Abstract
Background
SARS-CoV-2 emergence was a threat for armed forces. A COVID-19 outbreak occurred on the French aircraft carrier Charles de Gaulle from mid-March to mid-April 2020.
Aim
To understand how the virus was introduced, circulated then stopped circulation, risk factors for infection and severity, and effectiveness of preventive measures.
Methods
We considered the entire crew as a cohort and collected personal, clinical, biological, and epidemiological data. We performed viral genome sequencing and searched for SARS-CoV-2 in the environment.
Results
The attack rate was 65% (1,148/1,767); 1,568 (89%) were included. The male:female ratio was 6.9, and median age was 29 years (IQR: 24–36). We examined four clinical profiles: asymptomatic (13.0%), non-specific symptomatic (8.1%), specific symptomatic (76.3%), and severe (i.e. requiring oxygen therapy, 2.6%). Active smoking was not associated with severe COVID-19; age and obesity were risk factors. The instantaneous reproduction rate (Rt) and viral sequencing suggested several introductions of the virus with 4 of 5 introduced strains from within France, with an acceleration of Rt when lifting preventive measures. Physical distancing prevented infection (adjusted OR: 0.55; 95% CI: 0.40–0.76). Transmission may have stopped when the proportion of infected personnel was large enough to prevent circulation (65%; 95% CI: 62–68).
Conclusion
Non-specific clinical pictures of COVID-19 delayed detection of the outbreak. The lack of an isolation ward made it difficult to manage transmission; the outbreak spread until a protective threshold was reached. Physical distancing was effective when applied. Early surveillance with adapted prevention measures should prevent such an outbreak.
Keywords: SARS-CoV-2, COVID-19; Outbreak; Aircraft Carrier; Ship, Herd immunity
Introduction
Infectious diseases are a common threat in the armed forces [1], which can experience epidemics that impact their capabilities or, alternatively, personnel may introduce pathogens into naive populations [2]. Controlling infectious diseases in the armed forces is a challenge, and military health services must be able to detect, investigate, and react to the emergence of new pathogens and outbreaks [3]. For example, a military ship’s crew is a cohort-like population, with members living closely together in a confined space; such environments can be catalysts for virus transmissions. The emergence and spread of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus [4] and the related disease coronavirus disease (COVID-19) across Europe in early 2020 exemplify such a threat, as evidenced by COVID-19 outbreaks on the Diamond Princess cruise ship [5] and the USS Theodore Roosevelt aircraft carrier [6]. At that time, this virus, its transmission, and the symptoms of the disease were unknown [7,8].
In January 2020, the French Carrier Battle Group (CVBG), including the aircraft carrier Charles de Gaulle (PA-CDG) and its carrier air wing, left the city of Toulon, its home port in South-eastern France, for a 4-month mission. From February to April, the CVBG navigated between the Mediterranean and the North Sea, making only two stopovers in Limassol (Cyprus, 21–26 February) and Brest (Western France, 13–16 March). In addition, the PA-CDG, as a hub airport at sea, took many service members on board, directly from land or from the other ships of the CVBG. On 7 April 2020, a COVID-19 outbreak was reported on the Charles de Gaulle. An investigation team was sent on board to perform testing and confirm the diagnosis. Exhaustive case identification and systematic isolation was performed once the PA-CDG docked in Toulon on 13 April, and the crew disembarked.
Our aim was to describe the entire outbreak, including a hypothesis to explain how the virus was introduced on board. In addition, we present the clinical profile of the COVID-19 cases including risk factors for infection and severity, the effectiveness of preventive measures and the potential protective threshold in our setting.
Methods
Study design
The investigation was conducted as a retrospective cohort by the French Armed Forces Center for Epidemiology and Public Health (CESPA) among the 1,767 service members of the PA-CDG present on board between 21 February and 13 April 2020.
Our study started with the stopover in Limassol, as there was no SARS-CoV-2 circulation identified in France and Europe when the PA-CDG departed Toulon on 21 January 2020 [4]. The complete timeline of the PA-CDG journey is available in Supplementary Figure S1.
Data sources
From 23 to 30 April, each service member was phoned by investigators with experience conducting a retrospective survey, using a standardised questionnaire. We chose this type of investigation because service members were isolated or quarantined. The questions were about personal (sex, age, body mass index (BMI), active smoking, blood group and rhesus factor), clinical (medical history, presence of symptoms, and dates of symptom onset/disappearance), and epidemiological data (date of boarding, places where they slept/had meals/worked, possible exposure to COVID-19, 1-to-3 score (never/sometimes, often and always) for application of physical distancing > 1 m, face mask wearing, and hand hygiene). When necessary, we obtained additional information from medical records and consultation registers. The first 30 confirmed COVID-19 cases were more extensively interviewed for precise dates and close contacts and/or possible exposure to other COVID-19 cases during the 14 days before symptom onset.
