In March 2020, the COVID-19 disease was declared a pandemic by World Health Organization (WHO). To date, more than 570 million confirmed cases of COVID-19 along with 6.38 million deaths have been reported globally (https://coronavirus.jhu.edu/map.html). It is gradually becoming clear that patients recovered from COVID-19 are reporting various long-term ill-health consequences, but little is known about its long-term sequelae on bone health. The relevance of the skeletal system is supported by the fact that it is involved in calcium homeostasis, hematopoiesis, mobility, etc. The role of the skeletal system as a bona fide endocrine organ (osteocalcin—Ocn and fibroblast growth factor—FGF) in controlling the physiological energy metabolism and mineral ion homeostasis is well established [1]. Ocn is a bone matrix protein that in its gamma (γ)-carboxylated form regulates the size and shape of hydroxyapatites. However, the undercarboxylated form of Ocn regulates glucose metabolism, testosterone biosynthesis (by Leydig cells), etc. A study reported that daily injection of Ocn improved glucose tolerance and insulin sensitivity and prevented the development of type 2 diabetes in mice [2]. Consistent with this, a study reported that deficiency of Ocn hormone impaired glucose homeostasis in Ocn null mice [3]. Of note, recently a study showed that lower levels of Ocn can be employed as a good prognostic marker for monitoring stress-induced hyperglycemia in COVID-19 infected patients [4]. In addition, exosomes-ExoFlo™ generated from bone marrow mesenchymal stem cells (MSCs-osteoblast progenitors) increased the survival rate in COVID-19 disease patients, by increasing oxygenation, reducing the inflammatory environment, and considerably lowering the neutrophil count [5]. Together these studies emphasize the importance of bone in maintaining the physiological functioning of the body under both normal and disease conditions.

The intriguing interaction between the skeletal system and the host immune system reveals the fascinating feature supporting the adaptability of the skeletal system and its cells. An interdisciplinary field called “Osteoimmunology” was founded in 2000 by the Takayanagi et al. group as a result of the relationship between the immune system and bone [6]. In the past 2 decades, critical work in this enthralling field has resulted in the identification of the role played by the RANKL-OPG (osteoprotegerin) axis in the preservation of skeletal homeostasis, the earlier being a key regulator of osteoclastogenesis. Numerous immune cells, including activated T cells and B cells, which are crucial in the pathophysiology of numerous bone-related illnesses, including osteoporosis, express RANKL in addition to bone-forming OBs cells. Experimental evidence supports the idea that pro-inflammatory cytokines such as IL-1β, IL-6, IL-17, and TNF-α promote bone resorption by activating the RANK-RANKL axis, which causes the appearance of a variety of bone-related illnesses [7, 8] (Fig. 1). Immune system activation in response to SARS-CoV-2 infection also leads to the aggressive production and accumulation of these inflammatory cytokines (IL-1β, IL-6, IL-17, and TNF-α) resulting in an event termed as “Cytokine Storm” [9]. Enhancement in the level of inflammatory cytokines causes the influx of several immune cells such as macrophages, T cells, and neutrophils to the site of infection, resulting in devastating effects on the vascular barrier, capillaries, alveoli, cell-to-cell interactions ultimately leading to damage in multiple organs (including bone) in SARS-CoV-2-infected patients [9]. A study reported in 2005 demonstrated that during the SARS-CoV outbreak patients who were treated with corticosteroids showed lower bone mineral density (BMD) in comparison to normal controls in long-term studies [10]. In addition, WHO approved the use of corticosteroids to suppress the inflammatory response in critical COVID-19-infected patients thus alarming an enhanced fracture risk in SARS-CoV-2-infected patients. Accordingly, a better understanding of SARS-CoV-2 pathogenesis in inducing bone loss would result in improved therapeutic and preventative measures in a current pandemic. In the present review, we thus highlight the role of various factors underpinning the risk of developing skeletal disorders in various viral diseases including COVID-19 (Fig. 2). In addition, we further discuss the role of GM and probiotics in managing the long-term consequences of COVID-19 infection on bone health.

