Related Experiment Video
Updated: Dec 11, 2025

06:11
Author Spotlight: Exploring the Long-Term Health Impacts of Intracytoplasmic Sperm Injection on Offspring
Published on: May 17, 2024
951
[SARS-CoV-2 pandemic and assisted reproduction]
Summary
The SARS-CoV-2 virus impacts the reproductive system, with ACE2 receptors found in testes, ovaries, and embryos. Assisted reproduction centers adapted protocols during the pandemic based on scientific recommendations.
Area of Science:
- Reproductive endocrinology and virology.
- Infectious disease epidemiology.
Context:
- The COVID-19 pandemic necessitated rapid adaptation by assisted reproduction centers globally.
- Reduced activity during the acute phase has been followed by a resumption of services.
Purpose:
- To review current literature on SARS-CoV-2 and its effects on the human reproductive system.
- To analyze recommendations from scientific societies regarding assisted reproduction during the pandemic.
Summary:
- SARS-CoV-2 utilizes the ACE2 receptor, present in male and female reproductive organs (testes, ovaries, endometrium) and embryos.
- A comparative analysis of scientific society guidelines on infection screening, lab standards, and operational protocols is presented.
Impact:
- Provides a consolidated overview of the virus's reproductive implications for clinicians and researchers.
- Informs the ongoing safe practice of assisted reproduction in the context of viral pandemics.
More Related Videos
Related Concept Videos
Infertility in Males
460
Male infertility affects millions of couples worldwide, arising from various factors that impact different stages of the reproductive process. An endocrine imbalance resulting from conditions like hypogonadism, Klinefelter syndrome, or pituitary disorders can disrupt hormone levels and reduce sperm production. Testicular defects, such as tumors, cryptorchidism, atrophic testes, abnormal sperm morphology, and low sperm count or motility, may arise due to genetic factors, structural...
460
Infertility in Females
3.5K
Female infertility is defined as the inability to conceive after a year of regular, unprotected intercourse and affects about 10–15% of couples worldwide. The primary cause of female infertility is ovulatory disorders, which hinder the release of eggs. These disorders can be classified as hypothalamic amenorrhea, polycystic ovarian syndrome (PCOS), premature ovarian failure, and hyperprolactinemic anovulation disorders.
Endometriosis, a condition characterized by abnormal growth of...
Endometriosis, a condition characterized by abnormal growth of...
3.5K
CRISPR
56.6K
Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
56.6K
In Vitro Fertilization
733
In vitro fertilization (IVF) is a form of assisted reproductive technology where an egg is fertilized with sperm in a controlled laboratory environment before transferring the resulting embryo into the uterus. This process is designed to help individuals and couples experiencing difficulties conceiving.
The IVF process begins with ovarian stimulation, during which reproductive endocrinologists prescribe hormonal medications to stimulate the ovaries to produce multiple eggs instead of the single...
The IVF process begins with ovarian stimulation, during which reproductive endocrinologists prescribe hormonal medications to stimulate the ovaries to produce multiple eggs instead of the single...
733
Single Nucleotide Polymorphisms-SNPs
17.7K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
17.7K

