Identification of a Super-Spreading Chain of Transmission Associated with COVID-19 at the Early Stage of the Disease Outbreak in Wuhan

Article Information

Ke Hu1*, Yang Zhao1, Mengmei Wang1, Qiqi Zeng2, Xiaorui Wang2, Ming Wang3, Zhishui Zheng1, Xiaochen Li1, Yunting Zhang1, Tao Wang1, Shaolin Zeng1, Yan Jiang4, Dan Liu4, Wenzhen Yu1, Fang Hu2, Hongyu Qin2, Jingcan Hao5, Meng Jiang2, Binghong Zhang7, Bingyin Shi6, Chengsheng Zhang2,5,8*

1Department of Respiratory and Critical Care Medicine, Renmin Hospital of Wuhan University Zhangzhidong Road No. 99, Wuhan 430060, China

2Precision medicine center, The First Affiliated Hospital of Xi’an Jiaotong University, 277 Yanta West Road, Xi’an 710061, China

3Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China

4Division of Respiratory Disease, the Fifth Hospital of Wuhan City, Xianzheng street No. 122, Hanyang district, Wuhan 430050, China

5Cancer Center, The First Affiliated Hospital of Xi’an Jiaotong University, 277 Yanta West Road, Xi’an 710061, China

6Department of Endocrinology, the First Affiliated Hospital of Xi’an Jiaotong University, 277 Yanta West Road, Xi’an 710061, China

7East campus, Renmin Hospital of Wuhan University, Gaoxin 6th Road, East Lake New Technology Development Zone, Wuhan 430040, China

8The Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA

*Corresponding author: Chengsheng Zhang, MD, PhD, Precision Medicine Center, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an, China

Ke Hu, MD, Department of Respiratory Disease, Renmin Hospital of Wuhan University, Wuhan, China

Received: 19 July 2021; Accepted: 27 July 2021; Published: 30 July 2021

Citation:

Ke Hu, Yang Zhao, Mengmei Wang, Qiqi Zeng, Xiaorui Wang, Ming Wang, Zhishui Zheng, Xiaochen Li, Yunting Zhang, Tao Wang, Shaolin Zeng, Yan Jiang, Dan Liu, Wenzhen Yu, Fang Hu, Hongyu Qin, Jingcan Hao, Meng Jiang, Binghong Zhang, Bingyin Shi, Chengsheng Zhang. Identification of a Super-Spreading Chain of Transmission Associated with COVID-19 at the Early Stage of the Disease Outbreak in Wuhan. Archives of Clinical and Biomedical Research 5 (2021): 598-612.

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Abstract

Background: The super-spreading events were associated with the outbreaks of SARS and MERS, but their association with the outbreak of COVID-19 was unknown before we first published a report in medRxiv preprint in March 2020. Here, we reported a super-spreading transmission chain of SARS-CoV-2 involving an index patient, seven cancer patients, 40 health care workers and four family members.

Methods: We conducted a retrospective study to identify the index patient and the exposed individuals linked to a chain of transmission associated with COVID-19. We collected and analyzed the data on demographic features, exposure history, clinical presentation, laboratory investigation, radiological examination, and disease outcome of these patients.

Results: We identified the index patient and another presumptive “super-spreader”, who initiated and amplified a super-spreading transmission chain associated with COVID-19, respectively. There were 31 female and 21 male patients in this cohort, and the median age was 37 years (range: 22-79 years). Each of them had an exposure history with the index patient or his close contacts. Approximately 87% (45/52) of the patients had fever or other symptoms, 96% (50/52) had abnormal chest CT-scan findings, 86% of the tested patients (39/45) were positive for SARS-CoV-2 in the nasopharyngeal or throat swab specimen, 85% of the tested patients (29/34) were positive for SARS-CoV-2-specific IgM and/or IgG, 15% of the RT-PCR positive patients were tested negative for the specific IgM and/or IgG at the convalescent phase, and 15% of the RT-PCR negative patients were tested positive for the specific IgM and/or IgG. The severe patients experienced a significant decrease in oximetry saturation, lymphocyte, and platelet counts, along with a significant increase in C-reactive protein, D-dimer, and lactate dehydrogenase. All six fatal cases h

