Abstract
Raccoons (Procyon lotor), which are closely related to the family Mustelidae, might be susceptible to natural infection by SARS-CoV-2. This assumption is based on experimental evidence that confirmed the vulnerability of farmed fur-carnivore species, including Procyon lotor to SARS-CoV-2. To date, there are no reports of natural SARS-CoV-2 infections of raccoons in Germany. Here, we use RT-PCR to analyze 820 samples from raccoons hunted in Germany with a focus on 4 German federal states (Saxony-Anhalt, Thuringia, Hesse, North Rhine-Westphalia). Lung tissues were homogenized and processed for RNA extraction and RT-qPCR for detecting SARS-CoV-2 was performed. No viral RNA was detected in any samples (0/820). Next, we compared raccoons and human ACE-2 residues that are known to serve for binding with SARS-CoV-2 receptor binding domain (RBD). Interestingly, we found only 60% identity on amino acid level, which may have contributed to the absence of SARS-CoV-2 infections in raccoons. In conclusion, the chance of raccoons being intermediate reservoir hosts for SARS-CoV-2 seems to be very low.
Avoid common mistakes on your manuscript.
Introduction
The raccoon (Procyon lotor) is a nocturnal omnivorous mammalian species that was introduced in Germany originally from North America in 1835. However, due to animals escape or release in the wild, their number is exponentially increasing, which make Germany one of the focal points of the European raccoon population (Pagel and Spieß 2011; Leicht 2009; Niethammer 1963; Stope 2019). This population surge could be attributed to their ability to adapt to different habitants, utilize a wide range of animal and plant food, highly reproductive potential, and the significant decrease in natural predators in Europe. Consequently, wild raccoons successfully colonized suburban and urban habitats, and are living in a proximity to humans and their pets, eat garbage and come even into contact with sewage. In North America, wild raccoons are either intermediate or final hosts for multiple zoonotic pathogens. Nonetheless, little is reported about the pathogen spectrum in the German and European invasive raccoon species (Bharti et al. 2003; Beltrán-Beck et al. 2012). The raccoon population in Germany is genetically heterogenous (Fischer et al. 2015; Biedrzycka et al. 2014), and therefore populations in close proximity may even show a different pathogenic pattern (Stope 2019). This is indeed a potential risk and therefore surveillance of pathogens, especially zoonotic pathogens, in wild raccoons in Germany and Central Europe is inevitable (Stope 2019).
In 2019, severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) emerged and caused a global pandemic (Zhu et al. 2020; Chan et al. 2020). Procyonidae are a closely related family to mustelids; however, little is known about their susceptibility to SARS-CoV-2. Coronavirus infections were reported in raccoons as a juvenile raccoon in the USA succumbed to infection and positive antibodies were detected against in raccoons in Japan (Martin and Zeidner 1992; Aoki et al. 2017). Raccoon dogs may have played also a role in the transmission chain of SARS-CoV-1 in 2003 (Guan et al. 2003). For this reason, and because of the zoonotic nature of coronaviruses, surveillance of SARS-CoV-2 infections in musteloid species was evident. Given the high potential of SARS-CoV-2 viruses for mutated variants, the potential of reverse zoonotic infections to wildlife species is certainly also an issue. Moreover, co-infections of species-specific coronaviruses and SARS-CoV-2 might lead to novel chimeric viruses (Focosi and Maggi 2022; Banerjee et al. 2020; Boniotti et al. 2016). Until now, experimental studies showed that raccoons are not susceptible to SARS-CoV-2, since challenged animals did not develop clinical symptoms nor shed virus genomes or infectivity (Francisco et al. 2021; Bosco-Lauth et al. 2021). Nonetheless, a variety of factors that are difficult to simulate in experimental studies such as coinfections, immunodeficiencies, gestation, senescence, parasitic burdens, and environmental conditions may also contribute to their susceptibility. Therefore, searching for natural SARS-CoV-2 infections in raccoons and wildlife using a screening approach will provide supportive answers.
