Abstract:The African penguin (Spheniscus demersus) is an endangered seabird that breeds along the coast of Namibia and South Africa, and disease surveillance was identified as a priority for its conservation. Aiming for the establishment of baseline data on the presence of potential pathogens in this species, a comprehensive health assessment (blood smear examination, haematology, biochemistry and serology) was conducted on samples obtained from 578 African penguins at 11 breeding colonies and a rehabilitation centre. … Show more
“…Blood parasites were remarkably common in African penguins examined in this study, with Babesia being the most frequent (46% prevalence on admission, 72% infection ratio), whereas Borrelia was recorded only sporadically (1% prevalence on admission, 3% infection ratio) and Plasmodium was only recorded once. Although these parasites have long been known to infect wild African penguins (Coles, 1941; Fantham and Porter, 1944), their prevalence in this study was markedly higher than in apparently wild healthy adult African penguins sampled in previous studies (Parsons et al ., 2016; Espinaze et al ., 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Borrelia infections are significantly associated with a decreased survival probability in African penguin chicks admitted for rehabilitation at SANCCOB (Vanstreels et al, 2019), and in some cases, Borrelia infections are lethal to penguins (Yabsley et al, 2012;Parsons et al, 2018b). Although Babesia infections have yet to be implicated in the death of African penguins, they have been linked to haematological abnormalities in otherwise apparently healthy African penguins (Parsons et al, 2016) and their potential lethality has been demonstrated in other penguin species (Parsons et al, 2017(Parsons et al, , 2018b. Furthermore, the flea P. longicornis is speculated to serve as a mechanical facilitator to the transmission of Avipoxvirus to penguins (Kane et al, 2012).…”
We investigate the factors associated with the occurrence and abundance of external and blood parasites in African penguins (Spheniscus demersus), an endangered seabird that breeds exclusively on the coasts of Namibia and South Africa. External parasites were collected using the dust-ruffling method from 171 African Penguins admitted at a rehabilitation facility in the Western Cape, South Africa. Additionally, blood smears were obtained upon admission and weekly during rehabilitation and examined for blood parasites. Fleas Parapsyllus longicornis humboldti, ticks Ornithodoros capensis and lice Austrogoniodes demersus were recovered from 93, 63 and 40%, respectively, of the penguins upon admission to the centre. Rescue location and age group were identified as significant determinants of flea abundance, whereas month of admission was a significant determinant of tick abundance. Blood parasites were also common on admission, with Babesia being the most frequent (46% prevalence) whereas Borrelia was recorded sporadically (1.2%) and Plasmodium was recorded once. The prevalence and abundance of ticks on admission was positively associated with Babesia infection on admission. Our findings demonstrate the variability and contributing factor of parasite infections in an endangered species of penguin, and highlight the need for additional research on the parasite–host dynamics involving these potential disease vectors.
“…Blood parasites were remarkably common in African penguins examined in this study, with Babesia being the most frequent (46% prevalence on admission, 72% infection ratio), whereas Borrelia was recorded only sporadically (1% prevalence on admission, 3% infection ratio) and Plasmodium was only recorded once. Although these parasites have long been known to infect wild African penguins (Coles, 1941; Fantham and Porter, 1944), their prevalence in this study was markedly higher than in apparently wild healthy adult African penguins sampled in previous studies (Parsons et al ., 2016; Espinaze et al ., 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Borrelia infections are significantly associated with a decreased survival probability in African penguin chicks admitted for rehabilitation at SANCCOB (Vanstreels et al, 2019), and in some cases, Borrelia infections are lethal to penguins (Yabsley et al, 2012;Parsons et al, 2018b). Although Babesia infections have yet to be implicated in the death of African penguins, they have been linked to haematological abnormalities in otherwise apparently healthy African penguins (Parsons et al, 2016) and their potential lethality has been demonstrated in other penguin species (Parsons et al, 2017(Parsons et al, , 2018b. Furthermore, the flea P. longicornis is speculated to serve as a mechanical facilitator to the transmission of Avipoxvirus to penguins (Kane et al, 2012).…”
We investigate the factors associated with the occurrence and abundance of external and blood parasites in African penguins (Spheniscus demersus), an endangered seabird that breeds exclusively on the coasts of Namibia and South Africa. External parasites were collected using the dust-ruffling method from 171 African Penguins admitted at a rehabilitation facility in the Western Cape, South Africa. Additionally, blood smears were obtained upon admission and weekly during rehabilitation and examined for blood parasites. Fleas Parapsyllus longicornis humboldti, ticks Ornithodoros capensis and lice Austrogoniodes demersus were recovered from 93, 63 and 40%, respectively, of the penguins upon admission to the centre. Rescue location and age group were identified as significant determinants of flea abundance, whereas month of admission was a significant determinant of tick abundance. Blood parasites were also common on admission, with Babesia being the most frequent (46% prevalence) whereas Borrelia was recorded sporadically (1.2%) and Plasmodium was recorded once. The prevalence and abundance of ticks on admission was positively associated with Babesia infection on admission. Our findings demonstrate the variability and contributing factor of parasite infections in an endangered species of penguin, and highlight the need for additional research on the parasite–host dynamics involving these potential disease vectors.
