Volume 15, Number 8—August 2009
Entomologic and Virologic Investigation of Chikungunya, Singapore
Local transmission of chikungunya, a debilitating mosquito-borne viral disease, was first reported in Singapore in January 2008. After 3 months of absence, locally acquired Chikungunya cases resurfaced in May 2008, causing an outbreak that resulted in a total of 231 cases by September 2008. The circulating viruses were related to East, Central, and South African genotypes that emerged in the Indian Ocean region in 2005. The first local outbreak was due to a wild-type virus (alanine at codon 226 of the envelope 1 gene) and occurred in an area where Aedes aegypti mosquitoes were the primary vector. Strains isolated during subsequent outbreaks showed alanine to valine substitution (A226V) and largely spread in areas predominated by Ae. albopictus mosquitoes. These findings led to a revision of the current vector control strategy in Singapore. This report highlights the use of entomologic and virologic data to assist in the control of chikungunya in disease-endemic areas.
Chikungunya is a mosquito-borne infectious disease caused by chikungunya virus (CHIKV), which belongs to the family Togaviridae and genus Alphavirus. CHIKV causes a nonfatal, self-limiting disease characterized by abrupt onset of high fever, severe arthralgia, or arthritis, often associated with skin rash.
CHIKV was first isolated during an outbreak in Tanganyika (now Tanzania) in 1952–1953 (1). The virus is believed to have originated in Africa and subsequently was introduced into many regions of Asia (2). The first CHIKV isolation in Asia was in Thailand in 1958 (3), followed by India in 1963 (4). A 2002–2003 serosurvey on 531 healthy young adults in Singapore showed a low prevalence (0.3%) of chikungunya antibodies (5). Although CHIKV has caused several large-scale epidemics in Asia and the Pacific region, it largely was neglected until its reemergence in the Indian Ocean Islands in early 2005 (6). Since then, CHIKV has caused outbreaks in India (7), Sri Lanka (8), Singapore (9), Malaysia (10), and Italy (11), focusing global attention on this newly emerging disease.
CHIKV is an enveloped, positive strand RNA virus with a genome of ≈11.8 kb (12). Phylogenetic analysis of the CHIKV genome has identified 3 lineages; West African, Asian and East, and Central and South African (ECSA) (13). The Asian lineage circulated in Asia until it was replaced by the ECSA type, which emerged during the 2005–2006 outbreaks in the Indian Ocean Islands and India (6).
Unlike in Africa, where the virus is maintained in a sylvatic cycle, chikungunya in Asia has been an urban disease, typically found in dengue-endemic areas and transmitted largely by Aedes aegypti mosquitoes. However, the predominant Aedes sp. in locations such as Réunion Island, where chikungunya emerged in 2005, was Ae. albopictus (14). The spread of chikungunya into rural areas during the later stages of outbreaks in India further confirmed the potential of Ae. albopictus mosquitoes in transmitting CHIKV (15). These changes were concurrent with the emergence of a strain having an alanine to valine substitution at codon 226 (A226V) of the envelope 1 (E1) gene in Réunion Island (16) and India (17). This mutation is known to increase the transmissibility of the virus by Ae. albopictus mosquitoes (18).
Because there is no licensed vaccine or specific drug therapy available to cure the illness, intervention relies upon vector control and minimizing mosquito-human contact. The first chikungunya outbreak in Singapore during January 2008 was successfully contained by combining aggressive vector control operations with active case detection and isolation of patients (9). On February 21, 2008, 24 days (2 incubation periods) after the last reported case, the outbreak was declared closed (9). After 3 months of no cases, local chikungunya cases resurfaced in May 2008 causing an outbreak that is yet to be resolved. This outbreak coincided with a rise in chikungunya incidence in Malaysia (10). In this report, we focus on the virologic and entomologic investigations carried out in Singapore, which assisted in the effort against the emergence of chikungunya in 2008.
Singapore initiated a chikungunya surveillance system in late 2006. The medical community was apprised by the Ministry of Health to look out for chikungunya cases among febrile patients, especially when associated with symptoms and signs (e.g., arthralgia, rash) suggestive of chikungunya (9). At the Environmental Health Institute (EHI), a national public health laboratory, an active laboratory-based surveillance was set up among a network of general practitioners. Confirmed cases were categorized as imported or local based on detailed travel history. Virologic analysis described in this study was performed on samples received by the EHI as part of the national public health surveillance program designed for chikungunya in Singapore.
