Mycoplasma Pneumonia: Symptoms, Causes & Treatment Guide

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Mycoplasma pneumonia, commonly known as walking pneumonia, is a respiratory infection caused by the bacterium Mycoplasma pneumoniae. This atypical pneumonia typically causes milder symptoms than other types of pneumonia, including a persistent dry cough, low-grade fever, fatigue, and headache. Most cases resolve on their own, but some people may need antibiotic treatment. Understanding the symptoms, when to seek care, and how to prevent spread is essential for managing this common respiratory infection.

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Author: iMedic Medical Editorial Team

Quick Facts: Mycoplasma Pneumonia

ICD-10 Code
J15.7
CAP Cases
10-40%
Incubation
1-3 weeks
Peak Age
5-20 years
SNOMED CT
58750007
MeSH ID
D009175

Key Takeaways

  • Walking pneumonia is the common name for mycoplasma pneumonia because symptoms are often mild enough to continue daily activities
  • Persistent dry cough is the hallmark symptom, often lasting 4-6 weeks even after other symptoms resolve
  • Most cases resolve without treatment, but antibiotics (macrolides or doxycycline) may be needed for severe symptoms or pneumonia
  • Standard antibiotics don't work: Penicillin and amoxicillin are ineffective because mycoplasma lacks a cell wall
  • Highly contagious: Spreads through respiratory droplets; practice good hand hygiene and stay home when sick
  • Seek emergency care for severe breathing difficulty, high fever, rapid breathing, or confusion
  • No vaccine exists: Prevention relies on hygiene measures and avoiding close contact with infected individuals

What Is Mycoplasma Pneumonia?

Mycoplasma pneumonia is a respiratory infection caused by the bacterium Mycoplasma pneumoniae. Unlike typical bacterial pneumonia, it usually causes gradual-onset, mild to moderate symptoms. It's commonly called "walking pneumonia" because many people feel well enough to continue normal activities despite having the infection.

Mycoplasma pneumoniae is a unique type of bacteria that is among the smallest self-replicating organisms known. What makes it particularly distinctive is that it lacks a cell wall, which is why common antibiotics like penicillin and amoxicillin are ineffective against it. These antibiotics work by disrupting bacterial cell wall synthesis, but since mycoplasma has no cell wall to target, they simply don't work.

The infection primarily affects the upper and lower respiratory tract, causing symptoms that range from a simple cold to pneumonia. The term "atypical pneumonia" is often used because the clinical presentation differs from classic bacterial pneumonia caused by organisms like Streptococcus pneumoniae. While typical pneumonia often presents with sudden onset of high fever, productive cough with colored sputum, and distinct lung findings on examination, mycoplasma pneumonia tends to develop more gradually with dry cough, low-grade fever, and often minimal physical examination findings despite significant symptoms.

Epidemiologically, mycoplasma pneumonia is responsible for approximately 10-40% of all community-acquired pneumonia (CAP) cases worldwide, making it one of the most common causes of respiratory infections. The infection occurs in cyclical outbreaks, typically every 3-7 years, though this pattern has become less predictable in recent years. These outbreaks often begin in late summer and continue through fall and winter.

Who Is Most at Risk?

While mycoplasma pneumonia can affect anyone, certain populations are more susceptible to infection. Children between ages 5 and 15 have the highest incidence rates, likely due to their close contact in school settings and developing immune systems. Young adults, particularly those living in close quarters such as college dormitories or military barracks, also face elevated risk due to the ease of respiratory transmission in these environments.

Interestingly, children under 5 years of age typically experience milder infections, often presenting only as upper respiratory symptoms. Adults, particularly those over 40, are more likely to develop actual pneumonia when infected. People with compromised immune systems, chronic lung diseases, or sickle cell disease face higher risks of severe infection and complications.

What Are the Symptoms of Mycoplasma Pneumonia?

The main symptoms of mycoplasma pneumonia include a persistent dry, hacking cough that can last weeks, low-grade fever (typically 100-102°F/38-39°C), headache, fatigue, and sore throat. Symptoms usually develop gradually over 1-3 weeks and are often milder than other types of pneumonia, which is why it's called "walking pneumonia."

