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. 2020 Dec 22;91(4):e2020129. doi: 10.23750/abm.v91i4.10852

Exploring the emergence of vertical transmission of SARS-CoV-2: A Rapid Review

Vidhi Jain 1, Tanuj Kanchan 2, Kewal Krishan 3,
PMCID: PMC7927489  PMID: 33525238

Abstract

Novel Coronavirus, SARS-CoV-2 is responsible for the global pandemic of COVID-19. It has been shown to spread through respiratory droplets, direct contact and environmental fomites. The possibility of its spread by other modes viz. airborne, fecal-oral, vertical, etc. is being explored and can have implications in planning preventive strategies and disease management. A systematic analysis was carried out using the keywords; “COVID 19 vertical transmission”, “SARS-CoV-2 pregnancy”, and “SARS-CoV-2 vertical transmission”, and the cases suggestive of possible vertical transmission of SARS-CoV-2 were studied in detail. The available evidences point at a possibility of vertical transmission of SARS-CoV-2. (www.actabiomedica.it)

Keywords: Amniotic fluid, vertical transmission, SARS-CoV-2, COVID-19 pandemic

Introduction and background

SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus-2) is responsible for the global pandemic of COVID-19 (Coronavirus Disease 2019). The current research and evidence suggest that the novel coronavirus predominantly spreads from person to person through direct contact or by inhalation of droplets generated through coughing, sneezing and speaking, originating from the infected person (1,2). It has also been established that the virus may spread by touching the environmental fomites and infected surfaces (3). According to recent communications, it has been cautioned that the airborne transmission is an important factor and contributes to the spread of the virus especially in the crowed places with poor ventilation (4,5). After eight months of continuous research, not much is known about the modes of transmission of this novel virus, however, the possibility of its spread by some other modes of transmission such as the fecal-oral, vertical, through flatus, ocular surface, blood borne, animal-to-human etc. is being explored and can have implications in planning preventive strategies and disease management (6).

Vertical transmission of SARS-CoV-2 is plausible due to some of its unique features. For one, its receptor Angiotensin-converting enzyme -2 (ACE-2) is suitably expressed in the human placenta (7). Second, it has an alleged structural similarity to HIV-1 proteins (8) and shows therapeutic response to anti-retroviral drugs. Third, it is an RNA virus like Zika. Materno-fetal transfer is well-established in both Zika and HIV.

Clinically, COVID-19 can be suspected in adult patients with non-specific clinical presentations like fever, cough, sore throat, anosmia, body ache etc., the majority of cases remain asymptomatic and maternal diagnosis must therefore be established by laboratory testing. The clinical dilemma of diagnosing a neonate with COVID-19, especially asymptomatic presentations, also requires the same confirmatory test. While real time reverse transcriptase PCR on respiratory specimens for detection of SARS-CoV-2 RNA remains the gold standard for diagnosis of COVID-19 in all age groups (9). Various newer approaches like antigen testing, antibody detection and serum inflammatory markers have been tried worldwide with various degrees of diagnostic success (10).

Most of the existing reviews and meta-analysis on this topic have focussed on RT-PCR COVID-19 positive mothers and the possibility of vertical transmission in their outcomes. However, there is a paucity of reviews focussed solely on neonates with RT-PCR confirmed COVID-19 diagnosis soon after birth.

A review and analysis of studies regarding vertical transmission of SARS-CoV-2

With this background, a systematic analysis of the available literature was carried out using the keywords; “COVID 19 vertical transmission”, “SARS-CoV-2 pregnancy”, and “SARS-CoV-2 vertical transmission”. Among all reported COVID-19 pregnancies only those cases with RT-PCR confirmed new-borns were studied in detail for the plausibility of Vertical transmission of SARS-CoV-2. A total of 12 new-borns (11-17) with confirmed COVID-19 infections were identified in literature at the time of writing.

While a review of 55 pregnancies (7) did not show any evidence of vertical transmission, a total of 6 studies comprising 11 new-borns (11-15,18) has presented striking arguments in favour of vertical transmission of SARS CoV-2 (Table 1). Pregnancy with COVID-19 has been associated with pre-term birth in >20% cases and perinatal death in 7% which suggests that fetal risk associated with the infection is worth investigating (19).

Table 1.