Keywords

COVID-19; SARS-CoV-2; Super-spreading; Super-spreader; Nosocomial transmission

COVID-19 articles; SARS-CoV-2 articles; Super-spreading articles; Super-spreader articles; Nosocomial transmission articles

Article Details

1. Introduction

The initial outbreaks and the ongoing pandemic of coronavirus disease 2019 (COVID-19), which was caused by the SARS-CoV-2, have posed tremendous challenges to the international communities [1-12]. As of July 16, 2021, more than 188 million confirmed cases and over 4 million deaths worldwide have been reported to the World Health Organization [12]. This is the first pandemic caused by a coronavirus [12]. Coronaviruses (CoV) are a large family of RNA viruses that cause a variety of mild and severe diseases in humans and animals [13]. Prior to the COVID-19, there were two severe outbreaks of human coronavirus diseases in the past two decades, the severe acute respiratory syndrome (SARS) and the Middle East respiratory syndrome (MERS) [14-18], which were caused by SARS-CoV and MERS-CoV, respectively. SARS was first reported in November 2002 in Guangdong Province, China [19]. There were 8,422 confirmed SARS cases, including 919 deaths in 32 countries between November 2002 and August 2003 [19]. MERS was first identified in September 2012 in Saudi Arabia [20]. There were 2494 confirmed MERS cases, including 858 deaths in 27 countries between September 2012 and November 2019 [20].

The super-spreading events, by which an individual patient spread an infection to a large number of susceptible people, were associated with the outbreaks of SARS and MERS [21-24]. While case clusters with human-to-human transmission of SARS-CoV-2 were reported [25-27], it remained unknown whether super-spreading events occurred before we first published a report in medRxiv preprint in March 2020 [28]. Here, we conducted a retrospective study and identified a super-spreading chain of transmission associated with COVID-19.

2. Methods

2.1 Patients and data collection

This retrospective study was approved by the institutional review board of Renmin Hospital of Wuhan University (No. WDRY2020-K019). Oral consent was obtained from the patients or their family members, whereas written informed consent was waived by the Provincial and National Health Commissions in China under the exceptional circumstances for investigation of an ongoing disease outbreak. In this cohort, we identified a super-spreading chain of transmission involving 52 linked patients with COVID-19 in three separate hospitals in Wuhan, the epicenter of an outbreak of COVID-19 across China. The data we retrieved from the electronic medical records included demographic features, comorbidities, clinical presentation, laboratory investigation, RT-PCR testing for SARS-CoV-2, serum specific IgM and IgG antibodies, chest computed tomographic (CT) scan, and the disease outcome. The contact and exposure history were also collected through communications with the patients and/or their family members.

2.2 Case definition

All patients with COVID-19 enrolled in this study were diagnosed and classified according to World Health Organization interim guidance and the “Guidelines on the Diagnosis and Treatment of the Novel Coronavirus Infected Pneumonia” developed by the National Health Commission of People’s Republic of China [29-31].

The severe cases showed at least one of the following presentations: (1) Respiratory distress, Respiratory rate (RR)≥30 times/min; (2) At rest, oxygen saturation≤93%; (3) Arterial partial pressure of oxygen (PaO2) /Fraction of Inspired Oxygen (FiO2)≤300mmHg (1mmHg=0.133kPa). Patients who had close contact with the index patient were defined as secondary cases. Patients who contracted the disease from the secondary cases were classified as tertiary cases.

2.3 Laboratory investigations

The routine laboratory investigations were performed by the certified clinical diagnostic laboratories inside the designated hospitals. The RT-PCR testing for SARS-CoV-2 was conducted by the Standard Operation Procedures published previously [28, 29]. Serum specific IgM and IgG antibodies against SARS-CoV-2 were detected using the immunoassay kit provided by the YHLO Biotech Co., Ltd. (Shenzhen, China) and the fully-automated chemiluminescence immunoassay analyzer (UniCel DxI800, Beckman Coulter, Inc., USA) according to the instructions of the manufacturers.

