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Journal articles on the topic 'Ostriches – Immunology'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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1

Perelman, B., A. Gur‐Lavie, and Y. Samberg. "Pox in ostriches." Avian Pathology 17, no. 3 (January 1988): 735–39. http://dx.doi.org/10.1080/03079458808436491.

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2

Perelman, B., and E. S. Kuttin. "Aspergillosis in ostriches." Avian Pathology 21, no. 1 (January 1992): 159–63. http://dx.doi.org/10.1080/03079459208418830.

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3

Perelman, B., and E. Kuttin. "Zygomycosis in ostriches." Avian Pathology 21, no. 4 (December 1992): 675–80. http://dx.doi.org/10.1080/03079459208418889.

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4

Jardine, J. E., and D. J. Verwoerd. "Pancreatic cryptosporidiosis in ostriches." Avian Pathology 26, no. 3 (September 1997): 665–70. http://dx.doi.org/10.1080/03079459708419243.

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5

El-Attrache, J., P. Villegas, B. O'Connor, J. R. Buhr, and G. N. Rowland. "Adenovirus Pathogenicity in Immature Ostriches." Avian Diseases 45, no. 2 (April 2001): 442. http://dx.doi.org/10.2307/1592985.

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6

Allwright, D. M., M. Wilson, and W. J. J. vanRensburg. "Botulism in ostriches (Struthio camelus)." Avian Pathology 23, no. 1 (March 1994): 183–86. http://dx.doi.org/10.1080/03079459408418987.

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7

Perelman, B., and E. S. Kuttin. "Parsley‐induced photosensitivity in ostriches and ducks." Avian Pathology 17, no. 1 (January 1988): 183–92. http://dx.doi.org/10.1080/03079458808436437.

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8

Wings, Oliver, and P. Martin Sander. "No gastric mill in sauropod dinosaurs: new evidence from analysis of gastrolith mass and function in ostriches." Proceedings of the Royal Society B: Biological Sciences 274, no. 1610 (December 19, 2006): 635–40. http://dx.doi.org/10.1098/rspb.2006.3763.

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Polished pebbles occasionally found within skeletons of giant herbivorous sauropod dinosaurs are very likely to be gastroliths (stomach stones). Here, we show that based on feeding experiments with ostriches and comparative data for relative gastrolith mass in birds, sauropod gastroliths do not represent the remains of an avian-style gastric mill. Feeding experiments with farm ostriches showed that bird gastroliths experience fast abrasion in the gizzard and do not develop a polish. Relative gastrolith mass in sauropods (gastrolith mass much less than 0.1% of body mass) is at least an order of magnitude less than that in ostriches and other herbivorous birds (gastrolith mass approximates 1% of body mass), also arguing against the presence of a gastric mill in sauropods. Sauropod dinosaurs possibly compensated for their limited oral processing and gastric trituration capabilities by greatly increasing food retention time in the digestive system. Gastrolith clusters of some derived theropod dinosaurs (oviraptorosaurs and ornithomimosaurs) compare well with those of birds, suggesting that the gastric mill evolved in the avian stem lineage.
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9

Abolnik, Celia, Adriaan Olivier, Chevonne Reynolds, Dominic Henry, Graeme Cumming, Dionne Rauff, Marco Romito, Deryn Petty, and Claudia Falch. "Susceptibility and Status of Avian Influenza in Ostriches." Avian Diseases 60, no. 1s (February 10, 2016): 286. http://dx.doi.org/10.1637/11110-042815-reg.

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10

Woolcock, P. R., J. D. Moore, M. D. McFarland, and B. Panigrahy. "Isolation of Paramyxovirus Serotype 7 from Ostriches (Struthio camelus)." Avian Diseases 40, no. 4 (October 1996): 945. http://dx.doi.org/10.2307/1592323.