Materials and method
Here we collected 820 lung tissue samples from hunted raccoons mainly coming from four different German federal states representing regions with high hunting ranges (Saxony-Anhalt, Thuringia, Hesse, North Rhine-Westphalia; Fig. 1A–B) and examined them by reverse transcriptase real-time polymerase chain reaction (RT-qPCR). We selected these animal species because they are common in urban areas and therefore come into contact with the human population either through consumption of garbage or directly in wildlife rehabilitation centers or even zoos. The tissue samples were homogenized (TissueLyser II, Qiagen, Germany) and viral RNA was extracted (MagMax, Invitrogen; Thermo Fisher Automated Nucleic Acid Extraction Workstation). Extracted RNA was further examined by RT-qPCR using an envelope (E) gene and β-actin targets and CFX real-time PCR systems (Bio-Rad, Germany) as previously described (Corman et al. 2020). Next, we analyzed why these species are rather resistant to SARS-CoV-2 infections, both in experimental and natural settings (Francisco et al. 2021). We used bioinformatics and structural approaches (Geneious Prime® 2021.0.1.) to compare essential ACE-2 residues in raccoons and humans, and in species known to be fairly resistant (poultry and pigs).
RT-qPCR-based surveillance on wild raccoon populations to monitor natural infections by SARS-CoV-2 in Germany. A Schematic depiction of collection sites for the analyzed raccoon samples across Germany on county level. The more samples collected from certain site, the more opacity of the color (maximum capture places were 19 and were from Sachsen-Anhalt). B Representing the hunting ranges of raccoons in pieces/100 ha huntable area (reproduced with kind permission of WILD-Monitoring/Deutscher Jagdverband), samples were taken in areas with high hunting ranges. C Results of RT-qPCR represented by Ct values for E-Sarbeco and β-actin as a negative control for RNA. Positive (cell culture supernatants) and negative (clinical samples) controls were used across all the examined samples
Results
No SARS-CoV-2 specific viral RNA was detected in any of the examined animals (0/820) (Fig. 1C). Based on our results, wild raccoons are unlikely to be a reservoir or amplifying host for SARS-CoV-2. SARS-CoV-2 possess a trimeric structure called spike protein that determines cell and host tropism. Establishment of the infection requires a cleavage of S-protein by ubiquitous host proteases to S1, which contains the receptor binding domain (RBD), and S2, a fusion protein. Binding of the RBD to the host cellular receptor, angiotensin converting enzyme 2 (ACE2) is a prerequisite for viral infection. Zhai et al. proposed certain residues in ACE-2 receptors that are essential for binding to the viral RBD and determining virus host range and postulated that animals with more amino acid changes at the ACE2-S interface are at lower risk for SARS-CoV-2 infection (Zhai et al. 2020). Here we detected only 60% identity (Fig. 2B) between residual ACE-2 in humans and raccoons, which may explain the lack of susceptibility to SARS-CoV-2 in these species. Among these deviant amino acids are Gln24 that forms a hydrogen bond to S N487, His34 in the center of the binding site, Asp30 that forms the central salt bridge, Leu79 and Met82 that interact with Phe486 in the peripheral binding sites, and the N-glycosylation site Asn90. These amino acids were substituted in ACE2 of pigs (Q24L, D30E, H34L, L79I, M82T, N90T) and chickens (Q24E, D30A, H34V, L79N, M82R). Pigs and chickens are known to be resistant to SARS-CoV-2 (Vergara‐Alert et al. 2021; Suarez et al. 2020; Michelitsch et al. 2021). Interestingly, we have found that these five amino acids were also substituted in ACE-2 of raccoon species (Fig. 2B). For instance, the Gln24 was substituted to Leu and therefore hydrogen bonds cannot be formed. Also, the Asp30 residue was swapped to Glu that is negatively charged and therefore the salt bridge to S Lys417 remains intact. Moreover, the His34 that interact with Tyr453, Leu455, and Gln493 in the interaction surface is replaced by Asn. Further, the Leu79 that interacts with S Phe486 was replaced to Gln and also the Met82 to Thr. More importantly, the N-glycosylation site Asn90 was deleted due to replacement by Asp.