The immune activities were measured as a relative light unit (RLU). The analyzer automatically converts the RLU from the immunoassay into an absolute unit by fitting the standard master calibration curve. A cutoff value of ≥10.0 AU/ml is considered as positive for both antibodies.

2.4 Statistical analysis

For statistical analysis, all of the continuous variables were performed by Shaprio-wilk test and Levene test to analyze normality and homogeneity. Continuous variables were expressed as median (IQR) and compared with T test or Mann-Whitney U test. Categorical variables were expressed as number (n/N %) and compared by χ² test, continuity-adjusted χ² test or Fisher’s exact test. A two-sided α of less than 0.05 was considered statistically significant. Statistical analyses were done using the SPSS 22.0 software.

3. Results

In this report, we conducted a retrospective study and identified a super-spreading chain of transmission involving the index patient, seven cancer patients, 40 health care workers and four family members (Figure 1 and Table 1).

3.1 Identification of the index patient (C-1)

On January 3, 2020, a male patient in his 50s developed fever (38.8°C), headache, chest pain and myalgias when he visited his relative in a wardroom (Ward-X in Figure 1) shared by four female cancer patients at Hospital A.

He initially thought that he had a “cold” and continued to visit this ward until he was admitted to hospital B on January 10, 2020. His Chest CT-scan findings showed a rapid progression of bilateral infiltrates in the lungs (Figure 2). He received antibiotics treatment for one week but was ineffective. On January 18, he was tested positive for SARS-CoV-2 and diagnosed with COVID-19. He died of severe respiratory failure on January 26, 2020.

While the exact exposure history of this patient remained unclear, he did not visit the “Huanan Wet Market”, the suspected origin for this outbreak in Wuhan. Of note, the “Huanan Wet Market” is located in the Hankou District of Wuhan city, which is separated from the Wuchang District by the Yangtse River. The two hospitals (A and B) where the index patient visited were located in Wuchang District.

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Figure 1:

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Figure 2:

3.2 A super-spreading event initiated by the index patient

Eleven people presented fever and abnormal CT-scan findings after close contacts with the index patient C-1 between January 3 and January 10, 2020 (Figure 1 and Table 1). Below was a timeline for the initial transmission events. (1) C-1 visited his relative C-2 in Ward-X that was shared by other three cancer patients (C-3, C4, and C-5) at the Department-I of hospital A when he first developed fever and other symptoms on January 3. All four cancer patients had close contacts with C-1 and subsequently developed fever (38°C-40°C) and abnormal CT-scan findings between January 4 and January 15. All were RT-PCR positive for SARS-CoV-2, but the assays for the serum specific antibodies were not available at that time. All four patients did not have other exposure records and epidemiological history before their disease onsets. Three of them died of severe respiratory failure within 9-20 days after the onsets. C-2 developed symptoms on January 9 (6 days after the onset of C-1) and died on January 17. C-3 developed symptoms on January 4 (one day after her close contact with C-1) and died on January 24. C-4 developed symptoms on January 15 and transferred to a designated hospital on January 30, where she remained at a stable condition after the treatment. C-5 developed symptoms on January 15 and died on January 29.

(2) On January 3, C-1 also visited the office area of the health care workers at the Department-I of hospital A to discuss the treatment plan for his relative C-2. Four doctors (C-6, C-7, C-8 and C-9) and one nurse (C-10) developed fever and abnormal CT-scan findings between January 9 and January13 (within 10 days after close contacts with C-1). In addition, a cluster of eleven health care workers (C-17 to C-27) from the same department who had close contact with their co-workers (C-6 to C-10) presented fever and abnormal CT-scan findings between January 16 and January 21 (within 3-12 days after their exposure to the secondary cases). All the health care workers were previously healthy and did not have other exposure records and epidemiological history (Figure 1 and Table 1).

(3) On January 10, C-1 was admitted to hospital B, where he was diagnosed with COVID-19. Two doctors (C-51 and C-52) had close contacts with C-1 when they met with him on a medical consultation meeting to discuss his treatment plan. They presented fever and abnormal CT-scan findings on January 21 and January 26, respectively. Both of them were previously healthy and did not have other exposure records and epidemiological history. Our findings suggested that C-1 was the source patient and considered as a “super-spreader” who initiated this super-spreading chain of transmission.