A rapid review of cases suggesting possible vertical transmission of SARS-CoV-2

Parameter Wang et al (11) Dong et al (12) Zeng et al (13) Alzamora et al (14) Zamaniyan et al (15) Yu et al (18)
Number of new-borns 1 1 6 1 1 1
Gestational age 40 weeks (Emergency LSCS) 37 weeks, 6 days (Elective LSCS) Full -term (Elective LSCS) 33 weeks; pre-term 32 weeks; pre-term (Emergency LSCS) 39 weeks + 6 days (Emergency LSCS)
Clinical symptoms Asymptomatic Asymptomatic Asymptomatic Mild respiratory difficulty on day 6 Fever at birth Asymptomatic
Investigations undertaken on the new-borns:
Nasopharyngeal aspirate RT-PCR Positive after 36 hours of birth Negative Negative Positive at 16 hours of birth Positive after 1 week Positive at 6hrs of birth
Cord blood RT-PCR Negative Not done Not done Not done Negative Not done
Serum RT-PCR Not done Not done Negative Not done Not done Not done
Anti- SARS-CoV -2 IgM Not done Elevated (at 2 hours of birth) Elevated in 2 cases Negative Not done Not done
Anti- SARS-CoV-2 IgG Not done Elevated (at 2 hours of birth) Elevated in 5 cases Negative Not done Not done
Inflammatory cytokine IL-6 Not done Not done Elevated in all 6 cases Not done Not done Not done
Maternal investigations:
Nasopharyngeal swab RT-PCR Positive Positive Positive Positive Positive Positive
Amniotic fluid RT-PCR Negative Not done Not done Not done Positive Not done
Anti- SARS-CoV -2 IgM Not done Positive Elevated in 4 cases Positive on post-partum day 4 Not done Not done
Anti- SARS-CoV-2 IgG Not done Positive Elevated in 5 cases Positive on post-partum day 4 Not done Not done
Placental tissue RT-PCR Negative Not done Not done Not done Not done Not done
Vaginal secretion RT-PCR Not done Negative Not done Not done Negative Not done
Breast milk RT-PCR Negative Negative Not done Not done Not done Not done
Associated maternal mortality -- -- -- -- Yes (19 days post- LSCS) -
Pre-op prophylaxis Recombinant human interferon alfa 1b and Ganciclovir Details not mentioned Details not mentioned Hydroxychloroquine and Oseltamivir Hydroxychloroquine Lopinavir, ritonavir, and Oseltamivir Oseltamivir, ganciclovir, interferon + antibiotics
Our inferences on possibility of vertical transmission Neonatal Nasopharyngeal RT-PCR positive at 36 hours suggests possible vertical transmission Elevated neonatal IgM at birth suggests possible vertical transmission Elevated neonatal IgM at birth suggests possible vertical transmission Positive neonatal Nasopharyngeal RT-PCR at 16 hours suggests possible vertical transmission Positive amniotic fluid and neonatal Nasopharyngeal RT PCR suggests possible vertical transmission Positive neonatal Nasopharyngeal RT-PCR at 6 hours suggests possible vertical transmission

Among the reported cases, demonstration of SARS-CoV-2 RNA in amniotic fluid by RT-PCR at the time of delivery (15) is a strong argument in favour of vertical transmission, at least in cases where maternal infection was severe in peripartum period. The fact that the nasopharyngeal RT-PCR was positive in three neonates born by LSCS, which obviated the possibility of acquisition of the virus from the birth canal (11,14,15), further strengthens the possibility of vertical transmission. The neonates reviewed in this study had all been delivered via caesarean section, however, it has been previously established that there is no measurable safety of LSCS over vaginal birth in COVID-19 pregnancies (20).

Since all the maternal SARS-CoV-2 reports were confirmed before delivery, the claim of strict adherence to contact, droplet and airborne precautions during the peri and postpartum period in all these cases, is believable, rendering the possibility of nosocomial acquisition by the new-born very low. The detection of IgM in the new-born, also favours the possibility of in-utero contact with the virus, as being a large molecule, it does not cross the intact placenta and cannot be acquired from the mother.

The results of neonatal RT-PCR positivity alone may not be sufficient to prove vertical transmission. A recent review and meta-analysis may have pre-maturely asserted a vertical transmission rate of 3.2% based on a combination of positive neonatal nasopharyngeal, cord-blood, rectal swab and serology (21). We feel it would be prudent to gather more definitive evidence before a consensus opinion can be agreed upon.