The symptom presentation of mycoplasma pneumonia follows a characteristic pattern that distinguishes it from other respiratory infections. Unlike the sudden onset typical of bacterial pneumonia caused by Streptococcus pneumoniae, mycoplasma infection develops insidiously over days to weeks. This gradual progression often leads people to initially dismiss their symptoms as a prolonged cold or viral infection.

The incubation period, meaning the time from exposure to symptom onset, ranges from 1 to 3 weeks, which is considerably longer than most respiratory infections. This extended incubation period contributes to the difficulty in identifying the source of infection and in implementing timely isolation measures during outbreaks.

The Characteristic Dry Cough

The hallmark symptom of mycoplasma pneumonia is a persistent, dry, hacking cough. This cough is typically non-productive, meaning it doesn't bring up significant amounts of mucus or phlegm, especially in the early stages of illness. The cough often worsens at night and can be severe enough to cause chest soreness, disrupted sleep, and significant distress.

What makes this cough particularly notable is its duration. While other symptoms may resolve within 2-3 weeks, the cough frequently persists for 4-6 weeks or even longer. This extended cough duration is due to the inflammatory damage caused by the infection to the airway lining, which takes considerable time to heal completely. Some patients report lingering cough sensitivity for months after the acute infection has resolved.

Fever and Constitutional Symptoms

Fever in mycoplasma infection is typically low-grade, usually ranging from 100°F to 102°F (38°C to 39°C). High fevers above 103°F (39.5°C) are less common but can occur, particularly when pneumonia develops. The fever often follows a fluctuating pattern, being higher in the evening and lower in the morning, and may persist for 1-2 weeks.

Associated constitutional symptoms include significant fatigue and malaise that can persist well beyond the acute illness phase. Many patients describe feeling "wiped out" or having decreased energy levels for weeks after their fever resolves. Headache is another common symptom, reported by roughly half of patients, and can be quite prominent in some cases.

Upper Respiratory Symptoms

Before or alongside the cough, many patients experience upper respiratory symptoms including sore throat, often described as scratchy or irritated rather than severely painful. Hoarseness is common and results from inflammation of the larynx. Nasal congestion and runny nose may occur but are typically less prominent than in viral upper respiratory infections.

Mycoplasma Pneumonia Symptoms by Severity
Symptom Severity Duration Notes
Dry cough Prominent 4-6 weeks May become productive; worsens at night
Low-grade fever Mild-Moderate 1-2 weeks Usually 100-102°F; fluctuates
Fatigue Moderate-Severe 2-4 weeks Can persist longer than other symptoms
Headache Variable 1-2 weeks Present in ~50% of cases
Sore throat Mild-Moderate 1-2 weeks Scratchy rather than severe

When Pneumonia Develops

In some cases, mycoplasma infection progresses from bronchitis to pneumonia, involving actual lung tissue inflammation. When this occurs, symptoms typically worsen and may include increasing shortness of breath, particularly with activity. Chest discomfort or pain, especially when breathing deeply or coughing, may develop. The cough may become more productive, and fever may spike higher.

It's important to note that the term "walking pneumonia" can be misleading. While many people with mycoplasma pneumonia can continue their daily activities, others develop significant illness requiring rest, time off work or school, and medical treatment. The severity varies considerably from person to person.

When Should You See a Doctor for Mycoplasma Pneumonia?

See a doctor if you have a persistent cough lasting more than 2 weeks, especially with fever, worsening shortness of breath, or deteriorating symptoms. Seek emergency care immediately if you experience severe breathing difficulty, rapid breathing, confusion, chest pain, or bluish discoloration of lips or fingertips.

Knowing when to seek medical attention for respiratory symptoms can be challenging, particularly since many respiratory infections are mild and self-limiting. However, certain symptoms and circumstances warrant medical evaluation to rule out mycoplasma pneumonia or to assess whether treatment is needed.

The most important trigger for seeking care is symptom duration combined with severity. While a cold typically improves within 7-10 days, symptoms of mycoplasma infection often persist and may gradually worsen. A cough lasting more than 2 weeks, particularly when accompanied by fever that hasn't resolved, should prompt a medical visit. Similarly, if you notice that your breathing is becoming increasingly difficult or that you're becoming more short of breath with routine activities, evaluation is warranted.

