Identification and genotyping of feline infectious peritonitis-associated single nucleotide polymorphisms in the feline interferon-γ gene
© Hsieh and Chueh; licensee BioMed Central Ltd. 2014
Received: 31 October 2013
Accepted: 28 April 2014
Published: 21 May 2014
Feline infectious peritonitis (FIP) is an immune-mediated, highly lethal disease caused by feline coronavirus (FCoV) infection. Currently, no protective vaccine or effective treatment for the disease is available. Studies have found that some cats survive the challenge of virulent FCoV isolates. Since cellular immunity is thought to be critical in preventing FIP and because diseased cats often show a significant decrease in interferon-γ (IFN-γ) production, we investigated whether single nucleotide polymorphisms (SNP) in the feline IFN-γ gene (fIFNG) are associated with the outcome of infection. A total of 82 asymptomatic and 63 FIP cats were analyzed, and 16 SNP were identified in intron 1 of fIFNG. Among these SNP, the fFING + 428 T allele was shown to be a FIP-resistant allele (p = 0.03), and the heterozygous genotypes 01C/T and +408C/T were found to be FIP-susceptible factors (p = 0.004). Furthermore, an fIFNG + 428 resistant allele also showed a clear correlation with the plasma level of IFN-γ in FIP cats. For the identification of these three FIP-related SNP, genotyping methods were established using amplification refractory mutation system PCR (ARMS-PCR) and restriction fragment length polymorphisms (RFLP), and the different genotypes could easily be identified without sequencing. The identification of additional FIP-related SNP will allow the selection of resistant cats and decrease the morbidity of the cat population to FIP.
Feline infectious peritonitis (FIP) is an immune-mediated disease caused by feline coronavirus (FCoV) infection. Despite the vast number of studies conducted since the recognition of FIP, neither effective vaccines nor therapeutic agents are available for the prevention or treatment of this often fatal disease. Therefore, it remains one of the most important feline infectious diseases.
Despite the ubiquitous existence of FCoV in cat populations around the world, the development of FIP was only observed in fewer than 5% of the FCoV-infected cats. In addition, during the past few decades, several studies were conducted using various FCoV isolates, and regardless of the dose of virulent FCoV, some cats survived from the experimental infection[2–11]. Genetic polymorphisms in the host were suggested to be important in the resistance to FIP; however, no specific gene with a clear correlation to resistance to this disease has ever been identified.
The protective immunity to FIP is thought to result mainly from cell-mediated immunity (CMI), and changes in the expression of several cytokines have been observed in cats with either experimentally induced or naturally occurring FIP. The expression of one of the cytokines studied, interferon-γ (IFN-γ), was consistently decreased in diseased animals, and this gene is thought to play a protective role in the pathogenesis of FIP, since it is a key cytokine in CMI[6, 8, 12–14].
In recent decades, single nucleotide polymorphisms (SNP) in the IFN-γ gene (IFNG) have been found to be associated with various pathological conditions in humans as well as in ruminants and fowl[16–23]. Nevertheless, this gene has not been investigated in cats. To identify a possible association between feline IFNG (fIFNG) SNP and the outcome of FCoV infection, some regions of the fIFNG gene were sequenced and analyzed. Three SNP with statistical relevance were found to be associated with the occurrence of FIP, and polymerase chain reaction (PCR) assays based on these differences were designed as a potential screening test for the selection of FIP-resistant populations.
Materials and methods
Whole blood and buccal swabs were collected from 82 FCoV-infected asymptomatic cats and 64 FIP cats from 2005 to 2012 at the National Taiwan University Animal Hospital for the association analysis. All asymptomatic healthy cats were three years old or younger and had positive reverse transcription-nested PCR test results for FCoV infection in any of the following samples upon first arriving at the hospital: whole blood or nasal, oral, conjunctival, or rectal swabs. In addition, these cats showed no FIP-related symptoms when recruited into the study, and except for 12 cats, they stayed healthy for at least two years. All the FIP cases enrolled in this study were cats showing typical clinical signs of FIP and further confirmed by necropsy, histopathological examinations and FCoV detection in disease-associated tissues, i.e. body effusions, kidney, liver, spleen, mesenteric lymph node, lung, and/or brain.