Interactions of SARS-CoV-2 RBD, human and raccoons ACE2. A The amino acids that are essential for this interaction are shown in yellow. The figure was created by Geneious Prime® 2021.0.1. B Multiple-alignment of human and raccoons ACE-2, highlighting the difference in important residues for binding to SARS-CoV-2 receptor binding domain (RBD). Residues in red represents amino acids essential for binding of SARS-CoV-1 and SARS-CoV-2, while in green represents those essential for the contact of SARS-CoV-2 only. Residues in boxes are those substituted in Procyon lotor species and other SARS-CoV-2-resistant animal species
Conclusion
Together, our data are consistent with previous reports about the susceptibility of raccoons to SARS-CoV-2 and highlight that raccoons do not function as competent reservoirs for SARS-CoV-2 (Francisco et al. 2021). Since raccoons often living in close neighborhood to humans not only in rural areas but also in regions with high urbanization, they represent a source of zoonotic diseases that should not be underestimated. That reservoirs for SARS-CoV-2 can form in wildlife populations has been demonstrated by transmissibility and spread studies with mink and white-tailed deer (Hale et al. 2021). Wild individuals of these species susceptible to SARS-CoV-2 have been shown to transmit the virus within wild populations and can also transmit it to kept conspecifics or even humans when contact occurs (Munnink et al. 2021; Pickering et al. 2022). Surveillance projects to monitor such populations are necessary to quickly detect and control unrestraint spread of the virus. Such a project was launched in the European framework for monitoring mustelids (European Food Safety Authority et al. 2021). Other European wildlife species must also be considered to represent potential host for the virus (Delahay et al. 2021), e.g., bats, carnivores, and cervids. Especially those susceptible species with close relationships to other species like raccoon dogs and raccoons deserve a special attention. Further studies including other carnivorous animals, rodents, and others regarding distribution of the virus and receptor studies must be done in the future to show as comprehensive a picture as possible of the spread of SARS-CoV-2 in wildlife species. The results of such studies must be brought together for a superior valuation and coordination of necessary responses. The present study shows that raccoons, including those living in close proximity to humans, are currently not expected to pose an increased risk for humans and other wildlife species. However, in view of the constant emergence of new variants of the virus, it seems necessary to include raccoons in surveillance studies. In this context, attention should be paid to variants and selective alterations in the genome of the viruses that facilitate binding of the virus to the cellular receptors of the different species.
References
Aguirre AA, Catherina R, Frye H, Shelley L (2020) Illicit wildlife trade, wet markets, and COVID-19: preventing future pandemics. World Medical & Health Policy 12(3):256–265
Aoki E, Soma T, Yokoyama M, Matsubayashi M, Sasai K (2017) Surveillance for antibodies against six canine viruses in wild raccoons (Procyon lotor) in Japan. J Wildl Dis 53(4):761–768