Diagnosis of chikungunya was confirmed by detection of a fragment of the nonstructural protein 1 gene of CHIKV by a real-time reverse transcription–PCR (RT-PCR) protocol described previously (19). CHIKV RNA was extracted from serum by using QIAamp viral RNA mini kit (QIAGEN, Hilden, Germany), and the amplification was performed in a LightCycler 2.0 system by using LightCycler RNA Master SYBR Green I kit (Roche Diagnostics GMbH, Mannheim, Germany) according to manufacturers’ instructions. All tests included 2 negative controls: a PCR control and a negative extraction control of DNAse/RNAse-free water. The positive control was RNA extracted from a CHIKV culture with a known PFU titer determined by plaque assay. The presence of CHIKV was determined based on the melting peaks (83.07°C–84.17°C) of the positive control amplifications.
Design of Specific Primers for Sequencing
All primers were essentially constructed towards strains of the Indian Ocean and Central African origin using Gene Runner 3.05 (Hastings Software, Inc., Hastings, NY, USA) and Primer Select 5.03 (DNASTAR Inc., Madison, WI, USA) software. The primer sequences used are listed in Table 1.
Sequencing of the E1 Gene
Complimentary DNA was synthesized as described in SuperScript III First-Strand synthesis system for RT-PCR (Invitrogen Corp., Carlsbad, CA, USA). All templates were purified with the QIAquick PCR purification kit (QIAGEN) before sequencing. Sequencing was performed using BigDye Terminator Cycle Sequencing kit, according to manufacturer’s instructions (Applied Biosystems, Foster City, CA, USA).
The nucleotide sequences were assembled using the SeqMan II version 5.03 (DNASTAR) and aligned using Clustal W multiple alignment tool in the BioEdit Sequence Alignment Editor version 126.96.36.199 (20). The phylogenetic tree was inferred based on the 1,002-nt sequence of the E1 gene from aa residues 91 to 424, using the maximum-likelihood (ML) method as implemented in PAUP* version 4.0b10 (21). Bootstrapping to access the robustness of the ML tree topology was performed using the neighbor-joining method under the ML criterion based on 1,000 replicates.
Seven local transmission clusters representing major local outbreaks were selected for entomologic investigation: Little India (1°18′24′′N, 103°50′57′′E), Queen Street (1°17′ 52′′N, 103°51′05′′E), Teachers’ Estate (1°23′0′′N, 103° 49′43′′E), Kranji (1°25′30′′N, 103°45′43′′E), Sungei Kadut (1°25′1′′N, 103°45′2′′E), Mandai Estate (1°24′31′′N, 103°45′34′′E), and Bah Soon Pah Road (1° 24′45′′N, 103°49′E) (Figure 1). These areas were classified naturally into urban (Little India and Queen Street), suburban (Teachers’ Estate) and rural (Kranji, Sungei Kadut, Mandai Estate and Bah Soon Pah Road). The georeferenced Aedes larvae collection data from the chikungunya clusters were extracted from the Geographic Information System (ArcGIS) database of the National Environmental Agency, Singapore. The database, which is a part of the national vector control program, was assembled based on routine vector surveillance data obtained daily through area-wide inspection for mosquito breeding by ≈500 vector control officers.
The ultimate objective of this routine exercise was to identify as many active breeding places as possible in all residential and nonresidential premises within each cluster area. The collected larvae were separated into species based on morphologic identification before their numbers were counted. For this study, larval surveillance data were expressed as the larval abundance index, the ratio between the numbers of Ae. aegypti and Ae. albopictus larvae collected. For a single case, the number of larvae found within a 200-m radius of the case was used to calculate the larval abundance index, whereas the number of larvae found within the boundary of the cluster area was used in widespread clusters. Larval data collected 3 months before and after the first case reported from each cluster were used to calculate the index.
