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Proteomic analysis of extremely severe hand, foot and mouth disease infected by enterovirus 71
- Li Deng†1,
- Hong-Ling Jia†2,
- Chao-Wu Liu†4,
- Yu-Fen Xu1,
- Li-Jia Mao1,
- Chun-Hui He1,
- Gen-Quan Yin1,
- Jun-Hong Lin1,
- Jian-Ping Tao1 and
- Li Zhu3Email author
© Deng et al.; licensee BioMed Central Ltd. 2013
Received: 10 March 2013
Accepted: 16 August 2013
Published: 20 August 2013
To clarify the molecular mechanisms that participate in the severe hand, foot and mouth disease (HFMD) infected by Enterovirus 71 and to detect any related protein biomarkers, we performed proteomic analysis of protein extracts from 5 extremely severe HFMD children and 5 healthy children.
The protein profiles of them were compared using two-dimensional electrophoresis. Differentially expressed proteins were identified using mass spectrometry. Functional classifications of these proteins were based on the PANTHER. The interaction network of the differentially expressed protein was generated with Pathway Studio.
A total of 38 differentially expressed proteins were identified. Functional classifications of these proteins indicated a series of altered cellular processes as a consequence of the severe HFMD. These results provided not only new insights into the pathogenesis of severe HFMD, but also implications of potential therapeutic designs.
Our results suggested the possible pathways that could be the potential targets for novel therapy: viral protection, complement system and peroxide elimination.
Human enterovirus 71 (EV71) and coxsackievirus A16 (CA16) are two predominant pathogens causing HFMD. EV71 is more associated with major outbreaks and causes complications of greater severity, severe neurologic symptoms, and higher rates of mortality than other enteroviruses [1–4]. Outbreaks of EV71 have been reported since 1969 . Especially since the late 1990s, a significant increase in EV71 epidemics is observed, creating a serious threat to public health throughout the Asia-Pacific region [5–7]. For example, in 2007, more than 80,000 HFMD cases were reported with dozens of deaths in mainland China [8, 9].
The complications of severe HFMD include pneumonia, myocarditis, encephalitis, brain-stem encephalitis and acute flaccid paralysis. High mortality and severe sequelae can be anticipated when the disease is complicated by neurogenic pulmonary edema, rapid disease progression [10, 11].
Only a small fraction of the mild cases further develop to the severe and fatal cases. However, these cases often progress rapidly and cause failure and deaths before effective treatment take place. As the rapid progression of symptoms in fatal cases, rapid diagnosis is essential for severely EV71-infected patients to provide timely treatment . EV71 virus can be detected by testing viral antigens, viral genomic RNA and antiviral antibodies in HFMD patients [13–15], however, no quick method has been established to distinguish mild HFMD from severe HFMD during the rapid progression of symptoms in fatal cases of EV71 infection.
Two-dimensional gel electrophoresis (2-DE) and MALDI-TOF/TOF mass spectrometry have been extensively applied to identify differentially expressed proteins between different stages of disease, as well as those in healthy individuals, in a wide variety of biological systems . This strategy is able to detect potential biomarkers for disease diagnosis, progression and therapy while does not require much knowledge background of the disease. In this study, we used comparative proteomics to systemically study the protein profile changes in serum of extremely severe HFMD. The proteome map presented here may serve as an important basis for future studies.