Case definitions
A biologically confirmed COVID-19 case was any service member with a positive SARS-CoV-2 quantitative (q)RT-PCR test. A confirmed COVID-19 case was any service member with a positive SARS-CoV-2 qRT-PCR and/or presenting symptoms of anosmia and/or ageusia. We included anosmia and ageusia in the definition because of their high specificity for COVID-19 disease, in order to identify cases earlier in those whose qRT-PCR test was negative at the time of investigation [9].
For this investigation, we used the following four clinical profile definitions: (i) asymptomatic case (no symptoms within 14 days of a positive SARS-CoV-2 qRT-PCR test), (ii) specific symptomatic (with symptoms indicative of COVID-19, e.g. anosmia, ageusia, cough, or fever), (iii) non-specific symptomatic (with other symptoms), and (iv) severe (requiring oxygen therapy).
Biological confirmation and testing strategy
A first panel of 67 patients presenting ongoing symptoms was sampled on board on 8 April 2020, confirming SARS-CoV-2 as the pathogen responsible for the outbreak. Then, from 14 to 17 April, all the service members underwent clinical screening and testing after they disembarked. Sampling was performed under biosecurity conditions using nasopharyngeal swabs. The qRT-PCR tests were analysed using either the LightCycler480 System (Roche Diagnostics) with assays set-up by the French Armed Forces Biomedical Research Institute (IRBA, Brétigny-sur-Orge) for samples taken on 8 April, and for later samples the cobas 6800 system with cobas SARS-CoV-2 kits (Roche Diagnostics) to target the Orf1a/b domain, performed according to the manufacturer’s instructions. Results were qualitative and the Cq threshold for a positive test was 35. Biologically confirmed cases were isolated at a military compound or a hospital in the Toulon area depending on the severity of their case, and those who tested negative were quarantined for 14 days. They were monitored daily by medical staff and tested if symptoms arose. All the qRT-PCR results were collected and used for the investigation. A negative qRT-PCR was required to leave the quarantine.
SARS-CoV-2 qRT-PCR was also performed on environmental swabs sampled from several common objects or surfaces before disinfection and inside the air conditioning system of the aircraft carrier.
Viral genome sequencing
Viral genome sequencing was performed on the first 60 positive samples taken from the service members on 8 April to contribute to molecular epidemiological studies (method in Supplementary Material: viral genome sequencing). Viral sequences are available online in the GISAID database (https://www.gisaid.org). The anonymous individual identifiers, GISAID accession numbers, and other data can be found in the Supplementary Table S1.
Statistical analysis
All statistical analyses were done using R [10]. We first studied the outbreak dynamics based on the epidemic curves and the instantaneous reproduction rate (Rt; Supplementary Methods: study of instantaneous reproduction rate). Then, we studied the circulation of the virus between sleeping compartments and work areas; the results are summarised in a chord diagram. Finally, we identified risk factors for SARS-CoV-2 infection and severity of COVID-19 using stepwise logistic regression, a descending step-by-step method that considers variables with p < 0.25 in univariate analysis or having an effect already recognised in other studies (especially age). We also tested a random-effect model on sleeping compartments, mess halls, and work areas; it was only significant for work areas.
Results
Population
Of 1,767 service members on the PA-CDG, the overall attack rate for COVID-19-confirmed cases was 65.0% (1,148/1,767). Among these, 1,568 (88.7%) were included in the study (Figure 1) to describe the outbreak, and 199 (11.3%) did not participate in the outbreak description (177 did not answer their mobile phone despite several calls and information messages, and 22 declined the offer to participate). Both participating vs non-participating groups differed in their mean ages (31.0 vs 27.8, p < 0.001), and in their RT-PCR positivity rates (64.7% vs 43.8, p < 0.001).
Figure 1.
Flowchart of the COVID-19 outbreak investigation on the Charles de Gaulle aircraft carrier, April 2020
COVID-19: coronavirus disease; neg: negative; pos; positive.
See details of data inside the blue dashed line in Table 1.

