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RESEARCH POSTER PRESENTATION DESIGN © 2012 www.PosterPresentations.com QUICK START (cont.) How to change the template color theme You can easily change the color theme of your poster by going to the DESIGN menu, click on COLORS, and choose the color theme of your choice. You can also create your own color theme. You can also manually change the color of your background by going to VIEW > SLIDE MASTER. After you finish working on the master be sure to go to VIEW > NORMAL to continue working on your poster. How to add Text The template comes with a number of pre- formatted placeholders for headers and text blocks. You can add more blocks by copying and pasting the existing ones or by adding a text box from the HOME menu. Text size Adjust the size of your text based on how much content you have to present. The default template text offers a good starting point. Follow the conference requirements. How to add Tables To add a table from scratch go to the INSERT menu and click on TABLE. 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Go to PosterPresentations.com and click on the FB icon. © 2013 PosterPresentations.com 2117 Fourth Street, Unit C Berkeley CA 94710 posterpresenter@gmail.com (—THIS SIDEBAR DOES NOT PRINT—) DESIGN GUIDE This PowerPoint 2007 template produces a 36”x48” presentation poster. You can use it to create your research poster and save valuable time placing titles, subtitles, text, and graphics. We provide a series of online tutorials that will guide you through the poster design process and answer your poster production questions. To view our template tutorials, go online to PosterPresentations.com and click on HELP DESK. When you are ready to print your poster, go online to PosterPresentations.com Need assistance? Call us at 1.510.649.3001 QUICK START Zoom in and out As you work on your poster zoom in and out to the level that is more comfortable to you. Go to VIEW > ZOOM. Title, Authors, and Affiliations Start designing your poster by adding the title, the names of the authors, and the affiliated institutions. You can type or paste text into the provided boxes. The template will automatically adjust the size of your text to fit the title box. You can manually override this feature and change the size of your text. TIP: The font size of your title should be bigger than your name(s) and institution name(s). Adding Logos / Seals Most often, logos are added on each side of the title. You can insert a logo by dragging and dropping it from your desktop, copy and paste or by going to INSERT > PICTURES. Logos taken from web sites are likely to be low quality when printed. Zoom it at 100% to see what the logo will look like on the final poster and make any necessary adjustments. TIP: See if your school’s logo is available on our free poster templates page. Photographs / Graphics You can add images by dragging and dropping from your desktop, copy and paste, or by going to INSERT > PICTURES. Resize images proportionally by holding down the SHIFT key and dragging one of the corner handles. For a professional-looking poster, do not distort your images by enlarging them disproportionally. Image Quality Check Zoom in and look at your images at 100% magnification. If they look good they will print well. ORIGINAL DISTORTED Corner handles Good printing quality Bad printing quality Vibrio are bacteria species commonly found in estuaries, brackish waters and other marine communities. V. vulnificus, V. cholerae and V. parahaemolyticus are the three potentially pathogenic species of vibrio that were studied. The pathogenic strains of V. cholerae can cause the disease cholera, and the pathogenic strains of V. parahaemolyticus can cause gastrointestinal illness or septicemia. Pathogenic V. vulnificus strains cause infections that can be life threatening and have a mortality rate from 15% or 50% if the infection progresses into septicemia. V. vulnificus can be contracted through ingestion of raw seafood or though exposure to an open wound. Microbiology techniques are used to isolate the Vibrio strains and to confirm their species and the potential pathogenicity of the isolate. Introduction and Background Abstract The sampling and isolation process begins by a “surveillance” of two sampling sites in the Great Bay estuary of New Hampshire: Oyster River and Nannie Island. The two sites are sampled during low tide. Figure 2. Map of Great Bay Grab sample and hydrographic profile readings are recorded at both sites. This includes the depth, temperature, salinity, pH, dissolved oxygen (DO) concentration and DO %Saturation. Oyster, water, sediment and plankton (phytoplankton and zooplankton) are sampled from both sites. Once the samples are gathered they then proceed through a “pipeline” process back at the lab. Serial dilutions are made of each of the samples collected from both sites in alkaline peptone water. Then MPN (most probable number) dilutions are made of each in triplicate. They are then incubated over night. To proceed in the pipeline process the dilutions that show any form of turbidity are then streaked onto ChromVibrio Agar for isolation. This media is selective and differential for Vibrio species. Any Vv and Vc growth is indicated as blue and Vp grows as purple colonies. Both blue and purple isolated colonies are then moved on to tryptic soy agar (TSA), a nutrient rich media and incubated overnight. Then isolated colonies are moved to heart infusion broth (HI), another nutrient rich media, and incubated overnight for supplemental growth. Lysates are made from each isolate and run through PCR (Bio- Rad T100 Thermal Cycler) for DNA gene amplification. This tests for the presence of species identifying and possible virulence genes. Gel electrophoresis is run to visualize and confirm the presence, or lack of, any amplified genes. Materials and Methods During the 2015 summer there were 220 positive Vibrio isolates: 83.2 % were Vp Positive 15.9 % were Vv Positive 0.9 % were Vc Positive Results Future Works Isolates will be used for more in-depth analyses for multiple projects in the Vibrio research center at UNH. Vv isolates will be sent to Keene State College to be further analyzed. Vv isolates will be categorized phenotypically and genetically at KSC. References Bross, Michael, Kathleen Soch, Robert Moarales, and Rayford Mitchell, "Vibrio vulnificus Infection: Diagnosis and Treatment." Am Fam Physician. 76.4 (2007): 539-44. Web. 29 July 2015. Centers for Disease Control and Prevention. Centers for Disease Control and Prevention, 21 Oct. 2013. Web. 30 July 2015. Richardson, Tom. SAT of Great Bay. Digital image. NewEnglandBoating.com. N.p., 21 Oct. 2010. Web. 30 July 2015. Lemire, Astrid, David Goudenège, Typhaine Versigny, Bruno Petton, Alexandra Calteau, Yannick Labreuche, and Frédérique Le Roux. "Populations, Not Clones, Are the Unit of Vibrio Pathogenesis in Naturally Infected Oysters." The ISME Journal ISME J 9.7 (2014): 1523-531. Web Muller, Wesley. "Hancock Shrimper Says His Days on the Water Are over after Vibrio Infection." The Sun Herald. N.p., 21 July 2015. Web. 25 July 2015. Acknowledgments This research was supported by the National Science Foundations Grant to NH EPSCoR #1330641 A special thanks to Kari Hartman, Jackie Lemaire, Liz Deyett and Meg Hartwick. Vibrio species are bacteria found in coastal marine waters that can be harmful to humans if pathogenic strains of the bacteria are contracted. In particular, there are three species that cause health problems in people, Vibrio vulnificus (Vv), Vibrio cholerae (Vc) and Vibrio parahaemolyticus (Vp). Each of these species cause different medical issues, with V. vulnificus being the most detrimental of these species. The ultimate goal of studying these bacteria is to discover why they have become more prominent in local waters in recent years, by monitoring bacterial levels and environmental parameters that may affect levels. We study these bacteria by isolating them to determine the species and to test isolated strains for potential pathogenicity. Over the course of the 2015 field season, samples collected from Great Bay included oysters, sediment, plankton and water. The overwhelming majority of the species that were isolated and positively confirmed through polymerase chain reaction (PCR) assays and gel electrophoresis was V. parahaemolyticus, followed by V. vulnificus, and lastly very few V. cholerae isolates. The V. vulnificus isolates that were positive for having the species identifying gene vvh were additionally tested for a potential pathogenicity gene, viu-b, but all were found to be negative. Department of Biological Sciences, University of New Hampshire Katherine Kiley, Dr. Steve Jones, Dr. Steven Hale Isolation and Confirmation of Vibrio Species All positive V. vulnificus isolates were tested using the vui-B primer for the pathogenic virulence factor gene. All the Vv isolates tested negative for the possible pathogenicity gene viu-B. Figure 3. ChromVibrio Agar plates streaked with Vibrio bacteria Figure 1. Field Work Figure 4. !.2% Agarose Gel Figure 3. Graph of Vibrio Isolates
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