3.3 Another super-spreading event initiated by a doctor from Department-II in hospital A

Between January 14 and January 20, 2020, a total of twelve doctors and nurses (C-29 to C-40) from Department-II in hospital a developed fever and abnormal CT-scan findings (Figure 1 and Table 1). All twelve individuals were previously healthy, and none of them except C-29 had other exposure records and epidemiological history. C-29, a male doctor in his 50s, attended medical consultation meetings between January 3 and January 8 at the Department-I to discuss treatment plans for two lung cancer patients (C-2 and C-3). Of note, Department-I and Department-II were located at two separate buildings in hospital A. C-29 had close contact with the health care workers (C-6 to C-10) on the consultation meetings before he developed fever and abnormal CT-scan findings and was diagnosed with COVID-19 on January 14. All eleven co-workers (C-30 to C-40) had close contacts with C-29 before his disease onset. In addition, C-29’s relative (C-41) was diagnosed with COVID-19 on January 25. Our findings indicated that C-29 was likely the source patient who was responsible for introduction of COVID-19 into this cluster, and therefore was considered as a “super-spreader”.

3.4 A cluster of tertiary cases linked to a gastric cancer patient

C-13, a female with gastric cancer, was initially hospitalized in Ward-Y at Department-I in hospital A. She was transferred to Department-III on January 10 and had surgical operation on January 12. She had close contacts with C-9 and C-10 who were in charge of her treatment at Department-I, However, she did not present fever and other symptoms until January 15 (i.e. 3 days after her surgical operation). She was transferred to a designated hospital after her confirmation with COVID-19 on January 23 and remained at a stable condition. Two Doctors (C-14 and C-15) who conducted the operation procedures were diagnosed with COVID-19 on January 21 and January 22, respectively. In addition, C-16 (C-15’s relative) showed fever and other symptoms on January 23 after close contact with C-16 at home.

3.5 A cluster of tertiary cases linked to a colon cancer patient

C-42, a female colon cancer patient, was admitted to the same hospital wardroom (Ward-Y) as C-13 on January 10 and treated by the same medical team (C-9 and C-10). She developed fever (39.9°C) and other symptoms on January 16 and died of severe respiratory failure on January 18. She did not take CT-scan and RT-PCR testing due to her sudden death. C-43, a male doctor from Department-V examined C-42 on January 15 and was diagnosed with COVID-19 on January 23 (8 days after his close contact with C-42). Moreover, C-44 was accompanying his relative C-42 in hospital A and diagnosed with COVID-19 on January 17 (one day after the disease onset of C-42). Two doctors (C-45 and C-46) who conducted the medical treatment on C-44 at Department-V in hospital A were diagnosed with COVID-19 on January 24 and January 25, respectively. Furthermore, C-44 was transferred to hospital C on January 17. Four doctors (C-47, C-48, C-49, and C-50) at hospital C had close contacts with C-44, and developed fever and other symptoms between January 24 and January 27. Our findings also suggested that C-44 was a potential “super-spreader” since he transmitted the disease to six people who had direct contacts with him.

3.6 Additional tertiary cases

(1) C-11 was diagnosed with COVID-19 after direct contact with his relative C-10 at home. (2) C-12, a male doctor from the Department-VI, conducted medical treatment on C-4 and C-5 on January 14, and was diagnosed with COVID-19 on January 19 (5 days after direct contacts with C-4 and C-5). (3) C-28, a male liver cancer patient in his 60s (Ward-Z), was diagnosed with COVID-19 on January 20 (4 days after the disease onset of his doctor C-17) and died of respiratory failure on January 23, 2020.