In the study group (n = 1,568), the sex ratio was 6.9 (1,369 men/199 women), and median age was 29 years (interquartile range (IQR): 24–36). Median body mass index (BMI) was 24.2 (IQR: 22.2–26.1). Several service members (n = 21; 1.3%) presented risk factors for severe COVID-19: arterial hypertension (n = 14), respiratory disease (n = 6), and diabetes (n = 1). Of the 1,568, 568 (36.2%) were active smokers. There were 593 (38.3%) crew members, 773 (49.7%) non-commissioned officers, and 187 (12.0%) officers. In the study group, 1,064 (67.9%) were COVID-19-confirmed cases, including 1,001 (94.1%) biologically confirmed cases and 63 (5.9%) cases with an early onset of anosmia and/or ageusia and a negative qRT-PCR at the time of investigation.
Clinical presentation, risk factors and exposure of COVID-19 cases
Among the 1,001 biologically confirmed cases, we describe four clinical profiles: asymptomatic (n = 130; 13.0%), non-specific symptomatic (n = 81; 8.1%), specific symptomatic (n = 764; 76.3%), and severe (n = 26; 2.6%) (Table 1). Median duration of symptoms at the time of the investigation was 8 days (IQR: 4–12). Age (p < 0.001) and BMI (p < 0.02) increased with the intensity of the clinical profile, in contrast to active smoking, which decreased (p = 0.003).
Table 1. Demographic characteristics, risk factors, and symptoms according to clinical profile among biologically confirmed COVID-19 cases, Charles de Gaulle aircraft carrier, April 2020 (n = 1,001).
| Variables | Total positive RT-PCR n = 1,001a |
Clinical profile | p value for clinical profileb | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Asymptomatic n = 130a |
Non-specific symptomatic n = 81a |
Specific symptomatic n = 764a |
Severe n = 26a |
||||||||
| n | % | n | % | n | % | n | % | n | % | ||
| Sex | |||||||||||
| Female | 121 | 12.1 | 12 | 9.2 | 11 | 13.6 | 95 | 12.4 | 3 | 11.5 | 0.74 |
| Male | 880 | 87.9 | 118 | 90.8 | 70 | 86.4 | 669 | 87.6 | 23 | 88.5 | |
| Age (years) | |||||||||||
| 18–25 | 314 | 31.4 | 51 | 39.2 | 30 | 37.0 | 231 | 30.3 | 2 | 7.7 | < 0.001 |
| 26–35 | 414 | 41.4 | 56 | 43.1 | 34 | 42.0 | 321 | 42.1 | 3 | 11.5 | |
| 36–45 | 182 | 18.2 | 20 | 15.4 | 13 | 16.0 | 139 | 18.2 | 10 | 38.5 | |
| 46–60 | 90 | 9.0 | 3 | 2.3 | 4 | 4.9 | 72 | 9.4 | 11 | 42.3 | |
| Hypertension | |||||||||||
| No | 985 | 98.4 | 129 | 100.0 | 80 | 100.0 | 751 | 98.8 | 25 | 96.2 | 0.21 |
| Yes | 10 | 1.0 | 0 | 0.0 | 0 | 0.0 | 9 | 1.2 | 1 | 3.8 | |
| Respiratory illness | |||||||||||
| No | 990 | 98.9 | 129 | 100.0 | 80 | 100.0 | 755 | 99.3 | 26 | 100.0 | 0.67 |
| Yes | 5 | 0.5 | 0 | 0.0 | 0 | 0.0 | 5 | 0.7 | 0 | 0.0 | |
| Active smoking | |||||||||||
| No | 676 | 67.5 | 78 | 60.0 | 51 | 63.0 | 523 | 68.5 | 24 | 96.0 | 0.003 |
| Yes | 323 | 32.3 | 52 | 40.0 | 30 | 37.0 | 240 | 31.5 | 1 | 4.0 | |
| BMI ≥ 25 | |||||||||||
| No | 597 | 59.6 | 80 | 61.5 | 47 | 58.8 | 462 | 61.4 | 8 | 30.8 | 0.02 |
| Yes | 391 | 39.1 | 50 | 38.5 | 33 | 41.2 | 290 | 38.6 | 18 | 69.2 | |
| Symptoms | |||||||||||
| Fever | 449 | 44.9 | NA | NA | NA | NA | 425 | 55.6 | 24 | 92.3 | NA |
| Cough | 356 | 35.6 | NA | NA | 333 | 43.6 | 23 | 88.5 | |||
| Headache | 562 | 56.1 | 45 | 55.6 | 497 | 65.1 | 20 | 76.9 | |||
| Asthenia | 459 | 45.9 | 30 | 37.0 | 411 | 53.8 | 18 | 69.2 | |||
| Anosmia | 550 | 54.9 | NA | NA | 539 | 70.5 | 11 | 42.3 | |||
| Ageusia | 446 | 44.6 | NA | NA | 436 | 57.1 | 10 | 38.5 | |||