Fig. 1

SARS-CoV-2 infection induce bone loss: In physiological conditions, the homeostatic balance between osteoblasts and osteoclasts maintains the bone health, whereas upon SARS-CoV-2 infection enhanced production of inflammatory cytokines shifts balance towards the bone-resorbing osteoclasts that further augments bone loss

Fig. 2

Factors influencing COVID-19 disease severity and bone loss: various factors such as dysbiosis of gut microbiota (GM), cytokine storm, administration of steroidal therapies, deficiency of vitamin D, gender and, hormonal factors influence COVID-19 and bone health

Inflammatory bone loss in viral diseases

The role of virus-induced bone loss has long been neglected, but investigations in recent decades revealed the involvement of virus infections in the augmentation of bone loss. Available reports suggest that human immunodeficiency virus (HIV)-infected patients showed a higher prevalence of bone-related diseases, and the use of corticosteroids further augments this in HIV-infected patients [11]. In the case of HIV, it has been observed that disruption of the immune-skeleton interface enhanced bone loss and thus intensified the risk of fracture in infected patients. Patients with HIV experience bone loss due to a variety of causes, but recently, the significance of B cells in HIV-induced bone loss has also come to light. It has been observed that dysregulated expression of RANKL and OPG on B cells elicits bone loss in HIV-infected patients [12]. In addition, a study demonstrated that highly active anti-retroviral therapies (HAART) control viral replication but the regimens such as tenofovir disoproxil fumarate (TDF) may also accelerate bone loss by inducing osteolytic activity of OCs along with dampening the OBs bone-forming potential [13]. In contrast to this, a study demonstrated that HIV-infected patients showed a higher prevalence of reduced BMD, irrespective of their anti-retroviral therapies status [11]. Of note, it has been observed that HIV exhibits the potential of inducing bone loss by directly increasing the adhesion and bone degradation machinery of OCs. In particular, the viral protein “nef” induces bone loss by promoting the assembly of OCs on the bone-resorbing sealing zone by activating Src (a key regulator of podosome formation in OCs) [14]. Furthermore, a cross-sectional study reported that the use of nucleoside/nucleotide analogs such as tenofovir reduced the BMD in hepatitis B virus (HBV) infected patients thereby simultaneously enhancing the risk of developing osteoporosis-related fractures in the long run [15, 16]. Importantly, bone resorptive biochemical marker such as deoxypyridinoline in the urine of HBV-infected patients further supports its bone resorptive potential. Alphaviruses have also been reported to interfere with the bone remodeling process by inducing the production of inflammatory cytokine levels such as IL-6 that further by dysregulating the RANKL-OPG axis augments bone loss [17]. Various bone anomalies were also observed in SARS-CoV-recovered patients which are partly explained by the rampant use of various steroidal therapies. In 2009, a study reported that human monocytes (precursor of OCs) express ACE2 (a receptor of SARS-CoV) that aid the entry of SARS-CoV directly into OCs, and by expressing 3a/X1protein, SARS-CoV increase the nuclear factor kappa B (NFκB) activity and promote RANKL-induced osteoclastogenesis [18]. Long-term follow-up studies in SARS-CoV-infected patients demonstrated the distinct possible mechanisms such as prolonged use of steroidal therapies, and inflammatory conditions may further induce bone loss in recovered patients. According to a recent cohort study, 36% of COVID-19-infected patients had thoracic vertebral fractures (VFs) that could affect their ability to breathe in the future. This is suggestive of the evaluation of the morphometric VFs parameters in all the COVID-19 suspected and infected patients [19]. Together, these studies suggest an enhanced risk of fractures in COVID-19 recovered patients.

