Literature DB >> 25075637

Antibodies against MERS coronavirus in dromedary camels, Kenya, 1992-2013.

Victor M Corman, Joerg Jores, Benjamin Meyer, Mario Younan, Anne Liljander, Mohammed Y Said, Ilona Gluecks, Erik Lattwein, Berend-Jan Bosch, Jan Felix Drexler, Set Bornstein, Christian Drosten, Marcel A Müller.   

Abstract

Dromedary camels are a putative source for human infections with Middle East respiratory syndrome coronavirus. We showed that camels sampled in different regions in Kenya during 1992-2013 have antibodies against this virus. High densities of camel populations correlated with increased seropositivity and might be a factor in predicting long-term virus maintenance.

Entities:  

Keywords:  Kenya; MERS-CoV; Middle East respiratory syndrome coronavirus; antibodies; coronavirus; dromedary camels; reservoir; seroprevalence; viruses; zoonoses

Mesh:

Substances:

Year:  2014        PMID: 25075637      PMCID: PMC4111164          DOI: 10.3201/eid2008.140596

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


Middle East respiratory syndrome coronavirus (MERS-CoV) was discovered in a patient from Saudi Arabia in 2012 and has since caused ≥250 human infections and 93 deaths (). The evolutionary origins of MERS-CoV and related viral species belonging to the genus Betacoronavirus clade C were attributed to insectivorous bats in Europe and Africa (–). Seroprevalence studies of livestock from diverse species showed that dromedary camels from Oman, Saudi Arabia, the United Arab Emirates, Jordan, Qatar, Spain, and Egypt harbored antibodies against MERS-CoV antigens (–). Direct evidence for MERS-CoV infection in camels has been found in Qatar, Saudi Arabia, and Egypt. Close similarity of camel-associated and human-associated MERS-CoV sequences suggests that camels are sources of infection for humans and might constitute a zoonotic animal reservoir (,,). Where and when the putative introduction of MERS-CoV into camel populations took place and how the virus is maintained in camel populations remains obscure. Most livestock camels slaughtered in the Arabian Peninsula and in Egypt are imported from the Greater Horn of Africa, in particular Ethiopia, Somalia, Sudan, and Kenya (,). We investigated MERS-CoV antibody levels and distribution patterns in farmed and nomadic camels from Kenya.

The Study

Samples were obtained from 774 dromedary camels in 3 regions in Kenya (Northeastern, Eastern, and Rift Valley [former administrative provinces]) and 7 counties (Mandera, Wajir, Isiolo, Marsabit, Laikipia, Turkana, and Baringo) during 1992–2013 (Figure). Blood samples were obtained from farmed or nomadic camels by jugular vein puncture. Serum samples originated from the archives of the International Livestock and Research Institute (ILRI) (Nairobi, Kenya). Ethical clearance for collection was part of the agreement between the Government of Kenya and ILRI, which provided ILRI with approval to broadly investigate livestock disease in Kenya.
Figure

Greater Horn of Africa and Kenya. A) Arabian Peninsula and neighboring countries in the Greater Horn of Africa. B) Detailed map of Kenya showing sampling sites in 7 counties (Turkana, Baringo, Laikipia, Marsabit, Isiolo, Mandera, and Wajir) for Middle East respiratory syndrome coronavirus (MERS-CoV). Counties were assigned to 3 regions named after the former administrative provinces of Rift Valley, Eastern, and Northeastern (left to right). The 3 sampling regions are indicated in shades of green and other counties are indicated in gray. Percentages of camels positive for antibodies against MERS-CoV are shown with the density of camels (individuals/km2) for the analyzed regions during 2 periods (1991–2000 and 2000–2013). Serosurveys were performed during 1992–2013. Camel population numbers were determined for 1991–2000 and 2000–2013. Maps were created by using data from http://www.naturalearthdata.com.