| Rhinitis | 379 | 37.9 | 31 | 38.3 | 340 | 44.5 | 8 | 30.8 | |||
| Myalgia | 448 | 44.8 | 24 | 29.6 | 400 | 52.4 | 24 | 92.3 | |||
| Odynophagia | 155 | 15.5 | 10 | 12.3 | 142 | 18.6 | 3 | 11.5 | |||
| Earache | 35 | 3.5 | 0 | NA | 34 | 4.5 | 1 | 3.8 | |||
| Malaise | 31 | 3.1 | 0 | NA | 28 | 3.7 | 3 | 11.5 | |||
| Dyspnoea | 272 | 27.2 | 6 | 7.4 | 247 | 32.3 | 19 | 73.1 | |||
| Chest pain | 131 | 13.1 | 8 | 9.9 | 111 | 14.5 | 12 | 46.2 | |||
| Diarrhoea | 150 | 15.0 | 8 | 9.9 | 128 | 16.8 | 14 | 53.8 | |||
| Vomiting | 24 | 2.4 | 3 | 3.7 | 18 | 2.4 | 3 | 11.5 | |||
| Abdominal pain | 61 | 6.1 | 1 | 1.2 | 55 | 7.2 | 5 | 19.2 | |||
| Other | 61 | 6.1 | 4 | 4.9 | 54 | 7.1 | 3 | 11.5 | |||
BMI: body mass index; COVID-19: coronavirus disease; NA: not applicable.
a Missing data explain the differences between totals of each variable.
b Chi-squared test.
We examined risk factors for infection in the entire study group but excluding cases with missing data for the model (Table 2). Active smoking was associated with reduced infection (adjusted odds ratio (ORa): 0.57; 95% confidence interval (CI): 0.44–0.73), contrary to age group (46–60 vs 18–25 years) (ORa: 1.79; 95% CI: 1.03–3.20). Sex, blood group, BMI and a history of risk factors were not associated with SARS-CoV-2 infection.
Table 2. Logistic regression analysis of possible factors associated with COVID-19-confirmed cases, Charles de Gaulle aircraft carrier, April 2020 (n = 1,221a).
| Variables | Univariate analysis | Multivariate analysis | ||||
|---|---|---|---|---|---|---|
| OR | 95% CI | p value | ORa | 95% CI | p value | |
| Individual characteristics | ||||||
| Sex | ||||||
| Female | Ref | NA | ||||
| Male | 1.28 | 0.91–1.79 | 0.15 | |||
| Age (years)b | ||||||
| 18–25 | Ref | |||||
| 26–35 | 1.17 | 0.88–1.55 | 0.29 | 1.30 | 0.95–1.78 | 0.10 |
| 36–45 | 0.95 | 0.67–1.34 | 0.75 | 1.05 | 0.73–1.51 | 0.81 |
| 46–60 | 1.64 | 0.98–2.84 | 0.07 | 1.79 | 1.03–3.20 | 0.04 |
| Active smoking | ||||||
| No | Ref | |||||
| Yes | 0.55 | 0.43–0.71 | < 0.001 | 0.57 | 0.44–0.73 | < 0.001 |
| BMI ≥ 25 | ||||||
| No | Ref | NA | ||||
| Yes | 1.12 | 0.88–1.44 | 0.36 | |||
| Blood group | ||||||
| A | Ref | NA | ||||
| AB | 1.30 | 0.68–2.67 | 0.45 | |||
| B | 0.78 | 0.52–1.18 | 0.23 | |||
| O | 0.87 | 0.67–1.13 | 0.30 | |||
| Rhesus factor | ||||||
| Negative | Ref | NA | ||||
| Positive | 0.90 | 0.63–1.29 | 0.58 | |||
| Infection prevention measures | ||||||
| Physical distancing | ||||||
| Never/sometimes | Ref | |||||
| Often | 0.85 | 0.64–1.14 | 0.27 | 0.91 | 0.68–1.23 | 0.54 |
| Always | 0.51 | 0.37–0.69 | < 0.001 | 0.55 | 0.40–0.76 | < 0.001 |
| Hand hygiene | ||||||
| Never/sometimes | Ref | NA | ||||
| Often | 0.91 | 0.38–1.99 | 0.82 | |||
| Always | 0.75 | 0.33–1.58 | 0.47 | |||
| Environment | ||||||
| Mess hall | ||||||
| Crew | Ref | |||||
| Non-commissioned officer | 1.10 | 0.85–1.42 | 0.47 | 1.01 | 0.76–1.34 | 0.93 |
| Officer | 0.76 | 0.50–1.17 | 0.21 | 0.61 | 0.38–0.98 | 0.04 |
| Work Area | ||||||
| Flight deck | 4.03 | 2.10–8.72 | < 0.001 | 4.09 | 2.10–8.97 | < 0.001 |
| Other | Ref | |||||
| Sleeping compartment occupancy | ||||||
| 1–4 | Ref | NA | ||||
| 5–10 | 1.03 | 0.73–1.46 | 0.86 | |||
| 11–15 | 1.10 | 0.80–1.52 | 0.56 | |||
| > 15 | 1.12 | 0.77–1.63 | 0.55 | |||
BMI: body mass index; CI: confidence interval; COVID-19: coronavirus disease; NA: not applicable; OR: odds ratio; ORa: adjusted odds ratio; Ref.: reference.
