Views: 514 Author: Yammi Publish Time: 2026-05-14 Origin: Site
In recent years, Hantaviruses have continued to spread worldwide. Due to their high fatality rate and the risks of aerosol transmission and laboratory exposure, they have become one of the pathogens of primary concern in public health. With the continuous advancement of molecular diagnostic technologies, establishing safe and standardized molecular pathology laboratories has become increasingly important. Laboratory management and biosafety precautions are particularly critical during the detection of high-risk pathogens such as Hantaviruses. Next, we will explore the transmission routes of Hantavirus and the instruments and equipment commonly used in laboratory testing.
Infection with hantaviruses can lead to two types of severe diseases:
Hemorrhagic fever with renal syndrome (HFRS), also known as epidemic hemorrhagic fever, is the most common type of hantavirus infection. Typical clinical manifestations include fever, bleeding, and kidney damage. Severe cases may present with shock and multiple organ failure; without proper treatment, the case-fatality rate can exceed 10%.
Hantavirus Pulmonary Syndrome (HPS), which is primarily prevalent in the Americas, is characterized by pulmonary infiltrates and respiratory failure, and has an even higher case-fatality rate.
The prevalence of hantaviruses exhibits distinct seasonal patterns, with peak incidence typically occurring from November to January of the following year. In some regions, a minor peak may occur from May to July. The epidemic cycle is directly related to the activity patterns and population fluctuations of the rodent hosts.
Rodents are the primary source of Hantavirus infection, with the brown rat and the black-striped field mouse being the most common hosts in China. The virus is shed through the host animal’s blood, saliva, urine, and feces. Humans are primarily infected through the following routes:
Respiratory Transmission: Inhalation of aerosols contaminated with excreta from infected rodents is the most common route of infection. The risk of exposure is significantly higher in enclosed, poorly ventilated spaces (such as warehouses, basements, and field shelters).
Gastrointestinal Transmission: Consuming food or water contaminated with excreta from infected rodents allows the virus to enter the human body through the mouth or the mucous membranes of the digestive tract.
Contact transmission: Infection can also result from bites or scratches by infected rodents, or from contact between broken skin or mucous membranes and the excreta or secretions of infected rodents.
It is important to emphasize that human-to-human transmission of Hantavirus is extremely rare. Clustered transmission within households has been reported only in a very small number of specific cases. Routine contact with confirmed patients does not lead to infection, so there is no need for excessive panic.
The following groups are at significantly higher risk of Hantavirus infection than the general population and should take special precautions:
Residents of rural areas, particularly those engaged in agricultural production or fieldwork. This includes, but is not limited to, farmers, forestry workers, geological surveyors, and field construction workers.
Workers in farmers’ markets, grain warehouses, livestock farms, food processing plants, and warehousing and logistics facilities. Rodent activity is frequent in these environments, resulting in a higher probability of exposure to virus-contaminated materials.
Public health workers, medical laboratory technicians, and laboratory researchers. These individuals face occupational exposure risks when handling samples, conducting tests, or performing research.
Individuals with a recent history of camping, hiking, or staying in rural areas. This is particularly true for those who have visited forested or grassland areas with high rodent activity during the epidemic season.
The incubation period for Hantavirus infection is typically 7–14 days, ranging from a minimum of 4 days to a maximum of 45 days. Early clinical manifestations resemble those of the common cold or influenza, which can easily lead to missed or misdiagnoses. High vigilance is warranted when the following symptoms are present and there is a relevant epidemiological history:
Fever: Sudden onset of high fever, typically above 38°C, which may be accompanied by chills and shivering; the fever usually lasts 3–7 days.
Systemic Toxic Symptoms: Pronounced “three pains”—headache, lower back pain, and orbital pain. These may be accompanied by generalized muscle aches, fatigue, nausea, vomiting, abdominal pain, and diarrhea.
Signs of capillary damage: The “three reds” are observed, characterized by flushing and redness of the skin on the face, neck, and upper chest. Conjunctival hyperemia and edema are present, and some patients may exhibit petechiae or ecchymoses on the skin and mucous membranes.
Currently, there are no specific antiviral drugs for Hantavirus. Clinical management primarily involves symptomatic and supportive care, with early intervention for high fever, hypotensive shock, and renal failure being the cornerstone of treatment.
The core of Hantavirus prevention and control lies in interrupting transmission routes, controlling sources of infection, and protecting susceptible populations. Specific prevention and control measures include:
Rodent Prevention and Eradication: Reducing rodent populations by improving environmental hygiene, eliminating rodent habitats, and using physical trapping devices or approved rodenticides is the most fundamental measure for Hantavirus prevention and control.