Greater Horn of Africa and Kenya. A) Arabian Peninsula and neighboring countries in the Greater Horn of Africa. B) Detailed map of Kenya showing sampling sites in 7 counties (Turkana, Baringo, Laikipia, Marsabit, Isiolo, Mandera, and Wajir) for Middle East respiratory syndrome coronavirus (MERS-CoV). Counties were assigned to 3 regions named after the former administrative provinces of Rift Valley, Eastern, and Northeastern (left to right). The 3 sampling regions are indicated in shades of green and other counties are indicated in gray. Percentages of camels positive for antibodies against MERS-CoV are shown with the density of camels (individuals/km2) for the analyzed regions during 2 periods (1991–2000 and 2000–2013). Serosurveys were performed during 1992–2013. Camel population numbers were determined for 1991–2000 and 2000–2013. Maps were created by using data from http://www.naturalearthdata.com. All serum samples were tested for MERS-CoV antibodies by using a recombinant MERS-CoV spike protein subunit 1–based ELISA (rELISA) as described (). Serum samples were used at a 1:100 dilution, which had been shown to be optimal for screening (). A positive serum sample from recent studies (,) was used as a reference in all experiments. We used the assay-specific cutoff (optical density ratio 0.3) that had been validated in a previous study of camel serum samples (). A total of 228 (29.5%) of 774 dromedary camels were rated MERS-CoV positive by the rELISA (Table 1). All 228 rELISA-positive serum samples from these 228 camels were subsequently tested at a 1:40 dilution by using an established recombinant immunofluorescence assay and Vero cells expressing MERS-CoV spike protein (). This confirmatory assay showed that 213 (93.4%) of 228 rELISA-positive serum samples had MERS-CoV antibodies (Table 1).
Table 1

Analysis for MERS-CoV in serum samples of dromedary camel from 3 regions in Kenya, 1992–2013*

RegionCounty†Husbandry/ managementYearNo. samplesNo. rELISA positive samples (%)No. rIFA positive samples/rELISA positive samples (%)
NortheasternMandera/ Wajir‡Nomadic§200816291 (56.2)86/91 (94.5)
EasternIsioloNomadic§1998122 (16.7)1/2 (50.0)
MarsabitNomadic§19994132 (78.0)28/32 (87.5)
VariableNomadic§20007339 (53.4)38/39 (97.4)
MarsabitNomadic§20082112 (57.1)12/12 (100.0)
MarsabitNomadic§201377 (100.0)7/7 (100.0)
Rift ValleyLaikipia¶Ranch#1992221 (4.5)0/1 (0.0)
LaikipiaRanch#1996372 (5.4)2/2 (100.0)
LaikipiaRanch#1998500 (0.0)ND
LaikipiaRanch#199917532 (18.3)30/32 (93.8)
TurkanaNomadic**1999507 (14.0)6/7 (85.7)
LaikipiaRanch#2000562 (3.6)2/2 (100.0)
BaringoResearch center††2007280 (0.0)ND
LaikipiaRanch2013401 (2.5)1/1 (100.0)
Total774228 (29.5)213/228 (93.4)

*MERS-CoV, Middle East respiratory syndrome coronavirus; rELISA, recombinant ELISA for MERS-CoV subunit 1 spike protein (serum samples were tested at a dilution of 1:100); rIFA, recombinant immunofluorescence assay for MERS-CoV spike protein expression in Vero cells (serum samples were tested at a dilution of 1:40; ND, not done.
†Designated county refers to place of sampling or location in which camels were primarily located.
‡Data was merged because both counties had comparable antibody levels.
§High density of camels and regular contact between herds, including exchange of animals between herds in relation to lactation and reproduction status.
¶Formerly from Pakistan.
#Low density of camels and only sporadic contact between herds, with introduction of new animals only by purchase or livestock raiding, or restocking of camels.
**Low density of camels but more frequent contact between herds than on ranches This includes encounters at waterholes and night enclosures, as well as sharing of pastures with daily to weekly contact between herds.
††Isolated herd that originated in Wajir but was kept under quarantine-like isolation conditions for experimental work since 1998.