3.7 Clinical features and laboratory findings

(Figure 1, Table 1, and Table 2). There were 31 female and 21 male patients in this cohort, and the median age was 37 years (range: 22-79 years). None of them were linked to the “Huanan Wet Market”, the suspected origin for this outbreak in Wuhan. Each of them, however, had a contact history with the index patient C-1 or his close contacts. Approximately 87% (45/52) of the patients had fever or other symptoms, 96% (50/52) had abnormal chest CT-scan findings, 86% of the tested patients (39/45) were positive for SARS-CoV-2 in the nasopharyngeal or throat swab specimen, 85% of the tested patients (29/34) were positive for SARS-CoV-2-specific IgM and/or IgG, 15% of the RT-PCR positive patients were tested negative for the specific IgM and/or IgG at the convalescent phase, and 15% of the RT-PCR negative patients were tested positive for the specific IgM and/or IgG. The severe patients experienced a significant decrease in oximetry saturation, lymphocyte, and platelet counts, along with a significant increase in C-reactive protein, D-dimer, and lactate dehydrogenase. Five of the seven cancer patients (71%) died within 2-20 days of the disease onset. All six fatal cases had comorbidities, whereas all the health care workers were previously heathy individuals.

Table icon

Table 1: Demographics, clinical features and laboratory findings of patients associated with COVID-19.

All patients

Severe cases

Non-severe cases

P value

N

IQR or n/N

N

IQR or n/N

N

IQR or n/N

White blood cell count, × 109/L

44

4.26 ( 3.65– 5.94 )

9

5.87 ( 3.37 - 7.61 )

35

4.13 ( 3.72 – 5.50 )

0.163

<4

-

18/44 ( 41% )

-

3/9 (33% )

-

15/35 (43% )

0.89

≥4

-

26/44 ( 59% )

-

6/9 (67% )

-

20/35 (57% )

/

Neutrophil count, × 109 /L

44

2.74( 1.90 – 4.30 )

9

4.37 ( 1.78 – 6.34 )

35

2.65 ( 2.03 – 3.79 )

0.176

Lymphocyte count, × 109/L

44

0.95 ( 0.66 - 1.56 )

9

0.30 ( 0.20 – 0.62 )

35

1.08 ( 0.86 – 1.75 )

0.000

<1.0

-

24/44 (55% )

-

9/9 (100% )

-

15/35 ( 43% )

0.007

≥1.0

-

20/44 ( 45% )

-

0/9

-

20/35 ( 57% )

/

Haemoglobin, g/L

44

13.45( 11.50 – 14.50 )

9

13.30 ( 9.65 – 14.95 )

35

13.60 ( 12.10 - 14.50 )

0.423

Platelet count, × 109/L

43

172.00 (132.00 – 217.00 )

9

108.00 ( 64.50 - 153.50 )

34

184.00 ( 158.25 – 225.25 )

0.001

<162

-

18/43 ( 42% )

-

7/9 ( 78% )

-

11/34 ( 32% )

0.038

≥162

-

25/43 ( 58% )

-

2/9 ( 22% )

-

23/34 ( 68% )

/

Oximetry saturation, %

19

92.00 ( 88.0 – 98.0 )

9

88.0 ( 80.0 - 91.0 )

10

97.5 ( 94.0 - 98.0 )

0.006

C-reactive protein, mg/L

-

-

-

0.001

≤5

-

18/36 ( 50% )

-

0/9

-

18/27 ( 67% )

/

>5

18/36 ( 50% )

9/9 ( 100% )

9/27 ( 33% )

/

Fibrinogen, g/dL

27

2.89 ( 2.47 - 4.09 )

8

3.86 ( 2.31 - 4.36 )

19

2.87( 2.47 – 3.77 )

0.192

Prothrombin time, s

28

11.15 ( 10.53 – 11.86 )

9

10.90 (10.20 - 11.90 )

19

11.20 ( 10.60 – 11.90 )

0.694

Activated partial thromboplastin time, s

27

29.80 ( 27.40 – 32.80 )

8

29.90 ( 26.10 – 33.25 )

19

29.40 ( 27.40 – 32.30 )

0.777

D-dimer, mg/L

28

0.54 ( 0.20 – 2.01 )

9

2.35 ( 1.04 – 4.11 )

19

0.23 ( 0.17 – 0.54 )

0.000

Albumin, g/L

41

41.00 ( 36.25 – 42.55 )

9

33.40 ( 29.10 – 42.55 )

32

41.00 ( 38.88 – 42.68 )

0.053

Alanine aminotransferase, U/L

41

20.00 ( 12.00 – 32.00 )