Routine Medical Evaluation

You should schedule a medical appointment if you experience a cough persisting beyond 2 weeks without improvement, fever lasting more than 1 week, progressive worsening of symptoms despite rest and home care, symptoms that initially improved but then returned or worsened, or underlying conditions like asthma, COPD, heart disease, or immunocompromising conditions.

Children and elderly adults warrant earlier evaluation due to their higher risk of complications. Parents should seek care for children who seem unusually fatigued, have decreased appetite or fluid intake, or show signs of breathing difficulty such as rapid breathing or using accessory muscles to breathe.

Emergency Warning Signs - Seek Immediate Care

Call emergency services or go to an emergency department immediately if you or someone you're caring for experiences any of the following:

  • Severe difficulty breathing or gasping for air
  • Rapid breathing (more than 30 breaths per minute in adults)
  • Confusion or altered mental status
  • Bluish discoloration of lips, fingernails, or skin (cyanosis)
  • Chest pain that worsens with breathing
  • Inability to drink fluids or keep fluids down
  • Rapid deterioration of symptoms over hours
  • High fever above 104°F (40°C) that doesn't respond to fever reducers

Special Considerations

Certain populations should have a lower threshold for seeking medical care. Individuals with chronic lung conditions like asthma or COPD may experience exacerbation of their underlying disease with mycoplasma infection and should contact their healthcare provider at the first sign of respiratory infection. People with weakened immune systems, whether from medications, cancer treatment, or conditions like HIV, are at higher risk for severe infection and complications.

Pregnant women should also seek early evaluation, as respiratory infections can potentially affect both maternal and fetal health. While mycoplasma pneumonia during pregnancy is generally manageable with appropriate antibiotics safe for use during pregnancy, monitoring is important.

How Does Mycoplasma Pneumonia Spread?

Mycoplasma pneumonia spreads through respiratory droplets when an infected person coughs, sneezes, or talks. The bacteria can travel several feet in the air and survive briefly on surfaces. Close, prolonged contact increases transmission risk, which is why outbreaks often occur in schools, dormitories, military bases, and households.

Understanding how mycoplasma pneumonia spreads is essential for preventing transmission and protecting yourself and others. The primary route of transmission is through respiratory droplets, small particles of moisture expelled when an infected person coughs, sneezes, speaks, or even breathes. These droplets can travel up to 6 feet (about 2 meters) in the air before settling on surfaces or being inhaled by nearby individuals.

The close contact required for transmission explains why outbreaks are particularly common in settings where people live, work, or study in close proximity. Schools represent one of the most common outbreak settings, as children and adolescents spend extended periods in enclosed spaces with many other people. College dormitories and military barracks see frequent outbreaks for similar reasons. Healthcare facilities, nursing homes, and correctional facilities are also recognized outbreak settings.

Contagious Period and Incubation

People infected with mycoplasma become contagious during the incubation period, before they even realize they're sick. This pre-symptomatic transmission contributes significantly to the spread of infection. The most contagious period is typically during the first week of illness when coughing is most active and bacterial shedding is highest.

However, people can continue to shed the bacteria and potentially spread infection for weeks to months after symptoms begin, even after starting antibiotic treatment. This prolonged shedding period, combined with the gradual onset of symptoms that may not prompt people to stay home, contributes to the ease with which mycoplasma spreads through communities.

The incubation period of 1-3 weeks is notably longer than many other respiratory infections. This extended incubation means that by the time one person becomes symptomatic, they may have exposed numerous others over a period of weeks, making it difficult to trace transmission chains and implement timely containment measures.

Household and Close Contact Transmission

Household transmission rates for mycoplasma are significant, with studies showing that 50-90% of household members may become infected once the bacteria is introduced into a home. Children often bring the infection home from school, subsequently infecting parents and siblings. The close, sustained contact within households, shared living spaces, and the difficulty of avoiding exposure to respiratory droplets all contribute to high secondary attack rates.