*MERS-CoV, Middle East respiratory syndrome coronavirus; rELISA, recombinant ELISA for MERS-CoV subunit 1 spike protein (serum samples were tested at a dilution of 1:100); rIFA, recombinant immunofluorescence assay for MERS-CoV spike protein expression in Vero cells (serum samples were tested at a dilution of 1:40; ND, not done.
†Designated county refers to place of sampling or location in which camels were primarily located.
‡Data was merged because both counties had comparable antibody levels.
§High density of camels and regular contact between herds, including exchange of animals between herds in relation to lactation and reproduction status.
¶Formerly from Pakistan.
#Low density of camels and only sporadic contact between herds, with introduction of new animals only by purchase or livestock raiding, or restocking of camels.
**Low density of camels but more frequent contact between herds than on ranches This includes encounters at waterholes and night enclosures, as well as sharing of pastures with daily to weekly contact between herds.
††Isolated herd that originated in Wajir but was kept under quarantine-like isolation conditions for experimental work since 1998. As a final step, antibody specificity was confirmed by using a highly specific MERS-CoV microneutralization assay as described (). All 228 rELISA-positive serum samples were tested at a starting dilution of 1:80 and an ending dilution of 1:800 to identify animals with high neutralization titers. A total of 119 (52.2%) 228 rELISA-positive serum samples had MERS-CoV neutralizing antibody titers (range 1:80–1:800) and 14 (6.1%) of 228 had high (>1:800) titers. The highly reactive camel serum samples originated from 3 counties (Wajir, Mandera, and Marsabit) in 2 regions (Northeastern and Eastern). The highest determined endpoint titer was 1:5,120. Dromedary camels that had MERS-CoV antibodies were present at all sampling sites and during the 20-year sampling period (Table 1; Figure). With the exception of 1 county, seroprevalence was generally higher in the Northeastern and Eastern regions (range 53.4%–100%) than in the northern Rift Valley region (range 0%–17.5%). Serum samples from 28 dromedary camels from Wajir County that had been held at a research center in isolation conditions since 1998 were negative for MERV-CoV antibodies. To further confirm the observed seropositivity gradient, we compared those 129 camel serum samples with those that were obtained in the same year (2000) but at 2 locations (Eastern and northwestern Rift Valley regions). Antibody levels of nomadic dromedary camels from the Eastern region were significantly higher than those for farmed animals from the Rift Valley (corrected χ2 34.1, p<0.005) (Table 2). Adult animals in both regions had a 7%–10% higher seroprevalence than juvenile animals, which is consistent with results of a previous study ().
Table 2

Antibodies against MERS-CoV in dromedary camels in 2 regions of Kenya, 2000*

RegionCounty†HusbandrySexAgeNo. samples positive by rELISA/no. tested (%)
EasternMarsabitNomadic‡F/MA24/42 (57.1)
F/MJ15/31 (48.4)
Subtotal39/73 (53.4)
Rift ValleyLaikipiaRanch§F/MA2/28 (7.1)
F/MJ0/28 (0)
Subtotal2/56 (3.6)
Total41/129 (31.8)

*MERS-CoV, Middle East respiratory syndrome coronavirus; rELISA, recombinant ELISA; A, adult; J, juvenile.
†Designated county refers to place of sampling or location in which camels were primarily located.
‡Frequent herd contacts.
§Sporadic herd contacts.

*MERS-CoV, Middle East respiratory syndrome coronavirus; rELISA, recombinant ELISA; A, adult; J, juvenile.
†Designated county refers to place of sampling or location in which camels were primarily located.
‡Frequent herd contacts.
§Sporadic herd contacts. Because virus transmission might be influenced by population density, we attempted to correlate seroprevalence with dromedary camel population density across different regions. Data for dromedary camel density (Technical Appendix) were calculated on the basis of livestock counts conducted by the Department of Resource Surveys and Remote Sensing as part of an ongoing Kenya-wide rangeland monitoring program (). Increased seroprevalence showed a significant correlation (Spearman rank correlation coefficient 0.715, p<0.005) with higher densities of dromedary camel populations in the Northeastern region and the northern part of the Eastern region (range 0.73–2.9 animals/km2) than in the Rift Valley region (0.58–0.6 animals/km2) (Figure; Technical Appendix).