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11

Allwright, D. M., W. P. Burger, Adelaide Geyer, and A. W. Terblanche. "Isolation of an influenza A virus from ostriches (Struthio camelus)." Avian Pathology 22, no. 1 (March 1993): 59–65. http://dx.doi.org/10.1080/03079459308418900.

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12

de Sousa, Ricardo Luiz Moro, Helio José Montassier, and Aramis Augusto Pinto. "Detection and Quantification of Antibodies to Newcastle Disease Virus in Ostrich and Rhea Sera Using a Liquid Phase Blocking Enzyme-Linked Immunosorbent Assay." Clinical Diagnostic Laboratory Immunology 7, no. 6 (November 1, 2000): 940–44. http://dx.doi.org/10.1128/cdli.7.6.940-944.2000.

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ABSTRACT A liquid phase blocking ELISA (LPB-ELISA) was adapted for the detection and quantification of antibodies to Newcastle disease virus. Sera from vaccinated and unvaccinated commercial flocks of ostriches (Struthio camelus) and rheas (Rhea americana) were tested. The purified and nonpurified virus used as the antigen and the capture and detector antibodies were prepared and standardized for this purpose. The hemagglutination-inhibition (HI) test was regarded as the reference method. The cutoff point for the LPB-ELISA was determined by a two-graph receiver operating characteristic analysis. The LPB-ELISA titers regressed significantly (P < 0.0001) on the HI titers with a high correlation coefficient (r = 0.875). The two tests showed good agreement (κ = 0.82; P < 0.0001), relative sensitivity (90.91%) and specificity (91.18%), and accuracy (91.02%), suggesting that they are interchangeable.
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13

Herráez, P., F. Rodríguez, A. Espinosa de los Monteros, B. Acosta, J. R. Jaber, J. Castellano, and A. Castro. "Fibrino-Necrotic Typhlitis Caused by Escherichia fergusonii in Ostriches (Struthio camelus)." Avian Diseases 49, no. 1 (March 2005): 167–69. http://dx.doi.org/10.1637/7221-061104r.

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14

Kelly, Pamela, Hanne Jahns, Eugene Power, John Bainbridge, Kevin Kenny, Juan M. Corpa, Joseph P. Cassidy, and John J. Callanan. "Mycobacteriosis in Ostriches (Struthio camelus) due to Infection withMycobacterium bovisandMycobacterium aviumComplex." Avian Diseases 57, no. 4 (December 2013): 808–11. http://dx.doi.org/10.1637/10581-052313-case.1.

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15

Yüksek, Nazmi, Zahid Agaoglu, Abdullah Kaya, Logman Aslan, Hidayet Metin Erdoğan, and Yakup Akgul. "Stomach Impaction in Ostriches (Struthio camelus): Blood Chemistry, Hematology, and Treatment." Avian Diseases 46, no. 3 (July 2002): 757–60. http://dx.doi.org/10.1637/0005-2086(2002)046[0757:siiosc]2.0.co;2.

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16

Mushi, E. Z., J. F. W. Isa, R. G. Chabo, M. G. Binta, L. Modisa, and J. M. Kamau. "Impaction of the Stomachs in Farmed Ostriches (Struthio camelus) in Botswana." Avian Diseases 42, no. 3 (July 1998): 597. http://dx.doi.org/10.2307/1592688.

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17

Samberg, Y., D. U. Hadash, B. Perelman, and M. Meroz. "Newcastle disease in ostriches (Struthio camelus): Field case and experimental infection." Avian Pathology 18, no. 2 (April 1989): 221–26. http://dx.doi.org/10.1080/03079458908418597.

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18

Levy, A., B. Perelman, M. V. Grevenbroek, Clara V. Creveld, R. Agbaria, and R. Yagil. "Effect of water restriction on renal function in ostriches(Struthio camelus)." Avian Pathology 19, no. 2 (April 1990): 385–93. http://dx.doi.org/10.1080/03079459008418688.