SARS-CoV-2 infection and its implications on bone health

The initial step involved in the pathogenesis of COVID-19 is the invasion of the SARS-CoV-2 virus into target host cells. Spike protein (S) of SARS-CoV-2 aids the entry of the virus into the host cell via interacting with ACE2 receptors expressed on cellular targets such as alveolar cells of lungs, myocardial cells, testis, and bone cells (Fig. 3). The physiological functioning of ACE2 is to regulate the inflammatory condition by hydrolyzing the angiotensin II (inflammatory) of the renin-angiotensin system (RAS) to angiotensin 1–7 (anti-inflammatory). This leads to an enhancement in controlling the inflammatory conditions. However, it has been observed that upon infecting the target cells, SARS-CoV-2 downregulates the expression of ACE2 and enhances the levels of angiotensin II [20]. Increased angiotensin II further induces inflammatory conditions via upregulating the expression of E and P selectin, IL-8, chemokine ligands (CCL)-2 and 5. In addition, angiotensin II stimulates innate immunity by activating the toll-like receptor (TLR)-4 [21] and thus, facilitates the massive production of inflammatory responses in respective organs including the skeletal system. Shimizu et al. demonstrated that angiotensin II exhibits osteoclastogenic potential via enhancing the expression of RANKL on OBs, which further enhances differentiation of OCs thereby accelerating osteoporosis development in the rat model [22]. Of note, a study demonstrated enhancement in OCs number along with a robust reduction in several bone parameters in the COVID-19 mice model [23]. From the TRAP staining data, it has been observed that infection of SARS-CoV-2 significantly enhanced OCs number by 64%, OCs surface by 27%, and 38% enhancement in OCs per bone surface in COVID-19 disease mice model after 2 weeks of post-infection [23]. Thus, it is vital to delineate and understand the long-term sequelae of SARS-CoV-2 infection on bone loss in COVID-19-recovered patients. Moreover, it is correspondingly important to understand the mechanism of COVID-19-induced bone loss. In further sections, we discuss the possible mechanisms that may enhance bone deterioration in COVID-19-recovered patients under distinct categories.

Fig. 3

SARS-CoV-2 affects bone health either directly or via cytokine storm: A Various organs of the body including skeleton system express angiotensin convertase enzyme 2 (ACE2) receptor that aids the entry of SARS-CoV-2 inside host cells. (1): Internalization of COVID-19 into target cells, (2): after pyroptosis waning cells generate death-associated molecular patterns (DAMPs) and pathogen-associated molecular patterns (PAMPs), (3): virus-derived DAMPs and PAMPs engulfed by macrophages in turn produce pro-inflammatory cytokines, (4) interleukin (IL)-1β, IL-6, tumor necrosis factor (TNF)-α, chemokine (CC) ligand-2, CCL-3 and CXCL10, (5): recruitment of neutrophils and CD8+ T cells to the site of infection that further causes tissue injury in lung parenchyma, (6): “Cytokine Storm Syndrome”, i.e., flooding of cytokines into circulation that leads to multiorgan failure including skeleton system. B Inside the skeleton system, SARS-CoV-2 binds to ACE2 receptor on osteoclasts and induces its differentiation. Moreover, inflammatory cytokines further augment bone loss by binding to cytokine receptors. In addition, by inducing production of micro-RNA-4485, SARS-CoV-2 inhibits osteogenic ability of osteoblasts.