Food Safety Management: All food must be stored properly to prevent contamination by rodents. Drinking water must be boiled before consumption, and food that has been gnawed on by rodents or contaminated by their feces must not be eaten.
Personal Protection: When working or engaging in activities outdoors, avoid contact with rodents and their excrement as much as possible, and do not sit or lie on the grass. When necessary, wear a mask and gloves, dress in long-sleeved clothing, and promptly disinfect and bandage any broken skin.
Vaccination: Currently available inactivated Hantavirus vaccines provide over 90% protection against prevalent virus strains.
Laboratory testing is the cornerstone of Hantavirus diagnosis, and test results are critical for reducing the case fatality rate. Laboratory testing must strictly adhere to biosafety regulations. All procedures must be conducted in laboratories that meet biosafety level requirements.
Common sample types used for Hantavirus testing include serum, plasma, whole blood, urine, and throat swabs. The appropriate sample types vary depending on the stage of the disease:
Acute-phase samples: Serum/plasma samples collected within 1 week of symptom onset. Suitable for nucleic acid testing, virus isolation, and IgM antibody testing. Samples should be submitted for testing within 48 hours at 2–8°C after collection. If long-term storage is required, samples must be stored at temperatures below –70°C to avoid repeated freeze-thaw cycles.
Convalescent-phase samples: Serum samples collected 2 weeks or more after onset of illness. Suitable for IgG antibody testing. A fourfold or greater increase in IgG antibody titers between paired serum samples may serve as a basis for confirmation of diagnosis.
Strict personal protective measures must be followed during sample handling. All sample manipulation must be performed in a Class II biological safety cabinet to prevent aerosol generation. Instruments that have come into contact with samples must be disposed of in accordance with medical waste regulations to prevent cross-contamination.
During an outbreak of hantavirus, diagnostic testing typically follows a stepwise process. From rapid screening of exposed individuals to confirmatory testing after hospitalization, the process generally proceeds in the following order.
1. Nucleic acid testing (real-time quantitative reverse transcription polymerase chain reaction)
For patients in the early stages of infection, particularly within the first week after exposure, quantitative Real-time Fluorescence PCR Detection System (qRT-PCR) is widely used to directly detect Hantavirus RNA. In samples collected early in the course of the disease, the positive predictive value can exceed 90%.
qRT-PCR has the following characteristics:
High sensitivity
Simple operation
Low cost
Rapid test results
2. IgM Antibody Testing for Further Screening
For individuals with fever, a history of rodent exposure, or close contact with a confirmed case, rapid serological screening is typically the method of choice for further evaluation. IgM antibodies are usually detectable within 3 to 5 days after symptom onset, with a positive predictive value exceeding 95% during the first week of illness.
Common rapid screening methods include:
Gold particle method
Enzyme-linked immunosorbent assay (ELISA)
Immunofluorescence assay
The gold particle method is simple and rapid, making it suitable for emergency screening during outbreaks and in primary care settings.
3. Confirmatory Laboratory Diagnosis
Once suspected patients are admitted to a hospital or transferred to a specialized laboratory, more accurate confirmatory testing is performed.
Serological antibody testing: This method offers higher accuracy
A positive IgM result typically indicates a recent or active infection.
IgG antibodies usually rise 1 to 2 weeks after the onset of symptoms and may persist for several years. A fourfold increase in IgG titers between acute-phase and convalescent-phase serum samples is considered strong evidence of active infection.
During virus testing, nucleic acid extraction, and sample processing, laboratories are typically equipped with the following devices.
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Temperature range (℃) : 2~8 Temperature display : LED digital display Temperature Accuracy (℃) : 0.1℃ Refrigeration Method: Air Cooling Defrosting Method: Automatic Defrosting | -25°C Freezer Controller: Microprocessor Defrost: Manual | -86°C Ultra Cold Freezer |
Laboratory Liquid Nitrogen Tank
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Laboratory Liquid Nitrogen TankLN₂ Capacity (L) : 10 / 31.5 / 35.5 / 47 / 50 / 65 / 95 / 115 / 145 / 175 Neck Opening (mm) : 125 / 127 / 216 Static Evaporation Rate (L/day) : 0.42 / 0.35 / 0.36 / 0.36 / 0.45 / 0.78 / 0.97 / 0.94 / 0.96 / 0.95 Static Holding Time (day) : 24 / 90 / 97 / 130 / 110 / 83 / 98 / 122 / 151 / 184 | Cryobiobank Liquid Nitrogen Tank LN₂ Capacity (L) : 350 / 460 / 587 / 783 / 890 Neck Opening (mm) : 326 / 326 / 445 / 445 / 465 Usable Internal Height (mm) : 600 / 828 / 600 / 828 / 773 | Static Storage Liquid Nitrogen Tank Neck Opening (mm) : 80 / 125 / 50 / 50 / 50 / 50 / 50 / 80 / 125 / 50 / 80 / 125 / 127 / 125 Canister Diameter (mm) : 63 / 97 / 38 / 63 / 97 / 104 / 97 |
Prevents aerosol spread
Protects operators
Protects samples from contamination
One of the core pieces of equipment in a virology laboratory.