Interestingly, some people exposed to mycoplasma never develop symptoms despite evidence of infection. This asymptomatic carriage contributes to community spread as these individuals can still transmit the bacteria to others who may then develop symptomatic disease.

How Is Mycoplasma Pneumonia Treated?

Most mycoplasma infections resolve without antibiotic treatment, but antibiotics are recommended for pneumonia or severe symptoms. Effective antibiotics include macrolides (azithromycin, clarithromycin), doxycycline (for adults), or fluoroquinolones for severe cases. Common antibiotics like penicillin and amoxicillin do NOT work against mycoplasma because it lacks a cell wall.

Treatment decisions for mycoplasma infection depend on the severity of illness and whether pneumonia has developed. Understanding the available treatment options, including why certain antibiotics work while others don't, is crucial for effective management of this infection.

Many cases of mycoplasma respiratory infection, particularly those limited to upper respiratory symptoms or mild bronchitis, resolve spontaneously without antibiotic treatment. The immune system can effectively clear the infection over time, though this process may take several weeks. During this period, supportive care measures help manage symptoms and maintain comfort.

When Antibiotics Are Needed

Antibiotic treatment is generally recommended when there's evidence of pneumonia, when symptoms are severe or prolonged, for patients with underlying conditions that increase complication risk, and when there's concern about preventing spread to vulnerable individuals. The goal of antibiotic treatment is to shorten the duration of illness, reduce symptom severity, and decrease the period of contagiousness.

A critical point that cannot be overemphasized is that standard antibiotics like penicillin, amoxicillin, and cephalosporins are completely ineffective against mycoplasma. These antibiotics work by disrupting bacterial cell wall synthesis, but mycoplasma lacks a cell wall entirely. Prescribing these antibiotics for suspected mycoplasma infection represents a treatment failure and unnecessary antibiotic exposure.

Effective Antibiotic Options

The antibiotics effective against mycoplasma target different bacterial functions than cell wall synthesis. Macrolide antibiotics are first-line treatment, with azithromycin being most commonly prescribed due to its convenient dosing, tolerability, and effectiveness. A typical azithromycin course is 5 days: 500mg on day 1, followed by 250mg daily for days 2-5. Clarithromycin and erythromycin are alternative macrolides.

Doxycycline, a tetracycline antibiotic, is an equally effective alternative, particularly for adults. It's typically dosed at 100mg twice daily for 5-7 days. However, doxycycline should generally be avoided in children under 8 years and during pregnancy due to effects on developing teeth and bones.

Fluoroquinolones (levofloxacin, moxifloxacin) are reserved for patients who cannot take macrolides or doxycycline, those with severe infection, or cases where treatment failure has occurred. These antibiotics are highly effective but carry additional side effect risks and should be used judiciously.

Important: Antibiotic Resistance

Macrolide-resistant mycoplasma has emerged as a growing concern globally, with resistance rates varying by region. In some Asian countries, resistance rates exceed 80%, while rates in Europe and North America remain lower but are increasing. If symptoms don't improve within 48-72 hours of starting macrolide treatment, antibiotic resistance should be considered, and switching to doxycycline or a fluoroquinolone may be necessary.

Supportive Care Measures

Regardless of whether antibiotics are prescribed, supportive care measures form an important component of treatment. Rest is essential, particularly during the acute illness phase. While "walking pneumonia" implies mild illness, pushing through significant symptoms can prolong recovery and potentially worsen the infection.

Adequate hydration helps thin respiratory secretions and supports overall recovery. Warm beverages may provide soothing relief for throat discomfort and help with cough. Over-the-counter medications can help manage symptoms: acetaminophen or ibuprofen for fever and body aches, cough suppressants for nighttime use when cough interferes with sleep, and throat lozenges for sore throat relief.

Honey has been shown in studies to be as effective as some over-the-counter cough medicines for nighttime cough relief and can be given to children over 1 year of age. Using a humidifier to add moisture to the air may also help ease cough and throat irritation.

How Can You Prevent Mycoplasma Pneumonia?

There is no vaccine for mycoplasma pneumonia. Prevention relies on good hygiene practices: frequent handwashing, covering coughs and sneezes, avoiding close contact with infected individuals, and staying home when sick. During outbreaks, minimizing time in crowded settings and maintaining good ventilation can reduce transmission risk.