In each cluster area selected, adult mosquito surveillance was also conducted to determine the Aedes spp. composition and to confirm the presence of CHIKV in identified mosquitoes. Adult mosquitoes were collected using the sweep-net method, the Biogents (BG) Sentinel Trap (Biogents AG, Regensburg, Germany) or both. In each area, adult mosquito surveillance was conducted within 1-week from the beginning of the outbreaks, usually at the location from where the highest number of cases was reported. The survey was conducted once in all areas, except for Kranji Way, where it was carried out twice with a gap of 1 week between each collection. The number of locations surveyed ranged from 1 to 25 premises in each area, with higher number of premises in urban areas and lower numbers in rural areas in general. However, if a single case was reported from a cluster area, the adult mosquito survey was conducted in a few randomly selected premises within the neighboring area of the index case, even if it was an urban area. The sweep net method was performed in Little India and Teachers’ Estate areas. The BG Sentinel traps were deployed in Queen Street, Sungei Kadut, Mandai Estate, and Bah Soon Pah Road areas. The number of traps deployed in each area ranged from 4 to 15 traps, with a trapping duration of 12 to 24 hours on each occasion. The sweep net method and BG Sentinel traps were used in Kranji Way. Adult Aedes mosquitoes were crushed individually in minimum essential medium before RT-PCR was performed as for serum samples. The isolated viruses were sequenced and analyzed as described above.
From December 2006 through December 2007, a total of 1,375 samples were tested at the EHI for chikungunya; 10 of these cases were positive by PCR or immunoglobulin M testing. Epidemiologic investigation showed that all these cases were imported from India, Maldives, Sri Lanka, and Indonesia, which generally reflected the regional distribution of chikungunya during that time.
More than 7,000 samples from general practitioners, hospitals, and active case detection were tested from January through September 2008. In January 2008, the first locally acquired case of chikungunya was detected in the Little India area by a general practitioner involved in the chikungunya surveillance network (Figure 1). A total of 13 locally acquired chikungunya cases were confirmed by PCR before the outbreak was finally brought under control.
Between the first episode of transmission and May 2008, 6 cases imported from Sri Lanka (n = 2), Indonesia (n = 3), and Malaysia (n = 1) were diagnosed. By June, the number of imported cases increased, and the local scene remained relatively quiet with only 2 episodes of local transmission in Teachers’ Estate area in late May (2 cases) and Farrer Road area in early June (1 case) (Figure 1). Both of these episodes were in suburban residential areas. Active case detection did not show any additional cases associated with those 2 episodes. Locally acquired cases occurred again in July 2008 coinciding with a rise in imported cases from Malaysia. By the end of September 2008, there was a cumulative total of 231 cases comprising 108 imported and 123 locally acquired infections. Of the imported cases, 92% (n = 99) had travel history to Malaysia, largely to the state of Johor, whereas the 123 local cases were distributed across 25 different locations.
After July 2008, transmission was more active in rural industrial and farming areas of Singapore, with the biggest clusters being in Kranji, Sungei Kadut, and Bah Soon Pah Road (Figure 1). Notably, during the active case surveillance using PCR, 2 viremic cases were found 1 day before the onset of clinical manifestations, with viral loads of 750 pfu/mL and 40 pfu/mL of blood, determined by using an external standard curve generated by plotting 10-fold serially diluted virus from a concentration of 108 pfu/mL, against respective crossing-point values of real-time PCRs.
The E1 gene of CHIKV from 85 imported and locally acquired infections was analyzed. Because there were several groups of similar sequences, the phylogenetic tree was constructed by using only 17 sequences that represented all imported as well as locally acquired strains at different time points. The tree also included 5 CHIKV from Sri Lanka sequenced at the EHI and 17 global sequences retrieved from the GenBank database (Figure 2). Phylogenetic analysis showed that all viruses reported in Singapore after January 2008, except 1, were related to the ECSA genotype. CHIKV isolated from the remaining infection was of Asian lineage and was imported from Indonesia (Figure 2). All ECSA-type viruses formed a distinct clade, together with isolates from India, Sri Lanka, Italy, and the Indian Ocean Islands (Figure 2). In the phylogenetic tree, the viruses isolated during the first outbreak in the Little India area clustered closely with those reported in India in 2006. One isolate from an imported case from Maldives also clustered within this group. In contrast, viruses isolated during the second local episode in the Teachers’ Estate in May 2008 and in all other areas from July 2008 grouped with those imported from Malaysia. Similarly, CHIKV isolated during the third local episode in the Farrer Road area in June 2008 clustered separately with isolates from Sri Lanka (Figure 2).
