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Journal articles on the topic 'Blood agar'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Feinsod, Fred M., and Chang H. Kim. "Goat Blood Agar." Tropical Doctor 16, no. 3 (1986): 117–19. http://dx.doi.org/10.1177/004947558601600307.

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2

Gil-Setas, A., A. Mazon, J. Alfaro, P. Idigoras, M. Drancourt, and D. Raoult. "Blood Agar, Chocolate Agar, and Mycobacterium tuberculosis." Journal of Clinical Microbiology 41, no. 8 (2003): 4008. http://dx.doi.org/10.1128/jcm.41.8.4008.2003.

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3

Asna, Shah Md Zahurul Haque, Mousumi Karmaker, and Una Jessica Sarker. "Brain Heart Infusion Agar : A Surrogate of Agar Blood." Bangladesh Journal of Medical Microbiology 12, no. 1 (2018): 24–26. http://dx.doi.org/10.3329/bjmm.v12i1.51688.

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Blood agar is needed for culture of various organisms. As sheep blood is needed for it’s preparation, many small laboratories specially those of rural areas can not prepare it due to difficulty in collection of sheep blood. So, either they do not do the culture or do it without blood agar which cause missing of some important organisms. In this study Brain heart infusion agar was used together with Blood agar to assess it’s efficacy as an alternative of Blood agar. In total 1256 various samples were cultured, on Blood agar , Brain heart Infusion agar and MacConkey agar. Out of 1256 samples 404

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4

Kelly, M. T., E. M. Stroh, and J. Jessop. "Comparison of blood agar, ampicillin blood agar, MacConkey-ampicillin-Tween agar, and modified cefsulodin-Irgasan-novobiocin agar for isolation of Aeromonas spp. from stool specimens." Journal of Clinical Microbiology 26, no. 9 (1988): 1738–40. http://dx.doi.org/10.1128/jcm.26.9.1738-1740.1988.

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5

Niederstebruch, Nils, Doris Sixt, Benard Isah Benda, and Nestor Banboye. "A suitable blood agar containing human blood especially for the use in laboratories of developing countries." Journal of Infection in Developing Countries 11, no. 05 (2017): 399. http://dx.doi.org/10.3855/jidc.8957.

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Introduction: In developed countries, blood agar containing defibrinated sheep or horse blood is a standard tool for the isolation of bacteria from clinical samples. Several issues prevent blood agar containing animal blood from being used in many developing countries. However, the use of easily available human blood for blood agar is discouraged because of the common tenet that human blood in nutrient media results in poor bacterial isolation rates and hardly visible hemolysis or no hemolysis at all. We have developed a reconfigured and easily applicable composition for blood agar containing

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6

Mauel, Michael J., Cynthia Ware, and Pedro A. Smith. "Culture ofPiscirickettsia salmonison enriched blood agar." Journal of Veterinary Diagnostic Investigation 20, no. 2 (2008): 213–14. http://dx.doi.org/10.1177/104063870802000211.

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7

C Jomol P, Prejish. "Defibrinated vs. Citrated Blood Agar: Assessing the Impact of Blood Form on Bacterial Growth and Morphology." International Journal of Science and Research (IJSR) 13, no. 4 (2024): 1083–88. http://dx.doi.org/10.21275/sr24410122713.

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8

NYE, K. J., D. FALLON, B. GEE, S. MESSER, R. E. WARREN, and N. ANDREWS. "A comparison of blood agar supplemented with NAD with plain blood agar and chocolated blood agar in the isolation of Streptococcus pneumoniae and Haemophilus influenzae from sputum." Journal of Medical Microbiology 48, no. 12 (1999): 1111–14. http://dx.doi.org/10.1099/00222615-48-12-1111.