Preparation of serum samples
Blood samples from 5 HFMD children (five extremely severe) according to the ‘foot and mouth disease prevention control guide’ (2008 Edition) issued by the Ministry of Health, China (http://www.moh.gov.cn/publicfiles/business/htmlfiles/mohbgt/s9511/200805/34775.htm), were randomly selected to be analyzed with 2-D Gel Electrophoresis and MALDI-TOF-MS and clinical symptoms and laboratory test (EV71 nucleic acid detection kit) confirmed that the EV71 infections caused all these HFMD cases. In addition to meeting the above symptoms, these children all had encephalitis, pulmonary hemorrhage, and mechanical ventilation and other clinical symptoms. They were proven to have no other disease after a systematic check in the hospital. Another five blood samples from healthy children were collected as controls. The protocols applied in this study were approved by the Ethical Committee of Guangzhou Women and Children′s medical center. The parents of all participants of this study provided written informed consent. A pooled sample consists of equal amounts of each of 5 experimental samples. Blood sample was separated by centrifugation at 1000 g for 20 min. Aliquots of serum were collected and stored at -80°C until ready for use. Serum samples were processed using the ProteoExtract® Albumin/IgG Removal Kit (Merck, New jersey, USA) that selectively removes IgG and albumin from the serum sample. Serum samples were handled according to the manufacture’s instructions. To purify the protein extraction and determine the final protein concentration, the 2-D Clean-up Kit (GE healthcare, UK) and Bradford protein assay kit (Bio-Rad, USA) were used sequentially, following the manufacturer’s instructions.
Two-dimensional (2D) gel electrophoresis
Total proteins were mixed up to 250 μL of rehydration solution (8 M urea, 20 mM DTT, 2% CHAPS, and 0.5% IPG buffer). For each sample 300 μg of total protein were used for the experiment. 2-DE gel was performed with Amersham Biosciences IPGphor IEF System and Hoefer SE 600 (GE Healthcare) electrophoresis units using a 13-cm immobilized pH 3–10 nonlinear gradient IPG strips according to the protocol suggested by the manufacturer. The rehydration step was performed for 10 h at low voltage of 30 V. IEF was run by following a step-wise voltage increase protocol: 500 and 1000 V for 1 h each and 5000–8000 V for about 10 h with a total of 64 kVh. After IEF, the strips were subjected to two-step equilibration in equilibration buffers (6M urea, 2% SDS, 30% glycerol and 50 mM Tris–HCl pH 6.8) with 1% DTT w/v for the first step, and 2.5% iodoacetamide (w/v) for the second step. The equilibrated gel strip was placed on top of a 12.5% SDS-PAGE gel, sealed with 0.5% agarose containing a little bromophenol blue. SDS-PAGE was carried out at a constant current of 15 mA for 30 min per gel and then 30 mA per gel until the bromophenol blue reached the bottom of the gels. Proteins were detected by a silver nitrate staining.
Analytical gels were scanned on an Image Scanner (GE healthcare) at 300 dpi with 12-bit gray scale levels in tagged image file format (TIFF), images were analyzed using the ImageMaster 2D Platinum (GE Healthcare). All gels in the analyses were scanned with identical parameters. The individual spots of each gel were detected by their boundaries and the spot volumes corresponding to the protein abundance were calculated automatically. Each spot intensity volume was processed by background subtraction and total spot volume normalization. The resulting spot volume percentage was used for comparison. Only those spots that have statistical significance in differential expression, as judged by software analysis of the silver-stained gels, were excised from gels for analysis by MS.
Each gel piece was rinsed three with deionized water, destained in a 1:1 solution of 30 mM potassium ferricyanide and 100 mM sodium thiosulfate and then equilibrated in 50 mM ammonium bicarbonate to pH 8.0. After hydrating with acetonitrile and drying in a Speed Vac. The gel spots were rehydrated in a minimal volume of trypsin (Promega, USA) solution (20 μg/ml in 25 mM NH4HCO3) and incubated at 37°C overnight. The supernatants were transferred into a 200 μL microcentrifuge tube and the gels were extracted once with extraction buffer (67% acetonitrile containing 2.5% trifluoroacetic acid). The peptide extract and the supernatant of the gel spot were combined and then completely dried in a Speed Vac centrifuge.
Protein identification and data analysis
After digestion, tryptic peptides were lyophilized and resuspended in 2 μL of a 30% acetonitrile/0.1% TFA solution. 0.8 μL of the samples were spotted onto the MALDI sample target plate, followed by 0.4 μL of a saturated matrix solution of a-cyano-4-hydroxycinnamic acid prepared in 50% acetonitrile/0.1% TFA.