CHIKV isolated during the first local outbreak was wild-type (alanine) at aa residue 226 (A226) of the E1 gene, whereas, those detected during the second, third, and subsequent local episodes contained valine (A226V). Besides A226V, CHIKV isolated during the second local outbreak showed 2 synonymous mutations at nucleotide positions 300 (C300T) and 363 (A363G) of the E1 gene, which were not present in viruses involved in the first and third outbreaks. Of these isolates, C300T was unique to CHIKV strains imported from Malaysia. C300T and A363G were also found in all viruses detected in imported cases from Malaysia after June 2008. Similarly, CHIKV isolated in the third local episode was unique because it showed 2 synonymous mutations at nucleotide positions 105 (A105G), 1308 (C1308T) and a nonsynonymous mutation at nucleotide position 633 (A633C [K211N]) of the E1 gene, the combination of which was unique to CHIKV isolates from Sri Lanka. Therefore, we defined the combinations of C300T + A363G and A105G + A633C + C1308T as genetic signatures of isolates from Malaysia and Sri Lanka, respectively. These observations demonstrated that the first 3 episodes of chikungunya transmission in Singapore were most likely due to independent importations of distinct viruses from different geographic locations.
Aedes larval collection data showed that Ae. albopictus was the predominant species in all cluster areas, except Little India, an urban area where the first outbreak occurred (Table 2). In the Little India cluster, larval abundance index in the Clive Street area (2.14:1) was even higher than the generalized ratio for the whole cluster (1.77:1). The Clive Street area is a highly urbanized area and reported the highest number of chikungunya cases (n = 10) within the Little India cluster. This observation was further strengthened by adult mosquito surveillance, which yielded only Ae. aegypti in the Little India cluster. In contrast, Ae. albopictus (n = 164) was the only Aedes sp. caught in other cluster areas (Table 2). Adult Ae. albopictus mosquitoes from the Kranji Way and Bah Soon Pah Road areas were positive for CHIKV by RT-PCR. In Kranji Way, 7 (9.1%) of 77 female Ae. albopictus mosquitoes were positive for CHIKV, whereas 6 (13.5%) of 45 mosquitoes were positive in the Bah Soon Pah Road area. The E1 gene sequences of those 13 Ae. albopitcus-borne CHIKV were identical to sequences of strains imported from Malaysia. All mosquito-borne viruses possessed the A226V substitution.
Chikungunya is an emerging infectious disease of public health importance in Singapore. Owing to Singapore’s small size, tropical climate, presence of the vectors, and high population density, timely and effective disease control is required to minimize the risk for chikungunya outbreaks. Since its emergence on the local scene in January 2008, entomologic and virologic investigations have been used to elucidate the origin of the current outbreak of chikungunya in Singapore.
Phylogenetic data showed that the first, second, and third episodes of local transmission from January 14, 2008 to June 9, 2008, were due to 3 genetically distinct viruses of different geographic origins. The first outbreak in the Little India area in January 2008 was due to a CHIKV strain of Indian origin, whereas the second episode (2 cases) in Teachers’ Estate area in May was due to a strain closely related to viruses detected in cases imported from Malaysia. On the other hand, the CHIKV strain of the third episode (1 case) in Farrer Road area in June was closely related to isolates from Sri Lanka. According to epidemiologic data, no locally acquired chikungunya cases occurred between the first and the second episodes. Similarly, no cases were reported between the second and third episodes. Therefore, the possibility that CHIKV involved in the first outbreak evolved into genetically distinct strains detected in the second and third episodes was highly unlikely.
The unique genetic signatures among these viruses and the lack of local transmission between episodes indicated that the first 3 local episodes were most likely due to independent importations of CHIKV, most likely from India, Malaysia, and Sri Lanka. This finding was further supported by the fact that 6 imported cases reported during the first and second episodes included cases imported from Malaysia and 2 from Sri Lanka. However, all cases reported after July 2008 were due to a single strain, which was closely related to CHIKV detected in cases imported from Malaysia. This strain was genetically close to the virus that caused the second episode. Recently, it was reported that the 2007 chikungunya outbreak in Malaysia was due to a virus of the ECSA lineage (10). This evidence points to the interconnectedness of simultaneous chikungunya outbreaks in Singapore and Malaysia, which is not unexpected given the close proximity and porous borders between these 2 countries.