a Study group (n = 1,568) excluding cases with missing data for the model (n = 347).
b Age was forced into the model for the multivariate analysis.
Preventive measures
We evaluated the effectiveness of infection prevention measures. Application of physical distancing was associated with SARS-CoV-2 infection (ORa: 0.55; 95% CI: 0.40–0.76), contrary to the score of hand hygiene. Since face masks were required only for cases with symptoms indicative of COVID-19 on board in March, and for all service members once the epidemic was confirmed on 8 April, this prevention measure could not be studied in statistical analyses.
We also examined the infection risk in sleeping, eating, and working areas. Working on the flight deck led to greater odds of SARS-CoV-2 infection (ORa: 4.09; 95% CI: 2.10–8.97) than the other areas; it was where the outbreak began. The officers’ mess hall (which is like a restaurant where personnel density was low during meals) was associated with lower odds (ORa: 0.61; 95% CI: 0.38–0.98) than the mess hall used by the crew (self-service and high density).
Disease severity
A total of 29 severe cases were recorded. Of these, 26 had a positive qRT-PCR (details are in Table 1). Three cases required hospitalisation in an intensive care unit, none died. We examined risk factors for severity among confirmed COVID-19 cases: Active smoking was inversely associated with severe COVID-19 (ORa: 0.12; 95% CI: 0.01–0.57). Conversely, belonging to the oldest age group (ORa: 8.81; 95% CI: 1.01–61.08) and having a BMI above 25 (ORa: 3.12; 95% CI: 1.22–9.02) were risk factors for severity (Table 3).
Table 3. Logistic regression analysis of exposure factors linked to severity of COVID-19, Charles de Gaulle aircraft carrier, April 2020 (n = 845a).
| Variables | Univariate analysis | Multivariate analysis | ||||
|---|---|---|---|---|---|---|
| OR | 95% CI | p value | ORa | 95% CI | p value | |
| Sex | ||||||
| Female | Ref | NA | ||||
| Male | 0.88 | 0.29–3.79 | 0.83 | |||
| Age (years) | ||||||
| 18–25 | Ref | |||||
| 26–35 | 1.47 | 1.28–10.65 | 0.66 | 1.19 | 0.23–8.70 | 0.84 |
| 36–45 | 7.07 | 1.75–47.29 | 0.01 | 4.76 | 1.14–32.30 | 0.05 |
| 46–60 | 14.4 | 1.40–98.54 | 0.001 | 8.81 | 1.01–61.08 | 0.008 |
| Active smoking | ||||||
| No | Ref | |||||
| Yes | 0.09 | 0.01–0.45 | 0.02 | 0.12 | 0.01–0.57 | 0.04 |
| BMI ≥ 25 | ||||||
| No | Ref | |||||
| Yes | 3.92 | 1.57–11.08 | 0.005 | 3.12 | 1.22–9.02 | 0.02 |
| Blood group | ||||||
| A | Ref | NA | ||||
| AB | 1.16 | 0.06–6.59 | 0.89 | |||
| B | 1.01 | 0.15–4.13 | 0.99 | |||
| O | 1.20 | 0.47–3.18 | 0.70 | |||
| Rhesus factor | ||||||
| Negative | Ref | NA | ||||
| Positive | 0.98 | 0.33–4.24 | 0.98 | |||
BMI: body mass index; CI: confidence interval; COVID-19: coronavirus disease; NA: not applicable; OR: odds ratio; ORa: adjusted OR.
a COVID-19-confirmed cases (n = 1,001) in the study group, excluding cases with missing data for the model (n = 156).