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9

Novita, Rr Irma Dewi, and Indah Febrianti. "Pemanfaatan Penggunaan Darah Donor Yang Telah Kadaluwarsa Untuk Pembuatan Agar Darah Pada Pertumbuhan Staphylococcus aureus." Jurnal Pengelolaan Laboratorium Pendidikan 1, no. 2 (2019): 64–69. http://dx.doi.org/10.14710/jplp.1.2.64-69.

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The use of media so that sheep's blood for the growth of Staphylococcus aureus bacteria is still difficult to get the sheep's blood. Therefore, a way to find alternatives to sheep blood is sought, namely by using donor blood that has expired. In this study using blood agar media using blood donors and blood agar media using sheep blood as a control. Using a blood donor with a presentation of 4% and 5% of the colony diameter, zone of hemolysis, the color of the colony of Staphylococcus aureus is almost the same as supported grown in 4% sheep blood agar media. While 6%, 7% and 8% blood donors ar

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10

Anand, Chandar, Rhonda Gordon, Helene Shaw, Kevin Fonseca, and Merle Olsen. "Pig and Goat Blood as Substitutes for Sheep Blood in Blood-Supplemented Agar Media." Journal of Clinical Microbiology 38, no. 2 (2000): 591–94. http://dx.doi.org/10.1128/jcm.38.2.591-594.2000.

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In many developing countries sheep and horse blood, the recommended blood supplements in bacteriological media, are not readily available, whereas pig and goat blood are. Therefore, this study examined the use of pig and goat blood as potential substitutes for sheep blood in blood-supplemented bacteriologic media commonly used in clinical microbiology laboratories. In general, the growth characteristics and colony morphologies of a wide range of aerobic and anaerobic bacteria and Candida albicans were similar on media containing pig, goat, and sheep blood, although differences were found.Enter

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11

Moya-Salazar, Jeel, Liz Pio-Dávila, Alfonso Terán-Vásquez, and José Olivo-López. "Rendimiento diagnóstico del agar sangre con filtro versus agar karmali para el diagnóstico de Campylobacter en coprocultivo." Horizonte Médico (Lima) 16, no. 3 (2016): 58–65. http://dx.doi.org/10.24265/horizmed.2016.v16n3.09.

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12

Payne, Marie P., and Rebecca J. Morton. "Effect of Culture Media and Incubation Temperature on Growth of Selected Strains of Francisella Tularensis." Journal of Veterinary Diagnostic Investigation 4, no. 3 (1992): 264–69. http://dx.doi.org/10.1177/104063879200400307.

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The rate and amount of growth of 4 field isolates and reference strain ATCC 6223 of Francisella tularensis were evaluated on isolation media with 2 different agar bases and with different supplements and incubated at 25 C, 35 C, and 42 C. Biochemical reactions on conventional differential media with and without cysteine were evaluated. Two of the field isolates and the reference strain were F. tularensis subspecies tularensis (formerly biovar tularensis or Type A), and 2 isolates were subspecies holarctica (formerly subspecies palaearctica or Type B). Bacto cystine heart blood agar supplemente

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13

Filthuth, I., S. Emler, E. Jacobs, and R. Auckenthaler. "Isolation ofMycoplasma hominis on CDC anaerobic blood agar." European Journal of Clinical Microbiology & Infectious Diseases 15, no. 11 (1996): 896–97. http://dx.doi.org/10.1007/bf01691229.

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14

HOGAN, J. S., J. W. PANKEY, P. MURDOUGH, and D. B. HOWARD. "Survey of Bulk Tank Milk using Blood-Esculin Agar Counts1." Journal of Food Protection 49, no. 12 (1986): 990–93. http://dx.doi.org/10.4315/0362-028x-49.12.990.