Entomologic surveillance showed a difference between the vector species involved in the first and subsequent outbreaks in Singapore. All adult mosquitoes caught in the vicinity of the first outbreak area (Little India) were Ae. aegypti. The larval surveillance data also showed the predominance of Ae. aegypti mosquitoes in this area (Table 2). Little India is generally a highly urbanized area with sparse vegetation, which could explain the presence of more Ae. aegypti vectors than Ae. albopictus. On the other hand, subsequent chikungunya episodes were seen in less-urbanized areas (Table 2) where Ae. albopictus was the predominant vector species. Detection of CHIKV in Ae. albopictus mosquitoes further confirmed its role in CHIKV transmission in less urbanized areas. In general, large clusters of chikungunya were seen in less urbanized areas, with a high Ae. albopictus mosquito density near human habitations.
Of note, CHIKV strains isolated from Little India, an Ae. aegypti mosquito–abundant area, showed alanine at codon 226 (A226) of the E1 gene. In contrast, all CHIKV strains isolated during subsequent episodes showed A226V substitution and were distributed in areas that were mainly inhabited by Ae. albopictus mosquitoes. Recently, Tsetsarkin et al. showed that CHIKV strains with A226V substitution replicate better in Ae. albopictus mosquitoes than does the wild-type strain (18). Their findings indicated that although the transmission potential of the wild-type virus is optimum for Ae. aegypti mosquitoes, A226V substitution confers greater vector competence in Ae. albopictus mosquitoes, making the latter species a better vector of the mutated strain than Ae. aegypti (18). This finding may result in selection for the mutated strain in areas where Ae. albopictus mosquitoes are abundant. Although the competence of Ae. aegypti mosquitoes in transmitting the virus with A226V in Singapore remains uncertain, the known evidence may therefore explain why the mutant virus with A226V caused outbreaks in less urbanized areas in Singapore where Ae. albopictus mosquitoes dominate but had little effect on urbanized areas where Ae. aegypti mosquitoes dominate. Similarly, this finding could also explain the distribution of the wild-type (A226) strain in urban areas, where Ae. aegypti mosquitoes are predominantly found. A similar observation has also been made in India, where the emergence of CHIKV with A226V was first reported in rural areas of Kerala region that are predominantly inhabited by Ae. albopictus mosquitoes (15). The low transmission rate of the mutant virus in urban and suburban Singapore could also be due to the aggressive dengue control program, which targets mainly urban and suburban parts of the country.
Based on these observations, the National Environment Agency’s Aedes spp. control strategy was revised and expanded, especially in areas where Ae. albopictus mosquitoes are present. Because Ae. albopictus are generally outdoor mosquitoes, in contrast to Ae. aegypti, measures such as outdoor fogging and residual spray of external walls were conducted in chikungunya outbreak areas. The phylogenetic data was mainly used to trace the possible origins of viral strains causing the local chikungunya episodes. The longitudinal monitoring of E1 gene sequences of CHIKV is in progress to monitor local transmission of chikungunya in Singapore. Our results showed that Singapore, being a travel hub and a cosmopolitan city, is vulnerable to multiple importations of CHIKV. The aggressive A226V variant of the ECSA genotype that has established itself in the region is posing a challenge to Singapore. Because Ae. albopictus is a common vector species in the region, the establishment of the A266V CHIKV variant in the region may continue to pose challenges in the years to come.
Dr Ng heads the Environmental Health Institute, a national public health laboratory under the auspices of National Environmental Agency, Singapore. Her research interests include the epidemiology and control of vector-borne diseases.
We thank the Ministry of Finance for the Reinvestment Fund made available for surveillance and investigative work. We are also grateful to colleagues from the Environmental Health Department, who facilitated the field investigation; colleagues at EHI, who assisted in diagnostics; and Molecular Medicine Unit, Faculty of Medicine, University of Kelaniya, Sri Lanka, for providing CHIKV isolates from Sri Lanka for sequencing.
- Robinson MC. An epidemic of virus disease in Southern Province Tanganyika Territory, in 1952–53. I. Clinical features. Trans R Soc Trop Med Hyg. 1955;49:28–32.