SARS-CoV-2 and bone cells

Several studies demonstrated that SARS-CoV-2 exhibits the potential to infect the skeletal system by directly infecting the bone cells (OCs and OBs) and affecting the bone remodeling process. A study reported that along with owning the inflammatory potential, ACE2/Ang (1–7) axis is found to be linked with osteoporosis marked by the expression of ACE2 receptors on OBs and OCs [24] (Fig. 3). Moreover, it suggests that SARS-CoV-2 invades bone cells and may alter their ability to modulate bone health by targeting the ACE2 receptor. Furthermore, in situ immunofluorescence analysis and single-cell RNA sequencing data revealed that entry of SARS-CoV-2 in bone marrow macrophages (BMMs) is dependent on the expression of neuropilin-1 (NRP-1). The expression of NRP-1 on BMMs makes these cells target for SARS-CoV-2 [25]. However, the expression of NRP-1 is observed to be reduced upon differentiation of BMMs into mature OCs, thus indicating the reduced tendency of SARS-CoV-2 to infect mature OCs. A recent study described a novel method by which SARS-CoV-2 reduces the osteogenic potential of OBs by increasing the expression of microRNA-4485 via targeting TLR4 (found to perturb the fracture healing) in COVID-19 disease patients [26] (Fig. 3). Together these studies are indicative of the strong disruption of bone health in post-COVID-19 patients. Along with directly targeting the bone cells, SARS-CoV-2 can also influence bone health in multiple ways such as by either augmenting inflammatory conditions or even by causing the dysbiosis of GM. Thus, in further sections, we enlist these factors in detail.

Cytokine storm

In response to SARS-CoV-2, immediate activation of innate immune cells, viz. macrophages, neutrophils, etc. occurs that further limits the infection by causing the downstream activation of the long-lasting adaptive immune system to produce neutralizing antibodies and T cell response against the virus. Nevertheless, when inflammation does not resolve after serving its purpose then it can cause dysregulated hyperinflammation, i.e., “cytokine storm” and results in inhibition of the adaptive immune system thereby further escalating tissue damage and organ failure. Cytokine storm is manifested by unrestrained production of several inflammatory cytokines such as IL-6, IL-7, IL-2, IL-17, TNF-α, monocyte chemoattractant protein (MCP)-1, and macrophage inhibitory protein (MIP)-1α (Fig. 3) (Table 1). These cytokines are considerably higher in intensive care unit (ICU) patients infected with SARS-CoV-2 in comparison to non-ICU patients having the same viral load [27, 28]. Thus, these studies suggest that viral load is not the pertinent factor in determining the severity in COVID-19 patients. But the elevated levels of inflammatory cytokines by promoting hyperinflammation, acute respiratory distress syndrome (ARDS), and multiorgan failure define the severity of COVID-19 disease. In addition to inducing inflammatory conditions, disease severity is also marked by the reduced expression of anti-viral cytokine IFNγ by CD4+ T cells [29]. Both IL-6 and TNF-α cytokines via inducing apoptosis in T and B lymphocytes causes lymphopenia and increased IL-2 levels thereby causing activation induced cell death [28]. In addition, the expression of ACE2 on lymphocytes also aids the apoptosis of lymphocytes. In support of this, a study demonstrated (golden Syrian hamster model) that cytokine storm causes the loss of bone in the trabecular region of long bones and lumbar-vertebrae of SARS-CoV-2-infected model [30]. It has been observed that bone loss aggravates from the acute phase to the post-recovery phase. A mechanistic view of the enhanced bone loss deciphered the ability of inflammatory cytokines such as IL-1β, IL-6, and TNF-α in inducing pathological bone loss in the hamster model [30]. Since the immune system is strongly associated with the management of healthy bone and any dysregulation in the levels of inflammatory cytokines leads to unfavorable effects on bone health. To further emphasize the importance of the immune system in inflammatory bone loss conditions such as osteoporosis, Srivastava et al. have recently coined the term “Immunoporosis”, i.e., immunology of osteoporosis [31]. A recent study proved that higher levels of inflammatory cytokines such as IL-1β, IL-6, IL-17, and TNF-α in postmenopausal osteoporotic women enhance bone deterioration (low BMD) in comparison to the control group [32]. These inflammatory cytokines by causing an imbalance in the metabolism of the skeletal system favor bone resorption by promoting the expression RANKL on OBs. Altogether, these studies suggest that therapeutic strategies proven to be effective for treating inflammatory conditions in COVID-19 disease may also enhance the risk of developing secondary osteoporosis and destruction of joints in recovered patients.