Epidemiological description of the outbreak
Among all 1,064 confirmed COVID-19 cases, a date of symptom onset was available for 959 (90.1%), from which an epidemiological curve associated with the progression of estimated Rt (Figure 2) was generated. Final R during the outbreak was 2.86. Of all service members on board, the final proportion of COVID-19 confirmed cases was 65.0% (1,148/1,767; 95% CI: 62–68).
Figure 2.
A. Epidemiological curve of confirmed COVID-19 cases according to date of symptom onset and B. Instantaneous reproduction rate curve of the Charles de Gaulle aircraft carrier, April 2020 (n = 959a)
COVID-19: coronavirus disease; Rt: instantaneous reproduction rate.
a COVID-19 confirmed cases in the study group and with a date of symptoms onset
In panel B, the red line indicates the estimated Rt progression. The green shaded area represents the 95% confidence interval. The blues dotted lines delimit five Rt main changes.
The statistically significant changes in the epidemiological and Rt curves highlighted five phases in the progression of Rt: (i) an initial phase of low circulation with sporadic cases (1.1 < Rt < 2.2), (ii) an acceleration following the Brest stopover associated with Rt peaking at 3.9, (iii) a phase of moderate virus circulation starting between 21 and 24 March, with Rt between 1 and 2, (iv) an epidemic phase starting between 31 March and 1 April, with Rt peaking at 2.9, and (v) a slowing down of the epidemic, which began on 8 April and crossed the level of Rt = 1 on 13 April.
Interviews with the first 30 confirmed cases revealed that two early chains of transmission had started before the stopover in Brest, accounting for the ship’s first eight COVID-19 confirmed cases. The date of symptom onset of the first case was 28 February, leading to only one secondary case among sleeping compartment mates on 11 March (Figure 2). The second index case developed symptoms on 2 March. This case led to five secondary and tertiary cases between 6 and 17 March among individuals working on the flight deck and using a very densely occupied break room. During the 4-day stopover in Brest from 13 to 16 March, 97% of personnel disembarked. Some went to restaurants and bars while others met relatives who came from all over the country. Interviews identified two cases who had symptoms during the stopover, eliciting several additional virus introductions. After the stopover in Brest, SARS-CoV-2 actively circulated on board, and it was difficult to establish true transmission chains. We examined the possible spread of the virus by analysing back-and-forth movements of confirmed cases between sleeping compartments and work areas (Figure 3). Attack rates in work areas were between 56.0% and 78.1%, and in sleeping compartments between 56.9% and 75.0%. Only the flight deck work area and its associated sleeping compartments had a higher attack rate, at 87.5% and 85.0% respectively.
Figure 3.
Chord diagram between sleeping compartments and work areas of COVID-19- confirmed cases, Charles de Gaulle aircraft carrier, April 2020 (n = 1,064)
COVID-19: coronavirus disease.
The top half of the chord diagram represents five main sleeping areas. The bottom half represents 16 work areas; each work area was assigned a different colour. The size of the chords spanning across the two halves is proportional to the number of COVID-19-confirmed cases in common between two areas.
Phylogenetic analyses of subclades
To further examine viral introduction and spread, we performed phylogenetic and temporal analyses on the 51 strains available among the first 60 SARS-CoV-2-positive samples. Of these 51 strains, five separate groups were identified. Four groups were potentially linked to four separate introduction events (highlighted in blue, green, pink, and yellow in Figure 4; we observed an evolution of the strains with a successive accumulation of mutations. When compared with the known diversity at the time of the outbreak in France, most of the strains clustered with sequences originating from the Brittany, Hauts-de-France, and Auvergne-Rhône-Alpes regions. One strain (highlighted in purple in Figure 4) did not cluster with any other PA-CDG strain. Its positioning confirms that its origin was different than that of all the other 50 genomes analysed, reflecting an additional virus introduction event on the PA-CDG. Among all the samples, we observed no significant correspondence or proximity to isolates originating from Cyprus, Italy, Spain, Portugal, or the United Kingdom (some service members transited through these countries before boarding, see Supplementary Figure S1: Timeline of the main exposure events for SARS-CoV-2 introduction).