While there is currently no vaccine available to prevent mycoplasma pneumonia, understanding and implementing effective prevention strategies can significantly reduce your risk of infection. These measures become particularly important during outbreak periods or when someone in your household is infected.

Hand hygiene represents one of the most effective and accessible prevention measures. Respiratory droplets carrying mycoplasma can land on surfaces and be transferred to hands, which then touch the face, allowing entry of the bacteria through the nose, mouth, or eyes. Washing hands frequently with soap and water for at least 20 seconds, particularly after coughing or sneezing, before eating, and after touching commonly shared surfaces, can interrupt this transmission route.

Respiratory Hygiene

Practicing good respiratory hygiene, sometimes called "cough etiquette," helps prevent the spread of mycoplasma and other respiratory infections. When coughing or sneezing, cover your mouth and nose with a tissue, then dispose of the tissue immediately and wash your hands. If no tissue is available, cough or sneeze into your elbow rather than your hands, as this prevents contamination of hands that subsequently touch surfaces and other people.

If you're sick with respiratory symptoms, wearing a mask when around others can reduce the spread of respiratory droplets. This is particularly important when you must be in contact with household members or when seeking medical care.

Avoiding Exposure

During times when mycoplasma is circulating in your community, reducing exposure to potential sources of infection can be helpful. This doesn't mean complete isolation, but rather being mindful of risk factors. Avoid close, prolonged contact with people who have respiratory symptoms when possible. In crowded settings, maintaining some physical distance and ensuring good ventilation can reduce transmission risk.

If someone in your household is infected, certain measures can help limit spread to other family members. The infected person should stay in a separate room when possible and use a separate bathroom if available. Frequently touched surfaces should be cleaned regularly. Other household members should practice vigilant hand hygiene and monitor for symptoms.

Supporting Immune Function

While not specific to mycoplasma prevention, maintaining overall health supports immune function and the body's ability to fight off infections. Adequate sleep is particularly important, as sleep deprivation has been shown to impair immune function. A balanced diet providing essential nutrients, regular physical activity, stress management, and avoiding excessive alcohol consumption all contribute to immune system health.

What Are the Possible Complications of Mycoplasma Pneumonia?

Most mycoplasma infections resolve without complications, but in rare cases, serious complications can occur. These include severe pneumonia requiring hospitalization, neurological complications (encephalitis, meningitis), skin reactions (Stevens-Johnson syndrome), and blood disorders (hemolytic anemia). Early treatment and monitoring can reduce complication risks.

While the majority of mycoplasma infections are mild and self-limiting, it's important to be aware of potential complications that can occasionally occur. Understanding these possibilities helps in recognizing warning signs that warrant urgent medical attention and reinforces the importance of appropriate treatment when indicated.

The most common complication is progression of respiratory infection from bronchitis to pneumonia, or from mild to more severe pneumonia. Approximately 10-20% of mycoplasma infections progress to pneumonia, and a small percentage of these become severe enough to require hospitalization. Risk factors for severe pneumonia include older age, underlying lung disease, immunocompromised status, and delayed or inadequate treatment.

Neurological Complications

Neurological complications occur in approximately 0.1% of mycoplasma infections but can be serious when they develop. The most common neurological complication is encephalitis (inflammation of the brain), which can cause altered consciousness, confusion, seizures, and focal neurological deficits. Meningitis (inflammation of the membranes surrounding the brain and spinal cord) can also occur, presenting with severe headache, neck stiffness, and sensitivity to light.

The mechanism by which mycoplasma causes neurological complications is not fully understood but appears to involve both direct invasion of the nervous system and immune-mediated processes. These complications can occur during the acute infection or up to several weeks afterward, which sometimes makes the connection to the initial respiratory infection difficult to recognize.

Skin Reactions

Mycoplasma infection can trigger various skin reactions, ranging from mild rashes to severe conditions. The most serious skin complication is Stevens-Johnson syndrome (SJS) and its more severe form, toxic epidermal necrolysis (TEN). These conditions involve widespread blistering and peeling of skin and mucous membranes and represent medical emergencies requiring intensive care.

