Muhammad Shahid

Dr. Muhammad Shahid

Molecular Virology, National Centre of Excellence in Molecular Biology, University of the Punjab

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 December 2022 in Egyptian Liver Journal
Verified
Journal Article
Open access
PDF file
FBFatima Butt
Fatima Butt
MSMuhammad Shahid
Muhammad Shahid
MHMuhammad Hassan
Muhammad Hassan
FTFarah Tawakkal
Farah Tawakkal
IAIram Amin
Iram Amin
MIMuhammad Idrees
Muhammad Idrees
Background: Hepatitis C virus, a member of Flaviviridae is a single-stranded positive-sense RNA virus infecting 62–79 million people around the globe. This blood-borne virus is one of the leading causes of liver diseases worldwide. This review aims to identify novel potential genes linked to cellular host factors, as well as revise the roles of each gene in hepatitis C Virus infection. This review also aims to provide a comprehensive insight into therapeutic advancements against HCV. Methods: For this review article, 190 articles were searched via PubMed Central, Bio-One, National Academy of Science, Google Scholar, and Worldwide Science. 0ut of these 190 studies, 55 articles were selected for this review. The inclusion of articles was done on the criteria of high citation and Q1 ranking. Results: The information gathered from previously published articles highlighted a critical link between host-cellular factors that are important for HCV infection. Conclusion: Although many advancements in HCV treatment have been made like DAAs and HTAs, the development of a completely effective HCV therapy is still a challenge. Further research on combinations of DAAs and HTAs can help in developing a better therapeutic alternative. Keywords: Hepatitis C virus, Replication cycle, Non-structural proteins, Host-cellular factors, Treatment strategies


1 March 2019 in European Journal of Gastroenterology & Hepatology
Verified
Journal Article
Closed access
MSMuhammad Shahid
Muhammad Shahid
MIMuhammad Idrees
Muhammad Idrees
ABAzeem M. Butt
Azeem M. Butt
SRSyed M. Raza
Syed M. Raza
IAIram Amin
Iram Amin
RNRabia Nawaz
Rabia Nawaz
Hepatitis G virus (HGV) infection appears to be common in patients with chronic hepatitis C virus (HCV) infection. The aim of this study was to investigate the prevalence of HCV/HGV in patients with chronic hepatitis C (CHC) in Pakistan and to look for possible associations with various clinical and histopathological changes in HCV/HGV coinfection and HCV infection. The present study included 136 patients. Clinical, biochemical, virological and histological findings were compared between patients coinfected with HCV/HGV and patients with HCV alone. Of the 136 patients with CHC, 16 (11.76%) were coinfected with HCV/HGV. The mean age of coinfected patients was lower than in patients with HCV alone. HCV/HGV coinfected patients did not show significant differences in sex, clinical presentation, biochemical markers, and liver fibrosis as compared to those with HCV infection. Only the mean values of platelets count, mean corpuscular hemoglobin (MCH), and MCH concentration markers were significantly different in HCV/HGV coinfected patients as compare to patients with HCV alone. It was found that 11.76% of patients with CHC in Pakistan were associated with HCV/HGV coinfection. No significant differences were observed in clinical and histological features except for platelets count, MCH, and MCH concentration markers between HCV and HGV coinfected patients in comparison with HCV-infected patients.

30 April 2022 in Osong Public Health and Research Perspectives
Verified
Journal Article
Open access
IMIqra Mir
Iqra Mir
SASania Aamir
Sania Aamir
SSSyed Rizwan Hussain Shah
Syed Rizwan Hussain Shah
MSMuhammad Shahid
Muhammad Shahid
IAIram Amin
Iram Amin
MIMuhammad Idrees
Muhammad Idrees
The coronavirus disease 2019 (COVID-19) pandemic rapidly spread globally. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes COVID-19, is a positive-sense single-stranded RNA virus with a reported fatality rate ranging from 1% to 7%, and people with immune-compromised conditions, children, and older adults are particularly vulnerable. Respiratory failure and cytokine storm-induced multiple organ failure are the major causes of death. This article highlights the innate and adaptive immune mechanisms of host cells activated in response to SARS-CoV-2 infection and possible therapeutic approaches against COVID-19. Some potential drugs proven to be effective for other viral diseases are under clinical trials now for use against COVID-19. Examples include inhibitors of RNA-dependent RNA polymerase (remdesivir, favipiravir, ribavirin), viral protein synthesis (ivermectin, lopinavir/ritonavir), and fusion of the viral membrane with host cells (chloroquine, hydroxychloroquine, nitazoxanide, and umifenovir). This article also presents the intellectual groundwork for the ongoing development of vaccines in preclinical and clinical trials, explaining potential candidates (live attenuated-whole virus vaccines, inactivated vaccines, subunit vaccines, DNA-based vaccines, protein-based vaccines, nanoparticle-based vaccines, virus-like particles and mRNA-based vaccines). Designing and developing an effective vaccine (both prophylactic and therapeutic) would be a long-term solution and the most effective way to eliminate the COVID-19 pandemic.

10 November 2022 in Journal of Basic Microbiology
Verified
Journal Article
Closed access
RMRakhtasha Munir
Rakhtasha Munir
SRShazia Rafique
Shazia Rafique
AAAmjad Ali
Amjad Ali
IAIram Amin
Iram Amin
SASameen Ahmed
Sameen Ahmed
Muhammad Usman KhanMuhammad Usman Khan
Muhammad Usman Khan

25 February 2023 in Pakistan Journal of Zoology
Verified
Journal Article
Open access
MSMuhammad Shahid
Muhammad Shahid
MIMuhammad Idrees
Muhammad Idrees
ARAfza Rasul
Afza Rasul
IAIram Amin
Iram Amin
SASamia Afzal
Samia Afzal
Identification of Predictive Factors in Chronic Hepatitis C Patients with Non-Infected Individuals: A Comparative Analysis