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Biological Safety Cabinet Class II A2 Airflow System : 70% air recirculation, 30% air exhaust Work Surface Height : 750mm Front Window : Motorized, toughened glass | Biological Safety Cabinet Class II B2 Airflow System : 100% air exhaust Max Opening Height : 400 mm Downflow Velocity : 0.35±0.025 m/s Inflow Velocity : 0.52±0.025 m/s | Biological Safety Cabinet Class II A2 Work Surface Height : 800 mm Airflow Mode : 70% air recirculation, 30% air exhaust Front Window : Motorized, toughened glass 6 mm, Anti-UV |
High-Speed Refrigerated Centrifuge
Serum separation
Nucleic acid extraction
Virus sample pretreatment
The refrigeration function helps maintain RNA stability.
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High Speed Refrigerated Centrifuge Max Speed 20000r/min Max RCF 27000×g Max Capacity 4×100mL Motor Ac frequency conversion motor Speed Accuracy ±30r/min | Max Speed : 16000rpm Max RCF : 19040×g Max Volume : 6×10ml Angle rotor Speed Accuracy: ±10rpm | Benchtop High Speed Refrigerated Centrifuge Max Speed : 16000rpm Max RCF : 19040×g Max Volume : 6×10ml Angle rotor Temperature Accuracy: ±1℃ Speed Accuracy: ±10rpm |
Nucleic Acid Extraction System
Automated RNA extraction
Improves testing efficiency
Reduces human error
Suitable for high-throughput sample processing.
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Reagent Type : Magnetic bead method reagents Throughput : 1–32 samples Volume : 20–1000 μL Consumable : 96 deep well Plate + Magnetic rod's tip | Throughput : 1–16/ 1–32 samples Volume : 30–1000 μL Built-in : Protocol >500 Oscillatory Mixed Mode : Multi-level adjustable Display : 7-inch touch screen 10-inch touch screen |
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Ultra Water Purifier TOC : <3ppb; <3ppb; <5ppb; <20ppb Microorganism : <1cfu/ml | Ultra Water Purifier, Supereconomic Series TOC : <3ppb; <5ppb; <10ppb; <20ppb Microorganism : <1 CFU/mL | Ultra Water Purifier, Economic Series Total Organic Carbon(TOC) : ≤20 ppb Microorganism : <1 CFU/mL |
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Digital Dry Bath Temperature Setting Range (℃): 25~120 Temperature Range: RT.+5~120°C Temperature Control Accuracy (At 37°C): ± 0.5°C | Dry Bath with Heating Lid Display Accuracy : 0.1℃ Temp. Uniformity : ≤±0.3℃ (At 37℃) Heating Time : ≤12min (From 25℃ to 100℃) | Dry Bath with Heating & Cooling & Mixing Temperature Control Accuracy : ±0.5℃ (At 20~45℃) Temperature Setting Range(℃) : 0.1~100; 15~100; 15~100 Max. Heating Rate : 5.5℃/min |
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Vortex Mixer Rotating diameter : 4mm Motor type : DC Motor Speed range : 0~3000rpm | Thermostatic Mixer Temperature Control Precision : ±0.3°C Oscillation Speed Range : 200~1500 rpm/min | Rotary Mixer Timing Range : 1min ~99h59min Time for Pause : 1-5s Max. load : 6kg Mixing Method : Flip |
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Twelve-channel Adjustable Volume Pipette Increment : 0.1 ~ 5μL Test Volume : 1μL ~ 300μL | Eight-channel Electronic Pipette Increment : 0.01μL ~ 1μL Test Volume : 1μL ~ 300μL | Electronic Single Channel Pipette |
Primarily used for:
Viral RNA amplification
Quantitative detection
Viral load analysis
A key piece of equipment for molecular detection of Hantavirus.