Figure 4.
Maximum likelihood tree inferred from sequenced SARS-CoV-2 genomes, Charles de Gaulle aircraft carrier, April 2020 (n = 51), and the French SARS-CoV-2 sequences present in the GISAID database, 3 May 2020 (n = 246)
SARS-CoV-2: severe acute respiratory syndrome coronavirus 2.
The two SARS-CoV-2 Wuhan strains are coloured in dark blue text. Red circles indicate sequenced genomes from the Charles de Gaulle aircraft carrier. Blue, yellow, pink, purple, and green areas highlight the five different groups of SARS-CoV-2 strains detected on board. The authors acknowledge the originating and submitting laboratories of the sequences from GISAID’s EpiFlu Database used in the phylogenetic analysis.
Environmental analysis
In an examination of environmental samples, 11 swabs were positive for SARS-CoV-2 among 38 environmental samples collected inside the ship (on shared objects such as a table, handrail, control panel, joystick, toilet) as were several samples from the filters of the air conditioning system. Viral cultures were not performed.
Discussion
This outbreak in a monitored group of military personnel living in close quarters in a confined environment offered a unique opportunity to describe the natural progression of SARS-CoV-2 epidemic spread and infection characteristics in a young and healthy and predominantly male population. Our case definition, which considers RT-PCR results but also specific clinical signs, was sensitive enough to capture the real proportion of SARS-CoV-2 infected cases. The attack rate was 65%, close to the final 64% seroprevalence measured on the PA-CDG at the end of the 2-week isolation/quarantine period [11].
The outbreak began early in March 2020 among the personnel of the aircraft carrier’s ‘airport’. Case interviews, the epidemic curve, and virus sequencing corroborated the hypothesis of several introductions of the virus on board. Even when at sea, an aircraft carrier is a hub airport that regularly receives aircraft and passengers for the entire CVBG. The first chain of transmission was identified among the flight deck staff, and eventually the highest attack rate was observed in this sub-population. Other introductions occurred during the stopover in Brest 2 weeks later. This stopover represents a critical point in the outbreak. The national lockdown began 2 days later, on 17 March, as SARS-CoV-2 was spreading rapidly in Northern and Eastern France [12]. At that time, access to RT-PCR tests in France was limited. As a rule, ships should avoid stopovers in countries where an epidemic is occurring, and even more so in the case of an emerging pathogen, whose circulation may be underestimated. The results of viral genome sequencing were compatible with the transmission network inferred from the epidemiological data – all the clades identified but one came from France.
The epidemic then spread between sleeping compartments and work areas, moving back and forth, and the measures taken to stop these flows, e.g. remote working, cohorting according to activities, lockdown, caused the spread to slow [12]. This pattern may be the same in the general population between homes and workplaces. Mealtime also played a role in transmission, as the level of proximity in mess halls was associated with probability of infection. During the 15 days following the Brest stopover, preventive measures were forcefully applied, e.g. hand hygiene, decrease in the number of meetings, closing of bars, and particularly, physical distancing [13], which was significantly protective against SARS-CoV-2 infection on the PA-CDG, despite the confined environment and high attack rate, as on the USS-Roosevelt [14]. This also suggests that droplet transmission was predominant in the outbreak. We found viral RNA in the air conditioning system, illustrating the possibility of aerial transmission. Virus exposure through a contaminated environment was also possible, as one out of three environmental samples was positive. However, we cannot conclude on the degree to which aerial or environmental transmission played a role in the spread.
The prevention measures made it possible to contain the speed of virus transmission (1 < Rt < 2). As soon as these measures were lifted on 30 March, the outbreak expanded, with Rt increasing to almost 3. Eventually, Rt declined and the outbreak stopped. Mandatory face mask wearing for the entire crew as well as the systematic isolation of cases occurred well after the epidemic peak, too late to influence its natural course.
Our results suggest rather that once 65% (95% CI: 62–68) of the crew had been infected, that proportion appeared to be large enough to prevent the virus from circulating further. This threshold obtained from a real outbreak was consistent with the level of herd immunity deemed necessary to protect the population from the viral circulation [15]. With the emergence of more-contagious SARS-CoV-2 variants, this threshold would probably have to be raised [16].