9

27.00 ( 20.00 – 33.50 )

32

18.50 ( 11.25 – 32.50 )

0.313

Aspartate aminotransferase, U/L

41

22.00 ( 18.00 - 27.00 )

9

27.00 ( 21.50 – 40.00 )

32

21.00 ( 17.25 – 26.00 )

0.028

≤32

-

35/41 ( 85% )

-

5/9 ( 56% )

-

30/32 (94% )

0.015

>32

-

6/41 ( 15% )

-

4/9 ( 44% )

-

2/32 ( 6% )

/

Alkaline phosphatase , U/L

34

60.80 ( 51.00 – 76.18 )

8

94.75 ( 48.68– 143.13 )

26

59.05 (51.00 – 70.75 )

0.18

Bbilirubin, mmol/L

41

9.50 ( 7.55 – 13.05 )

9

13.00( 8.50 – 24.47 )

32

9.10 (7.33 – 12.08 )

0.041

Potassium, mmol/L

38

3.87 (3.63 - 4.18 )

8

3.50 ( 3.10– 4.13 )

30

3.93 ( 3.67 – 4.19 )

0.082

Urea, mmol/L

40

4.07 ( 3.54 – 5.48 )

8

7.12 ( 5.52 – 13.85 )

32

3.85 ( 3.38 – 4.56 )

0.003

Sodium, mmol/L

39

139.90 ( 138.20 - 141.10 )

9

137.30 ( 132.75 - 142.65 )

30

139.90 ( 138.40 - 141.20 )

0.223

Creatinine, μmol/L

41

57.0 ( 48.0 – 75.0 )

9

72.00 ( 43.00 – 98.30 )

32

57.00 ( 47.75 – 74.75 )

0.25

≤80

-

33/41 ( 80% )

-

5/9 ( 56% )

-

28/32 ( 88% )

0.097

>80

-

8/41 ( 20% )

-

4/9 ( 44% )

-

4/32 ( 12% )

/

Creatine kinase, U/L

35

72.00 ( 34.00 – 101.00 )

9

28.00 ( 20.00 – 216.50 )

26

74.50 ( 40.75 – 95.00 )

0.406

≤170

-

31/35 ( 89% )

-

6/9( 67% )

-

25/26 ( 96% )

0.044

>170

-

4/35 ( 11% )

-

3/9 ( 33% )

-

1/26 ( 4% )

/

Lactate dehydrogenase, U/L

35

193.0 ( 161.0 – 228.0 )

9

247.0 ( 202.5 – 361.0 )

26

184.0 ( 157.25 - 202.0 )

0.001

≤214

-

25/35 ( 71% )

-

3/9 ( 33% )

-

22/26 ( 85% )

0.007

>214

-

10/35 ( 29% )

-

6/9 ( 67% )

-

4/26 ( 15% )

/

Table 2: Laboratory findings of patients with COVID-19.

4. Discussion

In this study, we identified a super-spreading chain of transmission associated with COVID-19 at the early stage of the outbreak in Wuhan, China. In addition, we were able to find the index patient C-1 and C-29 as the presumptive “super-spreaders” who initiated and amplified this chain of transmission, respectively. We understand that “super-spreader” is still a vague term without a strict scientific definition; we followed a definition adopted by the epidemiologists during the SARS outbreak, which defined the “super-spreader” as an individual with transmission of SARS to at least eight contacts [21]. Therefore, C-1 and C-29 were considered as the super-spreaders because each of them passed the infection of SARS-CoV-2 on to at least eleven contacts. Since super-spreading events were associated with the outbreaks of SARS and MERS [21-24], it would be not a surprise to discover super-spreading events associated with COVID-19.