Peptide mass spectra were obtained on a MALDI-TOF/TOF mass spectrometer (4800 Proteomics Analyzer, Applied Biosystems, Foster City, CA, USA) in the positive ion reflectron mode. After an external calibration with a mixture of Gradykinin (Mr, 904.458), angiotensin I (Mr, 1296.685), Glul-Fibrinopeptide (Mr, 1570.677), ACTH clip 1–17 (Mr, 2093.08), ACTH clip 18–39 (Mr, 2465.199), ACTH clip 7-38(Mr, 3657.929), spectra were obtained in the mass range between 900 and 3500 Da with 500 laser shots. For each sample spot, a data dependent acquisition method was created to select the seven most intense peaks(S/N>50), excluding those from the matrix, due to trypsin autolysis or acrylamide peaks, for subsequent MS/MS data acquisition. MS/MS spectra were acquired with 1200 laser shots in the mass range from 10 Da to the mass of parent ion using an interpretation method present on instrument software, where the seven most intense peaks were selected and MS/MS spectra were generated automatically.
Database search spectra were processed and analyzed by the Global Protein Server Workstation (Applied Biosystems, Foster City, CA, USA), which uses internal Mascot (Matrix Science Ltd, UK)software for searching the peptide mass fingerprints and MS/MS data. Searches were performed against the uniport database with the taxonomy of Homo sapiens. Mass searches were performed using mass tolerance settings of 100 ppm for the precursor and 0.2 Da for the fragment masses. The following parameters were used in database searching: fixed modification, carbamidomethyl (cysteine), variable modification, oxidation (methionine), Up to one missed trypsin cleavage was allowed. To ensure a reliable identification, the results from both the MS and MS/MS spectra were used in the database search. Protein identification was accepted when the score reported by the Mascot search routine was higher than 62 and, whenever possible, confirmed with MW/pI values.
Protein categorization and network construction
Identified proteins were classified based on the PANTHER (Protein ANalysis THrough Evolutionary Relationships) system (http://www.pantherdb.org), a unique resource that classifies genes and proteins by their functions. The PANTHER ontology, a highly controlled vocabulary (ontology terms) by molecular function, protein class and biological process was used to categorize proteins into families and subfamilies with shared functions.
The interaction network of the differentially expressed protein was generated with Pathway Studio version 5.0 software (Ariadne Genomis, Rockville, MD) and Resnet 5 database. Common upstream regulators or downstream targets of multiple proteins were identified by using this software that facilitated the process of selecting potential mechanisms and key factors from the large number of differentially regulated proteins.
Western blot analysis
Protein extracts from serum of normal and extremely severe HFMD were separated by SDS-PAGE (12–15% acrylamide) and then electroblotted onto PVDF membranes. The membranes were incubated with Keratin type II cytoskeletal 6C(KRT6C),Serum amyloid P-component(APCS), Apolipoprotein A-1(APOA1) and Peroxiredoxin-2(PRDX2) antibodies at 4°C overnight, followed by incubation with corresponding secondary antibodies at room temperature for 2 h. Specific protein bands were visualized with the SuperSignal chemiluminescence system (ECL, Pierce, USA) and imaged by autoradiography.
Comparative proteomic analysis of extremely severe HFMD
Identification of differentially expressed proteins of extremely severe HFMD patients by MALDI-TOF/TOF
Protein score C.1.%
35 kDa inter-alpha-trypsin inhibitor heavy chain H4
Inter-alpha-trypsin inhibitor heavy chain H2
Serum albumin (Fragment)
Serum albumin (Fragment)
C2ORF3 variant 2
Pigment epithelium-derived factor
Ig alpha-2 chain C region
Cdna FLJ55673 highly similar to complement fator B
Clusterin alpha chain (Fragment)
Haptoglobin beta chain
Haptoglobin beta chain
Haptoglobin beta chain
Haptoglobin beta chain
Isoform 1 of Ficolin-3
Isoform 2 of Ficolin-3
complement component 4B preproprotein
DADB-112B14.11 Complement component 4B
Ig kappa chain V-III region WOL
Keratin, type II cytoskeletal 1
Keratin, type II cytoskeletal 6C
Serum amyloid P-component
Retinol-binding protein 4
Haptoglobin beta chain
HPR 47 kDa protein
Validation of differentially expressed proteins in extremely severe HFMD
Functional categories and biological interaction networking of identified proteins
There are no effective antiviral drugs and vaccines available against HFMD, therefore the timely and accurate diagnosis and monitoring is crucial for the treatment. In the present study, we took advantage of proteomics to identify potential markers which reflect the status of HFMD. The goals were to (i) define a set of differentially expressed proteins that may be used as potential biomarkers to facilitate the severe HFMD diagnosis and monitoring of therapy effectiveness and (ii) gain a deeper understanding of the early pathological processes in severe HFMD.