The vertical transmission of COVID-19 has remained a topic of debate since the last 8 months but can it be proven at all? Theoretically, it will require SARS-CoV-2 RNA to be demonstrable in the respiratory secretions of the mother and newborn, as well as in the placenta, membranes or other products on conception in the same delivery outcome. Those seeking the answer will have to adopt a planned prospective approach and conduct molecular testing of all the specimens enumerated above, perhaps more than once, to rule out false negatives.

The development of more sensitive viral nucleic acid load detection methods remains the need of the hour. The non-detection of viral nucleic acid in umbilical cord blood, placenta, amniotic fluid and breast milk (11) in some studies could simply be due to low viral load, poor sensitivity of existing techniques, flawed timing of amniocentesis and effective pre-operative antiviral administration.

Conclusion

In light of the above findings, there seems to be a strong possibility of vertical transmission of SARS-CoV-2, if the same can be virologically proven. If proven, there would be an urgent need to device sensitive and economical screening tests in pregnancy, effective pre-operative anti-viral regimens, operative protocols, guidelines for new-born screening and safety of breastfeeding etc. The current evidence is limited by the non-availability of Maternal Serum viral RNA load which, akin to HIV, may be tried as a predictor of the risk of vertical transmission, paired with amniotic fluid testing in severe maternal illness. The same may be considered before elective COVID-19 caesareans in future studies. Any publications on fetal outcomes of mothers with severe infection, who could not receive timely hydroxy-chloroquine and pre-operative antivirals, will also fill the gaps in our current understanding of the topic. Global reporting of all COVID-19 pregnancies using COVI-Preg, a structured data collection (22) will assist in swift formulation of management guidelines for the same.

Acknowledgements

Kewal Krishan is supported by a DST PURSE grant and UGC Centre of Advanced Study (CAS-II) awarded to the Department of Anthropology, Panjab University, Chandigarh, India.

Conflict of interest:

Each author declares that he or she has no commercial associations (e.g. consultancies, stock ownership, equity interest, patent/licensing arrangement etc.) that might pose a conflict of interest in connection with the submitted article

Authors’ contributions:

Vidhi Jain: Conceptualization, Writing - original draft, Writing - review & editing, final approval; Tanuj Kanchan: Writing - review & editing, final approval and supervising the work; Kewal Krishan: Writing - review & editing, final approval and supervising the work.