Conclusions

The present study showed that dromedary camels from Kenya have antibodies against MERS-CoV, which complements the current finding that MERS-CoV is a common pathogen in dromedary camel populations (,,,,). Our finding of MERS-CoV antibodies in dromedary camels as early as 1992 is consistent with findings of a recent report from Saudi Arabia, which suggested that MERS-CoV has been circulating in dromedary camels for ≥20 years (). To project and potentially control virus spread, the public health community must understand factors determining virus maintenance. Our group and others have demonstrated that young dromedary camels have lower seroprevalences and are more likely to carry infectious virus (,). Similar observations have been made for coronaviruses in their original chiropteran hosts wherein strong virus amplification occurred soon after the time of parturition (). Young, immunologically naive animals may thus facilitate virus amplification in dromedary camel populations. We also demonstrated that dromedary camel population density shows a positive correlation with MERS-CoV seropositivity, which suggests efficient MERS-CoV maintenance or spread if herd density is high. Different types of animal husbandry in the Northeastern and Eastern regions of Kenya might be better predictors of virus transmission among camels. Dromedary camels in this area are often nomadic following rainfall patterns, and are taken across borders into neighboring countries, such as Ethiopia, for trade purposes (). The observed increase in seropositivity from the Western region to the Northeastern and Eastern regions could be attributed to increased animal-to-animal contact in cross-border dromedary camel metapopulations. Conversely, dromedary camels that originated in the Northeastern region but had been held in isolation since 1998 were negative for MERS-CoV antibodies, which is consistent with absence of antibodies in dromedary camels bred in isolation in Dubai (). The combination of nomadic husbandry for a large population and presence of young virus-susceptible animals might facilitate virus maintenance. However, our retrospective study with archived samples could not assess hypotheses for each of the individual variables to determine their relative and absolute degrees of influence on virus circulation. Because exportation of dromedary camels is largely unidirectional from eastern Africa into the Arabian Peninsula (), our findings might facilitate the search for more ancestral MERS-CoV variants to clarify the natural history of acquisition of MERS-CoV by dromedary camels and its putative transmission to humans. Our recent finding of a MERS-CoV ancestor in bats from South Africa () highlights the need for wider investigations of viral reservoirs. The fact that no human MERS cases have been observed in eastern Africa could indicate less transmissibility of viruses in regional lineages or lack of detection and reporting of cases. Serosurveys of persons handling dromedary camels in this region could help to determine whether silent or unrecognized infections are being maintained in humans.

Technical Appendix

Dromedary camel population densities in 3 regions in Kenya during 2 periods and average numbers of dromedary camels in Kenya, 1992–2013.
  11 in total

1.  Seroepidemiology for MERS coronavirus using microneutralisation and pseudoparticle virus neutralisation assays reveal a high prevalence of antibody in dromedary camels in Egypt, June 2013.

Authors:  R A Perera; P Wang; M R Gomaa; R El-Shesheny; A Kandeil; O Bagato; L Y Siu; M M Shehata; A S Kayed; Y Moatasim; M Li; L L Poon; Y Guan; R J Webby; M A Ali; J S Peiris; G Kayali
Journal:  Euro Surveill       Date:  2013-09-05

2.  Circulation of group 2 coronaviruses in a bat species common to urban areas in Western Europe.

Authors:  Chantal B E M Reusken; Peter H C Lina; Annemarie Pielaat; Ankje de Vries; Cecile Dam-Deisz; Jeroen Adema; Jan Felix Drexler; Christian Drosten; Engbert A Kooi
Journal:  Vector Borne Zoonotic Dis       Date:  2010-01-07       Impact factor: 2.133

3.  Human betacoronavirus 2c EMC/2012-related viruses in bats, Ghana and Europe.

Authors:  Augustina Annan; Heather J Baldwin; Victor Max Corman; Stefan M Klose; Michael Owusu; Evans Ewald Nkrumah; Ebenezer Kofi Badu; Priscilla Anti; Olivia Agbenyega; Benjamin Meyer; Samuel Oppong; Yaw Adu Sarkodie; Elisabeth K V Kalko; Peter H C Lina; Elena V Godlevska; Chantal Reusken; Antje Seebens; Florian Gloza-Rausch; Peter Vallo; Marco Tschapka; Christian Drosten; Jan Felix Drexler
Journal:  Emerg Infect Dis       Date:  2013-03       Impact factor: 6.883

4.  Amplification of emerging viruses in a bat colony.

Authors:  Jan Felix Drexler; Victor Max Corman; Tom Wegner; Adriana Fumie Tateno; Rodrigo Melim Zerbinati; Florian Gloza-Rausch; Antje Seebens; Marcel A Müller; Christian Drosten
Journal:  Emerg Infect Dis       Date:  2011-03       Impact factor: 6.883