Our study has a number of unique features. (1) By coincidence, this transmission chain started from a hospital ward shared by four female cancer patients, and the female health care workers (total of 23) outnumbered the male co-workers (total of 17). As a result, there were 60% female (31/52) and 40% (21/52) male patients in this cohort, which were different from other reports [3-5]. (2) We were able to identify several distinct clusters of cases based on the exposed time and the date of disease onset, which helped connecting all the related activities and events. (3) There were seven cancer patients in this study, and five of them (71%) died of severe respiratory failure within 2-20 days of their disease onsets, suggesting that cancer patients were highly vulnerable to COVID-19 and had rapid disease progression and high mortality rate due to immune suppression and comorbidities. (4) Approximately 13.5% (7/52) of patients were asymptomatic individuals in this study (Table 1), it would be important to understand the potential contributions of these individuals to the disease transmission if similar portion of asymptomatic patients existed in the general populations with COVID-19 [27]. (5) Approximately 15% of the RT-PCR negative patients were tested positive for the specific IgM and IgG. On the other hand, 15% of the RT-PCR positive patients were tested negative for the specific IgM and/or IgG at the convalescent phase. The discrepancy between the results of the RT-PCR assay and serological testing suggested the existence of possible “false negative” and/or “false positive” with these assays. Both scenarios may significantly affect the clinical diagnosis and should be addressed accordingly by additional studies given the fact that strict clinical validation studies were not performed on any of these assays due to the urgent need for screening and diagnosis of COVID-19 during the disease outbreak. In particular, it would be a huge concern if a significant portion of SARS-CoV-2 infected patients were tested negative for the specific IgM and IgG at the convalescent phase.

A large number of health care workers were infected with SARS-CoV-2 in our cohort, which were consistent with a report that 41% of the 138 hospitalized patients at one of the major tertiary hospitals in Wuhan were hospital-related transmission [6]. These findings suggested that serious nosocomial transmission occurred at the early stage of this outbreak, which likely changed the dynamics of COVID-19 and contributed significantly to the widespread of the disease in a short period of time in Wuhan and other neighboring cities in Hubei Province.

We recognized that our study had a number of limitations and the findings need to be interpreted with caution. (1) Some cases had incomplete records of the exact exposure time and epidemiological history. (2) RT-PCR and serological testing were not carried out for some cases due to the irregular service during the early stage of the outbreak. (3) The viral genomes of SARS-CoV-2 in this cohort were not sequenced.

In conclusion, we identified a super-spreading chain of transmission associated with COVID-19 at the early stage of the disease outbreak in Wuhan, China. Given the fact that COVID-19 was spreading rapidly in many other countries worldwide, we believed at that time that more super-spreading events associated with COVID-19 would be identified in future. Indeed, many super-spreading events have been reported since our first report published in medRxiv preprint in March 2020 [28, 32].

Acknowledgment

We are extremely grateful to all the patients and their families for participation of this study and providing all the valuable information. We also thank our colleagues for their kind help and strong support.

Author’s Contribution

K.H., Y.Z., M.W., Q.Q.Z., X.R.W., B.H.Z., B.Y.S., C.Z participated in study design; K.H., Q.Q.Z., X.R.W., F.H., H.Y.Q., J.C.H., J.Y., R.S., M.J., X.D., B.Y.S., C.Z. performed data analysis

K.H., Y.Z., M.W., M.W., Z.S.Z., X.C.L., Y.T.Z., T.W., S.L.Z., Y.J., D.L., W.Z.Y., B.H.Z. recruited patients; K.H., Y.Z., M.W., Q.Q.Z., X.R.W., F.H., H.Y.Q., B.Y.S., C. Z. drafted the manuscript

K.H. and C.Z. were responsible for study conception; all authors provided critical review of the manuscript and approved the final draft for publication.

Funding

The Hubei province key project on novel coronavirus pneumonia (2020FCA002) and the Operational Funds of the First Affiliated Hospital of Xi’an Jiaotong University.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