Table 1 Cytokine storm and its effect on bone healthSteroidal therapies and bone health

Corticosteroid drugs are synthetic steroid hormones that are produced by the adrenal cortex, and it is employed to treat a wide range of inflammatory diseases. Corticosteroids include both glucocorticoids and mineralocorticoids. Primarily glucocorticoids such as dexamethasone are considered a double edge sword for treating critical COVID-19 patients (Table 2). Dexamethasone mimics the nature of natural compounds that the body produces to quell the inflammation and is used to treat various inflammatory disease conditions including chronic obstructive lung diseases (COLD), asthma, allergies, and skin conditions. Dexamethasone is being given in dosage ranging from 0.5 to 10 mg daily which in turn depends on the nature and severity of the disease. In the recovery clinical trial, it was observed that the use of dexamethasone also resulted in lowered mortality rate in COVID-19-infected patients who were receiving oxygen support or mechanical ventilation (The recovery collaborative group; https://www.nejm.org/doi/full/10.1056/nejmoa2021436). However, extended administration of glucocorticoids was found to be detrimental. Strikingly, epidemiological data suggest that glucocorticoid therapy enhanced the risk of fracture occurrence and was found to be the reason for iatrogenic osteoporosis commonly known as glucocorticoid-induced osteoporosis (GIOP) [33]. Glucocorticoids by altering the bone metabolism shift the balance of bone remodeling towards OCs thus enhancing bone loss. Recently, a cross-sectional study reported a confirmed case of osteonecrosis in a cohort of Wuhan COVID-19 patients treated with glucocorticoids [34, 35]. Moreover, dexamethasone via inhibiting the osteogenesis of stem cells reduced the ability of cells to repair the bone and thus lead to the onset of osteonecrosis. According to a longitudinal research, 58 percent of SARS-CoV-infected patients who received corticosteroid treatment went on to develop avascular osteonecrosis [36]. Debating the use of corticosteroids, led to disagreements about whether the short-term advantages may outweigh the severe side effects that are seen over the long term. The leading theory behind the observed consequences is that corticosteroid treatment leads to the accumulation of fat droplets in blood and swelling of fat cells inside BM that may further lead to clogging of small blood vessels thereby starving bone cells for oxygen and nutrients. Moreover, a study demonstrated that the treatment of rabbits with methylprednisolone activates the RAS system in bone and induces osteonecrosis by enhancing the expression of ACE receptors on OCs [36]. These advancements in research are  thus indicating a considerable increase in skeletal disorders in COVID-19-recovered patients, highlighting the need for a long-term follow-up studies.

Table 2 Corticosteroidal therapies given to COVID-19-infected patients and their impact on bone healthGender and hormonal influences

Across geographics, different findings reported the association between gender and the risk of developing worse outcomes due to COVID-19. Though the prevalence of COVID-19 infection is the same in both males and females, clinical data indicate a higher number of fatalities in males in comparison to females in most countries [37]. However, in some countries such as India, Nepal, Vietnam, and Slovenia, fatality rate due to COVID-19 is higher in women in comparison to men [38]. Further to investigate whether the observed disparities are linked with the alterations in the hormonal levels. It has been observed that sex steroids regulate the expression of ACE2, thus controlling the entry of SARS-CoV-2 inside the host cells. A cohort study demonstrated that testosterone concentration is inversely related to the concentrations of inflammatory cytokines such as IL-6, interferon-gamma inducible protein 10 (IP10), interleukin 1 receptor antagonist, and C-reactive protein (CRP) in COVID-19-infected males [39]. Moreover, gene enrichment analysis showed upregulation in hormone signaling pathways in both classical (CD14+CD16−) and non-classical (CD14−CD16+) monocytes, indicating that low testosterone levels activate the inflammatory signaling cascade and are associated with the disease severity [39]. This study clearly indicates that lower levels of testosterone hormone predispose men towards COVID-19 infection. Recently, a study reported that hospitalized women are less likely to die due to COVID-19 infection, but once severe symptoms develop the risk of mortality is similar in both females and males [40]. These shreds of evidence suggest that gonadal hormones in females mainly estrogen (E2) and progesterone (P4) give a likely explanation for the sexual dimorphism in the COVID-19 infection and disease severity. It has been observed that E2 and P4 favor the anti-inflammatory state in females via reducing the innate immunity along with enhancing the immune tolerance and antibody production in females. A study reported in mice showed that estradiol treatment reduces the expression of ACE2 in kidney and airway epithelial cells via activating the estrogen receptor alpha (ERα) thus inhibiting viral entry, whereas ovariectomy (estrogen-deficient condition) in mice enhances the expression of ACE2 in distinct tissues and thus may enhance virus entry [41] in elderly women. However, the protective effect of estrogen is diminished in postmenopausal women resulting in a higher incidence of COVID-19 in menopausal subjects (estrogen-deficient condition) [42]. Together, these studies represent the effects of sex hormones estrogen and testosterone in regulating the expression of receptors involved in SARS-CoV-2 virus entry, modulating the immune system, etc.

