Modelling of the human middle ear via the Port Hamiltonian approach

Author(s):  
Milka C. I. Madahana ◽  
Mohlalakoma Ngwako ◽  
Otis O. T. Nyandoro ◽  
John E. D. Ekoru
1998 ◽  
Vol 23 (3) ◽  
pp. 265-265 ◽  
Author(s):  
Hutton ◽  
Birchall ◽  
French ◽  
Kubba ◽  
Severn ◽  
...  

Author(s):  
Arwa Kurabi ◽  
Kwang Pak ◽  
Adam S. DeConde ◽  
Allen F. Ryan ◽  
Carol H. Yan

AbstractViral infections have already been implicated with otitis media and sudden sensorineural hearing loss. However, the pathophysiology of COVID-19 as it relates to otologic disorders is not well-defined. With the spread of SARS-CoV-2, it is important to evaluate its colonization of middle ear mucosa. Middle ear and nasal tissue samples for quantitative RT-PCR and histologic evaluations were obtained from post-mortem COVID-19 patients and non-diseased control patients. Here we present evidence that SARS-CoV-2 colonizes the middle ear epithelium and co-localizes with the primary viral receptor, angiotensin-converting enzyme 2 (ACE2). Both middle ear and nasal epithelial cells show relatively high expression of ACE2, required for SARS-CoV-2 entry. The epithelial cell adhesion molecule (EpCAM) was use as a biomarker of epithelia. Furthermore, we found that the viral load in the middle ear is lower than that present in the nasal cavity.


2013 ◽  
Vol 81 (3) ◽  
pp. 645-652 ◽  
Author(s):  
Kirsty R. Short ◽  
Patrick C. Reading ◽  
Lorena E. Brown ◽  
John Pedersen ◽  
Brad Gilbertson ◽  
...  

ABSTRACTInfluenza A virus (IAV) predisposes individuals to secondary infections with the bacteriumStreptococcus pneumoniae(the pneumococcus). Infections may manifest as pneumonia, sepsis, meningitis, or otitis media (OM). It remains controversial as to whether secondary pneumococcal disease is due to the induction of an aberrant immune response or IAV-induced immunosuppression. Moreover, as the majority of studies have been performed in the context of pneumococcal pneumonia, it remains unclear how far these findings can be extrapolated to other pneumococcal disease phenotypes such as OM. Here, we used an infant mouse model, human middle ear epithelial cells, and a series of reverse-engineered influenza viruses to investigate how IAV promotes bacterial OM. Our data suggest that the influenza virus HA facilitates disease by inducing a proinflammatory response in the middle ear cavity in a replication-dependent manner. Importantly, our findings suggest that it is the inflammatory response to IAV infection that mediates pneumococcal replication. This study thus provides the first evidence that inflammation drives pneumococcal replication in the middle ear cavity, which may have important implications for the treatment of pneumococcal OM.


1995 ◽  
Vol 105 (2) ◽  
pp. 188-191 ◽  
Author(s):  
Masayuki Furukawa ◽  
Nobuo Kubo ◽  
Toshio Yamashita

2008 ◽  
Vol 128 (12) ◽  
pp. 1303-1307 ◽  
Author(s):  
Jae-Jun Song ◽  
Jae Gu Cho ◽  
Soon-Jae Hwang ◽  
Chang Gun Cho ◽  
Seok-Won Park ◽  
...  

1981 ◽  
Vol 69 (S1) ◽  
pp. S43-S43 ◽  
Author(s):  
E. A. G. Shaw ◽  
M. R. Stinson

2003 ◽  
Vol 123 (3) ◽  
pp. 362-366 ◽  
Author(s):  
Jae Young Choi ◽  
Kyou-nam Cho ◽  
Joo-heon Yoon

2003 ◽  
Vol 113 (8) ◽  
pp. 1347-1351 ◽  
Author(s):  
Patrick J. Antonelli ◽  
Gregory S. Schultz ◽  
Karen M. Kim ◽  
John S. Cantwell ◽  
David J. Sundin ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-1 ◽  
Author(s):  
Shin Hye Kim ◽  
Sun Hwa Shin ◽  
Yoon Young Go ◽  
Sung-Won Chae ◽  
Jae-Jun Song

Sign in / Sign up

Export Citation Format

Share Document