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Infections of the skin or other soft tissues with the hard-to-treat MRSA (methicillin-resistant Staphylococcus aureus) bacteria appear to permanently compromise the lymphatic system, which is crucial to immune system function. Massachusetts General Hospital (MGH) investigators describe finding that MRSA infection impairs the ability of lymphatic vessels to pump lymphatic fluid to lymph nodes in mouse models, which may contribute to the frequent recurrences of MRSA infection experienced by patients.
MRSA produces toxins that kill the muscle cells critical to the pumping of lymph, MRSA with a genetic deficiency that lowers the amount of toxin produced does not kill lymphatic muscle cells, which both supports the role for bacterial toxins in the post-MRSA impairment of lymphatic function and may also suggest a possible treatment strategy. Patients with lymphedema – swelling and fluid buildup caused by damage to or blockage of the lymphatic system – are particularly prone to recurrent infections, which can exacerbate existing lymphedema.
In contrast to the cardiovascular system, in which blood is propelled through arteries and veins by the pumping of the heart, in the lymphatic system, lymphatic fluid – which carries immune cells and other important factors – is pumped along by the contraction of the lymphatic vessels , driven by lymphatic muscle cells. Experiments in mouse models of MRSA tissue infections – conducted by team members including lead author Dennis Jones, PhD – revealed that the infection itself cleared within 30 days and associated inflammation was gone within 60 days.
The lymphatic vessels in MRSA-infected tissues showed abnormalities – including increased vessel diameter and weaker, less frequent contractions – that were still present 120 days after the induction of infection. Close examination revealed that the number of lymphatic muscle cells surrounding lymphatic vessels was depleted as late as 260 days after infection. Lymph pumping was restored after the resolution of sterile inflammation, MRSA-induced impairment persisted long after the infection was resolved and the inflammation had stopped. This persistence long after bacteria have been cleared can be explained by the loss of lymphatic muscle cells.
Exposure of cultured mouse and human lymphatic or smooth muscle cells to the proteins produced by MRSA led to the death of these cells, and detailed analysis of MRSA-produced proteins identified a significant number of known pathogenic toxins. Since expression of many MRSA toxins is controlled by a genetic element called the accessory gene regulator (agr), the team tested a mutant form of MRSA lacking the agr against several types of cultured cells and in their animal model.
The agr-mutant MRSA did not produce the muscle-cell-killing proteins, and lymphatic function – including the strength and frequency of vessel contraction – was significantly better in mice infected with the mutant strain than in animals infected with a non-mutated strain. Targeting the action of the agr during and after MRSA infection may preserve lymphatic muscle cells and, as a result, lymphatic function.
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