References

  • 1.Chan JFW, Yuan S, Kok KH, To KKW, Chu H, Yang J, 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. 2020;395:514–523. doi: 10.1016/S0140-6736(20)30154-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. WHO, World Health Organization, Transmission of SARS-CoV-2: implications for infection prevention precautions, Available at: https://www.who.int/news-room/commentaries/detail/transmission-of-sars-cov-2-implications-for-infection-prevention-precautions , 2020 (Accessed on 23th October 2020) [Google Scholar]
  • 3.van Doremalen N, Bushmaker T, Morris DH, et al. Aerosol and surface stability of SARS-CoV-2 as compared with SARS-CoV-1. N Engl J Med. 2020;382:1564–1567. doi: 10.1056/NEJMc2004973. https://doi.org/10.1056/NEJMc2004973 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Morawska L, Cao J. 2020. Airborne transmission of SARS-CoV-2: the world should face the reality. Environ Int. 2020;139:105730. doi: 10.1016/j.envint.2020.105730. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Morawska L, Milton DK. It is Time to Address Airborne Transmission of COVID-19. Clin Infect Dis. 2020:ciaa939. doi: 10.1093/cid/ciaa939. https://doi.org/10.1093/cid/ciaa939 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Mukhra R, Krishan K, Kanchan T. Possible modes of transmission of Novel coronavirus SARS-CoV-2: a review. Acta Bio Med. 2020;91(3):e2020023. doi: 10.23750/abm.v91i3.10039. https://mattioli1885journals.com/index.php/actabiomedica/article/view/10039 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Dashraath P, Wong JLJ, Lim MXK, Lim LM, Li S, Biswas A, et al. Coronavirus Disease 2019 (COVID-19) Pandemic and Pregnancy. Am J Obstet Gynecol. 2020;222(6):521–531. doi: 10.1016/j.ajog.2020.03.021. DOI: 10.1016/j.ajog.2020.03.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Pradhan P, Pandey AK, Mishra A, Gupta P, Tripathi PK, Menon MB, Gomes J, Vivekanandan P, Kundu B. Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1 gp120 and Gag. bioRxiv. 2020 2020.01.30.927871, DOI: 10.1101/2020.01.30.927871. [Google Scholar]
  • 9.World Health Organization. (‎2020)‎. Laboratory testing strategy recommendations for COVID-19: interim guidance, 21 March 2020. World Health Organization. https://apps.who.int/iris/handle/10665/331509 . License: CC BY-NC-SA 3.0 IGO. (Accessed on 23th October 2020) [Google Scholar]
  • 10.Tang YW, Schmitz JE, Persing DH, Stratton CW. Laboratory Diagnosis of COVID- 19: Current Issues and Challenges. J Clin Microbiol. 2020;58(6):e00512–20. doi: 10.1128/JCM.00512-20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Wang S, Guo L, Chen L, Liu W, Cao Y, Zhang J, Feng L. A case report of neonatal COVID-19 infection in China. Clin Infect Dis. 2020;71(15):853–857. doi: 10.1093/cid/ciaa225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Dong L, Tian J, He S, et al. Possible vertical transmission of SARS- CoV-2 from an infected mother to her newborn. JAMA. 2020;323(18):1846–1848. doi: 10.1001/jama.2020.4621. DOI: 10.1001/jama.2020.4621. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Zeng H, Xu C, Fan J, et al. Antibodies in infants born to mothers with COVID-19 pneumonia. JAMA. 2020; 26;323(18):1848–9. doi: 10.1001/jama.2020.4861. DOI: 10.1001/ jama.2020.4861. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Alzamora MC, Paredes T, Caceres D, Webb CM, Valdez LM, La Rosa M. Severe COVID-19 during Pregnancy and Possible Vertical Transmission. Am J Perinatol. 2020;37(8):861–865. doi: 10.1055/s-0040-1710050. doi:10.1055/s-0040-1710050. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Zamaniyan M, Ebadi A, Aghajanpoor Mir S, Rahmani Z, Haghshenas M, Azizi S. Preterm delivery, maternal death, and vertical transmission in a pregnant woman with COVID-19 infection. Prenat Diagn. 2020 doi: 10.1002/pd.5713. 10.1002/pd.5713. doi:10.1002/pd.5713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Dumpa V, Kamity R, Vinci AN, Noyola E, Noor A. Neonatal Coronavirus 2019 (COVID-19) Infection: A Case Report and Review of Literature. Cureus. 2020;12(5):e8165. doi: 10.7759/cureus.8165. doi:10.7759/cureus.8165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Piersigilli F, Carkeek K, Hocq C, et al. COVID-19 in a 26-week preterm neonate. Lancet Child Adolesc Health. 2020;4(6):476–478. doi: 10.1016/S2352-4642(20)30140-1. doi:10.1016/S2352-4642(20)30140-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Yu N, Li W, Kang Q, et al. Clinical features and obstetric and neonatal outcomes of pregnant patients with COVID-19 in Wuhan, China: a retrospective, single-centre, descriptive study. Lancet Infect Dis. 2020;20(5):559–564. doi: 10.1016/S1473-3099(20)30176-6. doi:10.1016/S1473- 3099(20)30176-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Di Mascio D, Khalil A, Saccone G, Rizzo G, Buca D, Liberati M, et al. Outcome of Coronavirus spectrum infections (SARS, MERS, COVID-19) during pregnancy: a systematic review and meta-analysis. Am J Obstet Gynecol MFM. 2020;2(2):100107. doi: 10.1016/j.ajogmf.2020.100107. doi:10.1016/j.ajogmf.2020.100107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Yang Z, Liu Y. Vertical Transmission of Severe Acute Respiratory Syndrome Coronavirus 2: A Systematic Review. Am J Perinatol. 2020;37(10):1055–1060. doi: 10.1055/s-0040-1712161. doi:10.1055/s-0040-1712161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Kotlyar A, Grechukhina O, Chen A, Popkhadze S, Grimshaw A, Tal O, Taylor HS, Tal R. Vertical Transmission of COVID-19: A Systematic Review and Meta-analysis. Am J Obstet Gynecol. 2020 doi: 10.1016/j.ajog.2020.07.049. doi: https://doi.org/10.1016/j.ajog.2020.07.049 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Panchaud A, Favre G, Pomar L, Vouga M, Aebi-Popp K, Baud D, et al. An international registry for emergent pathogens and pregnancy. Lancet. 2020;395(10235):1483–1484. doi: 10.1016/S0140-6736(20)30981-8. doi:10.1016/S0140-6736(20)309. [DOI] [PMC free article] [PubMed] [Google Scholar]

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