesap en ingemaakte tamaties. Bederf word gekenmerk deur ’n medisinale reuk en guaiacol produksie. Daar is gevind dat hierdie endospoorvormers pasteurisasie teen 95 °C vir 2 min kan oorleef en kan groei by temperature tussen 25° en 60 °C en ‘n pH van 2.5 to 6.0. Plaaslik sowel as internasionaal is kennis van hierdie organisme beperk en die roete van kontaminasie van produkte is nog nie goed vasgestel nie. In hierdie studie is die vrugtekonsentraat-verwerkingsmilieu ondersoek as ‘n moontlike bron en roete van kontaminasie van die finale produk. Spesies van Alicyclobacillus is vanuit vrugteboordgrond, verskeie verwerkingstadia en van vrugtesap en vrugtesapkonsentraat geïsoleer. Die isolate is op grond van morfologiese, biochemiese en fisiologiese eienskappe geïdentifiseer. Identifikasie tot spesiesvlak is deur 16S rDNS sekwensering gedoen en stam differensiasie deur RAPD-PKR. Resultate het aangetoon dat A. acidoterrestris en A. acidocaldarius in vrugteboordgrond sowel as in alle stadia van die verwerkingsmilieu voorkom. Dit is die eerste verslag van die isolering van hierdie spesies uit die Suid-Afrikaanse vrugteverwerkingsmilieu, vrugteboordgrond en asynvlieë. Die 16 isolate, geïdentifiseer as A. acidoterrestris en in vier groepe geplaas op grond van hul RAPD-PKR bandpatrone, dui aan dat hulle aan minstens vier genotipiese groepe behoort. Isolate afkomstig van die vrugtekonsentraat, waswater en die grond buitekant die vrugteverwerkingsaanleg het een groep gevorm. Uit hierdie resultate kan afgelei word dat A. acidoterrestris, wat in die waswater en grond buite die aanleg voorkom, as ‘n moontlike bron van organismes vir die kontaminering van die finale vrugtekonsentraat kan dien. Goeie vervaardigingspraktyke speel dus ‘n noodsaaklike rol in die beheer van bederf veroorsaak deur hierdie bakterieë. Vrugtesappe kan behandel word met ultravioletlig (UV-C) met ‘n golflengte van 254 nm wat ‘n dodende effek op mikro-organismes het. Kraanwater, gebruikte waswater van ‘n vrugtesapvervaardigingsaanleg en druiwesapkonsentraat is met A. acidoterrestris spore geïnokuleer. Ultraviolet toedieningsvlakke (J L−1) van 0, 61, 122, 183, 244, 305 en 367 is aangewend met behulp van ‘n nuwe UV-C drukvloei stelsel. Daar is aangetoon dat die UV-behandelingsmetode ‘n betroubare vermindering (99.99%) van meer as 4 log10 per 0.5 kJ L-1 van ‘n UV-C dosis gee in al die vloeistowwe wat geïnokuleer is met A. acidoterrestris. Die toegepaste nuwe UV-tegnologie kan gebruik word as ‘n alternatief tot die hittebehandeling van vrugtesap vir die deaktivering van Alicyclobacillus spore of in die behandeling van gekontamineerde waswater. Ten slotte is hitte-deaktivering teen 95 °C van twee stamme van A. acidoterrestris, geïsoleer uit gekontamineerde vrugtesapkonsentraat, in ‘n 0.1% (m/v) peptoonbufferoplossing (pH 7.04) en druiwesap (pH 4.02, 15.5 °Brix), ondersoek. Die hitte-deaktivering van A. acidoterrestris spore het eerste-orde kinetika gevolg, wat aandui dat die mikrobe-populasie teen ‘n konstante tempo afsterf, wanneer blootgestel aan ‘n spesifieke hoë temperatuur. Die D-waardes in die bufferoplossing is bereken as 1.92 min en 2.29 min, terwyl daar gevind is dat die D-waardes in druiwesap 2.25 min en 2.58 min is vir die twee betrokke stamme. Vanuit hierdie studie is dit duidelik dat die D-waardes afhang van die betrokke stam, maar ook van die oplosbare vaste stowwe van die oplossing waarin die selle opgelos is. Die resultate dui daarop dat die spore van A. acidoterrestris, wat geïsoleer is uit Suid-Afrikaanse vrugtesapkonsentraat, die pasteurisasiebehandeling wat algemeen tydens vervaardiging toegepas word, kan oorleef. Aangesien die toepassing van strenger hittebehandeling om spore van A. acidoterrestris te deaktiveer onaanvaarbare organoleptiese veranderinge in die produk tot gevolg het, word dit aanbeveel dat die risiko van bederf verminder behoort te word deur die gebruik van goeie vervaardigingspraktyke gedurende vrugteverwerking.