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19

Watson, Rebecca R., Jonas Rubenson, Lisa Coder, Donald F. Hoyt, Matthew W. G. Propert, and Richard L. Marsh. "Gait-specific energetics contributes to economical walking and running in emus and ostriches." Proceedings of the Royal Society B: Biological Sciences 278, no. 1714 (December 2010): 2040–46. http://dx.doi.org/10.1098/rspb.2010.2022.

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A widely held assumption is that metabolic rate ( Ė met ) during legged locomotion is linked to the mechanics of different gaits and this linkage helps explain the preferred speeds of animals in nature. However, despite several prominent exceptions, Ė met of walking and running vertebrates has been nearly uniformly characterized as increasing linearly with speed across all gaits. This description of locomotor energetics does not predict energetically optimal speeds for minimal cost of transport ( E cot ). We tested whether large bipedal ratite birds (emus and ostriches) have gait-specific energetics during walking and running similar to those found in humans. We found that during locomotion, emus showed a curvilinear relationship between Ė met and speed during walking, and both emus and ostriches demonstrated an abrupt change in the slope of Ė met versus speed at the gait transition with a linear increase during running. Similar to human locomotion, the minimum net E cot calculated after subtracting resting metabolism was lower in walking than in running in both species. However, the difference in net E cot between walking and running was less than is found in humans because of a greater change in the slope of Ė met versus speed at the gait transition, which lowers the cost of running for the avian bipeds. For emus, we also show that animals moving freely overground avoid a range of speeds surrounding the gait-transition speed within which the E cot is large. These data suggest that deviations from a linear relation of metabolic rate and speed and variations in transport costs with speed are more widespread than is often assumed, and provide new evidence that locomotor energetics influences the choice of speed in bipedal animals. The low cost of transport for walking is probably ecologically important for emus and ostriches because they spend the majority of their active day walking, and thus the energy used for locomotion is a large part of their daily energy budget.
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20

Terzich, Mac, and Stanley Vanhooser. "Postmortem Findings of Ostriches Submitted to the Oklahoma Animal Disease Diagnostic Laboratory." Avian Diseases 37, no. 4 (October 1993): 1136. http://dx.doi.org/10.2307/1591926.

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21

Abolnik, Celia, Jeanni Fehrsen, Adriaan Olivier, Wouter van Wyngaardt, Geoffrey Fosgate, and Charlotte Ellis. "Serological investigation of highly pathogenic avian influenza H5N2 in ostriches (Struthio camelus)." Avian Pathology 42, no. 3 (June 2013): 206–14. http://dx.doi.org/10.1080/03079457.2013.779637.

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22

Mushi, E. Z., J. F. W. Isa, R. G. Chabo, M. G. Binta, J. Nyange, and L. Modisa. "Selenium—vitamin E responsive myopathy in farmed ostriches (Struthio camelus)in Botswana." Avian Pathology 27, no. 3 (June 1998): 326–28. http://dx.doi.org/10.1080/03079459808419346.

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23

Nguyen, Sam Thi, Yasuhiro Fukuda, Chika Tada, Vu Vy Huynh, Duc Tan Nguyen, and Yutaka Nakai. "Prevalence and molecular characterization of Cryptosporidium in ostriches (Struthio camelus) on a farm in central Vietnam." Experimental Parasitology 133, no. 1 (January 2013): 8–11. http://dx.doi.org/10.1016/j.exppara.2012.10.010.

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24

Clavijo, A., J. Riva, and J. Pasick. "Pathogenicity of a Ratite-Origin Influenza A H5 Virus in Ostriches (Struthio camelus)." Avian Diseases 47, s3 (September 2003): 1203–7. http://dx.doi.org/10.1637/0005-2086-47.s3.1203.

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25

Abolnik, Celia. "Molecular Characterization of H5N2 Avian Influenza Viruses Isolated from South African Ostriches in 2006." Avian Diseases 51, no. 4 (December 2007): 873–79. http://dx.doi.org/10.1637/7953-022107-regr.1.