To elucidate the role of host genetic background in the development of FIP, two viral pathogens, i.e. feline immunodeficiency virus (FIV) and feline leukemia virus (FeLV), that cause immunosuppression in cats were checked in FIP cats using nested PCR[25, 26], and the positive cats were omitted from the association analysis.
Identification of SNP in the partial fIFNG sequences
Primers used for the identification of SNP, ARMS-PCR and RFLP
Sequence (5′ - 3′)c
Identification of SNP
5′-PRRe - intron 1
−677 ~ -654
+629 ~ +607
5′-UTRf - exon 2
−44 ~ -25
+1390 ~ +1371
+320 ~ +341
+519 ~ +500
F (T allele)
+382 ~ +402
R (C allele)
+418 ~ +400
+320 ~ +341
+519 ~ +500
+288 ~ +307
+519 ~ +500
F (T allele)
+408 ~ +429
R (C allele)
+449 ~ +427
Linkage disequilibrium (LD) test and association analysis
An LD test and the creation of an LD plot were performed using LD2SNPing v 2.0 (Department of Electronics Engineering, National Kaohsiung University of Applied Science, Kaohsiung, Taiwan). The associations between SNP and the outcome of FCoV infection were analyzed. A Fisher’s exact test value of P < 0.05 was considered to represent a significant association.
Quantification of IFN-γ levels in the plasma samples of FIP cats
The plasma samples of FIP cats collected at the day of presentation were stored at −20 °C before use. The concentration of IFN-γ in the plasma samples was determined using an antigen capture ELISA (R & D system, McKinley Place NE, USA) following the procedure advised by the manufacturer’s instructions.
Genotyping of SNP by tetra-primer amplification refractory mutation system PCR (ARMS-PCR) and restriction fragment length polymorphisms (RFLP)
For the genotyping of SNP using ARMS-PCR, the PCR reactions contained 1 μL of template DNA, each primer at 500 nM, 200 μM dNTP, 1.5 mM MgCl2, and 0.4 U Phusion DNA polymerase (Thermo Scientific, Waltham, USA) in a total volume of 20 μL with 1× Phusion HF buffer. The primers and PCR conditions are listed in Table 1. The PCR products were resolved in 2% agarose gels and photographed using an imaging system. The PCR for the genotyping of SNP with RFLP was carried out with the same protocol, and the PCR products were digested with HpyCH4 III (New England Biolabs, Ipswich, USA) following the manufacturer’s instructions. The digested DNA was resolved in 2% agarose gels and photographed using an imaging system.
Polymorphisms in fIFNG
The SNP were then subjected to LD analysis. An LD plot of all the SNP for the whole population, including asymptomatic and FIP cats, was generated (Figure 1B). Three pairs of SNP were found to be significantly associated (r2 > 0.8): fIFNG + 230 T/C and fIFNG + 308A/C, fIFNG + 401 T/C and fIFNG + 408 T/C, and fIFNG + 524G/A and fIFNG + 1133G/C. fIFNG + 230 and fIFNG + 308 and fIFNG + 401 and fIFNG + 408 had a high degree of LD and were inherited together 100% of the time.
FIP-associated SNP in fIFNG identified in the whole cat population in this study
Control number (%)
FIP number (%)
OR (95% CI)
fIFNG + 428
FIP-associated SNP in fIFNG identified in the type I FCoV-infected cats
Control number (%)
FIP number (%)
OR (95% CI)
fIFNG + 401
fIFNG + 408
Production of IFN-γ in FIP cats carrying different genotypes
Genotyping for disease-related SNP
The occurrence of FIP is thought to be largely affected by viral virulence factors, and their roles in FIP have been intensely studied. Several viral genes, including spike[31–33], accessory gene 3c[34–36] and 7b[37–39], and membrane, have been proposed to play important roles in the development of the disease in FCoV-infected cats. As a disease with immunopathogenesis entity, the knowledge of the host genetic factors that affect FIP is still very limited, and only two studies have reported such factors[41, 42], in contrast to the considerable quantity of information on the virulence factors.