Banerjee A, Doxey AC, Tremblay BJ-M, Mansfield MJ, Subudhi S, Hirota JA, Miller MS, McArthur AG, Mubareka S, Mossman K (2020) Predicting the recombination potential of severe acute respiratory syndrome coronavirus 2 and Middle East respiratory syndrome coronavirus. J Gen Virol 101(12):1251–1260. https://doi.org/10.1099/jgv.0.001491
Beltrán-Beck B, García FJ, Gortázar C (2012) Raccoons in Europe: disease hazards due to the establishment of an invasive species. Eur J Wildl Res 58(1):5–15. https://doi.org/10.1007/s10344-011-0600-4
Bharti AR, Nally JE, Ricaldi JN, Matthias MA, Diaz MM, Lovett MA, Levett PN, Gilman RH, Willig MR, Gotuzzo E (2003) Leptospirosis: a zoonotic disease of global importance. Lancet Infect Dis 3(12):757–771
Biedrzycka A, Zalewski A, Bartoszewicz M, Okarma H, Jędrzejewska E (2014) The genetic structure of raccoon introduced in Central Europe reflects multiple invasion pathways. Biol Invasions 16(8):1611–1625
Boniotti MB, Papetti A, Lavazza A, Alborali G, Sozzi E, Chiapponi C, Faccini S, Bonilauri P, Cordioli P, Marthaler D (2016) Porcine epidemic diarrhea virus and discovery of a recombinant swine enteric coronavirus. Italy Emerg Infect Dis 22(1):83–87. https://doi.org/10.3201/eid2201.150544
Bosco-Lauth AM, Root JJ, Porter SM, Walker AE, Guilbert L, Hawvermale D, Pepper A, Maison RM, Hartwig AE, Gordy P (2021) Survey of peridomestic mammal susceptibility to SARS-CoV-2 infection. BioRxiv
Cahan E (2020) COVID-19 hits US mink farms after rip** through Europe. Science 80 (10.1126)
Chan JF-W, Yuan S, Kok K-H, To KK-W, Chu H, Yang J, **ng F, Liu J, Yip CC-Y, Poon RW-S (2020) A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster. The Lancet 395(10223):514–523
Corman VM, Landt O, Kaiser M, Molenkamp R, Meijer A, Chu DK, Bleicker T, Brünink S, Schneider J, Schmidt ML (2020) Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR. Eurosurveillance 25(3):2000045
Delahay RJ, La Fuente Jd, Smith GC, Sharun K, Snary EL, Flores Girón L, Nziza J, Fooks AR, Brookes SM, Lean FZX, Breed AC, Gortazar C (2021) Assessing the risks of SARS-CoV-2 in wildlife. One Health Outlook 3:7. https://doi.org/10.1186/s42522-021-00039-6
European Food Safety Authority, Centre E, for Disease Prevention Control, Boklund A, Gortázar C, Pasquali P, Roberts H, Nielsen SS, Stahl K, Stegeman A, Baldinelli F, Broglia A, Van Der Stede Y, Adlhoch C, Alm E, Melidou A, Mirinaviciute G (2021) Monitoring of SARS-CoV-2 infection in mustelids. EFSA J 19(3):e06459. https://doi.org/10.2903/j.efsa.2021.6459
Fischer ML, Hochkirch A, Heddergott M, Schulze C, Anheyer-Behmenburg HE, Lang J, Michler F-U, Hohmann U, Ansorge H, Hoffmann L (2015) Historical invasion records can be misleading: genetic evidence for multiple introductions of invasive raccoons (Procyon lotor) in Germany. PLoS ONE 10(5):e0125441
Focosi D, Maggi F (2022) Recombination in coronaviruses, with a focus on SARS-CoV-2. Viruses 14(6):1239
Francisco R, Hernandez SM, Mead DG, Adcock KG, Burke SC, Nemeth NM, Yabsley MJ (2021) Experimental susceptibility of North American raccoons (Procyon lotor) and striped skunks (Mephitis mephitis) to SARS-CoV-2. bioRxiv
Guan Y, Zheng BJ, He YQ, Liu XL, Zhuang ZX, Cheung CL, Luo SW, Li PH, Zhang LJ, Guan YJ, Butt KM, Wong KL, Chan KW, Lim W, Shortridge KF, Yuen KY, Peiris JSM, Poon LLM (2003) Isolation and characterization of viruses related to the SARS coronavirus from animals in Southern China. Science 302(5643):276–278. https://doi.org/10.1126/science.1087139
