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Coronaviruses Detected in Bats in Close Contact with Humans in Rwanda

Abstract

Bats living in close contact with people in Rwanda were tested for evidence of infection with viruses of zoonotic potential. Mucosal swabs from 503 bats representing 17 species were sampled from 2010 to 2014 and screened by consensus PCR for 11 viral families. Samples were negative for all viral families except coronaviruses, which were detected in 27 bats belonging to eight species. Known coronaviruses detected included the betacorona viruses: Kenya bat coronaviruses, Eidolon bat coronavirus, and Bat coronavirus HKU9, as well as an alphacoronavirus, Chaerephon Bat coronavirus. Novel coronaviruses included two betacorona viruses clustering with SARS-CoV, a 2d coronavirus, and an alphacoronavirus.

Introduction

Bats are natural reservoirs for a number of pathogens of public health concern (Plowright et al. 2015; Shi 2013). For example, in Southeast Asia, Pteropus fruit bats are the natural reservoirs of the zoonotic paramyxoviruses Hendra and Nipah (Chua et al. 2000). In 2002–2003, an epidemic of severe acute respiratory syndrome (SARS) caused by a novel coronavirus (SARS-CoV) emerged in China (Drosten et al. 2003, Ksiazek et al. 2003), and bats were determined to be natural reservoirs and the possible source of the virus (Ge et al. 2013; Lau et al. 2010). In 2012, a pathogenic paramyxovirus, Sosuga virus, which caused severe illness in a patient following contact with bats in Uganda, was subsequently detected in Egyptian fruit bats (Rousettus aegyptiacus) (Amman et al. 2015). In Africa, Egyptian fruit bats (R. aegyptiacus) are reservoirs of Marburg virus (Towner et al. 2008), and antibodies against Zaire ebola virus have been detected in the same species (Pourrut et al. 2009), while antibodies against Bombali ebolavirus have been detected in Little free-tailed bat (Chaerephon pumilus), Angolan free-tailed bat (Mops condylurus) (Goldstein et al. 2018).

To assess the risk presented by human-bat contact, the USAID Emerging Pandemic Threats PREDICT project has been conducting viral surveillance in wildlife in more than 35 countries to detect viruses of zoonotic potential, including in Rwanda (https://ohi.vetmed.ucdavis.edu/programs-projects/predict-project).

Rwanda is continental Africa’s most densely populated country (Butler 2004), and bats are frequently observed in/around urban centers and adjacent to wildlife protected areas. Ecotourism centered on mountain gorillas in Volcanoes National Park also drives tourism to the nearby bat roosting “Musanze Caves” (Spenceley et al. 2010; Joachim 2013).

Between 2010 and 2014, biological sampling of bats was conducted at urban and rural sites in Rwanda characterized by an intense human–wildlife interface, including in and around Volcanoes National Park and the Musanze Caves. Anthropogenic activities around sampling sites were classified according to human livelihoods and activities, including ecotourism, crop farming, and national parks.

A total of 503 bats belonging to 17 species were captured at 25 sites (Fig. 1) following established PREDICT protocols for bat capture and sampling (PREDICT 2017) (Table 1). Following capture, bats were photographed, measured, and identified to species level as close as possible (Kingdon et al. 2013; Patterson and Webala 2012). Date, site name, season, apparent species, sex, age class (determined by the degree of epiphyseal-diaphyseal fusion) (Anthony 1988), reproductive status, and mass data were recorded. For handling and restraining larger fruit bats, light anesthesia was induced using inhalational isoflurane and oxygen (Fluriso™, Teva UK, Limited, Castleford, UK). Smaller fruit bats and insectivorous bats were physically restrained during sampling. All bats were released at the capture site within 3 h of capture.

Figure 1
figure 1

Coronaviruses phylogenetic analysis performed in Anthony et al. (2017b). Sequences are collapsed into clades, representing operating taxonomic units (sequences sharing equal or more than 90%). The sequences included in this manuscript are indicated in the boxes.

Table 1 Bat Species Sampled at 25 Sites in Rwanda for 11 Viral Families, with Numbers and Percentages of Bats Testing Positive for CoV RNA.