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Real-time Fluorescence Quantitative PCR Sample Capacity : 0.1/0.2 mL PCR tubes×96, 8×12 PCR plate or 96 well plate ×1 MAX. Ramp Rate : 6 ℃/s Reaction Volume : 10-50 μL | Capacity : 96×0.2mL; 8×0.2 mL PCR strip tubes Sample Volume : 10-200 uL Thermal Cycle Mode : Peltier Uniformity : ﹤0.3 ℃ Temperature Control : Block\Tube | Real-time Fluorescence Quantitative PCR Sample Capacity : 16 wells, compatible with 0.2 mL PCR single tubes or PCR 8-strip tubes Reaction Volume : 10–50 μL Thermal Cycle Technology : Peltier Max.Temperature Change Rate : 6.0 °C/s |
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Volume Requirements : 0.3–2 μL Fluorescent Detector : Photodiode Spectral Resolution : 2 nm Detection Wavelength Range : 200–800/200–850 nm | Fluorescence Spectrophotometer Excitation Source : 150W xenon lamp(Hamamatsu) Wavelength Accuracy : ±1.0nm ±0.4nm ±1.0nm |
Used to measure the absorbance (OD value) after an ELISA reaction, thereby determining:
The presence of viral antibodies or antigens
The sample concentration
Whether the test result is positive or negative
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Automatic Elisa Plate Reader 96 Wells Plate Repeatability : [0, 3.0)≤0.3%, [3, 4.0)≤1% Resolution : 0.001Abs | Elisa Microplate Reader Wavelength Accuracy : 2 nm Wavelength Repeatability : 0.2 nm Microplate Type : 96/384 wells | Elisa Microplate Reader, 96/48-well Plate Resolution: 0.001 A Accuracy: ±0.008 A Reproducibility: ≤0.2% Stability: ±0.003 A |
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Automatic Gel Imaging and Analysis System Exposure : 1 ms-5000ms Photosensitive Efficiency : High QE: >79% Pixel Merge : 1×1 |
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Horizontal Gel Electrophoresis Tank Buffer Volume : 300/700 mL Sample Comb : 1.0/1.5/2.0 mm, 2/ 3/ 6/ 8/ 11/ 13/ 14/ 18/ 25/ 26 wells Gel size (W×L) : 60×60/ 60×75/ 60×120/120×60/ 120×120/ 130×150/ 130×200 mm | Vertical Electrophoresis Tank Number of Gels : 1-4 pcs Number of Samples : 10~40pcs Gel Thickness : Standard 1.0mm, optional 0.75 & 1.5mm | Horizontal Electrophoresis Tank Buffer Capacity : 800ml Blue Light Wavelength : 470nm Gel Tray(W×L)(mm) : 130×150, 130×200 |
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Electrophoresis Power Supply Display : LCD touchscreen Interface: USB Output Sockets: 4 sets | Electrophoresis Power Supply Testing Temperature: -20℃~+85℃ Input Range: 110-250V is suitable for different countries and regions |
Used for:
Sterilization of medical waste
Disinfection of laboratory equipment
Safe disposal of contaminants
An essential component of the laboratory biosafety system.
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Sterilization Temperature (℃) : 105~136 Max. Sterilization Pressure (Mpa) : 0.23 Drying Function : YES | Temperature (℃) : 121℃-134℃ Highest Working Pressure : 0.25Mpa Temp.Accuracy : 0.5℃ Design Pressure : 0.28~0.3Mpa ST-VLA series with drying function | Sterilization Temperature (℃) : 105~136 Max. Sterilization Pressure (Mpa) : 0.23 Drying Function : YES Water Injection Method : Built-in water tank Drying Time : 15min |
The accuracy of Hantavirus testing depends not only on advanced molecular diagnostic technologies but is also closely linked to laboratory biosafety management, sample handling procedures, and equipment configuration. Non-compliant operations, sample contamination, or inadequate equipment performance at any stage may lead to biased test results, thereby affecting disease diagnosis, outbreak surveillance, and clinical decision-making.
Therefore, establishing a comprehensive laboratory management system, equipping laboratories with reliable testing instruments, and strictly adhering to biosafety protocols are of critical importance for improving the accuracy of Hantavirus testing and ensuring the safety of laboratory personnel. With the continuous advancement of molecular diagnostic technologies, standardized, automated, and highly secure laboratory solutions will play an increasingly vital role in viral testing and public health prevention and control.