Vitamin D status

An active form of vitamin D (1,25-dihydroxy vitamin D) is responsible for the regulation of calcium and phosphate metabolism. Several studies reported that lower levels of vitamin D enhance the development of multiple immune-related diseases such as rheumatoid arthritis (RA), multiple sclerosis (MS), type 1 diabetes (T1D), and COVID-19. It has been observed that older patients with vitamin D deficiency (< 30 nmol/L) showed higher D-dimer levels and were found to be associated with worse outcomes of COVID-19 infection [43]. Consistent with this, a study recently demonstrated that COVID-19-positive patients with vitamin D levels > 30 ng/ml showed lower levels of D-dimer, CRP, and shorter hospital stays in contrast to COVID-19 patients with severe vitamin D deficiency (< 10 ng/ml) [44]. Thus, these studies suggest that vitamin D levels may be employed as a prognosis indicator. A clinical trial (NCT04344041): COVIT-TRIAL is a randomized clinical trial where a high-risk elderly population was supplemented with vitamin D and the outcome of the trial described that a high dose of vitamin D is found to be an effective and immediately approachable treatment for COVID-19 [45]. Furthermore, a vitamin D deficiency’s secondary effect is a disturbance in the process of bone mineralization, which results in bone loss, muscle weakness, and the onset of osteoporosis, which may eventually progress to osteomalacia [46]. Notably, the majority of patients admitted to ICU and dying concomitantly suffered from hypovitaminosis D. In agreement with this, a study showed that decreased serum vitamin D levels were linked to an increase in mortality in critically ill patients infected with SARS-CoV-2 [47]. Vitamin D is also a key modulator of the renin–angiotensin system which is exploited by the SARS-CoV-2 to enter the host cells [48]. In addition, vitamin D controls the immune system via dampening the pro-inflammatory immune response along with enhancing the anti-inflammatory immune response, anti-microbial peptides (AMPs), along with activating the macrophages thereby exhibiting the potential to destroy the SARS-CoV-2. According to a study, a feedback loop between vitamin D deficiency and the COVID-19-linked coagulopathy enhances platelet activation, which heightens thrombosis [49]. Notably, vitamin D insufficiency and low platelet count have been connected to illnesses that cause pathological bone loss, such as osteoporosis, and have also been proven to play a critical role in the metabolism of minerals and the preservation of bone health. Thus, to prevent the pathological bone loss caused by the SARS-CoV-2 infection, it is crucial to monitor both platelet count and vitamin D levels.

