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The Rapidly Changing Patterns in Bacterial Co-infections Reveal Peaks in Limited Gram-Negatives during COVID and Their Sharp Drop Post- Vaccinations Implying Potential Evolution of Co-protection during Vaccine-Virus-Bacterial Interplay
Said, K.B.; Alsolami, A.; Alshammari, K.F.; Moussa, S.; Alshammeri, F.; Alghozwi, M.H.; Alshammari, S.F.; Alharbi, N.F.; Khalifa, A.M.; Mahmoud, M.R.; Alshammari, K.; Ghoniem, M.E. The Rapidly Changing Patterns in Bacterial Co-Infections Reveal Peaks in Limited Gram Negatives during COVID-19 and Their Sharp Drop Post-Vaccination, Implying Potential Evolution of Co-Protection during Vaccine–Virus–Bacterial Interplay. Viruses2024, 16, 227.
Said, K.B.; Alsolami, A.; Alshammari, K.F.; Moussa, S.; Alshammeri, F.; Alghozwi, M.H.; Alshammari, S.F.; Alharbi, N.F.; Khalifa, A.M.; Mahmoud, M.R.; Alshammari, K.; Ghoniem, M.E. The Rapidly Changing Patterns in Bacterial Co-Infections Reveal Peaks in Limited Gram Negatives during COVID-19 and Their Sharp Drop Post-Vaccination, Implying Potential Evolution of Co-Protection during Vaccine–Virus–Bacterial Interplay. Viruses 2024, 16, 227.
Said, K.B.; Alsolami, A.; Alshammari, K.F.; Moussa, S.; Alshammeri, F.; Alghozwi, M.H.; Alshammari, S.F.; Alharbi, N.F.; Khalifa, A.M.; Mahmoud, M.R.; Alshammari, K.; Ghoniem, M.E. The Rapidly Changing Patterns in Bacterial Co-Infections Reveal Peaks in Limited Gram Negatives during COVID-19 and Their Sharp Drop Post-Vaccination, Implying Potential Evolution of Co-Protection during Vaccine–Virus–Bacterial Interplay. Viruses2024, 16, 227.
Said, K.B.; Alsolami, A.; Alshammari, K.F.; Moussa, S.; Alshammeri, F.; Alghozwi, M.H.; Alshammari, S.F.; Alharbi, N.F.; Khalifa, A.M.; Mahmoud, M.R.; Alshammari, K.; Ghoniem, M.E. The Rapidly Changing Patterns in Bacterial Co-Infections Reveal Peaks in Limited Gram Negatives during COVID-19 and Their Sharp Drop Post-Vaccination, Implying Potential Evolution of Co-Protection during Vaccine–Virus–Bacterial Interplay. Viruses 2024, 16, 227.
Abstract
The SARS-CoV-2 have caused a devastating pandemic of all times in the recent human history. However, there is a serious paucity in high quality data on aggravating factors and mechanisms of co-infection. This study aimed to identify the trending patterns of bacterial co-infections and types and associated outcomes in three phases of the pandemic. Using quality hospital data, we have investigated the SARS-CoV-2 fatality rates, profiles, and types of bacterial co-infections before, during, and after COVID-19 vaccinations. Out of 389 isolates used in different aspects, 298 was examined before and during the pandemic (n=149 before, n=149 during), death rates were 32% during compared to only 7.4% before pandemic with significant association (P value = 0.000000075). Death rate was 34% in co-infected (n = 170) compared to non-co-infected patients (n = 128) indicating a highly significant value (P value = 0.00000000000088). However, analysis of patients without other respiratory problems (n=28) indicated that among the remaining 270 patients, death was 30% in co-infected patients (n=150) and only 0.8% in non-coinfected (n=120) with high significant P value= 0.00000000076. The trending patterns of co-infections before, during, and after vaccinations showed a significant decline in Staphylococcus aureus with concomitant peaks in Gram-negatives in totals of (n= 149 before/n= 149 during): Klebsiella pneumonia (n = 11/49 before/during; E. coli n=10/24, A. baumannii n=8/25, and Ps. Aeruginosa n= 5/16, and S. aureus 13/1. Nevertheless, in post vaccination phase, (n= 91) gender-specific co-infections were examined for potential differences in susceptibility. Methicillin resistant S. aureus (MRSA) dominated both genders followed by E. coli in males and females with the latter gender showing higher rates of isolations in both species. Klebsiella pneumoniae declined to third place mostly in male patients. The drastic decline in K. pneumoniae and Gram-negatives post-vaccination strongly imply a potential co-protection in vaccines. Future analysis would gain more insights into molecular mimicry.
Public Health and Healthcare, Public Health and Health Services
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