“…There are no studies conclusively demonstrating Avian orthoreovirus infection in penguins, but Gough et al (2002) isolated reovirus-like particles from the tissues of African Penguins that died with gastrointestinal and respiratory lesions at a zoo in the UK. Previous surveys of Avian orthoreovirus in penguins found seroprevalences ranging from 0% to 23% (Karesh et al 1999;Travis et al 2006;Smith et al 2008;Parsons et al 2016). In addition, antibodies to this pathogen were also reported in other seabirds that share breeding habitat with Magellanic Penguins in Patagonia (Gallo et al 2013), and it therefore seems likely that wild penguins are sporadically exposed to Avian orthoreovirus.…”
Section: Reoviridaementioning
confidence: 95%
“…Given the low positive predictive value, we would interpret our findings as potentially false positive results. In contrast, enzyme-linked immunosorbent assay (ELISA) testing of African Penguins for antibodies against this virus found seroprevalence ranging from 1% to 5% in wild populations (Parsons et al 2016). It is unclear, however, whether these serological results can be attributed to exposure to Tremovirus A or to cross-reactivity with other antigenically similar agents.…”
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“…African penguins' vocalizations and the information they carry are important to social recognition, and ultimately the survival of their species (Favaro et al, 2015 (Parsons, Schaefer & Vanstreels, 2016;Sherley et al, 2013). The reason for this population decline is due mostly to low food availability, and breeding success that is inadequate to sustain their population (Crawford et al, 2003).…”
First of all, I would like to thank Dr. DeLong, my dedicated thesis advisor. This process has been rewarding and not nearly as stressful as I imagined it would be, thanks to you. Thanks for spending hours with me to design my procedure, and even more hours on top of that reading my drafts and providing feedback. I would like to also thank the other two members of my thesis committee, Dr. Condry and Dr. Herbert. Dr. Condry, thank you for helping with the design of the method. Your input on the habituation-dishabituation methodology made this experiment possible. Dr. Herbert, thank you for your direct and helpful edits to my thesis proposal, and your all-around support throughout the process of completing my thesis. I also sincerely thank the staff at the Seneca Park Zoo; especially the curator David Hamilton, and the penguin keepers Kevin Blakely, Kellee Wolowitz, and Hanna Kaiser. Thank you, Peter Cook, for giving me advice on how to design my experiment. I would like to thank Tyler Wilcox for helpful suggestions for the statistical analyses of my test data. I would also like to mention a few very special penguins. Sky, thank you for making me smile every time you stepped on my shoe, untied my boots, or followed me around the penguin habitat during set up. Obi, thank you for never leaving my sneakers tied at the end of equipment set up. Blanka, thank you for looking out for all the other penguins and making sure all your non-biological chicks are safe. Gizmo, thanks for the great picture, you are very photogenic and that shot will forever hold a place on my desk in a frame.
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