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Milk from bulk tanks of 2,931 dairy herds were sampled and evaluated using trypticase blood-esculin agar, somatic cell, standard plate and preliminary incubation counts. Percent samples with trypticase blood-esculin agar counts &gt;1 × 102 colony forming units/ml by organisms were Staphylococcus aureus, 33; Staphylococcus spp., 84; Streptococcus agalactiae, 47; esculin-positive streptococci, 72; coliforms, 73; and other microbes, 89. Trypticase blood-esculin agar counts were useful for identifying primary bacterial contaminants. Correlations were low between trypticase blood-esculin agar c

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15

Sethi, Sunil, Shreya Singh, SurinderSingh Banga, et al. "Revisiting blood agar for the isolation of Neisseria gonorrhoeae." Indian Journal of Sexually Transmitted Diseases and AIDS 41, no. 2 (2020): 221. http://dx.doi.org/10.4103/ijstd.ijstd_51_18.

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16

Drancourt, Michel, and Didier Raoult. "Cost-Effectiveness of Blood Agar for Isolation of Mycobacteria." PLoS Neglected Tropical Diseases 1, no. 2 (2007): e83. http://dx.doi.org/10.1371/journal.pntd.0000083.

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17

Muniaraj, M., A. K. Gupta, S. Narayan, D. Singh, P. K. Sinha, and P. Das. "Long-term preservation ofLeishmania donovanipromastigotes on blood-agar slants." Annals of Tropical Medicine & Parasitology 100, no. 2 (2006): 173–75. http://dx.doi.org/10.1179/136485906x86257.

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18

Nahar, S. Gul, M. Bulbul Hasan, Mst Rokeya Khatun, M. Nawshad Ali, and DK Mohanta. "Chromogenic Agar Medium : A Versatile Tool for the Diagnosis of UTI." TAJ: Journal of Teachers Association 25 (November 28, 2018): 64–71. http://dx.doi.org/10.3329/taj.v25i0.37561.

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Objective: The present study was done on Chromogenic agar media to identify uropathogens more efficiently by its characteristic colony colour for each of the organism.Methodology: A total 300 sample were collected from Rajshahi Medical College Hospital, Bangladesh. Urine samples of the suspected UTI cases, showing pus cells >5/HPF on microscopic examination were included for urine culture simultaneously onto Chromogenic agar media, Blood agar and MacConkey agar media.Results: Culture yielded 139 (46.33%) bacterial growth among them, 133 (44.33%) showed single organism and remaining 06 (2.00

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19

Monsen, T., S. Persson, H. Edebro, S. Granström, and J. Wiström. "Mueller–Hinton agar is superior to PDM blood agar for detection of methicillin-resistant Staphylococcus aureus." Clinical Microbiology and Infection 9, no. 1 (2003): 61–64. http://dx.doi.org/10.1046/j.1469-0691.2003.00462.x.

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20

Russell, F. M., S. S. N. Biribo, G. Selvaraj, et al. "As a Bacterial Culture Medium, Citrated Sheep Blood Agar Is a Practical Alternative to Citrated Human Blood Agar in Laboratories of Developing Countries." Journal of Clinical Microbiology 44, no. 9 (2006): 3346–51. http://dx.doi.org/10.1128/jcm.02631-05.

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21

Gardam, M. A., and M. A. Miller. "Optochin Revisited: Defining the Optimal Type of Blood Agar for Presumptive Identification of Streptococcus pneumoniae." Journal of Clinical Microbiology 36, no. 3 (1998): 833–34. http://dx.doi.org/10.1128/jcm.36.3.833-834.1998.

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To determine the optimal media for optochin susceptibility testing of Streptococcus pneumoniae, we measured inhibition zones for 72 S. pneumoniae and 22 Streptococcus viridans isolates on three blood-containing media. Because 15.3, 0, and 22.2% of S. pneumoniae organisms were misidentified on Columbia agar, Trypticase soy agar (TSA), and Mueller-Hinton agar, respectively, each containing sheep blood, we recommend that TSA-sheep blood agar be used.

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22

Hoppe, Jörg E., Anton Haug, and Konrad Botzenhart. "Bordetellae and Charcoal Horse Blood Agar: Inactivation of Antibiotics in Agar during Prolonged Incubation for Susceptibility Testing." Chemotherapy 34, no. 1 (1988): 36–39. http://dx.doi.org/10.1159/000238545.

