Short report | Open | Published:
Association of ABO blood groups with Chikungunya virus
Virology Journalvolume 7, Article number: 140 (2010)
Chikungunya virus (CHIKV) an emerging arboviral infection of public health concern belongs to the genus Alphavirus, family Togaviridae. Blood group antigens are generally known to act as receptors for various etiological agents. The studies defining the relationship between blood groups and CHIKV is limited and hence it is necessary to study these parameters in detail. In the present study 1500 subjects were enrolled and demographic data (Age, Gender, Blood group, CHIKV infection status, and CHIKV infection confirmation mode) was collected from them. The risk of acquiring CHIKV disease and its association with factors such as blood group, age and gender was analyzed statistically. The data of this study showed a possible association between blood group, age and gender of the study population with CHIKV infection. It is observed that CHIKV infections were higher in individuals with Rh positive blood group when compared to their Rh negative counterparts.CHIKV infections were found to be higher in Rh positive individuals of AB and A blood groups than that of Rh negative counterparts. Results also indicated that infections were higher in adults belonging to the age group > 30 years and also higher in males as compared to females enrolled in this study. These data present further evidence for the association of the blood groups, age and gender to susceptibility to CHIKV infection. Further studies are needed to confirm these findings. This is the second study showing the possible association of blood groups with chikungunya.
Chikungunya virus (CHIKV), belonging to the genus Alphavirus, family Togaviridae is transmitted by Aedes mosquitoes (Ae. aegyptii and Ae. albopictus). Ae. albopictus played a pivotal role in transmitting the CHIKV in the recent outbreaks of Reunion islands, North Eastern Italy and India [1–3]. The disease is usually characterized by fever, arthralgia and myalgia. It was first reported from Makonde plateau, Tanzania during 1952-53 and since then, has been held responsible for explosive epidemics in Africa, India and South East Asia [4, 5]. CHIKV, an enveloped virus containing positive sense single stranded RNA as its genetic material is about 11,805 nucleotides in length containing ORF1 and ORF2 of about 7422 and 3744 nucleotides in length respectively. Phylogenetic analysis based on partial E1 gene sequences showed the presence of three distinct CHIKV phylogroups. The first phylogroup contained all isolates from West Africa; the second phylogroup involved isolates from East, Central and South Africa (ECSA); and the third phylogroup contained Asian isolates. CHIKV one of the six major vector borne diseases endemic to India has reemerged causing severe mortality during the recent outbreak . It has been declared as a high priority pathogen by NIH . It affected 216 districts in India with an estimated 1.38 million people as its victims by the end of 2006 and which further declined to an estimated 59,535, 95,091 and 68,245 cases by the end of 2007, 2008 and 2009, respectively [8, 9]. Andhra Pradesh, the most affected state was first to report the CHIKV epidemic in December 2005 in India . RT-LAMP assay is a valuable tool used for rapid, real-time detection as well as quantification of CHIKV acute phase samples and will serve as an important tool for CHIKV surveillance in developing countries . The association of diseases with blood groups has always been under controversial discussion. The relationship of blood groups of population and their susceptibility to diseases like plague, small pox, malaria, cholera etc suggest the possible role of blood group antigen in the occurrence of diseases. During the past twenty years there are many reports documenting the role of blood group antigens as receptors for parasites, bacteria and viruses . Association of blood groups with HBV infection and fibrosis severity in HCV infection has been reported earlier . The studies defining the relationship between blood groups and CHIKV is limited and hence it is necessary to study these parameters in detail. Keeping this in view the present study was designed to determine the relationship between CHIKV infection and ABO/Rhesus blood groups, age and gender.
During January-February 2010, 1500 subjects from Sri Venkateswara University Campus, Andhra Pradesh, India were enrolled in the study. A questionnaire was prepared and demographic data recorded for each patient included age, gender, blood group, CHIKV infection status (Yes/No) and CHIKV infection confirmation mode (Self declared CHIKV cases (SDC)/CHIKV infection confirmed by a physician). The importance of the present study was explained to the patients and oral consent from all the patients were obtained prior to data collection. The statistical tools such as, Odds ratio (OR) with 95% confidence interval (C.I) is presented to know the likelihood of acquiring CHIKV disease with respect to different blood groups: O, A, B and AB (Both Rh positive and Rh Negative individuals) when compared to healthy individuals. Chi-square test (χ2 test) statistic was also carried out to observe the association between the blood groups and CHIKV infection. A p value < 0.05 was considered to be statistically significant.