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26

Ley, Elizabeth C., Teresa Y. Morishita, Brian S. Harr, Ram Mohan, and Thomas Brisker. "Serologic Survey of Slaughter-Age Ostriches (Struthio camelus) for Antibodies to Selected Avian Pathogens." Avian Diseases 44, no. 4 (October 2000): 989. http://dx.doi.org/10.2307/1593077.

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27

Andrade, Josiana Gomes de, Eulógio Carlos Queiroz de Carvalho, Clóvis de Paula Santos, and Renato Augusto DaMatta. "Mixed infection withLibyostrongylus dentatusandLibyostrongylus douglassiiinduces a heterophilic inflammatory infiltrate in the proventriculus of ostriches." Avian Pathology 40, no. 4 (August 2011): 367–70. http://dx.doi.org/10.1080/03079457.2011.585631.

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28

Manvell, R. J., C. English, P. H. Jorgensen, and I. H. Brown. "Pathogenesis of H7 Influenza A Viruses Isolated from Ostriches in the Homologous Host Infected Experimentally." Avian Diseases 47, s3 (September 2003): 1150–53. http://dx.doi.org/10.1637/0005-2086-47.s3.1150.

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29

Capua, Ilaria. "Crimean‐Congo haemorrhagic fever in ostriches: A public health risk for countries of the European Union?" Avian Pathology 27, no. 2 (April 1998): 117–20. http://dx.doi.org/10.1080/03079459808419311.

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30

Kelly, Patrick J., Norman Masanvi, Hilary F. Cadman, Suman M. Mahan, Lorenza Beati, and Didier Raoult. "Serosurvey for Cowdria ruminantium, Coxiella burnetii, and Spotted Fever Group Rickettsiae in Ostriches (Struthio camelus) from Zimbabwe." Avian Diseases 40, no. 2 (April 1996): 448. http://dx.doi.org/10.2307/1592243.

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31

Cadman, Hilary F., Patrick J. Kelly, Raramai Zhou, Frans Davelaar, and Peter R. Mason. "A Serosurvey Using Enzyme-Linked Immunosorbent Assay for Antibodies against Poultry Pathogens in Ostriches (Struthio camelus) from Zimbabwe." Avian Diseases 38, no. 3 (July 1994): 621. http://dx.doi.org/10.2307/1592088.

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32

Verwoerd, D. J., A. Olivier, B. Gummow, G. H. Gerdes, and R. Williams. "Experimental Infection of Vaccinated Slaughter Ostriches in a Natural, Open-Air Feedlot Facility with Virulent Newcastle Disease Virus." Avian Diseases 43, no. 3 (July 1999): 442. http://dx.doi.org/10.2307/1592641.

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33

Venter, Marietjie, Florette K. Treurnicht, Amelia Buys, Stefano Tempia, Rudo Samudzi, Johanna McAnerney, Charlene A. Jacobs, Juno Thomas, and Lucille Blumberg. "Risk of Human Infections With Highly Pathogenic H5N2 and Low Pathogenic H7N1 Avian Influenza Strains During Outbreaks in Ostriches in South Africa." Journal of Infectious Diseases 216, suppl_4 (September 15, 2017): S512—S519. http://dx.doi.org/10.1093/infdis/jix018.

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34

Jørgensen, P. H., O. L. Nielsen, H. C. Hansen, R. J. Manvell, J. Banks, and D. J. Alexander. "Isolation of influenza a virus, subtype H5N2, and avian paramyxovirus type 1 from a flock of ostriches in Europe." Avian Pathology 27, no. 1 (February 1998): 15–20. http://dx.doi.org/10.1080/03079459808419269.

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35

Razmyar, Jamshid, Seyed Mostafa Peighambari, and Amir Hossein Zamani. "Detection of a Newly Described Bacteriocin, Perfrin, Among Clostridium perfringensIsolates from Healthy and Diseased Ostriches and Broiler Chickens in Iran." Avian Diseases 61, no. 3 (September 2017): 387–90. http://dx.doi.org/10.1637/11580-010517-resnoter.