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23

TAKAHASHI, Masami, Eiichi YOSHIDA, Shigemi TERAKUBO, and Atsushi TERADA. "Diffuse growth of strains of Acinetobacter calcoaceticus on blood agar and their motility digging soft-agar medium." Nippon Saikingaku Zasshi 41, no. 4 (1986): 721–26. http://dx.doi.org/10.3412/jsb.41.721.

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24

Nahar, S. Gul, M. Bulbul Hasan, Mst Rokeya Khatun, and M. Nawshad Ali. "Comparative Study of Hicrome Agar Medium with Conventional Culture System for the Isolation of Uropathogens." TAJ: Journal of Teachers Association 24, no. 2 (2018): 128–35. http://dx.doi.org/10.3329/taj.v24i2.37542.

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Objective: The present study was done to compare the performance of chromogenic agar medium and conventional culture media for the isolation and presumptive identification of uropathogen.Methodology: A total 300 sample were collected from Rajshahi Medical College Hospital, Bangladesh during January to June, 2008. Urine samples of the suspected UTI cases, showing pus cells >5/HPF on microscopic examination were included for urine culture simultaneously onto 2 conventional media (Blood agar and MacConkey agar) and chromogenic agar medium (HiCrome UTI agar medium). Results: Culture yielded 139

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25

Arimi, S. M., R. W. A. Park, and C. R. Fricker. "Study of haemolytic activity of someCampylobacterspp. on blood agar plates." Journal of Applied Bacteriology 69, no. 3 (1990): 384–89. http://dx.doi.org/10.1111/j.1365-2672.1990.tb01528.x.

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26

Drancourt, M., P. Carrieri, M. J. Gevaudan, and D. Raoult. "Blood Agar and Mycobacterium tuberculosis: the End of a Dogma." Journal of Clinical Microbiology 41, no. 4 (2003): 1710–11. http://dx.doi.org/10.1128/jcm.41.4.1710-1711.2003.

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27

Drancourt, M., M. J. Gévaudan, C. Truffot, and V. Jarlier. "Growth on blood agar discriminates Mycobacterium avium and Mycobacterium intracellulare." Clinical Microbiology and Infection 9, no. 10 (2003): 1028–30. http://dx.doi.org/10.1046/j.1469-0691.2003.00706.x.

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28

Kolasinac, Sabina Sibcic, Lars Moe, Vibeke Rootwelt, and Henning Sørum. "Bacteria in Normal Canine Milk Analyzed by Blood Agar Medium." Animals 13, no. 13 (2023): 2206. http://dx.doi.org/10.3390/ani13132206.

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Studies of microbiota in normal canine milk from healthy dams are sparse. As is the case with blood and urine, it was considered that milk contains no microbiota. Any discovery of bacteria in canine milk is, therefore, often noted to be a result of contamination during sampling or interpreted as mastitis and treated with antibiotics. Milk was collected twice within 19 days after natural parturition from 11 lactating dams, with no general or local clinical signs of mastitis or other disease. The skin and teats were prepared with an antimicrobial protocol prior to each milk sampling. In total, 2

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29

Fawcett, Paul T., Kathleen M. Gibney, and Kathleen M. B. Vinette. "Helicobacter pylori Can Be Induced To Assume the Morphology of Helicobacter heilmannii." Journal of Clinical Microbiology 37, no. 4 (1999): 1045–48. http://dx.doi.org/10.1128/jcm.37.4.1045-1048.1999.