  1. Zhu N, Zhang D, Wang W, et al. A novel coronavirus from patients with pneumonia in China, 2019. N Engl J Med 382 (2020):727-733.
  2. Lu R, Zhao X, Li J, et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet 395 (2020): 565-574.
  3. Huang C, Wang Y, Li X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 395 (2020): 497-506.
  4. Li Q, Guan X, Wu P, et al. Early transmission dynamics in Wuhan, China, of novel coronavirus–infected pneumonia. N Engl J Med (2020).
  5. Chen N, Zhou M, Dong X, et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet 395 (2020): 507-513.
  6. Wang D, Hu B, Hu C, et al. Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus–infected pneumonia in Wuhan, China. JAMA 323 (2020):1061-1069.
  7. Guan W, Ni Z, Hu Y, et al. Clinical Characteristics of Coronavirus Disease 2019 in China. N Engl J Med 382 (2020): 1708-1720.
  8. Wu Z, McGoogan JM. Characteristics of and Important Lessons from the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72314 Cases from the Chinese Center for Disease Control and Prevention. JAMA 323 (2020): 1239-1242.
  9. Argenziano MG, Bruce SL, Slater CL, et al. Characterization and clinical course of 1000 patients with coronavirus disease 2019 in New York: retrospective case series. BMJ 369 (2020): m1996.
  10. Price-Haywood EG, Burton J, Fort D, Seoane L. Hospitalization and Mortality among Black Patients and White Patients with Covid-19. N Engl J Med 382 (2020): 2534-2543.
  11. Richardson S, et al. Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area. JAMA 323 (2020): 2052-2059.
  12. WHO Coronavirus (COVID-19) Dashboard. World Health Organization (2020).
  13. Fehr AR, Perlman S. Coronaviruses: an overview of their replication and pathogenesis. Coronaviruses. Humana Press, New York, NY (2015): 1-23.
  14. Lee N, Hui D, Wu A, et al. A major outbreak of severe acute respiratory syndrome in Hong Kong. N Engl J Med 348 (2003): 1986-1994.
  15. Peiris J, Lai S, Poon L, et al. Coronavirus as a possible cause of severe acute respiratory syndrome. Lancet 361 (2003): 1319-1322.
  16. Zaki AM, Van Boheemen S, Bestebroer TM, et al. Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia. N Engl J Med 367 (2012): 1814-1820.
  17. Zumla A, Hui DS, Perlman S. Middle East respiratory syndrome. Lancet 386 (2015): 995-1007.
  18. de Wit E, van Doremalen N, Falzarano D, Munster VJ. SARS and MERS: recent insights into emerging coronaviruses. Nat Rev Microbiol 14 (2016): 523.
  19. World Health Organization. Severe acute respiratory syndrome – SARS (2003).
  20. World Health Organization. Middle East respiratory syndrome coronavirus (MERS-CoV) (2019).
  21. Tsang KW, Ho PL, Ooi GC, et al. A cluster of cases of severe acute respiratory syndrome in Hong Kong. N Engl J Med 348 (2003): 1977-1978.
  22. Shen Z, Ning F, Zhou W, et al. Super spreading sars events, Beijing, 2003. Emerging Infect Dis 10 (2004): 256.
  23. Cho SY, Kang JM, Ha YE, et al. MERS-Cov outbreak following a single patient exposure in an emergency room in South Korea: an epidemiological outbreak study. Lancet 388 (2016): 994-1001.
  24. Kang CK, Song KH, Choe PG, et al. Clinical and epidemiologic characteristics of spreaders of Middle East respiratory syndrome coronavirus during the 2015 outbreak in Korea. J Korean Med Sci 32 (2017): 744-749.
  25. Chan JFW, Yuan S, Kok KH, et al. A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster. Lancet 395 (2020): 514-523.
  26. Phan LT, Nguyen TV, Luong QC, et al. Importation and human-to-human transmission of a novel coronavirus in Vietnam. N Engl J Med 382 (2020): 872-874.
  27. Rothe C, Schunk M, Sothmann P, et al. Transmission of 2019-nCoV infection from an asymptomatic contact in Germany. N Engl J Med 382 (2020): 970-971.
  28. Hu K, Yang Zhao Y, Wang M, et al. Identification of a super-spreading chain of transmission associated with COVID-19. medRxiv preprint (2020).
  29. World Health Organization. COVID-19: Surveillance, case investigation and epidemiological protocols (2020).
  30. World Health Organization. Laboratory testing for 2019 novel coronavirus (2019-nCoV) in suspected human cases (2020).
  31. Government of China. New coronavirus pneumonia prevention and control program (8nd Ed.) (2021).
  32. Majra D, Benson J, Pitts J, et al. SARS-CoV-2 (COVID-19) super spreader events. Journal of Infection (2020).

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