Sampling for viral family screening included collection oral and rectal mucosal or fecal swabs. Swabs were placed into viral transport media (BD Universal Viral Transport™ medium, Becton, Dickinson and Co., Sparks, Maryland) and NucliSENS Lysis Buffer (bioMerieux SA™, Marcy l’Etoile, France) and stored in liquid nitrogen for transport and transfer to a − 80 °C freezer.

We extracted RNA from oral and rectal swab samples using the Qiamp Viral Mini kit™ (Qiagen Inc., Valencia, CA) and reverse transcribed into cDNA using SuperScript III™ (Invitrogen Corp, Carlsbad, CA). Primers targeting the housekeeping gene β-actin were used to ensure the presence of amplifiable nucleic acid in RNA extracts (Goldstein et al. 2004). Samples were screened by consensus PCR targeting conserved gene fragments using established assays know to detect corona (Quan et al. 2010; Watanabe et al. 2010), alpha (Sánchez-Seco et al. 2001), arena (Lozano et al. 1997), bunya (Briese et al. 2007), filo (Zhai et al. 2007), flavi (Moureau et al. 2007), hanta (Raboni et al. 2005), influenza (Anthony et al. 2012), paramyxo (Tong et al. 2008), lenti (Courgnaud et al. 2001), and rhabdo (Wray et al. 2016) viruses. Bands of the expected size were excised from 1% agarose and purified using the Qiaquick kit (Qiagen Inc.). Purified PCR products were cloned (pCR4-TOPO vector; Invitrogen Corp.) and sequenced (ABI 3730 Capillary Electrophoresis Genetic Analyzer; Applied Biosystems, Inc., Foster City, CA). Sequences were analyzed and edited using Geneious (Version 6.0.3) and compared with known sequences in the Genbank database. Species identification of PCR-positive individuals was confirmed by DNA bar coding of the cytochrome b (Cytb) and cytochrome oxidase subunit 1 (CO1) mitochondrial genes (Townzen et al. 2008). Fisher’s exact test was used to examine the association of viral positivity with age and season using STATA 13.0 software. The level of significance was set at P ≤ 0.05 (Raymond and Rousset 1995).

No alpha, arena, bunya, filo, flavi, hanta, influenza, paramyxo, lenti, or rhabdo viruses were detected in oral or rectal swabs. Coronaviruses (CoV) were detected in 27 (5.4%) of the 503 bats sampled. Twenty-two of the 27 coronavirus positive bats belonged to three species: Straw-colored fruit bat (Eidolon helvum; 13 positives of 111 sampled, 11.7%), Geoffroy’s horseshoe bat (Rhinolophus clivosus; 5 of 24, 24.2%), and Egyptian fruit bat (Rousettus aegyptiacus; 4 of 36, 11.1%). Coronavirus positive bats were sampled at 11 different sites, including in the Musanze Caves (Table 1). Subadult bats were more likely to be positive for CoV than adults (6/36 vs. 21/429; P = 0.04). No coronaviruses were detected in juvenile bats (n = 11). There were no observed differences between seasons (Dry/Rainy; 3/90 vs. 24/386; P = 0.445).

Coronavirus sequences were classified as belonging to different viral species according to established cutoffs and methods (Anthony et al. 2017b). We detected four known coronaviruses (Table 2) and four new coronaviruses (Table 3; Fig. 1). One of the new betacoronaviruses, Coronavirus PREDICT_CoV-43, was detected in Hipposideros ruber and R. clivosus bats co-roosting in bat tourism caves (Site 10; Fig. 1; Table 3). Comparison of the conserved polymerase gene fragment sequences to other known coronaviruses indicated that Coronavirus PREDICT_CoV-43 clustered near the SARS-like coronaviruses but suggests it may be a distinct virus based on the conserved fragment sequence, as it showed only 84% nucleotide similarity to SARS-CoV (Genbank accession no. NC_009694). The second new betacoronavirus, PREDICT_CoV-44, was detected in two Hipposideros caffer bats trapped in Nyungwe National Park (Site No. 11) and in a R. clivosus bat in tourism caves at Site No. 10 (Fig. 2). Although the conserved sequence fragment also clustered with other betacoronaviruses, it was quite divergent, showing only 79% nucleotide similarity to others in the group.

Table 2 Known Coronaviruses Detected in Bats by Species and Specimen Type.
Table 3 Novel Coronaviruses Detected in Bats by Species and Specimen Type.
Figure 2
figure 2

Map of Rwanda showing the bats sampling sites for corona viral surveillance during the study.