Among 1500 subjects enrolled in the study, 860 (57.3%) were males and 640 (42.7%) were females. Among them 513(34.2%) reported to have acquired CHIKV infection and 987(65.8%) individuals reported absence of CHIKV fever. Among these 513 individuals 409 (79.7%) patients were previously confirmed of CHIKV infection by Medical Officer, S.V.University Health Center by RT-PCR/IgM strip analysis carried out at Viral diagnostic Laboratory, Department of Virology, S.V.University, Tirupati as described by us earlier . The remaining 104 (20.27%) individuals self declared to have acquired CHIKV infection (SDC) according to the CHIKV suspected case definition by NICD, New Delhi . Based on blood group antigens the individuals were kept in four groups A (324), B (483), AB (162) and O (531). Figure 1 depicts the representation between various blood groups and CHIKV disease of the present study. The cross tabulation between the Rh positive and Rh Negative subjects of different blood groups were associated with the CHIKV status (Table 1). χ2 test results showed the statistical significance at p < 0.05, which suggests that there exists an association between the blood groups and the risk of acquiring CHIKV. The Odds ratio is one of the familiar statistical measures used to know the likelihood of possessing the risk of acquiring CHIKV disease. The same measure is used here to know the likelihood of acquiring CHIKV disease between Rh positive and Rh negative individuals. The likelihood of acquiring CHIKV disease by O positive subjects was 2.2 times more than O negative individuals ie., ORO = 2.210 (95% C.I: 1.363, 3.585). The likelihood of acquiring CHIKV disease by A positive subjects is 2.8 times more than A negative subjects i.e. ORA = 2.825 (95% C.I: 1.666, 4.792). In the same manner the likelihood of acquiring CHIKV disease by B positive and AB positive subjects is 1.7 & 3 times more than B negative and AB negative subjects ORB = 1.774 (95% C.I: 1.094, 2.876) and ORAB = 3.033 (95% C.I: 1.454, 6.329)respectively. It is also observed that in A and AB blood groups, though the Rh positive and Rh negative subjects are almost proportionate in number, but the likelihood of acquiring CHIKV disease is more to Rh positive subjects. The association is observed statistically between blood groups and status of CHIKV focusing on the 'age' factor (Table 2). χ2 test results showed statistically significant differences at p < 0.05. The status of CHIKV across the age distribution is presented for all the blood groups (Figure 2). The individuals > 30 age group are found to be more susceptible in acquiring CHIKV disease. It is also observed that the association between gender and the status of CHIKV is statistically significant (χ2 = 5.926, p < 0.05) and the Odds RatioMale/Female = 1.306 (95% C.I: 1.053, 1.619). Therefore male individuals are 1.3 times more susceptible in acquiring CHIKV disease when compared to their female counterparts.
In conclusion our results implicate that blood group, age and gender are found to be associated with the status of CHIKV. It is observed that the Rh positive individuals are more susceptible when compared to their Rh negative counterparts in acquiring CHIKV disease. Using odds ratio (OR), the differences can be observed in between the Rh positive individuals and Rh negative individuals of AB and A blood groups followed by O and B blood groups, where the Rh positive individuals are likely to have more chance of acquiring CHIKV disease than that of Rh negative individuals. The interpretation on risk of acquiring CHIKV disease is given based on the OR value of each blood group with respect to their Rh positive and Rh negative blood groups. However, these results do not comply with the previously reported results where O positive individuals were shown to be more susceptible in acquiring CHIKV disease . The difference in the association of the blood groups and CHIKV infection of the present study to that of the previously documented report emphasizes the necessity of carrying out similar studies at multicentre level in order to generate more data. With increase in age (>30), the chances of acquiring CHIKV disease are more. Movement of people outdoors during day time when the activity of Ae.albopictus is at its peak, lesser personal protection (towards mosquitoes) and individual's differential immune response to diseases are some of the speculative reasons for increased susceptibility to CHIKV infection in higher age groups (> 30 years)[1, 17]. In the present study higher CHIKV infection rates were observed in males compared to their female counterparts, an observation which was also evidenced earlier in North eastern Italy and Southern India and differential exposure to Ae.albopictus mosquitoes is supposed to be the plausible reason [1, 18]. To the best of our knowledge, our study is the second report analyzing the possibility of an association of blood groups with CHIKV seropositivity. Identification of human cell surface receptor(s) for CHIKV is quite necessary for further understanding its pathophysiology in humans .Molecular and functional studies will necessarily be helpful in disclosing the association of blood group antigens and CHIKV infections. The role of blood group antigens as important key factors in disease development is evident from earlier studies  and hence their possible role on CHIKV susceptibility cannot be ruled out and needs further investigation.
Moro ML, Gagliotti C, Silvi G, Angelini R, Sambri V, Rezza G, Massimiliani E, Mattivi A, Grilli E, Finarelli AC, Saptaro N, Pierro AM, Seyler T, Macini P: Chikungunya virus in North-Eastern Italy: A Seroprevalence study. Am J Trop Med Hyg 2010, 82: 508-511. 10.4269/ajtmh.2010.09-0322
Philip Samuel P, Krishnamoorthi R, Hamzakoya KK, Agarwal CS: Entamo-epidemiological investigations on Chikungunya outbreak in the Lakshadweep islands, Indian Ocean. Indian J Med Res 2009, 129: 442-445.