We identified 38 differentially expressed spots which were detected in the serum of extremely severe HFMD patients compared with the healthy controls (Table 1). The known functions of these proteins are summarized in Figure 2. These proteins have previously been identified using proteomics approaches in mild and severe HFMD children . However, a change in their expression in relation to extremely severe HFMD had never been previously reported. Extremely severe HFMD represent the most acute and serious situation of this disease and usually life-threatening. Biomarkers for this stage can serve as a warning signal for an urgent treatment. A variety of cellular functions was covered from the identified proteins, including enzyme modulator, infection defense/immunity, signaling molecule, cytoskeleton maintenance, metabolism etc., reflecting the human body facing acute lesions.
Our study showed an apparent down regulation of Complement C3(C3), inter-alpha (globulin) inhibitor H2 (ITIH2), serum albumin (ALB), plasminogen (PLG) and retinol binding protein 4 (RBP4) [20–22]. The function of these proteins typically involve in virus invasion protection and elimination; histamine release and muscle smooth; colloidal osmotic pressure of blood regulation and retinol delivery. Thus, down regulation of the proteins indicated that the viral infection suppressed these reactions from HFMD patients, facilitating the disease progression. Inhibition of the viral protection enhances the virulence of the virus, leading to extremely severe symptoms and even fatal lesions. This suggested that antiviral therapies may help to control the disease progression in the extremely severe phase.
Previous studies have noted that many diseases, including the neurological diseases known as transmissible spongiform encephalopathies (TSEs), are due to inflammatory injury . EV71 infection can induce complement activation and an inflammatory response of the central nervous system. Inappropriate or excessive activation of the complement system can result in severe inflammation or tissue injury [24, 25]. It was known that complement C3 plays a key role in the activation of the complement system . From our study we found that the C3 was the most down regulated protein of the extremely severe HFMD. These information together with our results imply the activation of complement system due to EV71 infection and inflammatory is associated with complement activation. Whilst antiviral therapy is one possible approach, it is perhaps more important to inhibit the inflammatory response. Complement inhibition should greatly reduce the inflammatory reaction or tissue injury resulting from excess complement activation.
Peroxiredoxin-2 (PRDX2) was found extremely significant increased in extremely severe HFMD patient. It plays an important role in eliminating peroxides generated during metabolism. It participates the signaling cascades of growth factors and tumor necrosis factor-alpha by regulating the intracellular concentrations of H2O2. It is one of the most important antioxidant enzymes in humans [27, 28]. Previous studies showed that antioxidant enzymes activity, increased in severe HFMD patients and decreased significantly after vincristine–adriamycin– dexamethasone therapy . Therefore, we speculate that upregulation of PRDX2 may play significant roles in pathogenesis of severe HFMD and could be used as the potential drug targets.
We reported, for the first time, the analysis in a proteome level to identify proteins that change in expression in extremely severe HFMD. These proteins have the potential to be used, probably in combination, as potential molecular markers to monitor the progression of HFMD treatment. The results also suggested the crucial pathways in the development of the disease in extremely severe phase, providing important hints for the functional studies and therapy design of HFMD. Further validation with a much larger sample size is necessary to determine the biomarker set for clinical applications.
This work was supported by National Clinical Key Specialty Project Foundation, Guangdong Natural Science Foundation (9151008901000033), Applied Basic Research Program of Technology and Information Bureau Guangzhou City (2013J4100022), Dean Foundation (GW201238) of School of Public Health and Tropical Medicine, Southern Medical University.
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