The 2d betacoronavirus, PREDICT_CoV-66, was detected in one Rousettus angolensis bat in Nyungwe National Park (Site 11; Fig. 2) and showed 84% nucleotide similarity to the closest recognized coronavirus, Kenya bat Coronavirus BtKY84 (Genbank accession no. GU65428) found previously in E. helvum. The only alphacoronavirus PREDICT_CoV-42 was detected in a R. clivosus bat in tourism caves (Site No. 10). This virus sequence showed only 85% nucleotide similarity to the closest recognized coronavirus, Kenya bat Coronavirus BtKY69 (Genbank accession no. GU65413), found previously in horseshoe bats (Rhinolophus species).

Phylogenetic analyses of complete genome sequences of coronaviruses from bats, humans, and other vertebrates suggest that bats may be the reservoir hosts from which all coronavirus lineages originated (Vijaykrishna et al. 2007; Anthony et al. 2017a), and several studies document the diversity of bat coronaviruses globally (Dominguez et al. 2007; Annan et al. 2013; Anthony et al. 2017b).

In this study, sequences representing two novel coronaviruses that clustered with the SARS-like coronaviruses were detected in bat tourism caves and other sites where people and bats come into close contact in Rwanda. One virus (PREDICT CoV-43) was detected in both Sundevall’s roundleaf bat (H. ruber) and Geoffrey’s horseshoe bat (R. clivosus) that were co-roosting in the Musanze Caves (Site No. 10). The high sequence similarity of the viral fragment detected in both bat species suggests that this virus may have the ability to be maintained in more than one host or that cross-species transmission may occur. Studies have found that viral sharing and cross-species transmission may be important factors that contribute to emergence of novel coronaviruses and recombination of bat coronaviruses (Lau et al. 2010; Johnson et al. 2015).

While the known coronaviruses detected in this study have been identified in other geographical areas and in different bat species (Tao et al. 2012; Drexler et al. 2010), we report their first detection in Rwanda. The bat coronavirus HKU9 was previously detected in Rousettus leschenaulti bats in China (Tang et al. 2006), and now a strain of this virus has been detected in bats in Rwanda. Similarly, Kenya bat coronavirus/BtKY56/BtKY55 in R. aegyptiacus, Chaerephon bat coronavirus/Kenya/KY22/2006 in Chaerephon pumilus, and Eidolon bat coronavirus/Kenya/KY24/2006 in Eidolon helvum were first detected in Kenya in 2006 (Tao et al. 2012). We report the presence of these viruses in these same bat species in Rwanda, indicating a wider geographic distribution of these viruses in Eastern Africa, likely due to the widespread distribution of their bat hosts (Drexler et al. 2010; Gloza-Rausch et al. 2008).

In conclusion, bats in Rwanda carry novel and known coronaviruses, a family of viruses from which novel viruses have caused human pandemics. However, bats play important ecological roles and their elimination as a control measure is not recommended or warranted. We recommend additional surveillance and longitudinal studies to further understand the ecology of bat coronaviruses and the extent of human–bat interactions to identify strategies for public health protection and bat conservation.

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Acknowledgments

We thank the government of Rwanda for permission to conduct this work. This study was made possible by the generous support of the American people through the United States Agency for International Development (USAID) Emerging Pandemic Threats PREDICT project (cooperative agreement number GHN-A-OO-09-00010-00). The results from the study do not indicate the opinion of the United States of America government. Sampling was conducted under a University of California, Davis Animal Care and Use Committee approved protocol (UC Davis IACUC Protocol No. 16048). We thank also the One Health Institute Laboratory at University of California, Davis for viral sequencing, the RAB Wildlife Virology laboratory in Kigali for raw sample processing and storage, and Makerere University Walter Reed Project for viral family testing.

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Nziza, J., Goldstein, T., Cranfield, M. et al. Coronaviruses Detected in Bats in Close Contact with Humans in Rwanda. EcoHealth 17, 152–159 (2020). https://doi.org/10.1007/s10393-019-01458-8

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  • DOI: https://doi.org/10.1007/s10393-019-01458-8

Keywords

  • Rwanda
  • Bats
  • Coronaviruses
  • Human–wildlife interfaces