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36

Brown, Tom P., W. Roberts, and R. K. Page. "Acute Hemorrhagic Enterocolitis in Ratites: Isolation of Eastern Equine Encephalomyelitis Virus and Reproduction of the Disease in Ostriches and Turkey Poults." Avian Diseases 37, no. 2 (April 1993): 602. http://dx.doi.org/10.2307/1591696.

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37

Toffan, Anna, Adriaan Olivier, Marzia Mancin, Valentina Tuttoilmondo, Daniele Facco, Ilaria Capua, and Calogero Terregino. "Evaluation of different serological tests for the detection of antibodies against highly pathogenic avian influenza in experimentally infected ostriches (Struthio camelus)." Avian Pathology 39, no. 1 (January 19, 2010): 11–15. http://dx.doi.org/10.1080/03079450903431390.

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38

de Souza, Lara Pereira, Josiana Gomes de Andrade, Raphael Mansur Medina, Eulógio Carlos Queiroz de Carvalho, Leonardo Siqueira Glória, Renato Augusto DaMatta, and Clóvis de Paula Santos. "Anatomopathological changes, quantification and distribution of Libyostrongylus spp. in regions of the proventriculus and ventriculus of naturally- and experimentally-infected ostriches." Avian Pathology 48, no. 4 (May 20, 2019): 382–89. http://dx.doi.org/10.1080/03079457.2019.1607254.

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39

Blignaut, A., W. P. Burger, A. J. Morley, and D. U. Bellstedt. "Antibody Responses to La Sota Strain Vaccines of Newcastle Disease Virus in Ostriches (Struthio camelus) as Detected by Enzyme-Linked Immunosorbent Assay." Avian Diseases 44, no. 2 (April 2000): 390. http://dx.doi.org/10.2307/1592554.

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40

Ismail, Mahmoud Moussa, I. M. El-Sabagh, and Abdul-Rahman Al-Ankari. "Characterization and Phylogenetic Analysis of a Highly Pathogenic Avian Influenza H5N1 Virus Isolated from Diseased Ostriches (Struthio camelus) in the Kingdom of Saudi Arabia." Avian Diseases 58, no. 2 (June 2014): 309–12. http://dx.doi.org/10.1637/10723-111813-resnote.1.

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41

Abolnik, Celia, Gertruida H. Gerdes, Marna Sinclair, Boto W. Ganzevoort, James P. Kitching, Christina E. Burger, Marco Romito, et al. "Phylogenetic Analysis of Influenza A Viruses (H6N8, H1N8, H4N2, H9N2, H10N7) Isolated from Wild Birds, Ducks, and Ostriches in South Africa from 2007 to 2009." Avian Diseases 54, s1 (March 2010): 313–22. http://dx.doi.org/10.1637/8781-040109-reg.1.

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42

du Toit, C. J., A. Chinsamy, and S. J. Cunningham. "Cretaceous origins of the vibrotactile bill-tip organ in birds." Proceedings of the Royal Society B: Biological Sciences 287, no. 1940 (December 2, 2020): 20202322. http://dx.doi.org/10.1098/rspb.2020.2322.

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Some probe-foraging birds locate their buried prey by detecting mechanical vibrations in the substrate using a specialized tactile bill-tip organ comprising mechanoreceptors embedded in densely clustered pits in the bone at the tip of their beak. This remarkable sensory modality is known as ‘remote touch’, and the associated bill-tip organ is found in probe-foraging taxa belonging to both the palaeognathous (in kiwi) and neognathous (in ibises and shorebirds) clades of modern birds. Intriguingly, a structurally similar bill-tip organ is also present in the beaks of extant, non-probing palaeognathous birds (e.g. emu and ostriches) that do not use remote touch. By comparison with our comprehensive sample representing all orders of extant modern birds (Neornithes), we provide evidence that the lithornithids (the most basal known palaeognathous birds which evolved in the Cretaceous period) had the ability to use remote touch. This finding suggests that the occurrence of the vestigial bony bill-tip organ in all modern non-probing palaeognathous birds represents a plesiomorphic condition. Furthermore, our results show that remote-touch probe foraging evolved very early among the Neornithes and it may even have predated the palaeognathous–neognathous divergence. We postulate that the tactile bony bill-tip organ in Neornithes may have originated from other snout tactile specializations of their non-avian theropod ancestors.
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43