Erythema multiforme, presenting as distinctive target-shaped lesions on the skin, can also occur and may be accompanied by oral ulcers. While less severe than SJS/TEN, erythema multiforme can cause significant discomfort and requires medical evaluation.

Blood Disorders

Mycoplasma can trigger autoimmune hemolytic anemia, a condition where the immune system attacks and destroys red blood cells. This occurs because antibodies produced against the mycoplasma bacteria can cross-react with antigens on red blood cells. Symptoms include fatigue, pallor, dark urine, and jaundice. While usually mild and self-limited, severe cases may require treatment with corticosteroids or blood transfusion.

Long-term Outlook

For the vast majority of people, mycoplasma pneumonia resolves completely without lasting effects. The cough may persist for several weeks after other symptoms have resolved, but this typically improves gradually. Some people report lingering fatigue for weeks to months, but full recovery is expected. Repeated infections are possible since immunity following mycoplasma infection is not permanent.

How Is Mycoplasma Pneumonia Diagnosed?

Diagnosis of mycoplasma pneumonia typically involves clinical evaluation, chest X-ray to detect pneumonia, and specific tests including PCR (molecular testing) for bacterial DNA or serology (blood tests) for antibodies. PCR testing of respiratory samples is the most accurate method. However, many cases are diagnosed clinically based on symptoms and treated empirically.

Diagnosing mycoplasma pneumonia can be challenging because symptoms overlap significantly with other respiratory infections, and specific laboratory testing is not always readily available or practical. Healthcare providers often use a combination of clinical assessment, imaging, and sometimes laboratory testing to make the diagnosis.

The clinical presentation provides important diagnostic clues. The characteristic gradual onset, persistent dry cough, relatively mild constitutional symptoms despite prolonged illness, and the patient's age and exposure history all factor into the clinical suspicion for mycoplasma infection. Physical examination may reveal signs of pneumonia such as abnormal lung sounds, though findings are often minimal or absent despite significant symptoms, a phenomenon sometimes called "walking pneumonia" because the X-ray findings exceed what the physical examination suggests.

Imaging Studies

Chest X-ray is typically performed when pneumonia is suspected and can reveal characteristic patterns associated with mycoplasma infection. The findings are often described as reticulonodular infiltrates or patchy consolidation, frequently affecting the lower lobes and sometimes bilateral. Interestingly, the X-ray abnormalities in mycoplasma pneumonia are often more impressive than the patient's symptoms or physical examination findings would suggest.

CT scanning of the chest may be performed in complicated cases or when the diagnosis is uncertain, providing more detailed imaging of lung involvement. However, it's not routinely necessary for typical cases.

Laboratory Testing

Specific diagnosis of mycoplasma pneumonia can be confirmed through several laboratory methods. PCR (polymerase chain reaction) testing is the most sensitive and specific method, detecting mycoplasma DNA directly from respiratory specimens such as nasopharyngeal swabs, throat swabs, or sputum. Results are typically available within 24-48 hours, making PCR the preferred method when rapid diagnosis is needed.

Serological testing looks for antibodies against mycoplasma in the blood. IgM antibodies appear early in infection and suggest acute infection, while IgG antibodies develop later and persist longer. The limitation of serology is timing: a single test may not distinguish between current and past infection, and paired samples (acute and convalescent) showing rising antibody levels provide the most reliable diagnosis but require waiting 2-4 weeks.

In practice, many cases of suspected mycoplasma pneumonia are treated empirically based on clinical presentation without specific confirmatory testing, particularly in outpatient settings where testing may be unavailable or where the time required for results would delay treatment. This approach is reasonable given that the antibiotics effective against mycoplasma are also effective against other atypical pneumonia causes.

Frequently Asked Questions

Mycoplasma pneumonia is caused by the bacterium Mycoplasma pneumoniae and is classified as "atypical" pneumonia because it differs from typical bacterial pneumonia in several ways. Typical pneumonia (often caused by Streptococcus pneumoniae) usually has sudden onset with high fever, productive cough with colored sputum, and significant findings on physical examination. Mycoplasma pneumonia develops gradually over 1-3 weeks, typically causes dry cough, lower fever, and minimal physical examination findings despite significant symptoms. Additionally, mycoplasma lacks a cell wall, making common antibiotics like penicillin ineffective, requiring macrolides or tetracyclines instead.