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Cultures of Helicobacter pylori obtained from the American Type Culture Collection (strain 43504) were grown as isolated colonies or lawns on blood agar plates and in broth culture with constant shaking. Examination of bacterial growth with Gram-stained fixed preparation and differential interference contrast microscopy on wet preparations revealed that bacteria grown on blood agar plates had a morphology consistent with that normally reported for H. pylori whereas bacteria from broth cultures had the morphologic appearance of Helicobacter heilmannii. Bacteria harvested from blood agar plates

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30

Valdez, Yanet, Billie Velapatiño, Robert H. Gilman, Vilma Gutierrez, and Carlos León. "Antimicrobial Susceptibility of Helicobacter pylori Determined by the E Test Using Tetrazolium Egg Yolk Agar." Journal of Clinical Microbiology 36, no. 9 (1998): 2784–85. http://dx.doi.org/10.1128/jcm.36.9.2784-2785.1998.

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Metronidazole and tetracycline E tests were compared to an agar dilution method for the antimicrobial susceptibility testing ofHelicobacter pylori. Sixteen strains were tested by using tetrazolium egg yolk (TEY) agar. The characteristic E test inhibition ellipse was clearer on TEY agar than on standard blood agar and gave results comparable to those of the agar dilution test. The use of TEY medium is preferable to that of blood agar medium in E test MIC determinations for H. pylori.

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31

Niederstebruch, N., and D. Sixt. "Standard Nutrient Agar 1 as a substitute for blood-supplemented Müller–Hinton agar for antibiograms in developing countries." European Journal of Clinical Microbiology & Infectious Diseases 32, no. 2 (2012): 237–41. http://dx.doi.org/10.1007/s10096-012-1735-2.

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32

Maulana, Mochamad Rizal, та Maseva Wijayanti. "Kualitas Media Agar Darah Manusia dan Domba pada Pertumbuhan Streptococcus β hemolyticus". Borneo Journal of Medical Laboratory Technology 5, № 2 (2023): 320–24. http://dx.doi.org/10.33084/bjmlt.v5i2.4898.

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Sheep blood agar (ADD) is a growth medium for identifying pathogenic bacteria and is a standard medium for microbiological examination. Some countries experience difficulties multiplying ADD due to several factors, so another alternative is needed: using human blood agar (ADM) as a substitute. This study examines the feasibility of ADM as an alternative medium to replace ADD in growing Streptococcus β hemolyticus. This study used sheep and human blood agar, which were then observed at 24 and 48 hours of incubation to show differences in hemolysis in diameter. At 24 hours, the average hemolytic

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33

Farah, Tufail Hafiz Maqbool Ahmed Waqas Inayat. "THE SENSE OF DISTRIBUTION OF STAPHYLOCOCCUS AUREUS, ITS CHRACTRISTICS ON NUTRIENT AGAR, MANNITOL SALT AGAR, STEPH-110 MEDIUM AND BLOOD AGAR AND THEIR HEMOLYTIC PROPERTIES." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 10 (2018): 10464–75. https://doi.org/10.5281/zenodo.1467699.

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<em>Microorganisms, which are largely found in our environment, play an important role in stabilizing ecosystems such as primary energy and basic cycle. Microorganisms are everywhere like sea salts, high air pressure, very high and low temperatures. They are abundant in highly contaminated areas due to resistance. These organisms can be classified by ordinary carbon and energy sources converted into amino acids, starches, nucleotides, vitamins and different oils. Catalysts are mechanically extracted from microbes to perform different metabolic processes that are present in the world, and their

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34

Henriksen, S. D. "PASTEURELLA HAEMOLYTICA VAR. UREAE Action on Blood Agar and Serological Reactions." Acta Pathologica Microbiologica Scandinavica 53, no. 4 (2009): 425–29. http://dx.doi.org/10.1111/j.1699-0463.1961.tb00426.x.

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35

Payment, P., E. Coffin, and G. Paquette. "Blood agar to detect virulence factors in tap water heterotrophic bacteria." Applied and Environmental Microbiology 60, no. 4 (1994): 1179–83. http://dx.doi.org/10.1128/aem.60.4.1179-1183.1994.