Taniguchi, S., F. A. Neefhling, R. Oriol, T. Kobayashis, Y. Ye, M. Niekrasz, L. Peters, S. Kosanke, E. Koren, and D. K. C. Cooper. "Ratites (ostrich, emu) as potential heart donors for humans: Immunologic, anatomic, and physiologic considerations." Xenotransplantation 3, no. 3 (August 1996): 252–59. http://dx.doi.org/10.1111/j.1399-3089.1996.tb00145.x.

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44

Shinya, Kyoko, Akiko Makino, Makoto Ozawa, Jin Hyun Kim, Yuko Sakai-Tagawa, Mutsumi Ito, Quynh Mai Le, and Yoshihiro Kawaoka. "Ostrich Involvement in the Selection of H5N1 Influenza Virus Possessing Mammalian-Type Amino Acids in the PB2 Protein." Journal of Virology 83, no. 24 (September 30, 2009): 13015–18. http://dx.doi.org/10.1128/jvi.01714-09.

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ABSTRACT Amino acids at positions 627 and 701 in the PB2 protein (PB2-627 and PB2-701, respectively) of avian influenza A viruses affect virus replication in some mammalian cells. Highly pathogenic H5N1 influenza viruses possessing mammalian-type PB2-627 were detected during the Qinghai Lake outbreak in 2005 and spread to Europe and Africa. Via a database search, we found a high rate of viral isolates from Ratitae, including ostrich, possessing mammalian-type PB2-627 or -701. Here, we report that H5N1 avian influenza viruses possessing mammalian-type amino acids in PB2-627 or -701 are selected during replication in ostrich cells in vitro and in vivo.
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45

Fitzgerald, S. D., and P. G. Moisan. "Mycotic Rhinitis in an Ostrich." Avian Diseases 39, no. 1 (January 1995): 194. http://dx.doi.org/10.2307/1592003.

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46

Jehuda-Cohen, T. "The False-Positive Polymerase Chain Reaction and the Ostrich." Journal of Infectious Diseases 172, no. 5 (November 1, 1995): 1420. http://dx.doi.org/10.1093/infdis/172.5.1420.

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47

Sutherland, Jenni L., Ryno J. Naudé, and Willem Oelofsen. "The isolation and partial characterization of proelastase from the pancreas of the ostrich (Struthio camelus)." Comparative Biochemistry and Physiology Part C: Comparative Pharmacology 98, no. 2-3 (January 1991): 337–43. http://dx.doi.org/10.1016/0742-8413(91)90214-e.

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48

Jeffrey, J. S., R. P. Chin, H. L. Shivaprasad, C. U. Meteyer, and R. Droual. "Proventriculitis and Ventriculitis Associated with Zygomycosis in Ostrich Chicks." Avian Diseases 38, no. 3 (July 1994): 630. http://dx.doi.org/10.2307/1592090.

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49

Shivaprasad, H. L. "Hepatitis associated with Clostridium difficile in an ostrich chick." Avian Pathology 32, no. 1 (February 2003): 57–62. http://dx.doi.org/10.1080/0307945021000070723.

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50

Ley, Elizabeth C., Teresa Y. Morishita, Thomas Brisker, and Brian S. Harr. "Prevalence of Salmonella, Campylobacter, and Escherichia coli on Ostrich Carcasses and the Susceptibility of Ostrich-Origin E. coli Isolates to Various Antibiotics." Avian Diseases 45, no. 3 (July 2001): 696. http://dx.doi.org/10.2307/1592914.

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