COVID-19, gut microbiome, and bone health

Enormous variations among the COVID-19-infected patients are largely unknown and are described as “Immunological Dark Matter (IDM)”. Emerging evidence demonstrated that GM is likely to be a pertinent contributing factor to IDM. Though COVID-19 is a respiratory disease, several emerging pieces of evidence suggest that GM is also involved in the severity of the disease. GM harbors hundreds of bacterial genera that reside either in the luminal stream or adhere to the gut mucosa. It has been observed that SARS-CoV-2 infection alters the bacteriome and virome which could reflect the contribution of altered GM in the disease severity and recovery [50]. Since the major method of SARS-CoV-2 infection may involve respiratory droplets and fomite but the fecal–oral pathway may also be used to disseminate SARS-CoV-2 [51]. SARS-CoV-2 has likewise selected the GUT as its target because this organ also expresses ACE2 and TMPRSS2. In addition, SARS-CoV-2 viral RNA was also detected in the patient’s feces samples [51]. In consistent, the endoscopic evaluation revealed that individuals also suffered from colon injury when infected with SARS-CoV-2. Moreover, the fundamental etiology of post-acute COVID-19 syndrome (PACS) has been determined to be dysbiosis of the Gut microbiota. A 6-month follow-up study in COVID-19-recovered patients revealed the significant difference in the GM among the patients developing PACS and without PACS [52]. Moreover, patients with PACS showed reduced bacterial diversity and richness in comparison to healthy individuals. Together, these results point forth how GM dysbiosis contributes to the development of PACS and to the aggravation of COVID-19 illness.

A study demonstrated that Bacteroides spp. is observed to be inversely interrelated with the SARS-CoV-2 fecal load in hospitalized patients [53]. Bacteroides spp. has also been linked with the altered expression and functionality of the ACE2 receptor in the gut. Remarkably, Bacteroides were observed to modulate the lung heparan sulfate which is a glycosaminoglycan. In addition, the endoscopic evaluation revealed that the individuals had colon injury that in turn alters the adhesion of virion to the host cells [54]. In addition, a recent study showed a direct correlation with increased levels of inflammatory cytokines and markers such as CRP, aspartate aminotransferase (AAT), lactate dehydrogenase (LDH), and gamma-glutamyl transferase [53]. These studies highlight the involvement of GM in enhanced inflammation and disease severity in COVID-19 disease patients. Thus, strategies that can alter the GM should be employed to manage the long-term effects of COVID-19 in infected patients. This evidence supports the fact that altered GM and the associated leaky gut may also contribute to the multiorgan complications observed in long run. Growing evidence suggests that dysbiosis of the GM was also found to be the pivotal factor in augmenting bone loss which in turn promotes the development of several bone-related diseases such as RA and osteoporosis. A series of reports revealed that GM influences bone strength by altering the quality of bone tissue. The mechanism through which GM modulates bone health is via promoting the generation of regulatory metabolites such as indole derivatives, trimethylamine N-oxide (TMAO: amine oxide), short-chain fatty acids (SCFAs), and gasotransmitter such as hydrogen sulfide (H2S). It was observed that H2S-donating compound GYY4137 enhances bone health by activating the Wnt10b production thereby increasing bone formation with reducing the trabecular bone loss in the ovariectomy (ovx) induced postmenopausal osteoporotic mice model [55]. SCFAs such as acetate (C2), propionate (C3), and butyrate (C4) induce metabolic reprogramming in bone-resorbing cells viz. OCs resulting in enhanced glycolysis, thereby reducing the osteoclast’s specific genes such as NFATc1 and TRAF6, potent regulators of skeletal homeostasis [56].

The main producers of butyrate in the human gut are bacteria belonging to the phylum Firmicutes, mainly Faecalibacterium prausnitzii [57]. A study demonstrated that treatment with fermented products of Lactobacillus plantarum and Lactobacillus fermentum significantly improved the bone mass in the ovx mice model by enhancing the abundance of genus Faecalibacterium prausnitzii and Lactobacillus [58]. Notably, shotgun metagenome sequencing data of fecal samples collected from the 15 SARS-CoV-2-infected patients showed baseline abundance of Clostridium hathewayi, Clostridium ramosum, and Coprobacillus, and reduced levels of Faecalibacterium prausnitzii was observed to be associated with disease severity. These reports thereby strongly suggest that modulation of GM could also be employed to reduce the disease severity [