Santhosh SR, Dash PK, Parida MM, Khan M, Rao PVL: Appearance of E1: A226V mutant Chikungunya virus in Coastal Karnataka, India during 2008 outbreak. Virology Journal 2009, 6: 172. doi: 10.1186/1743-422X-6-172 10.1186/1743-422X-6-172
Edelman R, Tacket CO, Wasserman SS, Bodison SA, Perry JG, Mangiafico JA: Phase II safety and immunogenicity study of live chikungunya virus vaccine TSI-GSD-218. Am J Trop Med Hyg 2000, 62: 681-685.
Powers AM, Logue CH: Changing patterns of chikungunya virus: re-emergence of a zoonotic arbovirus. J Gen Virol 2007, 88: 2363-2377. 10.1099/vir.0.82858-0
Dhiman RC, Pahwa S, Dhillon GP, Dash AP: Climate change and threat of vector-borne diseases in India: are we prepared? Parasitol Res 2010, 106: 763-73. 10.1007/s00436-010-1767-4
Labadie K, Larcher T, Joubert C, Mannioui A, Delache B, Brochard P, Guigand L, Dubreil L, Lebon P, Verrier B, Lamballerie XD, Suhrbier A, Cherel Y, Grand RL, Roques P: Chikungunya disease in nonhuman primates involves long-term viral persistence in macrophages. J Clin invest 2010, 120: 894-906. 10.1172/JCI40104
NVBDCP: Epidemiological profile of chikungunya fever in the country. ( prov .).New Delhi: National Vector Borne Disease Control Programme; 2009. [http://nvbdcp.gov.in/Doc/chikun-update07.pdf]
NVBDCP: Status report on Dengue and Chikungunya as on 31.12.09(Dengue and chikungunya update).New Delhi: National Vector Borne Disease Control Programme; 2010. [http://nvbdcp.gov.in/Doc/Den_Chik_Dec09.pdf]
Ravi V: Re-emergence of Chikungunya virus in India. Indian J Med Microbiol 2006, 24: 83-84. 10.4103/0255-0857.25175
Parida MM, Santhosh SR, Dash PK, Tripathi NK, Lakshmi V, Mamidi N, Shrivastva A, Gupta N, Saxena P, Babu JP, Rao PV, Morita K: Rapid and real-time detection of Chikungunya virus by reverse transcription loop-mediated isothermal amplification assay. J Clin Microbiol 2007, 45: 351-357. 10.1128/JCM.01734-06
Garratty G: Relationship of blood groups to disease: do blood group antigens have a biological role? Rev Med Inst Mex Seguro Soc 2005,43(Suppl 1):113-121.
Behal R, Jain R, Behal KK, Dhole TN: Variation in the host ABO blood group may be associated with susceptibility to hepatitis C virus infection. Epidemiol Infect 2009. doi: 10.1017/S0950268809991117
Naresh Kumar CVM, Anthony Johnson AM, Sai Gopal DVR: Molecular characterization of chikungunya virus from Andhra Pradesh, India and phylogenetic relationship with Central African isolates. Indian J Med Res 2007, 126: 534-540.
National Institute of Communicable Disease, New Delhi: Chikungunya fever. CD Alert 2006, 10: 6-8.
Lokireddy S, Sarojamma V, Ramakrishna V: Genetic predisposition to chikungunya- a blood group study in chikungunya affected families. Virology Journal 2009, 6: 77. 10.1186/1743-422X-6-77
Staikowsky F, Le Roux K, Schuffenecker I, Laurent P, Grivard P, Develay A, Michault A: Retrospective survey of Chikungunya disease in Reunion island hospital staff. Epidemiol Infect 2008, 136: 196-206. 10.1017/S0950268807008424
Lakshmipathy DT, Dhanasekaran D: Molecular epidemiology of Chikungunya virus in Vellore distrct,Tamilnadu,India in 2006. East Afr J Public Health 2008, 5: 122-125.
Solignat S, Gay B, Higgs S, Briant L, Devaux C: Replication cycle of chikungunya: A re-emerging arbovirus. Virology 2009, 393: 183-197. 10.1016/j.virol.2009.07.024
CVMNK and NM greatly acknowledge, University Grants Commission, New Delhi for financial assistance in the form of UGC-JRF in Research Fellowship in Sciences for Meritorious Students Scheme (RFSMS). The research work of RVV is supported by DST-CMS project Lr. No.SR/S4/MS:516/07, Dt.21-04-2008.
The authors declare that they have no competing interests.
CVMNK designed and performed the experiment. CVMNK also performed statistical analysis, interpreted the statistical data and drafted the manuscript. NM performed the experiment and contributed in writing the manuscript. RVV has done the statistical analysis and interpretation of the results. DVRSG participated in the design and coordination of the study, analysis of the data and drafting of the manuscript. All authors read and approved the final manuscript.