Hale VL, Dennis PM, McBride DS, Nolting JM, Madden C, Huey D, Ehrlich M, Grieser J, Winston J, Lombardi D, Gibson S, Saif L, Killian ML, Lantz K, Tell R, Torchetti M, Robbe-Austerman S, Nelson MI, Faith SA, Bowman AS (2021) SARS-CoV-2 infection in free-ranging white-tailed deer (Odocoileus virginianus). bioRxiv. https://doi.org/10.1101/2021.11.04.467308
Leicht E (2009) Waschbär-kleiner Feldversuch mit großer Wirkung. AFZ-Der Wald 11:570–573
Martin H, Zeidner N (1992) Concomitant cryptosporidia, coronavirus and parvovirus infection in a raccoon (Procyon lotor). J Wildl Dis 28(1):113–115
Michelitsch A, Wernike K, Ulrich L, Mettenleiter TC, Beer M (2021) SARS-CoV-2 in animals: from potential hosts to animal models. Adv Virus Res 110:59–102. https://doi.org/10.1016/bs.aivir.2021.03.004
Munnink BBO, Sikkema RS, Nieuwenhuijse DF, Molenaar RJ, Munger E, Molenkamp R, Van Der Spek A, Tolsma P, Rietveld A, Brouwer M (2021) Transmission of SARS-CoV-2 on mink farms between humans and mink and back to humans. Science 371(6525):172–177
Niethammer G (1963) Einbürgerung von Säugetieren und Vögeln in Europa
Pagel T, Spieß W (2011) Der Zoologische Garten in Cöln eröffnet am 22. Juli 1860–150 Jahre Wildtierhaltung und-zucht. Zool Gart 80(3):117
Pickering B, Lung O, Maguire F, Kruczkiewicz P, Kotwa JD, Buchanan T, Gagnier M, Guthrie JL, Jardine CM, Marchand-Austin A, Massé A, McClinchey H, Nirmalarajah K, Aftanas P, Blais-Savoie J, Chee H-Y, Chien E, Yim W, Goolia M, Suderman M, Pinette M, Smith G, Sullivan D, Rudar J, Adey E, Nebroski M, Côté M, Laroche G, McGeer AJ, Nituch L, Mubareka S, Bowman J (2022) Highly divergent white-tailed deer SARS-CoV-2 with potential deer-to-human transmission. bioRxiv:2022.2002.2022.481551. https://doi.org/10.1101/2022.02.22.481551
Shi J, Wen Z, Zhong G, Yang H, Wang C, Huang B, Liu R, He X, Shuai L, Sun Z (2020) Susceptibility of ferrets, cats, dogs, and other domesticated animals to SARS–coronavirus 2. Science 368(6494):1016–1020
Stope M (2019) Wild raccoons in Germany as a reservoir for zoonotic agents. Eur J Wildl Res 65(6):1–7
Suarez DL, Pantin-Jackwood MJ, Swayne DE, Lee SA, DeBlois SM, Spackman E (2020) Lack of susceptibility to SARS-CoV-2 and MERS-CoV in poultry. Emerg Infect Dis 26(12):3074
Vergara-Alert J, Rodon J, Carrillo J, Te N, Izquierdo-Useros N, Rodríguez de la Concepción ML, Ávila-Nieto C, Guallar V, Valencia A, Cantero G (2021) Pigs are not susceptible to SARS-CoV-2 infection but are a model for viral immunogenicity studies. Transbound Emerg Dis 68(4):1721–1725
Zhai X, Sun J, Yan Z, Zhang J, Zhao J, Zhao Z, Gao Q, He W-T, Veit M, Su S (2020) Comparison of severe acute respiratory syndrome coronavirus 2 spike protein binding to ACE2 receptors from human, pets, farm animals, and putative intermediate hosts. J Virol 94(15):e00831-e1820
Zhu N, Zhang D, Wang W, Li X, Yang B, Song J, Zhao X, Huang B, Shi W, Lu R (2020) A novel coronavirus from patients with pneumonia in China 2019. N Engl J Med 382(8):727–733
Funding
Open Access funding enabled and organized by Projekt DEAL.
Author information
Authors and Affiliations
Corresponding author
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Hagag, I.T., Langner, T., Groschup, M.H. et al. Molecular surveillance revealed no SARS-CoV-2 spillovers to raccoons (Procyon lotor) in four German federal states. Eur J Wildl Res 68, 54 (2022). https://doi.org/10.1007/s10344-022-01605-7
Received:
Revised:
Accepted:
Published:
DOI: https://doi.org/10.1007/s10344-022-01605-7