People with mycoplasma infection become contagious during the incubation period (before symptoms appear) and remain contagious for extended periods. The most contagious period is during the first week of illness when coughing is most active. However, bacterial shedding can continue for weeks to months, even after antibiotic treatment begins. This prolonged shedding means that complete prevention of transmission is difficult. Generally, people are considered less contagious after 24-48 hours of appropriate antibiotic treatment, though they may still shed some bacteria for longer.

Yes, you can get mycoplasma pneumonia more than once. Unlike some infections that provide lifelong immunity, the immunity following mycoplasma infection is not permanent and wanes over time. Reinfection can occur months to years after the initial infection. Some studies suggest that subsequent infections may be milder than the first, but this is not always the case. The cyclical nature of mycoplasma outbreaks (typically every 3-7 years) partly reflects the waning of population immunity between outbreak periods.

Mycoplasma pneumonia during pregnancy is generally manageable with appropriate treatment. The infection itself is not known to cause birth defects or directly harm the developing baby. However, any serious illness during pregnancy, including pneumonia, warrants close monitoring. The main concern is ensuring appropriate antibiotic treatment while avoiding medications potentially harmful during pregnancy. Azithromycin is generally considered safe during pregnancy and is the first-line treatment. Doxycycline and fluoroquinolones should be avoided. Pregnant women with respiratory symptoms should seek medical care promptly to receive appropriate treatment and monitoring.

A prolonged cough lasting 4-6 weeks or longer is a characteristic feature of mycoplasma infection and doesn't necessarily indicate ongoing infection or treatment failure. The persistent cough results from inflammation and damage to the airway lining caused by the infection. Even after the bacteria are eliminated, the airways remain irritated and hyperreactive, triggering cough in response to minor stimuli. Healing of the damaged airway tissue takes time, which is why the cough gradually improves rather than stopping abruptly. If your cough is worsening rather than improving, or if you develop new symptoms like fever or increased shortness of breath, you should seek medical reevaluation.

References & Sources

This article is based on peer-reviewed medical research and international clinical guidelines. All medical claims are supported by Level 1A evidence (systematic reviews and randomized controlled trials) where available.

  1. Waites KB, Xiao L, Liu Y, et al. Mycoplasma pneumoniae from the Respiratory Tract and Beyond. Clinical Microbiology Reviews. 2017;30(3):747-809. doi:10.1128/CMR.00114-16
  2. Metlay JP, Waterer GW, Long AC, et al. Diagnosis and Treatment of Adults with Community-acquired Pneumonia: An Official Clinical Practice Guideline of the American Thoracic Society and Infectious Diseases Society of America. American Journal of Respiratory and Critical Care Medicine. 2019;200(7):e45-e67. doi:10.1164/rccm.201908-1581ST
  3. Martin-Loeches I, Torres A, Nagavci B, et al. ERS/ESICM/ESCMID/ALAT guidelines for the management of severe community-acquired pneumonia. European Respiratory Journal. 2023;61:2200735. doi:10.1183/13993003.00735-2022
  4. World Health Organization. WHO Pocket Book of Hospital Care for Children: Guidelines for the Management of Common Childhood Illnesses. 2nd edition. Geneva: WHO; 2013.
  5. Bradley JS, Byington CL, Shah SS, et al. The Management of Community-Acquired Pneumonia in Infants and Children Older Than 3 Months of Age: Clinical Practice Guidelines by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America. Clinical Infectious Diseases. 2011;53(7):e25-e76. doi:10.1093/cid/cir531
  6. Atkinson TP, Balish MF, Waites KB. Epidemiology, clinical manifestations, pathogenesis and laboratory detection of Mycoplasma pneumoniae infections. FEMS Microbiology Reviews. 2008;32(6):956-973. doi:10.1111/j.1574-6976.2008.00129.x

Editorial Team

This article was created by the iMedic Medical Editorial Team, a group of licensed specialist physicians with expertise in pulmonology, infectious disease, and internal medicine.

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