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36

Oktari, A., N. Vanawati, and U. I. Kurniawati. "The optimization of Human Blood Agar (HBA) for Streptococcus pneumonia growth." Journal of Physics: Conference Series 1280 (November 2019): 022002. http://dx.doi.org/10.1088/1742-6596/1280/2/022002.

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37

Stjernquist-Desatnik, ANNA, DAYA N. Kurl, and POUL Christensen. "REPEATED PASSAGE OF FRESHLY ISOLATED GROUP A STREPTOCOCCI ON BLOOD AGAR." Acta Pathologica Microbiologica Scandinavica Series B: Microbiology 94B, no. 1-6 (2009): 405–8. http://dx.doi.org/10.1111/j.1699-0463.1986.tb03075.x.

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38

Coban, A. Y., K. Bilgin, M. Uzun, et al. "Susceptibilities of Mycobacterium tuberculosis to Isoniazid and Rifampin on Blood Agar." Journal of Clinical Microbiology 43, no. 4 (2005): 1930–31. http://dx.doi.org/10.1128/jcm.43.4.1930-1931.2005.

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39

Bellon, J., B. Weise, G. Verschraegen, and M. De Meyere. "Selective streptococcal agar versus blood agar for detection of group A beta-hemolytic streptococci in patients with acute pharyngitis." Journal of Clinical Microbiology 29, no. 9 (1991): 2084–85. http://dx.doi.org/10.1128/jcm.29.9.2084-2085.1991.

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40

ISHII, Eiji, and Teruhiko KISHI. "Differences in Susceptibility of Helicobacter pylori to Macrolide and Other Antibiotics in Tests Using Blood Agar and Albumin Agar." Journal of the Japanese Association for Infectious Diseases 67, no. 2 (1993): 137–42. http://dx.doi.org/10.11150/kansenshogakuzasshi1970.67.137.

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41

Bale, Martha J., Carol Yang, and Michael A. Pfaller. "Evaluation of growth characteristics on blood agar and eosin methylene blue agar for the identification of Candida (Torulopsis) glabrata." Diagnostic Microbiology and Infectious Disease 28, no. 2 (1997): 65–67. http://dx.doi.org/10.1016/s0732-8893(97)00009-6.

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42

Reddy, Ashok Kumar, Upputuri Brahmaiah, Nitesh Narayen, et al. "Is blood agar an alternative to sabouraud dextrose agar for the isolation of fungi in patients with mycotic keratitis." International Ophthalmology 33, no. 3 (2012): 251–54. http://dx.doi.org/10.1007/s10792-012-9683-5.

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AlRubaye, AbdulRahman, and Amina N. Al-Thwaini. "Advancements in Helicobacter pylori: A Novel Culture AA-Medium for Helicobacter pylori Detection." Technium BioChemMed 8 (June 5, 2024): 83–90. http://dx.doi.org/10.47577/biochemmed.v8i.10790.

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This research provides crucial insights into the detection and culturing of Helicobacter pylori, a significant pathogen associated with gastric diseases. New culture media were prepared as X1, X2 and X3 in comparison with Columbia blood agar. Culturing success varied between Columbia blood agar and the novel X1-media which named as AA-media, while it failed on X2-media and X3-media. 48.8% of the positive samples were successfully cultured on Columbia blood agar and AA-media. Remarkably, colonies on AA-media displayed larger and distinct features within the first 24 hours, a stage achieved on C

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Gong, Yanshan, Yongsheng Yang, Yan Chen, et al. "Characterization of the hemolytic activity of Riemerella anatipestifer." Microbiology 166, no. 5 (2020): 436–39. http://dx.doi.org/10.1099/mic.0.000896.