- Carey DE. Chikungunya and dengue: a case of mistaken identity? J Hist Med Allied Sci. 1971;26:243–62.
- Hammon WM, Sather GE. Virological findings in the hemorrhagic fever epidemic (dengue) in Thailand. Am J Trop Med Hyg. 1964;13:629–41.
- Shah KV, Gibbs CJ, Banerjee G. Virological investigation of the epidemic of hemorrhagic fever in Calcutta: isolation of three strains of chikungunya virus. Indian J Med Res. 1964;52:676–83.
- Ministry of Health. Singapore. Chikungunya virus disease. Epidemiol News Bull. 2006 [cited 2009 Jun 2]. Available from http://www.moh.gov.sg/mohcorp/publicationsnewsbulletins.aspx?id=19542
- Parola P, de Lamballerie X, Jourdan J, Rovery C, Vaillant V, Minodier P, Novel chikungunya virus variant in travelers returning from Indian Ocean Islands. Emerg Infect Dis. 2006;12:1493–9.
- Yergolkar PN, Tandale BV, Arankalle VA, Sathe PS, Sudeep A, Gandhe SS, Chikungunya outbreaks caused by African genotype, India. Emerg Infect Dis. 2006;12:1580–3.
- Hapuarachchi HA, Bandara KB, Hapugoda MD, Williams S, Abeyewickreme W. Laboratory confirmation of dengue and chikungunya co-infection. Ceylon Med J. 2008;53:104–5.
- Ministry of Health. Singapore. Singapore’s first chikungunya outbreak – surveillance and response. Epidemiol News Bull. 2008 [cited 2009 Jun 2]. Available from http://www.moh.gov.sg/mohcorp/publicationsnewsbulletins.aspx?id=19542
- Noridah O, Paranthaman V, Nayar SK, Masliza M, Ranjit K, Norizah I, et al. Outbreak of chikungunya due to virus of Central/East African genotype in Malaysia. Med J Malaysia. 2007;62:323–8.
- Rezza G, Nicoletti L, Angelini R, Romi R, Finarelli AC, Panning M, Infection with chikungunya virus in Italy: an outbreak in a temperate region. Lancet. 2007;370:1840–6.
- Khan AH, Morita K, Parquet Md, Mdel C, Hasebe F, Mathenge EG, et al. Complete nucleotide sequence of chikungunya virus and evidence for an internal polyadenylation site. J Gen Virol. 2002;83:3075–84.
- Powers AM, Brault AC, Tesh RB, Weaver SC. Reemergence of chikungunya and o’nyong-nyong viruses: evidence for distinct geographical lineages and distant evolutionary relationships. J Gen Virol. 2000;81:471–9.
- Reiter P, Fontenille D, Paupy C. Aedes albopictus as an epidemic vector of chikungunya virus: another emerging problem? Lancet Infect Dis. 2006;6:463–4.
- Kumar NP, Joseph R, Kamaraj T, Jambulingam P. A226V mutation in virus during the 2007 chikungunya outbreak in Kerala, India. J Gen Virol. 2008;89:1945–8.
- Santhosh SR, Dash PK, Parida MM, Khan M, Tiwari M, Lakshmana Rao, PV. Comparative full genome analysis revealed E1 A226V shift in 2007 Indian chikungunya virus isolates. Virus Res. 2008;135:36–41.
- Schuffenecker I, Iteman I, Michault A, Murri S, Frangeul L, Vaney MC, Genome microevolution of chikungunya viruses causing the Indian Ocean outbreak. PLoS Med. 2006;3:e263.
- Tsetsarkin KA, Vanlandingham DL, McGee CE, Higgs S. A single mutation in chikungunya virus affects vector specificity and epidemic potential. PLoS Pathog. 2007;3:e201.
- Hasebe F, Parquet MC, Pandey BD, Mathenge EGM, Morita K, Balasubramaniam V, Combined detection and genotyping of chikungunya virus by a specific reverse transcription-polymerase chain reaction. J Med Virol. 2002;67:370–4.
- Hall TA. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 1999;41:95–8.
- Swofford DL. PAUP*. Phylogenetic analysis using parsimony (*and other methods). Version 4. Sunderland (MA): Sinauer Associates; 1999.