We calculated an asymptomatic case rate of 13%, close to that measured on the USS-Roosevelt (19.8%) [17] and in other outbreaks that we have investigated [18,19]. This rate was lower compared with passengers on the Diamond Princess (57.7%), but authors only collected respiratory symptoms [20,21]. More generally, a systematic review carried out by Buitrago et al. highlighted an asymptomatic rate of 20% (95% CI: 17–25) [22]. The low percentage of asymptomatic cases could also have been caused by the very low rate of air renewal on the PA-CDG, as it has been described that the SARS-CoV-2 inoculum could be linked to the clinical profiles of COVID-19 [13].
We had 29 severe cases (2.6%) that required hospitalisation with oxygen, which justified the shortening of the military mission; all recovered. Our findings confirmed that age and BMI were risk factors for increasing COVID-19 intensity [23]. Surprisingly, previous usual active smoking behaviour had lower odds of infection and its severity, although we expected that smoking areas were at risk because of increased close contact. Many studies find that smoking is instead a risk factor for COVID-19 [24-26]. We obtained this result among a young population with no comorbidities, who were not yet suffering from the complications of smoking. According to other studies which found similar results, hypothesised mechanisms of interaction between smoking and COVID-19 were a possible anti-inflammatory effect of nicotine, diminished immune and cytokine responses, or an increase of nitric oxide in the respiratory tract [27,28]. Blood group was not associated with the infection or with its severity.
The ship did not have an isolation ward with a separate ventilation system, so it was not possible to isolate and quarantine the numerous cases and their close contacts on board, once the epidemic was underway. An early warning and countermeasures would have changed the course of the epidemic. The first sign that could have early alerted medical staff was the increase of patients with upper respiratory symptoms and/or anosmia. However, in France, these symptoms were not associated with COVID-19 disease before April 2020. This underlines the important role of epidemiological surveillance [29], in particular syndromic epidemiological surveillance based on pre-diagnosis data collection, for emerging disease detection and management [30]. The deployment of multiplex PCR automates would have made it possible to exclude routine diagnosis as influenza or rhinovirus, leading to the suspicion of an unusual pathogen circulating. In the future, wastewater viral surveillance would also enable early warnings on shipboard viral circulation to be issued [31].
Our study has some limitations. Our findings are from observational retrospective data. Recollection and misrepresentation biases may have led to errors. There were some differences between participants and non-participants. However, selection bias should be limited, as only 11.3% of the services members did not participate to the study. The study group included mainly young males, so that our results cannot be extrapolated to the general population.
Conclusion
Such an epidemic causes the saturation of care capacities, the decline in the availability of staff and the disorganisation of activities, impacting the operation of the community on board in the end. Communities such as armed forces should protect themselves from such incidents by strengthening adapted prevention and early detection capabilities in order to be better prepared for outbreaks.
Statements
Ethical statement: This was not an experimental protocol, but an outbreak investigation with routine care provided to infected individuals, so no ethical approval from any named institutional and/or licensing/ethics committee was required. We obtained individual informed consent to analyse data. No administrative authorisation was required to access and use medical records. We chose not to provide certain details and to aggregate certain data in order to maintain patient anonymity. All methods were carried out in accordance with relevant guidelines and regulations.
Data availability statement: The datasets generated and/or analysed during the current study are not publicly available as they represent confidential medical information, but they are available from the corresponding author upon reasonable request.
Acknowledgements
We wish to thank Laurent Richecoeur, Isabelle Delplanque, Patrick Augier, Simon Cauchemez, Christian Hupin, and Rémy Michel, as well as the French Navy for making available additional personnel for the investigation. We acknowledge the authors, originating and submitting laboratories of the sequences from GISAID’s EpiFlu Database on which this research is based (see Figure 4). All submitters of data may be contacted directly via the GISAID website: www.gisaid.org.
Supplementary Data
Conflict of interest: None declared.
Authors’ contributions: Care of patients: Vanessa Marbac, Jacques Cobola, Fabien Dutasta. Outbreak investigation and management: Franck de Laval, Jean-Baptiste Meynard, Vincent Pommier de Santi. Data collection: Franck de Laval, Constance Lacrosse, Aissata Dia, Vanessa Marbac, Flavie Letois. Biological analyses: Frédéric Janvier. Viral genome sequencing: Olivier Gorgé, Flora Nolent, Jean-Nicolas Tournier. Data analysis: Hervé Chaudet, Olivier Gorgé, Joffrey Marchi, Bakridine Mmadi Mrenda, Gaëtan Texier, Charles Chapus, Véronique Sarilar, Anthony Levasseur. Writing: Franck de Laval, Vincent Pommier de Santi. PA-CDG COVID-19 investigation group: Care of patients, data collection or viral genome sequencing.
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