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Riemerella anatipestifer infection causes serious economic losses in the duck industry worldwide. Acute septicemia and high blood bacterial loading in R. anatipestifer infected ducks indicate that R. anatipestifer may be able to obtain iron and other nutrients by lysing duck erythrocytes to support its rapid growth and proliferation in the blood. However, so far, little is known about the hemolytic activity of R. anatipestifer to duck erythrocytes. In this study, 29 of 52 R . anatipestifer strains showed hemolytic activity on duck blood agar, whereas all the tested dba+ (with hemolytic activit

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Puschner, Birgit, Marguerite M. Basso, and Thomas W. Graham. "Thallium toxicosis in a dog consequent to ingestion of Mycoplasma agar plates." Journal of Veterinary Diagnostic Investigation 24, no. 1 (2011): 227–30. http://dx.doi.org/10.1177/1040638711425941.

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A 1-year-old dog ingested a mixture of blood agar and Mycoplasma agar plates. The Mycoplasma agar plates contained thallium acetate, which resulted in an estimated minimum dose of 5 mg thallium acetate/kg bodyweight. Clinical signs over the course of 2–3 weeks included vomiting, diarrhea, weight loss, alopecia, dysphonia, ataxia, paresthesia, intension tremors, megaesophagus with subsequent aspiration pneumonia, and several seizure episodes. The dog was treated with intravenous fluids and placement of a gastric feeding tube. Thallium concentrations in hair were 8.2 µg/g in samples taken on day

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46

Kargaltseva, N. M., V. I. Kocherovets, A. Yu Mironov, and O. Yu Borisova. "BRAIN-HEART MEDIA FOR BLOOD CULTURES." Russian Clinical Laboratory Diagnostics 65, no. 6 (2020): 375–81. http://dx.doi.org/10.18821/0869-2084-2020-65-6-375-381.

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When diagnosing bloodstream infection (BI) the culture medium is the basis for growth of microorganisms and obtaining the blood culture. Pancreatic digest from fish meal is the basis of all culture media in Russia. In European countries brain-heart media (BHM) are used for detecting microorganisms in blood. In Russia BHM is not produced. The aim is to work out the formulation and the way of the BHM (broth and agar) preparation in order to improve the efficiency of obtaining blood culture. There were defined the physical and chemical indices and biological parameters of the BHM. The microbiolog

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NYE, K. J., D. FALLON, B. GEE, et al. "A comparison of the performance of bacitracin-incorporated chocolate blood agar with chocolate blood agar plus a bacitracin disk in the isolation of Haemophilus influenzae from sputum." Journal of Medical Microbiology 50, no. 5 (2001): 472–75. http://dx.doi.org/10.1099/0022-1317-50-5-472.

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48

Aydın, Elif, and Özkan Yener. "Identification of Enterococci in MALDI-TOF MS by Comparison with Slanetz and Bartley and Blood Agar Media." Flora the Journal of Infectious Diseases and Clinical Microbiology 28, no. 1 (2023): 87–93. http://dx.doi.org/10.5578/flora.20239908.

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Introduction: Matrix assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) has been used frequently in the last decade as a fast and reliable method for the identification of microorganisms. The fact that only one gram-negative selective medium is recommended in this method causes problems in the diagnosis. There is no information in the scientific literature that Slanetz and Bartley (SB) agar used in the study can be used in MALDI-TOF MS to identify bacteria. Materials and Methods: In this study, it was aimed to compare the identification performance of enteroco

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Hornitzky, M. A. Z., and P. J. Nicholls. "J Medium is Superior to Sheep Blood Agar and Brain Heart Infusion Agar for the Isolation ofBacillus Larvaefrom Honey Samples." Journal of Apicultural Research 32, no. 1 (1993): 51–52. http://dx.doi.org/10.1080/00218839.1993.11101287.

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Niederstebruch, N., and D. Sixt. "Erratum to: Standard Nutrient Agar 1 as a substitute for blood-supplemented Müller–Hinton agar for antibiograms in developing countries." European Journal of Clinical Microbiology & Infectious Diseases 32, no. 2 (2012): 243. http://dx.doi.org/10.1007/s10096-012-1792-6.

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