5.  Close relative of human Middle East respiratory syndrome coronavirus in bat, South Africa.

Authors:  Ndapewa Laudika Ithete; Samantha Stoffberg; Victor Max Corman; Veronika M Cottontail; Leigh Rosanne Richards; M Corrie Schoeman; Christian Drosten; Jan Felix Drexler; Wolfgang Preiser
Journal:  Emerg Infect Dis       Date:  2013-10       Impact factor: 6.883

6.  MERS coronaviruses in dromedary camels, Egypt.

Authors:  Daniel K W Chu; Leo L M Poon; Mokhtar M Gomaa; Mahmoud M Shehata; Ranawaka A P M Perera; Dina Abu Zeid; Amira S El Rifay; Lewis Y Siu; Yi Guan; Richard J Webby; Mohamed A Ali; Malik Peiris; Ghazi Kayali
Journal:  Emerg Infect Dis       Date:  2014-06       Impact factor: 6.883

7.  Middle East respiratory syndrome coronavirus neutralising serum antibodies in dromedary camels: a comparative serological study.

Authors:  Chantal B E M Reusken; Bart L Haagmans; Marcel A Müller; Carlos Gutierrez; Gert-Jan Godeke; Benjamin Meyer; Doreen Muth; V Stalin Raj; Laura Smits-De Vries; Victor M Corman; Jan-Felix Drexler; Saskia L Smits; Yasmin E El Tahir; Rita De Sousa; Janko van Beek; Norbert Nowotny; Kees van Maanen; Ezequiel Hidalgo-Hermoso; Berend-Jan Bosch; Peter Rottier; Albert Osterhaus; Christian Gortázar-Schmidt; Christian Drosten; Marion P G Koopmans
Journal:  Lancet Infect Dis       Date:  2013-08-09       Impact factor: 25.071

8.  Middle East respiratory syndrome coronavirus in dromedary camels: an outbreak investigation.

Authors:  Bart L Haagmans; Said H S Al Dhahiry; Chantal B E M Reusken; V Stalin Raj; Monica Galiano; Richard Myers; Gert-Jan Godeke; Marcel Jonges; Elmoubasher Farag; Ayman Diab; Hazem Ghobashy; Farhoud Alhajri; Mohamed Al-Thani; Salih A Al-Marri; Hamad E Al Romaihi; Abdullatif Al Khal; Alison Bermingham; Albert D M E Osterhaus; Mohd M AlHajri; Marion P G Koopmans
Journal:  Lancet Infect Dis       Date:  2013-12-17       Impact factor: 25.071

9.  Middle East respiratory syndrome coronavirus infection in dromedary camels in Saudi Arabia.

Authors:  Abdulaziz N Alagaili; Thomas Briese; Nischay Mishra; Vishal Kapoor; Stephen C Sameroff; Peter D Burbelo; Emmie de Wit; Vincent J Munster; Lisa E Hensley; Iyad S Zalmout; Amit Kapoor; Jonathan H Epstein; William B Karesh; Peter Daszak; Osama B Mohammed; W Ian Lipkin
Journal:  mBio       Date:  2014-02-25       Impact factor: 7.867

10.  Antibodies against MERS coronavirus in dromedary camels, United Arab Emirates, 2003 and 2013.

Authors:  Benjamin Meyer; Marcel A Müller; Victor M Corman; Chantal B E M Reusken; Daniel Ritz; Gert-Jan Godeke; Erik Lattwein; Stephan Kallies; Artem Siemens; Janko van Beek; Jan F Drexler; Doreen Muth; Berend-Jan Bosch; Ulrich Wernery; Marion P G Koopmans; Renate Wernery; Christian Drosten
Journal:  Emerg Infect Dis       Date:  2014-04       Impact factor: 6.883

View more
  114 in total

1.  Middle-East respiratory syndrome coronavirus: Is it worth a world panic?

Authors:  Ahmed S Abdel-Moneim
Journal:  World J Virol       Date:  2015-08-12

2.  No Serologic Evidence of Middle East Respiratory Syndrome Coronavirus Infection Among Camel Farmers Exposed to Highly Seropositive Camel Herds: A Household Linked Study, Kenya, 2013.

