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A Comprehensive Guide to Hantavirus Prevention and Control: Transmission Routes, Risks, and Laboratory Testing

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.

Classification of Hantaviruses

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.

Transmission Routes of Hantaviruses

Primary Transmission Routes

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.

High-Risk Populations and Settings

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.

Clinical Recognition and Prevention and Control Principles

Recognition of Early Symptoms

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.

Key Points for Daily Prevention and Control

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.

Key Points of Laboratory Testing

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.

1. Sample Collection and Processing

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.

2. Common Diagnostic Methods

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.

Laboratory Equipment Potentially Used for Hantavirus Testing

During virus testing, nucleic acid extraction, and sample processing, laboratories are typically equipped with the following devices.

Sample and Reagent Storage

Medical Refrigerator

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Economic -25°C Freezer
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Laboratory Refrigerator

Temperature range (℃) : 2~8

Temperature display : LED digital display

Temperature Accuracy (℃) : 0.1℃

Refrigeration Method: Air Cooling

Defrosting Method: Automatic Defrosting

-25°C Freezer
Range (℃) at RT.10~32℃:  -10~-25
Sensor: NTC; PTC

Controller: Microprocessor

Defrost: Manual
Display: Digital display

-86°C Ultra Cold Freezer
Temperature Range (℃) at RT.10~32℃ : -40~-86
Sensor PTC
Refrigerant R4001 (CFC Free)
Defrost Manual

Laboratory Liquid Nitrogen Tank

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Cryobiobank 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 Under Platform Vapor Storage(L) : 55 / 55 / 80 / 80 / 135

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
LN₂ Capacity (L) : 10 / 10 / 13 / 15 / 20 / 25 / 31.5 / 31.5 / 31.5 / 35.5 / 35.5 / 35.5 / 47 / 50

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

Sample and Reagent Preparation

Biosafety Cabinet

Prevents aerosol spread

Protects operators

Protects samples from contamination

One of the core pieces of equipment in a virology laboratory.

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Class IIA2 Biological Safety Cabinet

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.

Benchtop High Speed Refrigerated Centrifuge, CFG-T20HRII
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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

Mini Centrifuge

Max Speed : 16000rpm

Max RCF : 19040×g

Max Volume : 6×10ml Angle rotor
Temperature Accuracy: ±1℃

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

Water Purification

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Ultra Water Purifier
Conductivity : <0.055μs/cm

TOC : <3ppb; <3ppb; <5ppb; <20ppb

Microorganism : <1cfu/ml

Ultra Water Purifier, Supereconomic Series
Conductivity : <0.055 μs/cm

TOC : <3ppb; <5ppb; <10ppb; <20ppb

Microorganism : <1 CFU/mL

Ultra Water Purifier, Economic Series
Pure Water Quality : 15–17 MΩ•㎝ (25℃)

Total Organic Carbon(TOC) : ≤20 ppb

Microorganism : <1 CFU/mL

Dry Block Incubators

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Digital Dry Bath
Functions: Heating

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
Temp. Accuracy : ≤±0.3℃ (At 37℃)

Display Accuracy : 0.1℃

Temp. Uniformity : ≤±0.3℃ (At 37℃)

Heating Time : ≤12min (From 25℃ to 100℃)

Dry Bath with Heating & Cooling & Mixing
Display : TFT

Temperature Control Accuracy : ±0.5℃ (At 20~45℃)

Temperature Setting Range(℃) : 0.1~100; 15~100; 15~100

Max. Heating Rate : 5.5℃/min

Vortex Mixer

Vortex Mixer VMX-5
Thermostatic Mixer TMX-1500C
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Vortex Mixer
Oscillation mode : Circular oscillation

Rotating diameter : 4mm

Motor type : DC Motor

Speed range : 0~3000rpm

Thermostatic Mixer
Temperature Control Range : 0~100°C

Temperature Control Precision : ±0.3°C

Oscillation Speed Range : 200~1500 rpm/min

Rotary Mixer
Shaking Speed : 10~100rpm(Precisely Adjustable)

Timing Range : 1min ~99h59min

Time for Pause : 1-5s

Max. load : 6kg

Mixing Method : Flip

Pipettes

Twelve-channel Adjustable Volume Pipette
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Electronic Single Channel Pipette

Twelve-channel Adjustable Volume Pipette
Volume Range : 0.5μL ~ 300μL

Increment : 0.1 ~ 5μL

Test Volume : 1μL ~ 300μL

Eight-channel Electronic Pipette
Volume Range : 0.5μL ~ 300μL

Increment : 0.01μL ~ 1μL

Test Volume : 1μL ~ 300μL

Electronic Single Channel Pipette
Volume Range : 0.5μL ~ 1000μL
Increment : 0.01μL ~ 5μL
Test Volume : 1μL ~ 1000μL

Nucleic acid amplification and detection

qRT-PCR Instrument

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

Gradient Thermal Cycler

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

Spectrophotometer

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Fluorescence Spectrophotometer FL 97 Series

UV-Vis Spectrophotometer

Volume Requirements : 0.3–2 μL

Fluorescent Detector : Photodiode

Spectral Resolution : 2 nm

Detection Wavelength Range : 200–800/200–850 nm

Fluorescence Spectrophotometer
Emission Wavelength : 200-900nm

Excitation Source : 150W xenon lamp(Hamamatsu)

Wavelength Accuracy : ±1.0nm ±0.4nm ±1.0nm

Elisa Microplate Reader

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
Wavelength Range : 340~880nm

Repeatability : [0, 3.0)≤0.3%, [3, 4.0)≤1%

Resolution : 0.001Abs

Elisa Microplate Reader
Wavelength Range : 200~1000 nm

Wavelength Accuracy : 2 nm

Wavelength Repeatability : 0.2 nm

Microplate Type : 96/384 wells

Elisa Microplate Reader, 96/48-well Plate
Reading Range: 0.000–4.000 A

Resolution: 0.001 A

Accuracy: ±0.008 A

Reproducibility: ≤0.2%

Stability: ±0.003 A

Auxiliary ldentification

Gel Imaging System

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Automatic Gel Imaging and Analysis System
Pixel : 6 million pixels

Exposure : 1 ms-5000ms

Photosensitive Efficiency : High QE: >79%

Pixel Merge : 1×1

Electrophoresis Tank

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Vertical Electrophoresis Tank ET-V04
Horizontal Electrophoresis Tank ET-H03I

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
Sample Comb : 10 samples

Number of Gels : 1-4 pcs

Number of Samples : 10~40pcs

Gel Thickness : Standard 1.0mm, optional 0.75 & 1.5mm

Horizontal Electrophoresis Tank
Sample Comb : 14, 18, 26 samples

Buffer Capacity : 800ml

Blue Light Wavelength : 470nm

Gel Tray(W×L)(mm) : 130×150, 130×200

Electrophoresis Power Supply

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Electrophoresis Power Supply
Output Sockets : 4 sets

Display : LCD touchscreen

Interface: USB

Output Sockets: 4 sets

Electrophoresis Power Supply
Parallel Output: 4 groups

Testing Temperature: -20℃~+85℃

Input Range: 110-250V is suitable for different countries and regions

Waste disposal

Autoclave

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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Vertical Pressure Steam Sterilizer, ST-VLA Series
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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

Conclusion

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.

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