Studies conducted on host genetic polymorphisms and their associations with FIP
Grouping (number of cats)
Polymorphism associated with FIP
1. Clonal sequence analysis
DSHb and Pure breed
1. FIP (8)
2. Carrier (4)
3. Transient (10)
4. Resistant (3)
SNP gene chip
1. FIP (34)
1. A2.191286425 - ELMO1
2. Healthy (151)
2. A1.196617776 - ERAP1, 2
3. A1.206840008 - ERAP1, 2
4. Un.59861682 - ERAP1, 2
5. E2.65509996 - UI c
PCR and sequencing
DSH and Pure breed
1. FIP (63)
1. fIFNG + 401
2. Healthy (82)
2. fIFNG + 408
3. fIFNG + 428
Recently, several FIP-associated SNP were identified by a massive screen of Birman cats using a commercialized SNP gene chip, and the candidate genes were located from 69 kb to more than 1 Mb away from the identified SNP (Table 4). In contrast to that report, the SNP were located within the candidate gene, fIFNG, in our study, which demonstrates a stronger linkage of the analyzed SNP to the candidate gene. In addition, the cat populations enrolled in this study, including approximately 50% DSH and another 50% pure breed or mixed breed cats, were more variable, and the SNP associated with the disease may have been better represented on the entire cat population.
IFN-γ is a crucial regulatory cytokine in CMI and is important for the control of intracellular pathogens. In FCoV infection, decreased IFN-γ production in FIP cats was consistently observed in multiple studies[6, 8, 12–14]. In addition, in FCoV-infected non-FIP cats, the peripheral blood mononuclear cells showed a significant increase in the IFN-γ response upon stimulation with the FCoV antigen when compared to the FIP cats. The expression of IFN-γ was thought to protect against FCoV infection. In several studies on human viral infections, i.e., human immunodeficiency virus, hepatitis B and hepatitis C[44, 45], a similar correlation between the magnitude of the IFN-γ response and disease manifestation was identified. The polymorphisms in IFNG were associated with the diseases caused by these viruses[46–48].
The SNP associated with FIP are located in the intron 1 region. Therefore, it is unlikely that they mediate the outcome of the infection directly by altering the function of IFN-γ. In humans, IFNG polymorphisms have been found that correlate with the expression of IFN-γ. In the promoter region, SNP at positions −183 and −155 were found to influence the binding of activating transcription factor-1 and the nuclear factor-associated T-cell site[49, 50]. In addition, the number of CA microsatellite repeats was found to be tightly associated with the SNP at position +874 and to influence the production of IFN-γ by altering the binding activity of nuclear factor kappa-light-chain-enhancer of activated B cells. In ewes, despite the polymorphisms in INFG at position -641, the microsatellite showed a significant effect on IFNG expression in the spleen, although the mechanism that mediates this effect remains unknown. In the present study, a clear correlation between the IFN-γ responses and the genotype at position +428 was observed (Figure 2B). The resistant T allele at position +428 may serve as a major factor to enhance the IFN-γ production upon infections of intracellular pathogens. Despite lacking correlation with the IFN-γ level, the SNP at positions +401 and +408 might still play a minor role in the alteration of the production of IFN-γ. Since the three FIP-related SNP identified in this study are located in a small cluster, it is possible that these polymorphisms alter the binding of one or more transcription factors and work together to influence the immune response to FCoV infection. However, the actual mechanism for the altered expression of IFN-γ remains to be investigated.
In this study, three SNP in fIFNG were found to be associated with the outcome of FCoV infection. Using the ARMS-PCR and RFLP tests established, the three SNP could be distinguished in the ordinary diagnostic laboratory without sequencing, and cats bearing either the susceptible or resistant genotypes could be identified. Since the disease outcome is usually influenced by multiple host genes, other candidate genes, i.e., tumor necrosis factor-α[51, 52], interleukin-12 and CD209, are currently being surveyed. A combination of all the FIP-related SNP into a single genotyping microarray will allow the selection of resistant cats before breeding and eventually decrease the morbidity of the cat population to FIP.
This work was supported by the grant NSC 102-2313-B-002- 027 from the National Science Council, Taiwan.
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