Authors:  Peninah Munyua; Victor Max Corman; Austine Bitek; Eric Osoro; Benjamin Meyer; Marcel A Müller; Erik Lattwein; S M Thumbi; Rees Murithi; Marc-Alain Widdowson; Christian Drosten; M Kariuki Njenga
Journal:  Am J Trop Med Hyg       Date:  2017-06       Impact factor: 2.345

3.  Seroepidemiology of Middle East respiratory syndrome (MERS) coronavirus in Saudi Arabia (1993) and Australia (2014) and characterisation of assay specificity.

Authors:  M G Hemida; R A Perera; R A Al Jassim; G Kayali; L Y Siu; P Wang; K W Chu; S Perlman; M A Ali; A Alnaeem; Y Guan; L L Poon; L Saif; M Peiris
Journal:  Euro Surveill       Date:  2014-06-12

Review 4.  Middle East respiratory syndrome coronavirus: another zoonotic betacoronavirus causing SARS-like disease.

Authors:  Jasper F W Chan; Susanna K P Lau; Kelvin K W To; Vincent C C Cheng; Patrick C Y Woo; Kwok-Yung Yuen
Journal:  Clin Microbiol Rev       Date:  2015-04       Impact factor: 26.132

Review 5.  MERS coronavirus: diagnostics, epidemiology and transmission.

Authors:  Ian M Mackay; Katherine E Arden
Journal:  Virol J       Date:  2015-12-22       Impact factor: 4.099

6.  A Highly Immunogenic and Protective Middle East Respiratory Syndrome Coronavirus Vaccine Based on a Recombinant Measles Virus Vaccine Platform.

Authors:  Anna H Malczyk; Alexandra Kupke; Steffen Prüfer; Vivian A Scheuplein; Stefan Hutzler; Dorothea Kreuz; Tim Beissert; Stefanie Bauer; Stefanie Hubich-Rau; Christiane Tondera; Hosam Shams Eldin; Jörg Schmidt; Júlia Vergara-Alert; Yasemin Süzer; Janna Seifried; Kay-Martin Hanschmann; Ulrich Kalinke; Susanne Herold; Ugur Sahin; Klaus Cichutek; Zoe Waibler; Markus Eickmann; Stephan Becker; Michael D Mühlebach
Journal:  J Virol       Date:  2015-09-09       Impact factor: 5.103

7.  Link of a ubiquitous human coronavirus to dromedary camels.

Authors:  Victor M Corman; Isabella Eckerle; Ziad A Memish; Anne M Liljander; Ronald Dijkman; Hulda Jonsdottir; Kisi J Z Juma Ngeiywa; Esther Kamau; Mario Younan; Malakita Al Masri; Abdullah Assiri; Ilona Gluecks; Bakri E Musa; Benjamin Meyer; Marcel A Müller; Mosaad Hilali; Set Bornstein; Ulrich Wernery; Volker Thiel; Joerg Jores; Jan Felix Drexler; Christian Drosten
Journal:  Proc Natl Acad Sci U S A       Date:  2016-08-15       Impact factor: 11.205

8.  Rooting the phylogenetic tree of middle East respiratory syndrome coronavirus by characterization of a conspecific virus from an African bat.

Authors:  Victor Max Corman; Ndapewa Laudika Ithete; Leigh Rosanne Richards; M Corrie Schoeman; Wolfgang Preiser; Christian Drosten; Jan Felix Drexler
Journal:  J Virol       Date:  2014-07-16       Impact factor: 5.103

9.  Transgene expression in the genome of Middle East respiratory syndrome coronavirus based on a novel reverse genetics system utilizing Red-mediated recombination cloning.

Authors:  Doreen Muth; Benjamin Meyer; Daniela Niemeyer; Simon Schroeder; Nikolaus Osterrieder; Marcel Alexander Müller; Christian Drosten
Journal:  J Gen Virol       Date:  2017-10       Impact factor: 3.891

Review 10.  The next-generation coronavirus diagnostic techniques with particular emphasis on the SARS-CoV-2.

Authors:  Maged G Hemida
Journal:  J Med Virol       Date:  2021-03-26       Impact factor: 2.327

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.